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Journal of Medicine and Pharmacy","Tạp chí Y Dược học Cần Thơ",{"EN":487,"VI":488},"\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">04\u002F10\u002F2015 Ministry of Information and Communications allowed Can Tho journal of medicine and pharmacy to operate (102 \u002FGP-BTTTT)\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">07\u002F16\u002F2015 Can Tho journal of medicine and pharmacy is internationally recognized: ISSN 2354-1210\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">In 2016, The journal has been included in the list of medical science journals by The State Council for professorship which is awarded a work score of 0-0.5 points for a published article.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Can Tho Journal of Medicine and Pharmacy welcome original works that haven’t been submitted or published in other medical journals. Posts must contain content related to one of the journal’s categories.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The content published\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The journal is divided into 3 categories:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Scientific research article: are valuable scientific works, which have been researched and accepted.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Overview of medicine, biology and pharmacy: serving the objective of continuing training in the fields of medicine, biology and pharmacy; to systematize classical and modern knowledge.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Update information on new knowledge about medicine, biology, pharmacy in the country and in the world.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Scope\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Publication and introduction of scientific research in the fields:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Medicine (internal medicine, surgery, pediatrics, obstetrics and gynecology, odonto-stomatology, laboratory, oncology, traditional medicine, nursing).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Biology (genetics, biotechnology).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">+ Pharmacology (pharmaceutics, drug quality analysis-control, synthetic pharmaceutical chemistry, biochemistry, pharmacognosy, botany, clinical pharmacy).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- To enhance the quality of undergraduate, postgraduate education, scientifically researching and meet the necessary treatment in hospital.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Introducing the updated domestic and oversea information about science technology to promote scientific research and exchanging technology in local, other universities.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">- Exchanging pharmaceutical and medical information for social health developing in the Mekong Delta and Vietnam.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">The object\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Postgraduate students, student of Can Tho University of Medicine and Pharmacy, scientists from schools, research institutes, hospitals, health centers, pharmaceutical companies of the Mekong Delta; other provinces and regions in Vietnam and other country.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Address\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Headquarters of Can Tho Journal of Medicine and Pharmacy, located Scientific Research and International Cooperation Office: 179 Nguyen Van Cu Street, An Khanh Ward, Ninh Kieu District, Can Tho City, Vietnam.\u003C\u002Fspan>\u003C\u002Fp>","\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Ngày 16\u002F7\u002F2015, Tạp chí Y Dược học Cần Thơ được cấp chỉ số quốc tế: ISSN 2354-1210.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 4\u002F2016, Tạp chí đã được Hội đồng Giáo sư ngành Y đưa vào danh sách các tạp chí khoa học Y học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Năm 2020 Tạp chí Y Dược học Cần Thơ đã được phê duyệt vào danh mục của các Hội đồng Giáo sư ngành Dược học được tính điểm công trình 0-0,5 điểm cho một bài báo đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ ra 12 số\u002Fnăm, 180-200 trang\u002Fsố.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Từ tháng 12\u002F2022 Tạp chí Y Dược học Cần Thơ là thành viên của hệ thống Crossref và từ tháng 01\u002F2023 tạp chí thực hiện bình duyệt online kín 2 chiều nhằm tăng tính minh bạch, tin cậy của các công trình nghiên cứu khoa học và đảm bảo tốt nhất chất lượng khoa học của bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ, mục đích và phạm vi của tạp chí\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tôn chỉ và mục đích hoạt động của tạp chí: xuất bản nhằm mục đích phổ biến kết quả từ các đề tài nghiên cứu khoa học; giao lưu trao đổi khoa học, chia sẻ kinh nghiệm, học tập, đồng thời cập nhật thông tin khoa học mới trong các lĩnh vực y, sinh, dược học trong và ngoài nước.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phạm vi của tạp chí: Tạp chí xuất bản được chia thành 3 chuyên mục: (i) Bài báo nghiên cứu khoa học là kết quả công trình nghiên cứu khoa học có giá trị đã được triển khai nghiên cứu, (ii) Bài tổng quan y, sinh, dược học: phục vụ mục tiêu đào tạo liên tục trong lĩnh vực y, sinh, dược học; nhằm hệ thống hóa những kiến thức kinh điển và hiện đại; (iii) Thông tin cập nhật kiến thức mới về y, sinh, dược học trong nước và trên thế giới.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Chính sách truy cập mở\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ áp dụng chính sách truy cập mở đối với các bài báo đã xuất bản đến với độc giả, nhằm mở rộng cơ hội tiếp cận các kết quả nghiên cứu chất lượng cao và tăng cường trao đổi kiến thức. Tạp chí đăng tải trực tuyến (miễn phí) toàn văn các bài báo được công bố trên website của Tạp chí (https:\u002F\u002Ftapchi.ctump.edu.vn).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đạo đức xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ cam kết tuân thủ đạo đức xuất bản phù hợp với các hướng dẫn và tiêu chuẩn của the Committee on Publication Ethics (COPE), tuân thủ các nguyên tắc của COPE’s Core Practices, Best Practices Guidelines for Journal Editors và Guidelines on Good Publication Practices.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Bản thảo bài báo chỉ được chấp nhận khi được tác giả chịu trách nhiệm chính cam kết các nội dung sau: Các nội dung của bản thảo chưa được đăng tải toàn bộ hoặc một phần ở các tạp chí khác; Tất cả các tác giả đều có đóng góp một cách đáng kể vào quá trình nghiên cứu hoặc chuẩn bị bản thảo và cùng chịu trách nhiệm về các nội dung của bản thảo; Tuân thủ các biện pháp đảm bảo đạo đức nghiên cứu (ví dụ thỏa thuận đồng ý tham gia nghiên cứu).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Cam kết bảo mật\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí cam kết thực hiện và tuân thủ các quy định của luật và các văn bản hướng dẫn liên quan đến bảo mật thông tin cá nhân trên không gian mạng. Các thông tin mà người dùng (tác giả, độc giả, biên tập viên, người phản biện) nhập vào các biểu mẫu trên Hệ thống Quản lý xuất bản trực tuyến của tạp chí chỉ được sử dụng vào các mục đích đã được tuyên bố rõ ràng và sẽ không được cung cấp cho bất kỳ bên thứ ba nào khác, hay dùng vào bất kỳ mục đích nào khác.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Phí gửi bài\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng bài: 1.000.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Lệ phí gửi đăng nhanh: 1.500.000đ\u002Fbài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với tác giả là cán bộ viên chức thuộc Trường Đại học Y Dược Cần Thơ thì được hỗ trợ 50% lệ phí gửi đăng bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Đối với sinh viên thực hiện đề tài nghiên cứu khoa học cấp trường được hỗ trợ 100% lệ phí đăng bài ( Tác giả gửi đính kèm “ Quyết định về việc giao tổ chức thực hiện đề tài nghiên cứu khoa học cấp Trường của sinh viên”).\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Hình thức nộp lệ phí:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Tiền mặt:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Nộp trực tiếp tại Phòng Tài chính - Kế toán, Trường Đại học Y Dược Cần Thơ, số 179 Nguyễn Văn Cừ, P. An Khánh, Q. Ninh Kiều, thành phố Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Chuyển khoản:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tên Tài khoản: Trường ĐHYD Cần Thơ, Số TK: 0111000115668, tại ngân hàng Vietcombank chi nhánh Cần Thơ.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Thời gian: Áp dụng từ ngày 01\u002F02\u002F2023.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">* Phí gửi bài không được hoàn trả khi bài viết bị từ chối hoặc tác giả xin rút bài viết.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Quy trình phản biện bài báo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tạp chí Y Dược học Cần Thơ thực hiện quy trình phản biện kín hai chiều nghiêm ngặt. Danh tính của những người phản biện không được tiết lộ cho các tác giả và ngược lại. Quy trình thẩm định bài báo đăng gồm các bước sau:\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tiếp nhận bản thảo\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Tác giả liên hệ gửi bản thảo đến Tạp chí qua hệ thống trực tuyến tại website: https:\u002F\u002Ftapchi.ctump.edu.vn. Hướng dẫn về cách đăng ký, gửi bài và chuẩn bị bản thảo được cung cấp trên website của Tạp chí.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sàng lọc sơ bộ\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Sau khi Tòa soạn nhận được bài báo của tác giả, Ban Thư ký sẽ tiến hành kiểm tra sơ bộ bài báo (các yêu cầu về nội dung và hình thức). Những bài báo không đúng quy cách hoặc có nội dung không phù hợp hoặc vi phạm bản quyền sẽ bị từ chối (Ban Thư ký thông báo phản hồi đến tác giả trong vòng 1 tuần). Những bài báo đủ điều kiện, được Ban Thư ký tòa soạn chuyển đến Ban Biên tập có cùng chuyên môn với nội dung bài báo để đề xuất người phản biện. Thời gian kể từ khi Ban Biên tập nhận bài báo đến khi đề xuất người phản biện bài báo chậm nhất là 5 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Vòng phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký gửi bài và yêu cầu phản biện đến 02 phản biện độc lập.