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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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In a comprehensive treatise of pathogen population genetics, this review summarizes global knowledge of genetic diversity among isolates sampled at various spatial and temporal scales, examines the mechanisms that generate this diversity and explores the implications of pathogen diversity and plasticity to resistance breeding. Despite their different modes of reproduction, there is large variation among isolates of all three species originating from different countries and continents. With a few exceptions, haplotype diversity ranges from 60 to 100% even within populations from individual fields. In \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic>, over 90% of the variation is found within populations, even when samples are collected from areas as small as 0.25 m\u003Cjats:sup>2\u003C\u002Fjats:sup>. Variation among populations is low (4–8%) with negligible population subdivision. This indicates a high level of gene flow (\u003Cjats:italic>N\u003C\u002Fjats:italic>\u003Cjats:sub>m\u003C\u002Fjats:sub> = 8–71) with linkage equilibrium for the majority of selectively neutral molecular marker loci analysed. These findings for \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic> point to large random mating populations driven by occasional outcrossing, high gene flow across large geographical distances and a relatively low host‐mediated directional selection. Similar conclusions can be drawn for the Canadian population of \u003Cjats:italic>F. pseudograminearum\u003C\u002Fjats:italic>, but not for populations from Australia, where different pathogen ecology may have reduced the frequency of sexual recombination. Phylogenetic analyses indicate delineation of lineages in \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic>, often along geographically separated lines, while the related \u003Cjats:italic>F. pseudograminearum\u003C\u002Fjats:italic> is a single recombining species with limited or no lineage development. The anamorphic \u003Cjats:italic>F. culmorum\u003C\u002Fjats:italic> shows no obvious clonal structure in its population as might have been expected. High levels of diversity within fields may have been caused by balancing selection from frequent alternation between saprophytic and parasitical life cycle and\u002For a hidden or recently extinct teleomorph. Other mechanisms including parasexual cycles or active transposable elements may also be involved but these have not been investigated as yet. Crosses between and among \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic> lineages have shown a rather simple, additive inheritance of pathogenicity and aggressiveness with frequent transgressive segregation in crosses among isolates with moderate aggressiveness. This raises the spectre of highly aggressive and\u002For toxigenic isolates evolving if a limited range of quantitative trait locus for FHB resistance is deployed on a large scale. Combining more than one genetically distinct sources of resistance, possibly with different modes of action against the pathogen, will be necessary to avoid severe FHB outbreaks in the future.