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Các phản biện gởi nhận xét cho Ban Thư ký. Thời gian từ khi gửi bài cho phản biện đến khi nhận ý kiến của phản biện tối đa là 20 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xử ký kết quả phản biện\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Nếu ý kiến đồng ý cho đăng và không cần chỉnh sửa, Ban Thư ký tiếp tục đăng bài theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Nếu ý kiến đồng ý đăng và cần chỉnh sửa, Ban Thư ký sẽ thông tin đến tác giả chỉnh sửa theo yêu cầu của người phản biện. Thời gian chỉnh sửa và gửi lại kéo dài không quá 2 tuần, từ khi tác giả bài báo nhận được thông tin (Quá trình này có thể lặp lại tối đa 2 lần\u002F1 bài báo). Khi có sự thống nhất, đồng ý của người phản biện; bài báo được tiếp tục đăng theo qui trình.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Những bài báo có chất lượng không đạt yêu cầu, cả 2 phản biện không đồng ý cho đăng sẽ bị Tòa soạn từ chối đăng.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">Xuất bản\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">1. Ban Thư ký tổng hợp các bản thảo đã được tác giả hoàn thiện sau thẩm định trình Ban Biên tập xem xét, Tổng Biên tập phê duyệt, quyết định bài đăng theo các tiêu chí: sự phù hợp nội dung với tôn chỉ và mục đích, thể loại bài viết (ưu tiên các bài có bài có nghiên cứu chuyên sâu, hàm lượng khoa học cao), đóng góp mới bài báo, bài báo được ưu tiên đăng trong số gần nhất của Tạp chí theo thứ tự: tính thời sự, chất lượng bài báo và thời gian gửi bài.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">2. Ban Biên tập và Ban Thư ký biên tập bản thảo, chế bản, đọc rà soát lỗi. Thời gian hoàn thành từ 10-15 ngày.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">3. Ban Thư ký có trách nhiệm thông báo cho tác giả bài báo (bằng e-mail) về tình hình phê duyệt bài báo, thời gian, số kỳ, tập xuất bản bài báo theo qui định.\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>\u003Cp>\u003Cspan style=\"color: rgb(0, 0, 0);\">4. Danh sách bài báo theo số Tạp chí được in ấn và phát hành trong năm định kỳ được công bố chính thức trên website: https:\u002F\u002Ftapchi.ctump.edu.vn\u003C\u002Fspan>\u003C\u002Fp>\u003Cp>\u003Cbr>\u003C\u002Fp>",{"VOID":490},"wcQ1uqwAAAAJ","2023-05-30T08:17:21.868+00:00",[],[494],{"id":495,"createTime":28,"updateTime":28,"relativeEntities":496,"slug":28,"properties":497,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":507,"parentIds":508,"statistic":28},"6413896b-eca9-442b-a73f-182a58a0ce40",[],{"title":498,"address":501,"country":504,"abbreviation":505},{"EN":499,"VI":500},"Can Tho University of Medicine and Pharmacy","Trường Đại học Y Dược Cần Thơ",{"EN":502,"VI":503},"No 179, Nguyen Van Cu street, An Khanh ward, Ninh Kieu district, Can Tho city, Vietnam","Số 179, đường Nguyễn Văn Cừ, phường An Khánh, quận Ninh Kiều, thành phố Cần Thơ, Việt Nam",{"VOID":15},{"VOID":506},"ctump","http:\u002F\u002Fwww.ctump.edu.vn\u002F",[],[],"https:\u002F\u002Ftapchi.ctump.edu.vn\u002Findex.php\u002Fctump",{"impactFactor":32,"impactFactorByYear":512,"i10Index":32,"i10IndexLast5Year":32,"totalPublication":514,"totalPublicationByYear":515,"totalCitation":520,"totalCitationByYear":521,"totalCitationPerPublication":108,"totalCitationPerPublicationByYear":523,"hindexLast5Year":45,"hindex":45},{"2022":513,"2023":111,"2024":106},0.01,1556,{"2020":47,"2021":516,"2022":517,"2023":518,"2024":519,"2025":122},57,306,801,358,161,{"2021":146,"2022":280,"2023":522},99,{"2021":524,"2022":318,"2023":104},0.23,{"impactFactor":28,"impactFactorByYear":28,"i10Index":123,"i10IndexLast5Year":123,"totalPublication":526,"totalPublicationByYear":527,"totalCitation":526,"totalCitationByYear":528,"totalCitationPerPublication":40,"totalCitationPerPublicationByYear":531,"hindexLast5Year":49,"hindex":49},476,{"0":205,"2019":123,"2021":139,"2022":459,"2023":451,"2024":357,"2025":49,"2026":48},{"2021":42,"2022":123,"2023":161,"2024":529,"2025":360,"2026":530},136,83,{"2021":105,"2022":513,"2023":532,"2024":127,"2025":533,"2026":534},0.62,25.43,13.83,{"id":536,"createTime":537,"updateTime":382,"relativeEntities":538,"slug":539,"properties":540,"entityType":25,"verifyStatus":26,"verifyTime":28,"verifyNote":28,"languages":552,"translateLanguages":28,"viewCount":133,"subjectFields":553,"manageAffiliations":554,"indexDatabases":555,"url":556,"thumbnailPath":557,"statistic":558,"gsStatistic":594,"type":55,"analyzePriority":28},"6984a56a-db70-403b-9cc4-4013e1ceaffa","2023-05-09T06:47:40.346+00:00",[],"T%E1%BA%A1p%20ch%C3%AD%20Nghi%C3%AAn%20c%E1%BB%A9u%20n%C6%B0%E1%BB%9Bc%20ngo%C3%A0i",{"country":541,"issn":542,"title":544,"introduce":547,"gsId":550},{"VOID":15},{"VOID":543},"25252445",{"EN":545,"VI":546},"VNU Journal of Foreign Studies","Tạp chí Nghiên cứu nước ngoài",{"EN":548,"VI":549},"{\"ops\":[{\"insert\":\"\\n\\nThe \\n\"},{\"attributes\":{\"italic\":true},\"insert\":\"VNU Journal of Science\"},{\"insert\":\"\\n was established in 1985 for the publication of national and international research papers in all fields of natural sciences and technology, social sciences and humanities. 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Number of deaths (World) by cause. Available from:http:\u002F\u002Fapps.who.int\u002Fgho\u002Fdata\u002Fnode.main.CODWORLD?lang=en. Last accessed 31 October 2013.",{},{"id":28,"text":1210,"url":28,"identifiers":1211},"Bray F, 2014, World cancer report 2014",{},{"id":28,"text":1213,"url":28,"identifiers":1214},"Ferlay J, 2013, GLOBOCAN 2012 cancer incidence and mortality worldwide: IARC cancerbase No. 11",{},{"id":28,"text":1216,"url":28,"identifiers":1217},"United Nations Population Division (UNPD), World population prospects, the 2010 revision",{},{"id":28,"text":1219,"url":28,"identifiers":1220},"10.1038\u002Fnrc1948",{"doi":1219},{"id":28,"text":1222,"url":28,"identifiers":1223},"Forman D, 2013, Cancer incidence in five continents, vol. X (electronic version)",{},{"id":28,"text":1225,"url":28,"identifiers":1226},"10.1002\u002Fijc.2910550604",{"doi":1225},{"id":28,"text":1228,"url":28,"identifiers":1229},"World Health Organisation (WHO) Databank, Health statistics and information systems",{},{"id":28,"text":1231,"url":28,"identifiers":1232},"Mathers C, 2005, Counting the dead and what they died from: an assessment of the global status of cause of death data, Bull World Health Org, 83, 171",{},{"id":28,"text":1234,"url":28,"identifiers":1235},"National Disease Surveillance System monitoring causes of death 2010, 2012, Chinese Center for Disease Control and Prevention",{},{"id":28,"text":1237,"url":28,"identifiers":1238},"Curado MP, 2007, Cancer incidence in five continents, vol. IX",{},{"id":28,"text":1240,"url":28,"identifiers":1241},"WHO, 1993, International Statistical Classification of Diseases and Related Health Problems. Tenth Revision, vol. 2",{},{"id":28,"text":1243,"url":28,"identifiers":1244},"10.1002\u002Fijc.25516",{"doi":1243},{"id":28,"text":1246,"url":28,"identifiers":1247},"United Nations Development Programme.Human development report.2013. Available at:http:\u002F\u002Fhdr.undp.org\u002Fen. Last accessed 12 February 2013.",{},{"id":28,"text":1249,"url":28,"identifiers":1250},"10.1016\u002Fj.ejca.2012.12.027",{"doi":1249},{"id":28,"text":1252,"url":28,"identifiers":1253},"10.1016\u002Fj.ejca.2004.09.007",{"doi":1252},{"id":28,"text":1255,"url":28,"identifiers":1256},"Segi M, 1960, Cancer mortality for selected sites in 24 countries (1950–57)",{},{"id":28,"text":1258,"url":28,"identifiers":1259},"10.1007\u002F978-3-642-85849-9",{"doi":1258},{"id":28,"text":1261,"url":28,"identifiers":1262},"10.1002\u002Fijc.2910410205",{"doi":1261},{"id":28,"text":1264,"url":28,"identifiers":1265},"Parkin DM, 1984, Estimates of the worldwide frequency of twelve major cancers, Bull WHO, 62, 163",{},{"id":28,"text":1267,"url":28,"identifiers":1268},"10.1016\u002F0277-5379(90)90278-2",{"doi":1267},{"id":28,"text":1270,"url":28,"identifiers":1271},"Sankaranarayanan R, 2011, IARC Scientific Publications vol. 162. ISBN 978‐92‐832‐2162‐3",{},{"id":28,"text":1210,"url":28,"identifiers":1273},{},{"id":28,"text":1275,"url":28,"identifiers":1276},"10.1016\u002FS1470-2045(12)70137-7",{"doi":1275},false,{"id":1279,"createTime":1280,"updateTime":1281,"relativeEntities":1282,"slug":1283,"properties":1284,"entityType":971,"verifyStatus":26,"verifyTime":1300,"verifyNote":973,"languages":1301,"translateLanguages":1302,"viewCount":32,"primaryUrl":1303,"fullTextUrl":28,"authors":1304,"publicationType":1139,"publisherRelationship":1399,"citationCount":1449,"citationInfo":1450,"publishDate":1466,"publishYear":1451,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":1467,"openAccess":28,"references":1468,"isForceReanalyzing":1277},"bf18410c-ee57-4e18-8e56-49b5220c5972","2024-09-21T11:32:58.448+00:00","2025-01-14T18:23:29.319+00:00",[],"Estimates-of-worldwide-burden-of-cancer-in-2008-GLOBOCAN-2008",{"mag":1285,"keywords":1287,"openalex":1289,"abstract":1291,"title":1294,"pm":1297,"doi":1299},{"VOID":1286},"1981989535",{"VI":1288},"",{"VOID":1290},"W1981989535",{"EN":1292,"VI":1293},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Estimates of the worldwide incidence and mortality from 27 cancers in 2008 have been prepared for 182 countries as part of the GLOBOCAN series published by the International Agency for Research on Cancer. In this article, we present the results for 20 world regions, summarizing the global patterns for the eight most common cancers. Overall, an estimated 12.7 million new cancer cases and 7.6 million cancer deaths occur in 2008, with 56% of new cancer cases and 63% of the cancer deaths occurring in the less developed regions of the world. The most commonly diagnosed cancers worldwide are lung (1.61 million, 12.7% of the total), breast (1.38 million, 10.9%) and colorectal cancers (1.23 million, 9.7%). The most common causes of cancer death are lung cancer (1.38 million, 18.2% of the total), stomach cancer (738,000 deaths, 9.7%) and liver cancer (696,000 deaths, 9.2%). Cancer is neither rare anywhere in the world, nor mainly confined to high‐resource countries. Striking differences in the patterns of cancer from region to region are observed.