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Homothallic \u003Cjats:italic>Fusarium graminearum\u003C\u002Fjats:italic> (teleomorph \u003Cjats:italic>Gibberella zeae\u003C\u002Fjats:italic>) và anamorphic \u003Cjats:italic>F. culmorum\u003C\u002Fjats:italic> là những tác nhân gây hại phá hoại gây ra bệnh phấn đầu Fusarium (FHB) trên các loại ngũ cốc nhỏ trên toàn cầu, trong khi \u003Cjats:italic>F. pseudograminearum\u003C\u002Fjats:italic> (jats:italic>G. coronicola\u003C\u002Fjats:italic>) có lẽ chỉ giới hạn ở Australia như là một tác nhân gây bệnh FHB. Trong một bài tổng quan toàn diện về di truyền quần thể của các tác nhân gây bệnh, bài viết này tóm tắt kiến thức toàn cầu về sự đa dạng di truyền giữa các mẫu được lấy ở nhiều quy mô không gian và thời gian khác nhau, xem xét các cơ chế tạo ra sự đa dạng này và khám phá ý nghĩa của sự đa dạng và tính linh hoạt của các tác nhân gây bệnh đối với việc chọn giống kháng bệnh. Mặc dù có các cách sinh sản khác nhau, vẫn có sự khác biệt lớn giữa các mẫu của cả ba loài xuất phát từ các quốc gia và châu lục khác nhau. Với một số ngoại lệ, độ đa dạng haplotype dao động từ 60 đến 100% ngay cả trong các quần thể từ những cánh đồng riêng lẻ. Trong \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic>, hơn 90% sự biến đổi được tìm thấy trong các quần thể, ngay cả khi các mẫu được thu thập từ các khu vực nhỏ tới 0.25 m\u003Cjats:sup>2\u003C\u002Fjats:sup>. Sự biến đổi giữa các quần thể là thấp (4–8%) với sự phân loại quần thể không đáng kể. Điều này cho thấy một mức độ lưu thông gen cao (\u003Cjats:italic>N\u003C\u002Fjats:italic>\u003Cjats:sub>m\u003C\u002Fjats:sub> = 8–71) với trạng thái cân bằng liên kết cho phần lớn các loci đánh dấu phân tử trung lập đã phân tích. Những phát hiện này cho \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic> chỉ ra các quần thể giao phối ngẫu nhiên lớn được thúc đẩy bởi sự giao phối ngẫu nhiên, lưu thông gen cao qua các khoảng cách địa lý lớn và áp lực chọn lọc hướng vào chủ thể thấp tương đối. Những kết luận tương tự có thể được rút ra cho quần thể Canada của \u003Cjats:italic>F. pseudograminearum\u003C\u002Fjats:italic>, nhưng không cho các quần thể từ Australia, nơi sinh thái tác nhân gây bệnh khác nhau có thể đã giảm tần suất tái tổ hợp giới tính. Phân tích phả hệ cho thấy đường phân định các nhánh trong \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic>, thường theo các đường địa lý tách biệt, trong khi \u003Cjats:italic>F. pseudograminearum\u003C\u002Fjats:italic> là một loài tái tổ hợp duy nhất với sự phát triển nhánh hạn chế hoặc không có. Anamorphic \u003Cjats:italic>F. culmorum\u003C\u002Fjats:italic> không có cấu trúc vô tính rõ ràng trong quần thể như có thể đã được mong đợi. Mức độ đa dạng cao trong các cánh đồng có thể được gây ra bởi sự chọn lọc cân bằng từ việc thay đổi thường xuyên giữa chu kỳ sống saprophytic và ký sinh và\u002Fhoặc một teleomorph ẩn hoặc gần như tuyệt chủng gần đây. Các cơ chế khác bao gồm chu kỳ parasexual hoặc các yếu tố di chuyển chủ động cũng có thể liên quan nhưng chưa được điều tra. Các phép giao phối giữa và trong các nhánh \u003Cjats:italic>F. graminearum\u003C\u002Fjats:italic> đã cho thấy một di truyền khá đơn giản, bổ sung về độc lực và tính xâm lấn với sự phân tách vượt qua thường xuyên trong các phép giao phối giữa các mẫu có tính xâm lấn vừa phải. Điều này nâng cao mối lo ngại về khả năng các mẫu xâm lấn mạnh mẽ và\u002Fhoặc độc tố sẽ phát sinh nếu một phạm vi giới hạn của locus tính trạng định lượng cho kháng FHB được áp dụng trên quy mô lớn. Kết hợp hơn một nguồn kháng di truyền khác nhau, có thể với các cơ chế khác nhau chống lại tác nhân gây bệnh, là cần thiết để tránh những đợt bùng phát FHB nghiêm trọng trong tương lai.