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Các ước tính về tỷ lệ mắc và tỷ lệ tử vong toàn cầu từ 27 loại ung thư trong năm 2008 đã được thực hiện cho 182 quốc gia như một phần của loạt tài liệu GLOBOCAN được công bố bởi Cơ quan Quốc tế Nghiên cứu Ung thư. Trong bài viết này, chúng tôi trình bày kết quả cho 20 khu vực trên thế giới, tóm tắt các mẫu hình toàn cầu cho tám loại ung thư phổ biến nhất. Tổng cộng, ước tính có 12,7 triệu ca ung thư mới và 7,6 triệu ca tử vong do ung thư xảy ra trong năm 2008, với 56% ca ung thư mới và 63% ca tử vong do ung thư xảy ra ở các khu vực kém phát triển hơn trên thế giới. Các loại ung thư được chẩn đoán phổ biến nhất trên toàn cầu là ung thư phổi (1,61 triệu ca, 12,7% tổng số), ung thư vú (1,38 triệu ca, 10,9%) và ung thư đại trực tràng (1,23 triệu ca, 9,7%). Nguyên nhân phổ biến nhất gây tử vong do ung thư là ung thư phổi (1,38 triệu ca, 18,2% tổng số), ung thư dạ dày (738.000 ca tử vong, 9,7%) và ung thư gan (696.000 ca tử vong, 9,2%). Ung thư không phải là hiếm ở bất kỳ nơi nào trên thế giới, cũng như không chỉ tập trung chủ yếu ở các quốc gia có nguồn lực cao. Những khác biệt nổi bật trong các mẫu hình ung thư từ khu vực này sang khu vực khác được quan sát thấy.\u003C\u002Fjats:p>",{"EN":1295,"VI":1296},"Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008","Ước tính gánh nặng ung thư toàn cầu năm 2008: GLOBOCAN 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Cancer incidence, mortality and prevalence worldwide IARC CancerBase No. 5 [Internet]. Version 2.0",{},{"id":28,"text":1497,"url":28,"identifiers":1498},"United Nations, Population division, World population prospects, the 2008 revision [Internet]",{},{"id":28,"text":1500,"url":28,"identifiers":1501},"Curado MP, 2007, IARC Scientific Publications No. 160",{},{"id":28,"text":1503,"url":28,"identifiers":1504},"Parkin DM, 2005, IARC CancerBase No. 7 [Internet]",{},{"id":28,"text":1506,"url":28,"identifiers":1507},"World Health Organisation (WHO) Databank, WHO statistical information system [Internet]",{},{"id":28,"text":1509,"url":28,"identifiers":1510},"World Health Organization, 2010, World health statistics 2010 [Internet]",{},{"id":28,"text":1512,"url":28,"identifiers":1513},"World Health Organization, 2008, The global burden of disease: 2004 update",{},{"id":28,"text":1515,"url":28,"identifiers":1516},"10.1002\u002F1097-0258(20000715)19:13\u003C1741::AID-SIM496>3.0.CO;2-O",{"doi":1515},{"id":28,"text":1518,"url":28,"identifiers":1519},"10.1002\u002Fsim.1481",{"doi":1518},{"id":28,"text":1521,"url":28,"identifiers":1522},"Cancer Registry of Norway. 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Lyon: IARC, 1990.",{},{"id":28,"text":1984,"url":28,"identifiers":1985},"Parkin, 1988, Int J Cancer, 41, 184, 10.1002\u002Fijc.2910410205",{"doi":1261},{"id":28,"text":1987,"url":28,"identifiers":1988},"Parkin, 1993, Int J Cancer, 54, 594, 10.1002\u002Fijc.2910540413",{"doi":1480},{"id":28,"text":1990,"url":28,"identifiers":1991},"Pisani, 1993, Int J Cancer, 55, 891, 10.1002\u002Fijc.2910550604",{"doi":1225},{"id":28,"text":1993,"url":28,"identifiers":1994},"Parkin, 1999, Int J Cancer, 80, 827, 10.1002\u002F(SICI)1097-0215(19990315)80:6\u003C827::AID-IJC6>3.0.CO;2-P",{"doi":1483},{"id":28,"text":1996,"url":28,"identifiers":1997},"Pisani, 1999, Int J Cancer, 83, 18, 10.1002\u002F(SICI)1097-0215(19990924)83:1\u003C18::AID-IJC5>3.0.CO;2-M",{"doi":1488},{"id":28,"text":1999,"url":28,"identifiers":2000},"Hakulinen, 1986, Int J Epidemiol, 15, 227, 10.1093\u002Fije\u002F15.2.226",{"doi":2001},"10.1093\u002Fije\u002F15.2.226",{"id":28,"text":2003,"url":28,"identifiers":2004},"Estimates and projections of mortality by cause: a global overview, 1970-2015. In: eds. Evolving health sector priorities in developing countries. Washington: Population, Health and Nutrition Division, The World Bank, 1989.",{},{"id":28,"text":2006,"url":28,"identifiers":2007},"The global burden of disease. Cambridge, MA: Harvard University Press, 1996.",{},{"id":28,"text":2009,"url":28,"identifiers":2010},"Murray, 1997, Lancet, 349, 1436, 10.1016\u002FS0140-6736(96)07495-8",{"doi":2011},"10.1016\u002FS0140-6736(96)07495-8",{"id":28,"text":2013,"url":28,"identifiers":2014},"Mortality patterns in national populations. New York: Academic Press, 1976.",{},{"id":28,"text":2016,"url":28,"identifiers":2017},"et al. GLOBOCAN 2000: cancer incidence, mortality and prevalence worldwide, version 1.0. IARC Cancer Base No. 5. Lyon: IARC, 2001.",{},{"id":28,"text":2019,"url":28,"identifiers":2020},"et al., eds. Cancer registration principles and methods. IARC Sci. Publ. No. 95. Lyon: IARC, 1991.",{},{"id":28,"text":2022,"url":28,"identifiers":2023},"et al., Eds. Cancer incidence in five continents, vol. VII. No. 143. Lyon: IARC, 1997. p 1028-9.",{},{"id":28,"text":2025,"url":28,"identifiers":2026},"et al., eds. SEER cancer statistics review 1973-1994. NIH Publication No. 97-2789. Bethesda, MD: U.S. Dept. of Health and Human Services, NCI, 1997.",{},{"id":28,"text":2028,"url":28,"identifiers":2029},"et al. Survival of cancer patients in Europe. The EUROCARE-2 study. IARC Sci. Publ. No. 151. Lyon: IARC, 1999.",{},{"id":28,"text":2031,"url":28,"identifiers":2032},"eds. Cancer survival in developing countries. IARC Sci. Publ. No. 145. Lyon: IARC, 1998.",{},{"id":28,"text":2034,"url":28,"identifiers":2035},"et al. Cancer prevention in developing countries. Nagoya, Japan: University of Nagoya Press (for UICC), 1982.",{},{"id":28,"text":1993,"url":28,"identifiers":2037},{"doi":1483},{"id":28,"text":2039,"url":28,"identifiers":2040},"Modern epidemiology, 2nd ed. Philadelphia: Lippincot-Raven, 1998.",{},{"id":28,"text":2042,"url":28,"identifiers":2043},"et al. EUCAN: cancer incidence, mortality and prevalence in the European Union 1996, version 3.1. IARC Cancer Base No. 4. Lyon: IARC, 1999. Limited version available from: URL: http:\u002F\u002Fwww-dep.iarc.fr\u002Feucan\u002Feucan.htm",{},{"id":28,"text":2045,"url":28,"identifiers":2046},"Pisani, Int J Cancer",{},{"id":28,"text":2048,"url":28,"identifiers":2049},"United Nations. World population prospects: the 1998 revision. vol. 1: comprehensive tables. New York: United Nations, 1999.",{},{"id":28,"text":2051,"url":28,"identifiers":2052},"Hakama, 1975, Cancer, 36, 2227, 10.1002\u002Fcncr.2820360941",{"doi":2053},"10.1002\u002Fcncr.2820360941",{"id":28,"text":2055,"url":28,"identifiers":2056},"Feldman, 1986, N Engl J Med, 315, 1394, 10.1056\u002FNEJM198611273152206",{"doi":2057},"10.1056\u002FNEJM198611273152206",{"id":28,"text":2059,"url":28,"identifiers":2060},"Tulinius, 1982, Acta Path Microbiol Scand, 100, 146",{},{"id":28,"text":2062,"url":28,"identifiers":2063},"Hewitt, 1999, J Natl Cancer Inst, 91, 1480, 10.1093\u002Fjnci\u002F91.17.1480",{"doi":2064},"10.1093\u002Fjnci\u002F91.17.1480",{"id":28,"text":2066,"url":28,"identifiers":2067},"Capocaccia, 1990, Cancer Causes Control, 1, 23, 10.1007\u002FBF00053180",{"doi":2068},"10.1007\u002FBF00053180",{"id":28,"text":2070,"url":28,"identifiers":2071},"Merrill, 2000, Int J Epidemiol, 29, 197, 10.1093\u002Fije\u002F29.2.197",{"doi":2072},"10.1093\u002Fije\u002F29.2.197",{"id":28,"text":2074,"url":28,"identifiers":2075},"Coldman, 1992, Stat Med, 11, 1579, 10.1002\u002Fsim.4780111205",{"doi":2076},"10.1002\u002Fsim.4780111205",{"id":28,"text":2078,"url":28,"identifiers":2079},"Murray, 1974, J Natl Cancer Inst, 52, 3, 10.1093\u002Fjnci\u002F52.1.3",{"doi":2080},"10.1093\u002Fjnci\u002F52.1.3",{"id":28,"text":2082,"url":28,"identifiers":2083},"Murray, 1994, Bull World Health Org, 72, 429",{},{"id":28,"text":2085,"url":28,"identifiers":2086},"Morrow, 1995, Am J Public Health, 85, 1356, 10.2105\u002FAJPH.85.10.1356",{"doi":2087},"10.2105\u002FAJPH.85.10.1356",{"id":2089,"createTime":2090,"updateTime":2091,"relativeEntities":2092,"slug":2093,"properties":2094,"entityType":971,"verifyStatus":26,"verifyTime":2090,"verifyNote":973,"languages":2110,"translateLanguages":2111,"viewCount":32,"primaryUrl":2112,"fullTextUrl":28,"authors":2113,"publicationType":1139,"publisherRelationship":2223,"citationCount":2273,"citationInfo":2274,"publishDate":2281,"publishYear":2275,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":2282,"openAccess":28,"references":2283,"isForceReanalyzing":1277},"fea25157-bb46-41ee-9470-3623ff245ef0","2024-08-30T11:18:26.484+00:00","2025-01-14T18:24:26.887+00:00",[],"Cancer-statistics-for-the-year-2020-An-overview",{"mag":2095,"keywords":2097,"openalex":2098,"abstract":2100,"title":2103,"pm":2106,"doi":2108},{"VOID":2096},"3147142721",{"VI":1288},{"VOID":2099},"W3147142721",{"EN":2101,"VI":2102},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Our study briefly reviews the data sources and methods used in compiling the International Agency for Research on Cancer (IARC) GLOBOCAN cancer statistics for the year 2020 and summarises the main results. National estimates were calculated based on the best available data on cancer incidence from population‐based cancer registries (PBCR) and mortality from the World Health Organization mortality database. Cancer incidence and mortality rates for 2020 by sex and age groups were estimated for 38 cancer sites and 185 countries or territories worldwide. There were an estimated 19.3 million (95% uncertainty interval [UI]: 19.0‐19.6 million) new cases of cancer (18.1 million excluding non‐melanoma skin cancer) and almost 10.0 million (95% UI: 9.7‐10.2 million) deaths from cancer (9.9 million excluding non‐melanoma skin cancer) worldwide in 2020. The most commonly diagnosed cancers worldwide were female breast cancer (2.26 million cases), lung (2.21) and prostate cancers (1.41); the most common causes of cancer death were lung (1.79 million deaths), liver (830000) and stomach cancers (769000).