\u003C\u002Fjats:p>",{"EN":984,"VI":985},"Population Genetics of Three Important Head Blight Pathogens \u003Ci>Fusarium graminearum, F. pseudograminearum\u003C\u002Fi> and \u003Ci>F. culmorum\u003C\u002Fi>","Di truyền quần thể của ba tác nhân gây bệnh phấn đầu quan trọng \u003Ci>Fusarium graminearum, F. pseudograminearum\u003C\u002Fi> và \u003Ci>F. culmorum\u003C\u002Fi>",{"VI":987},"",{"VOID":989},"10.1111\u002Fj.1439-0434.2007.01394.x","PUBLICATION","Auto Verify",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1439-0434.2007.01394.x",[996,1015,1034],{"id":997,"sortIndex":32,"researcher":28,"roles":998,"affiliations":999,"properties":1008,"displayName":1012,"givenName":28,"familyName":28},"6b958128-71d8-4ac7-81b4-b79e80e595bf",[],[1000],{"id":1001,"sortIndex":32,"affiliation":1002,"properties":28},"49867333-3bad-427f-ae87-e3627d356d2d",{"id":1001,"createTime":28,"updateTime":28,"relativeEntities":1003,"slug":28,"properties":1004,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1007,"statistic":28},[],{"title":1005},{"EN":1006},"Authors’ addresses: University of Hohenheim, State Plant Breeding Institute, 70593 Stuttgart, Germany",[],{"orcid":1009,"title":1011,"openalex":1013},{"VOID":1010},"https:\u002F\u002Forcid.org\u002F0000-0002-9541-3726",{"EN":1012},"Thomas Miedaner",{"VOID":1014},"A5080862387",{"id":1016,"sortIndex":40,"researcher":28,"roles":1017,"affiliations":1018,"properties":1027,"displayName":1031,"givenName":28,"familyName":28},"3beb50a9-a8d8-4bb3-b317-15ffc51b1a17",[],[1019],{"id":1020,"sortIndex":32,"affiliation":1021,"properties":28},"53687454-0893-4da7-96fd-776ca6039f05",{"id":1020,"createTime":28,"updateTime":28,"relativeEntities":1022,"slug":28,"properties":1023,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1026,"statistic":28},[],{"title":1024},{"EN":1025},"Crop Protection Cluster, University of the Philippines, Los Baños College, Laguna 4031, Philippines.",[],{"orcid":1028,"title":1030,"openalex":1032},{"VOID":1029},"https:\u002F\u002Forcid.org\u002F0000-0002-5676-657X",{"EN":1031},"Christian Joseph R. 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U, 2006, Development of a Fusarium graminearum Affymetrix GeneChip for profiling fungal gene expression in vitro and in planta, Fungal Genet Biol, 10, 2006",{},{"id":28,"text":1257,"url":28,"identifiers":1258},"10.1111\u002Fj.0032-0862.2004.01061.x",{"doi":1257},{"id":28,"text":1260,"url":28,"identifiers":1261},"10.1093\u002Fgenetics\u002F160.4.1451",{"doi":1260},{"id":28,"text":1263,"url":28,"identifiers":1264},"Lee J, 2004, The alignment between physical and genetic maps of Gibberella zeae, Phytopathology, 94, 58",{},{"id":28,"text":1266,"url":28,"identifiers":1267},"Leonard KJ, 2003, Fusarium Head Blight of Wheat and 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Available at:http:\u002F\u002Fwww.msu.edu\u002F~trail\u002Findex1.htm(verified Aug 10 2006).",{},{"id":28,"text":1402,"url":28,"identifiers":1403},"10.1023\u002FA:1026086510156",{"doi":1402},{"id":28,"text":1405,"url":28,"identifiers":1406},"10.1094\u002FPDIS.2001.85.4.404",{"doi":1405},{"id":28,"text":1408,"url":28,"identifiers":1409},"10.1073\u002Fpnas.142307199",{"doi":1408},{"id":28,"text":1411,"url":28,"identifiers":1412},"10.1111\u002Fj.1469-1809.1949.tb02451.x",{"doi":1411},{"id":28,"text":1414,"url":28,"identifiers":1415},"10.1094\u002FPHYTO.2003.93.7.874",{"doi":1414},{"id":28,"text":1417,"url":28,"identifiers":1418},"10.1046\u002Fj.1365-294X.2004.02098.x",{"doi":1417},false,{"id":1421,"createTime":1422,"updateTime":1423,"relativeEntities":1424,"slug":1425,"properties":1426,"entityType":990,"verifyStatus":26,"verifyTime":1422,"verifyNote":991,"languages":1440,"translateLanguages":1441,"viewCount":32,"primaryUrl":1442,"fullTextUrl":28,"authors":1443,"publicationType":1053,"publisherRelationship":1514,"citationCount":324,"citationInfo":1577,"publishDate":1580,"publishYear":1578,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":1581,"openAccess":28,"references":1582,"isForceReanalyzing":1419},"5f98fdfd-5084-4359-af65-f8c197878447","2024-12-04T05:24:08.418+00:00","2025-01-19T20:48:34.358+00:00",[],"Gas-Exchange-and-Emission-of-Chlorophyll-Fluorescence-during-the-Monocycle-of-Rust-Angular-Leaf-Spot-and-Anthracnose-on-Bean-Leaves-as-a-Function-of-their-Trophic-Characteristics",{"openalex":1427,"mag":1429,"abstract":1431,"title":1434,"keywords":1437,"doi":1438},{"VOID":1428},"W2034758892",{"VOID":1430},"2034758892",{"EN":1432,"VI":1433},"\u003Cjats:p>Measurements