\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Nghiên cứu của chúng tôi tóm tắt ngắn gọn các nguồn dữ liệu và phương pháp được sử dụng để biên soạn thống kê ung thư GLOBOCAN của Tổ chức Quốc tế nghiên cứu ung thư (IARC) cho năm 2020 và tóm tắt các kết quả chính. Ước tính quốc gia được tính toán dựa trên dữ liệu tốt nhất có sẵn về tỷ lệ mắc ung thư từ các đăng ký ung thư theo dân số (PBCR) và tỷ lệ tử vong từ cơ sở dữ liệu tử vong của Tổ chức Y tế Thế giới. Tỷ lệ mắc và tỷ lệ tử vong do ung thư năm 2020 theo giới tính và nhóm tuổi đã được ước tính cho 38 loại ung thư và 185 quốc gia hoặc vùng lãnh thổ trên toàn thế giới. Ước tính có 19.3 triệu (khoảng tin cậy 95% [UI]: 19.0‐19.6 triệu) trường hợp ung thư mới (18.1 triệu không bao gồm ung thư da không tế bào hắc tố) và gần 10.0 triệu (UI 95%: 9.7‐10.2 triệu) ca tử vong do ung thư (9.9 triệu không bao gồm ung thư da không tế bào hắc tố) trên toàn cầu trong năm 2020. Những loại ung thư thường được chẩn đoán nhất trên toàn thế giới là ung thư vú nữ (2.26 triệu trường hợp), ung thư phổi (2.21 triệu) và ung thư tuyến tiền liệt (1.41 triệu); những nguyên nhân phổ biến nhất gây ra tử vong do ung thư là ung thư phổi (1.79 triệu ca tử vong), ung thư gan (830000) và ung thư dạ dày (769000).\u003C\u002Fjats:p>",{"EN":2104,"VI":2105},"Cancer statistics for the year 2020: An overview","Thống kê ung thư năm 2020: Một cái nhìn tổng 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Accessed March 15 2021.",{},{"id":28,"text":2333,"url":28,"identifiers":2334},"10.1080\u002F0284186X.2019.1657586",{"doi":2333},{"id":2336,"createTime":2337,"updateTime":2338,"relativeEntities":2339,"slug":2340,"properties":2341,"entityType":971,"verifyStatus":26,"verifyTime":2357,"verifyNote":973,"languages":2358,"translateLanguages":2359,"viewCount":32,"primaryUrl":2360,"fullTextUrl":28,"authors":2361,"publicationType":1139,"publisherRelationship":2378,"citationCount":2427,"citationInfo":2428,"publishDate":2441,"publishYear":2429,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":2442,"openAccess":28,"references":2443,"isForceReanalyzing":1277},"9f2e0af3-b61c-4ccc-bd93-918ad7862754","2024-09-12T06:20:18.807+00:00","2025-01-14T18:25:25.048+00:00",[],"The-global-health-burden-of-infection-associated-cancers-in-the-year-2002",{"mag":2342,"keywords":2344,"openalex":2345,"abstract":2347,"title":2350,"pm":2353,"doi":2355},{"VOID":2343},"2140481064",{"VI":1288},{"VOID":2346},"W2140481064",{"EN":2348,"VI":2349},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Several infectious agents are considered to be causes of cancer in humans. The fraction of the different types of cancer, and of all cancers worldwide and in different regions, has been estimated using several methods; primarily by reviewing the evidence for the strength of the association (relative risk) and the prevalence of infection in different world areas. The estimated total of infection‐attributable cancer in the year 2002 is 1.9 million cases, or 17.8% of the global cancer burden. The principal agents are the bacterium \u003Cjats:italic>Helicobacter pylori\u003C\u002Fjats:italic> (5.5% of all cancer), the human papilloma viruses (5.2%), the hepatitis B and C viruses (4.9%), Epstein‐Barr virus (1%), human immunodeficiency virus (HIV) together with the human herpes virus 8 (0.9%). Relatively less important causes of cancer are the schistosomes (0.1%), human T‐cell lymphotropic virus type I (0.03%) and the liver flukes (0.02%). There would be 26.3% fewer cancers in developing countries (1.5 million cases per year) and 7.7% in developed countries (390,000 cases) if these infectious diseases were prevented. The attributable fraction at the specific sites varies from 100% of cervix cancers attributable to the papilloma viruses to a tiny proportion (0.4%) of liver cancers (worldwide) caused by liver flukes. © 2006 Wiley‐Liss, Inc.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Một số tác nhân gây nhiễm được xem là nguyên nhân gây ung thư ở người. Tỷ lệ của các loại ung thư khác nhau, và tất cả các loại ung thư trên toàn cầu và ở các khu vực khác nhau, đã được ước lượng bằng nhiều phương pháp; chủ yếu là bằng cách xem xét các bằng chứng về độ mạnh của mối liên hệ (rủi ro tương đối) và tỷ lệ mắc nhiễm trong các khu vực trên thế giới. Tổng số trường hợp ung thư do nhiễm trùng gây ra trong năm 2002 được ước tính là 1,9 triệu trường hợp, chiếm 17,8% gánh nặng ung thư toàn cầu. Các tác nhân chính bao gồm vi khuẩn \u003Cjats:italic>Helicobacter pylori\u003C\u002Fjats:italic> (5,5% tổng số ung thư), virus papilloma người (5,2%), virus viêm gan B và C (4,9%), virus Epstein‐Barr (1%), virus suy giảm miễn dịch của người (HIV) cùng với virus herpes người loại 8 (0,9%). Những nguyên nhân gây ung thư tương đối kém quan trọng hơn bao gồm schistosoma (0,1%), virus lymphotropic T của người loại I (0,03%) và sán lá gan (0,02%). Sẽ có 26,3% số ca ung thư ít hơn ở các nước đang phát triển (1,5 triệu ca mỗi năm) và 7,7% ở các nước phát triển (390.000 ca) nếu các bệnh nhiễm trùng này được phòng ngừa. Phân đoạn có thể quy cho các vị trí cụ thể khác nhau từ 100% ung thư cổ tử cung có thể quy cho virus papilloma đến tỷ lệ rất nhỏ (0,4%) ung thư gan (trên toàn cầu) do sán lá gan gây ra. © 2006 Wiley‐Liss, Inc.\u003C\u002Fjats:p>",{"EN":2351,"VI":2352},"The global health burden of infection‐associated cancers in the year 2002","Gánh nặng sức khỏe toàn cầu từ các loại ung thư liên quan đến nhiễm trùng trong năm 2002",{"VOID":2354},"16404738",{"VOID":2356},"10.1002\u002Fijc.21731","2024-09-12T06:20:18.806+00:00",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fijc.21731",[2362],{"id":2363,"sortIndex":32,"researcher":28,"roles":2364,"affiliations":2365,"properties":2374,"displayName":1104,"givenName":28,"familyName":28},"896ff3bd-6799-48ab-907c-645740e3f7d7",[],[2366],{"id":2367,"sortIndex":32,"affiliation":2368,"properties":28},"e08dd3d5-b071-4875-8ef1-feb116d78e67",{"id":2367,"createTime":28,"updateTime":28,"relativeEntities":2369,"slug":28,"properties":2370,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2373,"statistic":28},[],{"title":2371},{"EN":2372},"Clinical Trials Service Unit and Epidemiological Studies Unit, University of Oxford, Headington, UK. max.parkin@ctsu.ox.ac.uk",[],{"orcid":2375,"title":2376,"openalex":2377},{"VOID":1102},{"EN":1104},{"VOID":1106},{"url":28,"publisher":2379,"properties":2421},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":2380,"slug":872,"properties":2381,"entityType":25,"verifyStatus":884,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":2386,"manageAffiliations":2395,"indexDatabases":2406,"url":943,"thumbnailPath":28,"statistic":28,"gsStatistic":28,"type":28,"analyzePriority":28},[],{"country":2382,"eissn":2383,"issn":2384,"title":2385},{"VOID":875},{"VOID":877},{"VOID":879},{"EN":881},[2387,2391],{"id":887,"createTime":28,"updateTime":28,"relativeEntities":2388,"label":2389,"description":2390,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":890},{},{"id":893,"createTime":28,"updateTime":28,"relativeEntities":2392,"label":2393,"description":2394,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":896},{},[2396,2401],{"id":900,"createTime":28,"updateTime":28,"relativeEntities":2397,"slug":28,"properties":2398,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2400,"statistic":28},[],{"title":2399},{"EN":904},[],{"id":907,"createTime":28,"updateTime":28,"relativeEntities":2402,"slug":28,"properties":2403,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2405,"statistic":28},[],{"title":2404},{"EN":911},[],[2407,2414],{"id":915,"indexDatabase":2408,"url":921,"indexYears":922,"academicFieldIds":2413,"indexDatabaseRanking":926},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":2409,"label":2410,"description":2411,"key":781,"publicationTags":2412,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[924,925],{"id":928,"indexDatabase":2415,"url":940,"indexYears":28,"academicFieldIds":2420,"indexDatabaseRanking":28},{"id":930,"createTime":28,"updateTime":28,"relativeEntities":2416,"label":2417,"description":2418,"key":937,"publicationTags":2419,"standard":28},[],{"EN":933,"VI":933},{"EN":935,"VI":936},[939,813],[942],{"issue":2422,"pages":2423,"volume":2425},{"VOID":1444},{"VOID":2424},"3030-3044",{"VOID":2426},"118",2829,{"total":2427,"publishYear":2429,"statisticByYear":2430},2006,{"2012":2431,"2013":2432,"2014":2433,"2015":2434,"2016":215,"2017":2435,"2018":520,"2019":2436,"2020":2437,"2021":2438,"2022":2439,"2023":2440,"2024":280},211,215,234,220,175,157,147,141,113,96,"2006-06-15",[939,926],[2444,2447,2450,2453,2456,2459,2462,2465,2468,2471,2474,2477,2481,2484,2487,2490,2493,2496,2499,2502,2505,2508,2511,2514,2517,2520,2523,2526,2529,2532,2535,2538,2541,2544,2547,2550,2553,2556,2559,2562,2565,2568,2571,2574,2577,2580,2583,2586,2589,2593,2596,2599,2602,2605,2608,2611,2614,2617,2620,2623,2626,2629,2632,2635,2638,2641,2644,2647,2650,2653,2656,2659,2662,2665,2668,2671,2674,2677,2680,2683,2686,2689,2692,2695,2698,2701,2705,2708,2711,2714,2717,2720,2723,2726,2729,2733,2736,2739,2742,2745,2748,2751,2755,2758,2761,2764,2767,2770,2773,2776,2779,2782,2785,2789,2792,2795,2798,2801,2804,2807,2810,2813,2816,2819,2822,2825,2828,2831,2834,2837,2840,2843,2846,2849,2852,2855,2858,2861,2864,2867,2870,2873,2876,2879,2882,2885,2888,2891,2895,2898,2901,2904,2907,2910],{"id":28,"text":2445,"url":28,"identifiers":2446},"Parkin DM, 1999, 5",{},{"id":28,"text":2448,"url":28,"identifiers":2449},"Ferlay J, 2004, GLOBOCAN 2002. 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Gann monograph on cancer research (Japanese), J Cancer Res, 39, 129",{},{"id":28,"text":2802,"url":28,"identifiers":2803},"Verdier M, 1984, AIDS in Africa, 173",{},{"id":28,"text":2805,"url":28,"identifiers":2806},"10.1002\u002Fijc.2910430618",{"doi":2805},{"id":28,"text":2808,"url":28,"identifiers":2809},"Tajima K, 1985, Estimation of incidence rate of ATL among ATLV carriers in Kyushu, Japan (Japanese), J Clin Oncol, 15, 423",{},{"id":28,"text":2811,"url":28,"identifiers":2812},"Tokudome S, 1989, Incidence of adult T‐cell leukaemia\u002Flymphoma among human T‐lymphotropic virus type I carriers in Saga (Japanese), Cancer Res, 49, 226",{},{"id":28,"text":2814,"url":28,"identifiers":2815},"10.1002\u002F(SICI)1097-0215(20000201)85:3\u003C319::AID-IJC4>3.0.CO;2-B",{"doi":2814},{"id":28,"text":2817,"url":28,"identifiers":2818},"10.1002\u002Fijc.2910430214",{"doi":2817},{"id":28,"text":2820,"url":28,"identifiers":2821},"10.1093\u002Fjnci\u002F87.13.1009",{"doi":2820},{"id":28,"text":2823,"url":28,"identifiers":2824},"Levine PH, 1992, The epidemiology of human virus associated haematologic maligancies, Leukemia, 6, 54S",{},{"id":28,"text":2826,"url":28,"identifiers":2827},"10.1002\u002Fijc.2910480302",{"doi":2826},{"id":28,"text":2829,"url":28,"identifiers":2830},"10.1002\u002Fijc.2910590412",{"doi":2829},{"id":28,"text":2832,"url":28,"identifiers":2833},"10.1002\u002Fijc.21146",{"doi":2832},{"id":28,"text":2835,"url":28,"identifiers":2836},"Chung CS, 1976, An epidemiological study of primary liver carcinomas in Pusan area with special reference to clonorchiasis (Korean), J Pathology, 10, 33",{},{"id":28,"text":2838,"url":28,"identifiers":2839},"10.1093\u002Fije\u002F25.5.933",{"doi":2838},{"id":28,"text":2841,"url":28,"identifiers":2842},"Parkin DM, 1993, Cholangiocarcinoma: epidemiology, mechanisms of carcinogenesis and prevention, Cancer Epidemiol Biomarkers Prev, 2, 537",{},{"id":28,"text":2844,"url":28,"identifiers":2845},"1995, WHO Control of Food borne trematode infections",{},{"id":28,"text":2847,"url":28,"identifiers":2848},"10.1002\u002Fpath.1296",{"doi":2847},{"id":28,"text":2850,"url":28,"identifiers":2851},"10.1136\u002Fmp.53.5.255",{"doi":2850},{"id":28,"text":2853,"url":28,"identifiers":2854},"10.1002\u002Fijc.2910600513",{"doi":2853},{"id":28,"text":2856,"url":28,"identifiers":2857},"10.1053\u002Fj.gastro.2003.09.025",{"doi":2856},{"id":28,"text":2859,"url":28,"identifiers":2860},"10.1002\u002Fijc.20205",{"doi":2859},{"id":28,"text":2862,"url":28,"identifiers":2863},"10.1002\u002Fijc.20257",{"doi":2862},{"id":28,"text":2865,"url":28,"identifiers":2866},"10.1056\u002FNEJM199007123230202",{"doi":2865},{"id":28,"text":2868,"url":28,"identifiers":2869},"10.1093\u002Faje\u002Fkwh039",{"doi":2868},{"id":28,"text":2871,"url":28,"identifiers":2872},"The Gambia Hepatitis Study Group, 1987, The Gambia Hepatitis Intervention Study (GHIS), Cancer Res, 47, 5782",{},{"id":28,"text":2874,"url":28,"identifiers":2875},"Sun Z, 1991, Design and compliance of HBV vaccination trial on newborns to prevent hepatocellular carcinoma and 5‐year results of its pilot study, Cancer Detect Prev, 15, 313",{},{"id":28,"text":2877,"url":28,"identifiers":2878},"World Health Organization (WHO).Immunization surveillance assessment and monitoring.http:\u002F\u002Fwww.who.int\u002Fimmunization_monitoring\u002Fen\u002F(Accessed October 2005).",{},{"id":28,"text":2880,"url":28,"identifiers":2881},"10.1056\u002FNEJM199706263362602",{"doi":2880},{"id":28,"text":2883,"url":28,"identifiers":2884},"10.1056\u002FNEJMoa020586",{"doi":2883},{"id":28,"text":2886,"url":28,"identifiers":2887},"10.1016\u002FS0140-6736(04)17398-4",{"doi":2886},{"id":28,"text":2889,"url":28,"identifiers":2890},"10.1016\u002FS1470-2045(05)70101-7",{"doi":2889},{"id":28,"text":2892,"url":28,"identifiers":2893},"SkjeldestadFE.Prophylactic quadrivalent human papillomavirus (HPV) (types 6 11 16 18) L1 virus‐like particle (VLP) vaccine (Gardasil(tm)) reduces cervical intraepithelial neoplasia (CIN) 2\u002F3 risk. Presented at the 2005 meeting of the Infectious Diseases Society of America. San Francisco CA. Abstract LB‐8a.",{"doi":2894},"10.1016\u002FS1359-6349(05)82013-0",{"id":28,"text":2896,"url":28,"identifiers":2897},"10.1002\u002Fijc.20244",{"doi":2896},{"id":28,"text":2899,"url":28,"identifiers":2900},"10.1016\u002FS0140-6736(96)01501-2",{"doi":2899},{"id":28,"text":2902,"url":28,"identifiers":2903},"10.1046\u002Fj.1365-2036.2002.01204.x",{"doi":2902},{"id":28,"text":2905,"url":28,"identifiers":2906},"10.1001\u002Fjama.291.2.187",{"doi":2905},{"id":28,"text":2908,"url":28,"identifiers":2909},"10.1001\u002Fjama.291.2.244",{"doi":2908},{"id":28,"text":2911,"url":28,"identifiers":2912},"United Nations(2003)World population prospects. The 2002 revision. Population database.http:\u002F\u002Fesa.un.org\u002Funpp\u002F.",{},{"id":2914,"createTime":2915,"updateTime":2916,"relativeEntities":2917,"slug":2918,"properties":2919,"entityType":971,"verifyStatus":26,"verifyTime":2915,"verifyNote":973,"languages":2935,"translateLanguages":2936,"viewCount":32,"primaryUrl":2937,"fullTextUrl":28,"authors":2938,"publicationType":1139,"publisherRelationship":3007,"citationCount":3057,"citationInfo":3058,"publishDate":3062,"publishYear":3059,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":3063,"openAccess":28,"references":3064,"isForceReanalyzing":1277},"e1285350-142f-4eec-90a4-223efc68130d","2024-11-29T10:54:08.703+00:00","2025-01-14T18:26:23.767+00:00",[],"Production-of-a-mouse-monoclonal-antibody-reactive-with-a-human-nuclear-antigen-associated-with-cell-proliferation",{"mag":2920,"keywords":2922,"openalex":2923,"abstract":2925,"title":2928,"pm":2931,"doi":2933},{"VOID":2921},"2154536753",{"VI":1288},{"VOID":2924},"W2154536753",{"EN":2926,"VI":2927},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The production of a mouse monoclonal antibody, Ki‐67, is described. The Ki‐67 antibody recognized a nuclear antigen present in proliferating cells, but absent in resting cells. Immunostainings with Ki‐67 revealed nuclear reactivity in cells of germinal centres of cortical follicles, cortical thymocytes, neck cells of gastrointestinal mucosa, un‐differentiated spermatogonia and cells of a number of human cell lines. The Ki‐67 antibody did not react with cells known to be in a resting stage, such as lymphocytes, monocytes, parietal cells and Paneth's cells of gastrointestinal mucosa, hepatocytes, renal cells, mature sperm cells, brain cells, etc. Expression of the antigen recognized by Ki‐67 could be induced in peripheral blood lymphocytes after stimulation with phytohaemagglutinin, whereas it disappeared from HL‐60 cells stimulated with phorbol esters to differentiate into mature macrophages in a resting stage. These findings suggest that Ki‐67 is directed against a nuclear antigen associated with cell proliferation. A first series of immunostainings of tumour biopsies indicated that Ki‐67 may be a potent tool for easy and quick evaluation of the proportion of proliferating cells in a tumour.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Bài báo mô tả việc sản xuất kháng thể đơn dòng chuột, Ki‐67. Kháng thể Ki‐67 nhận diện một kháng nguyên hạt nhân có mặt ở các tế bào đang phân chia, nhưng không có ở các tế bào trạng thái nghỉ. Việc nhuộm miễn dịch với Ki‐67 cho thấy có phản ứng hạt nhân ở các tế bào của trung tâm sinh sản của các nang vỏ, thyocyte vỏ, tế bào cổ họng của niêm mạc tiêu hóa, tế bào tinh nguyên không phân hóa và tế bào của một số dòng tế bào người. Kháng thể Ki‐67 không phản ứng với các tế bào được biết đến là ở trạng thái nghỉ, chẳng hạn như lymphocyte, monocyte, tế bào chính và tế bào Paneth của niêm mạc tiêu hóa, hepatocyte, tế bào thận, tế bào tinh trùng trưởng thành, tế bào não, v.v. Biểu hiện của kháng nguyên được Ki‐67 nhận diện có thể được kích thích ở lymphocyte trong máu ngoại vi sau khi tiếp xúc với phytohaemagglutinin, trong khi đó nó biến mất từ các tế bào HL‐60 được kích thích bằng ester phorbol để phân hóa thành đại thực bào trưởng thành ở trạng thái nghỉ. Những phát hiện này gợi ý rằng Ki‐67 hướng đến một kháng nguyên hạt nhân liên quan đến sự gia tăng tế bào. Một loạt nhuộm miễn dịch đầu tiên từ các mẫu sinh thiết khối u cho thấy Ki‐67 có thể là một công cụ mạnh mẽ để đánh giá một cách dễ dàng và nhanh chóng tỷ lệ các tế bào đang phân chia trong một khối u.",{"EN":2929,"VI":2930},"Production of a mouse monoclonal antibody reactive with a human nuclear antigen associated with cell proliferation","Sản xuất kháng thể đơn dòng chuột phản ứng với kháng nguyên hạt nhân người liên quan đến sự gia tăng tế 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H., 1969, Handbuch der allgemeinen Pathologie, 496",{},{"id":28,"text":3075,"url":28,"identifiers":3076},"10.1111\u002Fj.1749-6632.1964.tb40692.x",{"doi":3075},{"id":28,"text":3078,"url":28,"identifiers":3079},"Gerdes J., 1980, Xenoantiserum to human C3 receptors: its preparation and effect on the C3b and C3d receptors of tonsil cells and the C3b receptors of erythrocytes and neutrophils, Immunology, 39, 75",{},{"id":28,"text":3081,"url":28,"identifiers":3082},"10.1016\u002F0014-2964(74)90148-0",{"doi":3081},{"id":28,"text":3084,"url":28,"identifiers":3085},"10.1073\u002Fpnas.71.3.685",{"doi":3084},{"id":28,"text":3087,"url":28,"identifiers":3088},"10.1007\u002FBF01632381",{"doi":3087},{"id":28,"text":3090,"url":28,"identifiers":3091},"10.1111\u002Fj.1600-065X.1979.tb00293.x",{"doi":3090},{"id":28,"text":3093,"url":28,"identifiers":3094},"Mitrou P. S., 1969, Kombinierte autoradiographisch‐cytophotometrische Unter‐suchungen von Keimzentrumszellen der menschlichen Tonsille, Virchows Arch. Abt. 