related to gas exchange and chlorophyll fluorescence emission were taken from healthy and diseased bean leaves with rust, angular leaf spot, and anthracnose during lesion development for each disease. The experiments were performed at different temperatures of plant incubation, and using two bean cultivars. The main effect of temperature of plant incubation was in disease development. There was no significant difference between cultivars in relation to disease development and in magnitude of physiological alterations when disease severity was the same for each cultivar. These diseases reduced the net photosynthetic rate and increased the dark respiration of infected leaves after the appearance of visible symptoms and the differences between healthy and diseased leaves increased with disease development. The transpiration rate and stomatal conductance were stable during the monocycle of rust, however, these two variables decreased in leaves with angular leaf spot and anthracnose beginning with symptom appearance and continuing until lesion development was complete. Carboxylation resistance was probably the main factor related to reduction of photosynthetic rate of the apparently healthy area of leaves with rust and angular leaf spot. Reduction of the intercellular concentration of CO\u003Cjats:sub>2\u003C\u002Fjats:sub>, due to higher stomatal resistance, was probably the main factor for leaves with anthracnose. Chlorophyll fluorescence assessments suggested that there was no change in electron transport capacity and generation of ATP and NADPH in apparently healthy areas of diseased leaves, but decreases in chlorophyll fluorescence emission occurred on visibly lesioned areas for all diseases. Minimal fluorescence was remarkably reduced in leaves with angular leaf spot. Maximal fluorescence and optimal quantum yield of photosystem II of leaves were reduced for all three diseases. Bean rust, caused by a biotrophic pathogen, induced less damage to the regulation mechanisms of the physiological processes of the remaining green area of diseased leaves than did bean angular leaf spot or anthracnose, caused by hemibiotrophic pathogens. The magnitude of photosynthesis reduction can be related to the host–pathogen trophic relationships.\u003C\u002Fjats:p>","\u003Cjats:p>Các phép đo liên quan đến trao đổi khí và phát thải huỳnh quang diệp lục đã được thực hiện trên lá đậu khỏe mạnh và bị bệnh với các triệu chứng gỉ sét, đốm lá góc và thối đen trong suốt quá trình phát triển tổn thương của từng bệnh. Các thí nghiệm được thực hiện ở các nhiệt độ ủ cây khác nhau, sử dụng hai giống đậu khác nhau. Ảnh hưởng chính của nhiệt độ ủ cây là đối với sự phát triển của bệnh. Không có sự khác biệt đáng kể giữa các giống liên quan đến sự phát triển của bệnh và về độ lớn của các biến đổi sinh lý khi mức độ nghiêm trọng của bệnh giống nhau cho mỗi giống. Các bệnh này làm giảm tỷ lệ quang hợp ròng và tăng hô hấp tối của lá bị nhiễm sau khi xuất hiện triệu chứng rõ ràng và sự khác biệt giữa lá khỏe mạnh và lá bị bệnh gia tăng theo sự phát triển của bệnh. Tỷ lệ thoát hơi nước và độ dẫn khí khép kín ổn định trong suốt chu kỳ đơn của bệnh gỉ sét, tuy nhiên, hai biến này đã giảm ở lá có đốm lá góc và bệnh thối đen bắt đầu với sự xuất hiện triệu chứng và tiếp tục cho đến khi quá trình phát triển tổn thương hoàn tất. Khả năng chống lại quá trình carboxylation có thể là yếu tố chính liên quan đến sự giảm tỷ lệ quang hợp của vùng lá rõ ràng khỏe mạnh có gỉ sét và đốm lá góc. Sự giảm nồng độ CO\u003Cjats:sub>2\u003C\u002Fjats:sub> trong tế bào, do