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Hämatologie und Bluttransfusion, 33",{},{"id":28,"text":3146,"url":28,"identifiers":3147},"Uchanska‐Ziegler B. The human promyelocytic cell line HL‐60 as a model for the study of granulocyte and monocyte differentiationin vitro: selective chemical induction and phenotypic surface analysis by monoclonal antibodies.Ph. D. Thesis Biological Faculty University of Tübingen (1982).",{},{"id":3149,"createTime":3150,"updateTime":3151,"relativeEntities":3152,"slug":3153,"properties":3154,"entityType":971,"verifyStatus":26,"verifyTime":3150,"verifyNote":973,"languages":3170,"translateLanguages":3171,"viewCount":32,"primaryUrl":3172,"fullTextUrl":28,"authors":3173,"publicationType":1139,"publisherRelationship":3210,"citationCount":3259,"citationInfo":3260,"publishDate":3263,"publishYear":3261,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":3264,"openAccess":28,"references":3265,"isForceReanalyzing":1277},"e7e2d70b-9931-4d72-a99d-3d7c2e153ff3","2024-09-02T16:09:40.697+00:00","2025-01-14T18:27:23.405+00:00",[],"Establishment-and-characterization-of-a-human-histiocytic-lymphoma-cell-line-U-937-",{"mag":3155,"keywords":3157,"openalex":3158,"abstract":3160,"title":3163,"pm":3166,"doi":3168},{"VOID":3156},"2133764756",{"VI":1288},{"VOID":3159},"W2133764756",{"EN":3161,"VI":3162},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>A human hematopoietic cell line (U‐937) with exceptional characteristics was derived from a patient with generalized histiocytic lymphoma. The morphology of the cell line was identical to that of the tumor cells in the pleural effusion from which the line was derived. Since Epstein‐Barr virus (EBV) carrying diploid lymphoblastoid cell lines unrelated to the tumor population often become established in vitro from non‐Burkitt lymphoma explants, several parameters were studied to discriminate the U‐937 from such lines: morphology in vitro, growth characteristics, cytochemistry, surface receptor pattern, Ig production, lysozyme production, β\u003Cjats:sub>2\u003C\u002Fjats:sub>‐micro‐globulin production, presence of EBV genome and karyotype. In all these respects U‐937 differed from prototype lymphoblastoid cell lines. The histiocytic origin of the cell line was shown by its capacity for lysozyme production and the strong esterase activity (naphtol AS‐D acetate esterase inhibited by NaF) of the cells. It is therefore concluded that the U‐937 is a neoplastic, histiocytic cell line.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Một dòng tế bào huyết học người (U‐937) với các đặc điểm ngoại lệ đã được phân lập từ một bệnh nhân mắc bệnh u lympho mô bào toàn thân. Hình thái của dòng tế bào này giống hệt với tế bào khối u trong dịch màng phổi từ đó dòng tế bào được chiết xuất. Kể từ khi virus Epstein‐Barr (EBV) mang các dòng tế bào lymphoblastoid diploid không liên quan đến dân số khối u thường được thiết lập in vitro từ các mẫu mô không phải Burkitt lymphoma, nhiều thông số đã được nghiên cứu để phân biệt U‐937 với các dòng tế bào như vậy: hình thái in vitro, đặc tính tăng trưởng, hóa ứng động tế bào, kiểu thụ thể bề mặt, sản xuất immunoglobulin, sản xuất lysozyme, sản xuất β\u003Cjats:sub>2\u003C\u002Fjats:sub>-microglobulin, sự hiện diện của bộ gen EBV và kiểu hình nhiễm sắc thể. Trong tất cả các khía cạnh này, U‐937 khác với các dòng tế bào lymphoblastoid mẫu. Xuất xứ histiocytic của dòng tế bào này đã được xác nhận bởi khả năng sản xuất lysozyme của nó và hoạt tính esterase mạnh (esterase naphtol AS‐D acetate bị ức chế bởi NaF) của các tế bào. Do đó, kết luận rằng U‐937 là một dòng tế bào histiocytic ác tính.\u003C\u002Fjats:p>",{"EN":3164,"VI":3165},"Establishment and characterization of a human histiocytic lymphoma cell line (U‐937)","Thành lập và đặc trưng của dòng tế bào u lympho mô bào người (U‐937)",{"VOID":3167},"178611",{"VOID":3169},"10.1002\u002Fijc.2910170504",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fijc.2910170504",[3174,3193],{"id":3175,"sortIndex":32,"researcher":28,"roles":3176,"affiliations":3177,"properties":3186,"displayName":3190,"givenName":28,"familyName":28},"523e2cfc-093a-4aed-85cd-00fc74b76a1c",[],[3178],{"id":3179,"sortIndex":32,"affiliation":3180,"properties":28},"3e537838-3e0d-4fb0-9c66-f480a6d67192",{"id":3179,"createTime":28,"updateTime":28,"relativeEntities":3181,"slug":28,"properties":3182,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3185,"statistic":28},[],{"title":3183},{"EN":3184},"Deparment of Pathology and Wallenberg Laboratory, University of Uppsala, Uppsala, Sweden",[],{"orcid":3187,"title":3189,"openalex":3191},{"VOID":3188},"https:\u002F\u002Forcid.org\u002F0000-0002-8160-5647",{"EN":3190},"Christer Sundström",{"VOID":3192},"A5051340130",{"id":3194,"sortIndex":40,"researcher":28,"roles":3195,"affiliations":3196,"properties":3203,"displayName":3207,"givenName":28,"familyName":28},"b28c99e8-1364-4859-a4bf-b1f06b1869f8",[],[3197],{"id":3179,"sortIndex":32,"affiliation":3198,"properties":28},{"id":3179,"createTime":28,"updateTime":28,"relativeEntities":3199,"slug":28,"properties":3200,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3202,"statistic":28},[],{"title":3201},{"EN":3184},[],{"orcid":3204,"title":3206,"openalex":3208},{"VOID":3205},"https:\u002F\u002Forcid.org\u002F0000-0002-0093-5725",{"EN":3207},"Kenneth Nilsson",{"VOID":3209},"A5002202838",{"url":28,"publisher":3211,"properties":3253},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":3212,"slug":872,"properties":3213,"entityType":25,"verifyStatus":884,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":3218,"manageAffiliations":3227,"indexDatabases":3238,"url":943,"thumbnailPath":28,"statistic":28,"gsStatistic":28,"type":28,"analyzePriority":28},[],{"country":3214,"eissn":3215,"issn":3216,"title":3217},{"VOID":875},{"VOID":877},{"VOID":879},{"EN":881},[3219,3223],{"id":887,"createTime":28,"updateTime":28,"relativeEntities":3220,"label":3221,"description":3222,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":890},{},{"id":893,"createTime":28,"updateTime":28,"relativeEntities":3224,"label":3225,"description":3226,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":896},{},[3228,3233],{"id":900,"createTime":28,"updateTime":28,"relativeEntities":3229,"slug":28,"properties":3230,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3232,"statistic":28},[],{"title":3231},{"EN":904},[],{"id":907,"createTime":28,"updateTime":28,"relativeEntities":3234,"slug":28,"properties":3235,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3237,"statistic":28},[],{"title":3236},{"EN":911},[],[3239,3246],{"id":915,"indexDatabase":3240,"url":921,"indexYears":922,"academicFieldIds":3245,"indexDatabaseRanking":926},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":3241,"label":3242,"description":3243,"key":781,"publicationTags":3244,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[924,925],{"id":928,"indexDatabase":3247,"url":940,"indexYears":28,"academicFieldIds":3252,"indexDatabaseRanking":28},{"id":930,"createTime":28,"updateTime":28,"relativeEntities":3248,"label":3249,"description":3250,"key":937,"publicationTags":3251,"standard":28},[],{"EN":933,"VI":933},{"EN":935,"VI":936},[939,813],[942],{"issue":3254,"pages":3255,"volume":3257},{"VOID":1185},{"VOID":3256},"565-577",{"VOID":3258},"17",2451,{"total":3259,"publishYear":3261,"statisticByYear":3262},1976,{"2012":149,"2013":689,"2014":137,"2015":140,"2016":132,"2017":136,"2018":129,"2019":140,"2020":132,"2021":122,"2022":130,"2023":135,"2024":49},"1976-05-15",[939,926],[3266,3269,3272,3275,3278,3281,3284,3287,3290,3293,3296,3299,3302,3305,3308,3312,3315,3318,3321,3324,3327,3330,3333,3336,3339,3342,3345,3348,3351,3354,3357,3360,3363,3366,3369,3372,3375,3378,3381,3384,3387,3390,3393,3396,3399,3402,3405,3409,3412,3415,3418,3421,3424,3427,3430,3433,3436,3439,3442,3445,3448,3451,3454,3457,3460,3463,3466,3469,3472,3475,3478,3481,3484,3487],{"id":28,"text":3267,"url":28,"identifiers":3268},"Abbrederis K., 1969, Zur Differentialdiagnose akuter Leukämien mittels zytochemischer Methoden, Schweiz. med. Wschr., 99, 1425",{},{"id":28,"text":3270,"url":28,"identifiers":3271},"10.1111\u002Fj.2164-0947.1951.tb01007.x",{"doi":3270},{"id":28,"text":3273,"url":28,"identifiers":3274},"10.1177\u002F10.6.741",{"doi":3273},{"id":28,"text":3276,"url":28,"identifiers":3277},"10.1016\u002F0014-4827(74)90791-5",{"doi":3276},{"id":28,"text":3279,"url":28,"identifiers":3280},"10.1002\u002Fijc.2910110107",{"doi":3279},{"id":28,"text":3282,"url":28,"identifiers":3283},"10.1084\u002Fjem.137.6.1532",{"doi":3282},{"id":28,"text":3285,"url":28,"identifiers":3286},"10.1177\u002F14.2.167",{"doi":3285},{"id":28,"text":3288,"url":28,"identifiers":3289},"10.1016\u002F0014-4827(71)90426-5",{"doi":3288},{"id":28,"text":3291,"url":28,"identifiers":3292},"Clarkson B. D., 1969, Immunoglobulin synthesis by human reticulum sarcoma cells in vivo and during long‐term culture in vitro, Cancer Res., 29, 823",{},{"id":28,"text":3294,"url":28,"identifiers":3295},"10.1084\u002Fjem.112.6.983",{"doi":3294},{"id":28,"text":3297,"url":28,"identifiers":3298},"10.1084\u002Fjem.118.6.991",{"doi":3297},{"id":28,"text":3300,"url":28,"identifiers":3301},"10.1002\u002F1097-0142(196403)17:3\u003C329::AID-CNCR2820170309>3.0.CO;2-G",{"doi":3300},{"id":28,"text":3303,"url":28,"identifiers":3304},"10.1093\u002Fjnci\u002F34.2.231",{"doi":3303},{"id":28,"text":3306,"url":28,"identifiers":3307},"10.1002\u002F1097-0142(197412)34:6\u003C1851::AID-CNCR2820340602>3.0.CO;2-4",{"doi":3306},{"id":28,"text":3309,"url":28,"identifiers":3310},"Evrin P. E., 1974, β2‐microglobulin production in vitro by human hematopoietic, mesenchymal and epithelial cells, J. Immunol., 112, 137, 10.4049\u002Fjimmunol.112.1.137",{"doi":3311},"10.4049\u002Fjimmunol.112.1.137",{"id":28,"text":3313,"url":28,"identifiers":3314},"10.1084\u002Fjem.138.1.89",{"doi":3313},{"id":28,"text":3316,"url":28,"identifiers":3317},"10.3181\u002F00379727-127-32692",{"doi":3316},{"id":28,"text":3319,"url":28,"identifiers":3320},"10.1007\u002FBF01487816",{"doi":3319},{"id":28,"text":3322,"url":28,"identifiers":3323},"10.1016\u002FS0014-4827(63)80014-2",{"doi":3322},{"id":28,"text":3325,"url":28,"identifiers":3326},"10.1016\u002FS0308-2261(72)80004-3",{"doi":3325},{"id":28,"text":3328,"url":28,"identifiers":3329},"Hertzog A. J., 1938, The phagocytic activity of human leukocytes with special reference to their type and maturity, Amer. J. Path., 14, 595",{},{"id":28,"text":3331,"url":28,"identifiers":3332},"10.1146\u002Fannurev.mi.19.100165.002011",{"doi":3331},{"id":28,"text":3334,"url":28,"identifiers":3335},"10.1007\u002FBF02052975",{"doi":3334},{"id":28,"text":3337,"url":28,"identifiers":3338},"10.1159\u002F000230091",{"doi":3337},{"id":28,"text":3340,"url":28,"identifiers":3341},"Huber Ch. Sundström Ch. Nilsson K. andWigzell H. Surface receptors on human hematopoietic cell lines.Clin. Exp. Immunol. in press (1976).",{},{"id":28,"text":3343,"url":28,"identifiers":3344},"10.1002\u002Feji.1830050616",{"doi":3343},{"id":28,"text":3346,"url":28,"identifiers":3347},"10.1056\u002FNEJM197404112901501",{"doi":3346},{"id":28,"text":3349,"url":28,"identifiers":3350},"Jobin M. E., 1974, Long term establishment of monocytoid cell lines derived from a patient with myelomonocytic leukemia, In Vitro, 10, 333",{},{"id":28,"text":3352,"url":28,"identifiers":3353},"10.1084\u002Fjem.136.2.207",{"doi":3352},{"id":28,"text":3355,"url":28,"identifiers":3356},"Jondal M., 1973, Human lymphocyte subpopulations: classification according to surface markers and\u002For functional characteristics, Transplant. Rev., 16, 163",{},{"id":28,"text":3358,"url":28,"identifiers":3359},"10.3181\u002F00379727-129-33360",{"doi":3358},{"id":28,"text":3361,"url":28,"identifiers":3362},"Kaplow L. S., 1975, Substitute for benzidine in myeloperoxidase stains, Amer J. clin. Path., 65, 451",{},{"id":28,"text":3364,"url":28,"identifiers":3365},"Kissmeyer‐Nielsen F., 1967, Histocompatibility testing, 381",{},{"id":28,"text":3367,"url":28,"identifiers":3368},"Klein E., 1968, Surface IgM‐kappa specificity on a Burkitt lymphoma cell in vivo and in derived culture lines, Cancer Res., 28, 1300",{},{"id":28,"text":3370,"url":28,"identifiers":3371},"10.1073\u002Fpnas.71.8.3283",{"doi":3370},{"id":28,"text":3373,"url":28,"identifiers":3374},"10.1084\u002Fjem.128.5.991",{"doi":3373},{"id":28,"text":3376,"url":28,"identifiers":3377},"Lennert K., 1975, Cytological and functional criteria for the classification of malignant lymphomata, Brit. J. Cancer, 31, 29",{},{"id":28,"text":3379,"url":28,"identifiers":3380},"Lillie R. D., 1948, Histopathologic technic",{},{"id":28,"text":3382,"url":28,"identifiers":3383},"10.1002\u002Fijc.2910130605",{"doi":3382},{"id":28,"text":3385,"url":28,"identifiers":3386},"10.1007\u002FBF01506146",{"doi":3385},{"id":28,"text":3388,"url":28,"identifiers":3389},"10.1177\u002F15.11.680",{"doi":3388},{"id":28,"text":3391,"url":28,"identifiers":3392},"10.1002\u002F1097-0142(197410)34:8 \u003C1488::AID-CNCR2820340822>3.0.CO;2-C",{"doi":3391},{"id":28,"text":3394,"url":28,"identifiers":3395},"10.1038\u002F158202a0",{"doi":3394},{"id":28,"text":3397,"url":28,"identifiers":3398},"Mathé G., 1975, Progress in the classification of lymphoid and\u002For monocytoid leukemias and of lympho and reticulosarcomas (non‐Hodgkin's lymphomas), Biomedicine, 22, 177",{},{"id":28,"text":3400,"url":28,"identifiers":3401},"Minowada J., 1972, Brief communication: Rosette‐forming human lymphoid cell lines. Establishment and evidence for origin of thymus‐derived lymphocytes, J. nat. Cancer Inst., 49, 891",{},{"id":28,"text":3403,"url":28,"identifiers":3404},"10.1177\u002F8.3.200",{"doi":3403},{"id":28,"text":3406,"url":28,"identifiers":3407},"Morris M. W., 1975, Immunologic and cytochemical properties of histiocytic and mixed histiocyticlymphocytic lymphomas, Amer. J. clin. Path., 63, 403, 10.1093\u002Fajcp\u002F63.3.403",{"doi":3408},"10.1093\u002Fajcp\u002F63.3.403",{"id":28,"text":3410,"url":28,"identifiers":3411},"10.1002\u002F1097-0142(196901)23:1\u003C64::AID-CNCR2820230107>3.0.CO;2-M",{"doi":3410},{"id":28,"text":3413,"url":28,"identifiers":3414},"10.1002\u002Fijc.2910070303",{"doi":3413},{"id":28,"text":3416,"url":28,"identifiers":3417},"10.1002\u002Fijc.2910080311",{"doi":3416},{"id":28,"text":3419,"url":28,"identifiers":3420},"10.1002\u002Fijc.2910150217",{"doi":3419},{"id":28,"text":3422,"url":28,"identifiers":3423},"10.1002\u002Fijc.2910130609",{"doi":3422},{"id":28,"text":3425,"url":28,"identifiers":3426},"10.1038\u002Fnewbio233103a0",{"doi":3425},{"id":28,"text":3428,"url":28,"identifiers":3429},"10.1084\u002Fjem.124.5.921",{"doi":3428},{"id":28,"text":3431,"url":28,"identifiers":3432},"10.1111\u002Fj.1699-0463.1948.tb00655.x",{"doi":3431},{"id":28,"text":3434,"url":28,"identifiers":3435},"Pearse A. G. E., 1960, Histochemistry. Theoretical and applied",{},{"id":28,"text":3437,"url":28,"identifiers":3438},"10.1016\u002FS0025-7125(16)32288-X",{"doi":3437},{"id":28,"text":3440,"url":28,"identifiers":3441},"10.1016\u002F0024-3205(67)90114-2",{"doi":3440},{"id":28,"text":3443,"url":28,"identifiers":3444},"Pope J. H., 1967, Burkitt lymphoma in New Guinea: establishment of a line of lymphoblasts in vitro and description of their fine structure, J. nat. Cancer Inst., 39, 933",{},{"id":28,"text":3446,"url":28,"identifiers":3447},"10.1136\u002Fjcp.18.3.261",{"doi":3446},{"id":28,"text":3449,"url":28,"identifiers":3450},"Raff M. C., 1970, Two distinct populations of peripheral lymphocytes in mice distinguishable by immunofluorescence, Immunology, 19, 637",{},{"id":28,"text":3452,"url":28,"identifiers":3453},"Ralph P. Moore M. A. S. andNilsson K. Lysozyme synthesis by established human and murine histiocytic lymphoma cell lines.J. Exp. Med. in press.",{},{"id":28,"text":3455,"url":28,"identifiers":3456},"Rappaport H., 1966, Atlas of Tumor Pathology. Section III, Fascicle 8",{},{"id":28,"text":3458,"url":28,"identifiers":3459},"10.1002\u002Fijc.2910110302",{"doi":3458},{"id":28,"text":3461,"url":28,"identifiers":3462},"10.1111\u002Fj.1365-2141.1968.tb00366.x",{"doi":3461},{"id":28,"text":3464,"url":28,"identifiers":3465},"Rutenburg A. M., 1965, An improved histochemical method for the demonstration of leukocyte alkaline phosphatase activity: Clinical application, J. lab. clin. Med., 65, 698",{},{"id":28,"text":3467,"url":28,"identifiers":3468},"10.1002\u002Fpath.1700590142",{"doi":3467},{"id":28,"text":3470,"url":28,"identifiers":3471},"10.1172\u002FJCI106999",{"doi":3470},{"id":28,"text":3473,"url":28,"identifiers":3474},"10.1016\u002FS0140-6736(72)92215-5",{"doi":3473},{"id":28,"text":3476,"url":28,"identifiers":3477},"Van Furth R., 1972, Synthesis of immunoglobulins by biopsied tissues and cell lines from Burkitt's lymphoma, Immunology, 22, 847",{},{"id":28,"text":3479,"url":28,"identifiers":3480},"10.1093\u002Fajcp\u002F55.3.283",{"doi":3479},{"id":28,"text":3482,"url":28,"identifiers":3483},"10.1111\u002Fj.1365-3083.1972.tb03306.x",{"doi":3482},{"id":28,"text":3485,"url":28,"identifiers":3486},"10.1002\u002Fijc.2910170108",{"doi":3485},{"id":28,"text":3488,"url":28,"identifiers":3489},"10.1038\u002Fnewbio237189a0",{"doi":3488},{"id":3491,"createTime":3492,"updateTime":3493,"relativeEntities":3494,"slug":3495,"properties":3496,"entityType":971,"verifyStatus":26,"verifyTime":3492,"verifyNote":973,"languages":3512,"translateLanguages":3513,"viewCount":32,"primaryUrl":3514,"fullTextUrl":28,"authors":3515,"publicationType":1139,"publisherRelationship":3552,"citationCount":3601,"citationInfo":3602,"publishDate":3605,"publishYear":3603,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":3606,"openAccess":28,"references":3607,"isForceReanalyzing":1277},"4c28725f-98ef-4be5-ad7b-ae43c28a67d5","2024-09-19T12:15:46.330+00:00","2025-01-14T18:28:21.059+00:00",[],"Binding-of-soluble-form-of-fibroblast-surface-protein-fibronectin-to-collagen",{"mag":3497,"keywords":3499,"openalex":3500,"abstract":3502,"title":3505,"pm":3508,"doi":3510},{"VOID":3498},"2024373128",{"VI":1288},{"VOID":3501},"W2024373128",{"EN":3503,"VI":3504},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Fibronectin, a plasma protein immunologically identical with a major surface protein of normal fibroblasts, was found to bind to collagen and gelatin. A solid phase enzyme immunoassay was used for the binding tests. Collagen, gelatin or various control proteins were adsorbed to a plastic surface. Binding of fibronectin was detected using purified fibronectin antibodies conjugated to alkaline phosphatase. Circulating fibronectin and fibronectin obtained from fibroblast cultures both showed specific binding to collagen and gelatin. Preparative affinity chromatography of plasma on gelatin coupled to Sepharose gave electrophoretically and immunologically pure fibronectin in high yields. Malignantly transformed fibroblasts lack surface fibronectin. Our findings suggest the possibility that this results in a lack of anchorage to the surrounding intercellular matrix, which could contribute to the malignant growth behavior.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Fibronectin, một protein huyết tương có độ giống miễn dịch với một protein bề mặt chính của các nguyên bào sợi bình thường, đã được phát hiện có khả năng liên kết với collagen và gelatin. Một phương pháp miễn dịch enzyme pha rắn đã được sử dụng để tiến hành các thử nghiệm liên kết. Collagen, gelatin hoặc các protein kiểm soát khác được hấp phụ vào bề mặt nhựa. Sự liên kết của fibronectin được phát hiện bằng cách sử dụng kháng thể fibronectin tinh khiết được nối với phosphatase kiềm. Fibronectin lưu hành và fibronectin thu được từ các nuôi cấy nguyên bào sợi đều cho thấy sự liên kết đặc hiệu với collagen và gelatin. Chromatography phân tử affinity chuẩn bị từ huyết tương trên gelatin liên kết với Sepharose cung cấp fibronectin tinh khiết về mặt điện di và miễn dịch với sản lượng cao. Các nguyên bào sợi bị biến đổi ác tính thiếu fibronectin bề mặt. Các phát hiện của chúng tôi gợi ý rằng điều này có thể dẫn đến sự thiếu sót về neo giữ vào ma trận liên bào xung quanh, điều này có thể góp phần vào hành vi tăng trưởng ác tính.",{"EN":3506,"VI":3507},"Binding of soluble form of fibroblast surface protein, fibronectin, to collagen","Sự liên kết của dạng hòa tan của protein bề mặt nguyên bào sợi, fibronectin, với collagen",{"VOID":3509},"903179",{"VOID":3511},"10.1002\u002Fijc.2910200102",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fijc.2910200102",[3516,3535],{"id":3517,"sortIndex":32,"researcher":28,"roles":3518,"affiliations":3519,"properties":3528,"displayName":3532,"givenName":28,"familyName":28},"290a5c08-7a71-4b28-9ff2-8971538a60f4",[],[3520],{"id":3521,"sortIndex":32,"affiliation":3522,"properties":28},"6408cee2-e27c-42e4-8c34-4bc6d217020e",{"id":3521,"createTime":28,"updateTime":28,"relativeEntities":3523,"slug":28,"properties":3524,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3527,"statistic":28},[],{"title":3525},{"VI":3526},"Division of Immunology, City of Hope National Medical Center, Duarte, California 91010 USA",[],{"orcid":3529,"title":3531,"openalex":3533},{"VOID":3530},"https:\u002F\u002Forcid.org\u002F0000-0003-1375-7566",{"EN":3532},"Eva Engvall",{"VOID":3534},"A5012218478",{"id":3536,"sortIndex":40,"researcher":28,"roles":3537,"affiliations":3538,"properties":3545,"displayName":3549,"givenName":28,"familyName":28},"3a37be06-81be-4bd8-a40e-ffacfb5ab0d2",[],[3539],{"id":3521,"sortIndex":32,"affiliation":3540,"properties":28},{"id":3521,"createTime":28,"updateTime":28,"relativeEntities":3541,"slug":28,"properties":3542,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3544,"statistic":28},[],{"title":3543},{"VI":3526},[],{"orcid":3546,"title":3548,"openalex":3550},{"VOID":3547},"https:\u002F\u002Forcid.org\u002F0000-0003-2496-3445",{"EN":3549},"Erkki Ruoslahti",{"VOID":3551},"A5088477154",{"url":28,"publisher":3553,"properties":3595},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":3554,"slug":872,"properties":3555,"entityType":25,"verifyStatus":884,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":3560,"manageAffiliations":3569,"indexDatabases":3580,"url":943,"thumbnailPath":28,"statistic":28,"gsStatistic":28,"type":28,"analyzePriority":28},[],{"country":3556,"eissn":3557,"issn":3558,"title":3559},{"VOID":875},{"VOID":877},{"VOID":879},{"EN":881},[3561,3565],{"id":887,"createTime":28,"updateTime":28,"relativeEntities":3562,"label":3563,"description":3564,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":890},{},{"id":893,"createTime":28,"updateTime":28,"relativeEntities":3566,"label":3567,"description":3568,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":896},{},[3570,3575],{"id":900,"createTime":28,"updateTime":28,"relativeEntities":3571,"slug":28,"properties":3572,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3574,"statistic":28},[],{"title":3573},{"EN":904},[],{"id":907,"createTime":28,"updateTime":28,"relativeEntities":3576,"slug":28,"properties":3577,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3579,"statistic":28},[],{"title":3578},{"EN":911},[],[3581,3588],{"id":915,"indexDatabase":3582,"url":921,"indexYears":922,"academicFieldIds":3587,"indexDatabaseRanking":926},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":3583,"label":3584,"description":3585,"key":781,"publicationTags":3586,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],[924,925],{"id":928,"indexDatabase":3589,"url":940,"indexYears":28,"academicFieldIds":3594,"indexDatabaseRanking":28},{"id":930,"createTime":28,"updateTime":28,"relativeEntities":3590,"label":3591,"description":3592,"key":937,"publicationTags":3593,"standard":28},[],{"EN":933,"VI":933},{"EN":935,"VI":936},[939,813],[942],{"issue":3596,"pages":3597,"volume":3599},{"VOID":3052},{"VOID":3598},"1-5",{"VOID":3600},"20",1968,{"total":3601,"publishYear":3603,"statisticByYear":3604},1977,{"2012":47,"2013":122,"2014":49,"2015":126,"2016":145,"2017":48,"2018":48,"2019":48,"2020":48,"2021":49,"2022":45,"2023":45},"1977-07-15",[939,926],[3608,3611,3614,3617,3620,3623,3626,3629,3632,3635,3638,3641,3644,3647,3650,3654,3657,3660,3663,3666,3669,3672,3675,3678,3681],{"id":28,"text":3609,"url":28,"identifiers":3610},"10.1016\u002F0005-2795(71)90132-2",{"doi":3609},{"id":28,"text":3612,"url":28,"identifiers":3613},"Engvall E., 1975, Detection of human antibodies to Trichinella spiralis by enzyme‐linked immunosorbent assay, ELISA, Acta path. microbiol. scand. Sect. C, 83, 231",{},{"id":28,"text":3615,"url":28,"identifiers":3616},"Engvall E., 1972, Enzyme‐linked immunosorbent assay, ELISA. III. Quantitation of specific antibodies by enzyme‐labeled anti‐immunoglobulin in antigen coated tubes, J. Immunol., 109, 129",{},{"id":28,"text":3618,"url":28,"identifiers":3619},"10.1021\u002Fbi00789a030",{"doi":3618},{"id":28,"text":3621,"url":28,"identifiers":3622},"10.1073\u002Fpnas.70.12.3329",{"doi":3621},{"id":28,"text":3624,"url":28,"identifiers":3625},"10.1073\u002Fpnas.71.2.489",{"doi":3624},{"id":28,"text":3627,"url":28,"identifiers":3628},"10.1073\u002Fpnas.70.11.3170",{"doi":3627},{"id":28,"text":3630,"url":28,"identifiers":3631},"10.1016\u002F0092-8674(74)90114-7",{"doi":3630},{"id":28,"text":3633,"url":28,"identifiers":3634},"10.1016\u002F0006-291X(77)90359-X",{"doi":3633},{"id":28,"text":3636,"url":28,"identifiers":3637},"10.1002\u002Fijc.2910170215",{"doi":3636},{"id":28,"text":3639,"url":28,"identifiers":3640},"10.1038\u002F250248a0",{"doi":3639},{"id":28,"text":3642,"url":28,"identifiers":3643},"10.1084\u002Fjem.142.1.41",{"doi":3642},{"id":28,"text":3645,"url":28,"identifiers":3646},"10.1021\u002Fja01189a080",{"doi":3645},{"id":28,"text":3648,"url":28,"identifiers":3649},"10.1016\u002F0005-2795(75)90294-9",{"doi":3648},{"id":28,"text":3651,"url":28,"identifiers":3652},"Mosher D. F., 1975, Cross‐linking of cold‐insoluble globulin by fibrin‐stabilizing factor, J. biol. Chem., 250, 6614, 10.1016\u002FS0021-9258(19)41110-1",{"doi":3653},"10.1016\u002FS0021-9258(19)41110-1",{"id":28,"text":3655,"url":28,"identifiers":3656},"10.1016\u002F0005-2795(77)90056-3",{"doi":3655},{"id":28,"text":3658,"url":28,"identifiers":3659},"10.1038\u002F262497a0",{"doi":3658},{"id":28,"text":3661,"url":28,"identifiers":3662},"10.1038\u002F2151491a0",{"doi":3661},{"id":28,"text":3664,"url":28,"identifiers":3665},"10.1038\u002F248789a0",{"doi":3664},{"id":28,"text":3667,"url":28,"identifiers":3668},"10.1084\u002Fjem.141.2.497",{"doi":3667},{"id":28,"text":3670,"url":28,"identifiers":3671},"10.1016\u002F0005-2795(73)90310-3",{"doi":3670},{"id":28,"text":3673,"url":28,"identifiers":3674},"Stemberger A., 1976, Affinity chromatography on immobilized fibrinogen and fibrin monomer, II. Behavior of cold‐insoluble globulin, Hoppe‐Seyler's Z. Physiol. Chem., 357, 1003",{},{"id":28,"text":3676,"url":28,"identifiers":3677},"10.1002\u002Fijc.2910130502",{"doi":3676},{"id":28,"text":3679,"url":28,"identifiers":3680},"10.1084\u002Fjem.142.2.530",{"doi":3679},{"id":28,"text":3682,"url":28,"identifiers":3683},"10.1073\u002Fpnas.73.4.1217",{"doi":3682},{"id":3685,"createTime":3686,"updateTime":3687,"relativeEntities":3688,"slug":3689,"properties":3690,"entityType":971,"verifyStatus":26,"verifyTime":3686,"verifyNote":973,"languages":3706,"translateLanguages":3707,"viewCount":32,"primaryUrl":3708,"fullTextUrl":28,"authors":3709,"publicationType":1139,"publisherRelationship":3780,"citationCount":3829,"citationInfo":3830,"publishDate":3838,"publishYear":3831,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":3839,"openAccess":28,"references":3840,"isForceReanalyzing":1277},"0976aaa0-82be-4590-ba73-3637604be5cd","2024-11-25T07:10:01.750+00:00","2025-01-14T18:29:18.244+00:00",[],"Global-estimates-of-cancer-prevalence-for-27-sites-in-the-adult-population-in-2008",{"mag":3691,"keywords":3693,"openalex":3694,"abstract":3696,"title":3699,"pm":3702,"doi":3704},{"VOID":3692},"2089569798",{"VI":1288},{"VOID":3695},"W2089569798",{"EN":3697,"VI":3698},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Recent estimates of global cancer incidence and survival were used to update previous figures of limited duration prevalence to the year 2008. The number of patients with cancer diagnosed between 2004 and 2008 who were still alive at the end of 2008 in the adult population is described by world region, country and the human development index. The 5‐year global cancer prevalence is estimated to be 28.8 million in 2008. Close to half of the prevalence burden is in areas of very high human development that comprise only one‐sixth of the world's population. Breast cancer continues to be the most prevalent cancer in the vast majority of countries globally; cervix cancer is the most prevalent cancer in much of Sub‐Saharan Africa and Southern Asia and prostate cancer dominates in North America, Oceania and Northern and Western Europe. Stomach cancer is the most prevalent cancer in Eastern Asia (including China); oral cancer ranks as the most prevalent cancer in Indian men and Kaposi sarcoma has the highest 5‐year prevalence among men in 11 countries in Sub‐Saharan Africa. The methods used to estimate point prevalence appears to give reasonable results at the global level. The figures highlight the need for long‐term care targeted at managing patients with certain very frequently diagnosed cancer forms. To be of greater relevance to cancer planning, the estimation of other time‐based measures of global prevalence is warranted.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Các ước tính gần đây về tỉ lệ mắc bệnh ung thư và tỷ lệ sống sót toàn cầu đã được sử dụng để cập nhật các số liệu trước đây về tỉ lệ mắc bệnh trong thời gian giới hạn đến năm 2008. Số lượng bệnh nhân được chẩn đoán mắc bệnh ung thư trong khoảng thời gian từ 2004 đến 2008 vẫn còn sống vào cuối năm 2008 trong dân số trưởng thành được mô tả theo khu vực thế giới, quốc gia và chỉ số phát triển con người. Tỉ lệ mắc bệnh ung thư toàn cầu trong vòng 5 năm ước tính là 28,8 triệu vào năm 2008. Gần một nửa gánh nặng tỉ lệ mắc bệnh nằm ở các khu vực có chỉ số phát triển con người rất cao, chỉ chiếm một phần sáu dân số thế giới. Ung thư vú tiếp tục là loại ung thư phổ biến nhất ở phần lớn các quốc gia trên toàn cầu; ung thư cổ tử cung là loại ung thư phổ biến nhất ở nhiều khu vực của châu Phi cận Sahara và Nam Á, trong khi ung thư tuyến tiền liệt chiếm ưu thế ở Bắc Mỹ, châu Đại Dương và Bắc cũng như Tây Âu. Ung thư dạ dày là loại phổ biến nhất ở Đông Á (bao gồm cả Trung Quốc); ung thư miệng đứng đầu trong số các loại ung thư ở nam giới Ấn Độ và sarcoma Kaposi có tỷ lệ mắc bệnh 5 năm cao nhất ở nam giới tại 11 quốc gia ở châu Phi cận Sahara. Phương pháp ước tính tỷ lệ mắc bệnh theo thời điểm dường như cho kết quả hợp lý ở cấp độ toàn cầu. Các con số này nhấn mạnh nhu cầu chăm sóc lâu dài nhằm quản lý bệnh nhân mắc các loại ung thư thường xuyên được chẩn đoán. 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