độ kháng khí khép kín cao hơn, có thể là yếu tố chính đối với lá có bệnh thối đen. Đánh giá huỳnh quang diệp lục gợi ý rằng không có sự thay đổi nào trong khả năng vận chuyển electron và sinh ATP và NADPH ở các vùng dường như khỏe mạnh của lá bị bệnh, nhưng sự giảm phát thải huỳnh quang diệp lục xảy ra ở các vùng tổn thương rõ ràng cho tất cả các bệnh. Huỳnh quang tối thiểu đã bị giảm đáng kể ở lá có đốm lá góc. Huỳnh quang tối đa và hiệu suất lượng tử tối ưu của hệ thống quang hợp II của lá bị giảm cho cả ba loại bệnh. Bệnh gỉ sét trên đậu, do một tác nhân sinh trưởng sinh học gây ra, đã gây ra thiệt hại ít hơn cho các cơ chế điều chỉnh của các quá trình sinh lý của vùng xanh còn lại của lá bị bệnh hơn là bệnh đốm lá góc hoặc bệnh thối đen, do các tác nhân sinh trưởng bán sinh lý gây ra. Độ lớn của sự giảm quang hợp có thể được liên kết với mối quan hệ dinh dưỡng giữa vật chủ và tác nhân gây bệnh.\u003C\u002Fjats:p>",{"EN":1435,"VI":1436},"Gas Exchange and Emission of Chlorophyll Fluorescence during the Monocycle of Rust, Angular Leaf Spot and Anthracnose on Bean Leaves as a Function of their Trophic Characteristics","Trao đổi khí và phát thải huỳnh quang diệp lục trong chu kỳ đơn của bệnh gỉ sét, đốm lá góc và bệnh thối đen trên lá đậu tương dưới tác động của đặc điểm dinh dưỡng của chúng",{"VI":987},{"VOID":1439},"10.1046\u002Fj.1439-0434.2002.00714.x",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1046\u002Fj.1439-0434.2002.00714.x",[1444,1463,1480,1497],{"id":1445,"sortIndex":32,"researcher":28,"roles":1446,"affiliations":1447,"properties":1456,"displayName":1460,"givenName":28,"familyName":28},"7a9b4ff8-6b8e-4593-b1ad-8fa5a623a8f3",[],[1448],{"id":1449,"sortIndex":32,"affiliation":1450,"properties":28},"46088742-7010-47a8-a357-909f2efde195",{"id":1449,"createTime":28,"updateTime":28,"relativeEntities":1451,"slug":28,"properties":1452,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1455,"statistic":28},[],{"title":1453},{"EN":1454},"Depto. de Entomologia, Fitopatologia e Zoologia Agrícola da Escola Superior de Agricultura `Luiz de Queiroz', Universidade de São Paulo, C. 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B., 2000, Análise das trocas gasosas em feijoeiro com ferrugem, mancha angular e antracnose, Fitopatologia Brasileira, 25, 643",{},{"id":28,"text":1587,"url":28,"identifiers":1588},"Bassanezi R. B., 2001, Eficiência fotossintética de folhas de feijoeiro infectadas com o vírus do mosaico‐em‐desenho, Uromyces appendiculatus e Phaeoisariopsis griseola, Summa Phytopathologica, 27, 5",{},{"id":28,"text":1590,"url":28,"identifiers":1591},"Bassanezi R. B., 1997, Efeito da antracnose na eficiência fotossintética do feijoeiro, Fitopatologia Brasileira, 22, 520",{},{"id":28,"text":1593,"url":28,"identifiers":1594},"10.1094\u002FPhyto-81-611",{"doi":1593},{"id":28,"text":1596,"url":28,"identifiers":1597},"10.1007\u002FBF01974664",{"doi":1596},{"id":28,"text":1599,"url":28,"identifiers":1600},"10.2134\u002Fagronj1980.00021962007200020001x",{"doi":1599},{"id":28,"text":1602,"url":28,"identifiers":1603},"Daly J. 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Blackwell Science Oxford UK.",{"doi":1638},"10.1046\u002Fj.1365-3059.1998.0223e.x",{"id":28,"text":1640,"url":28,"identifiers":1641},"10.1016\u002FS0048-4059(86)80003-0",{"doi":1640},{"id":28,"text":1643,"url":28,"identifiers":1644},"10.1094\u002FPhyto-80-677",{"doi":1643},{"id":28,"text":1646,"url":28,"identifiers":1647},"10.1046\u002Fj.0016-8025.2001.00737.x",{"doi":1646},{"id":28,"text":1649,"url":28,"identifiers":1650},"Moll S., 1995, In vivo chlorophyll fluorescence in rust‐infected bean plants, Angewandte Bot., 69, 163",{},{"id":28,"text":1652,"url":28,"identifiers":1653},"O'Connell R. S. B. Perfect R. Hughes J.Carzaniga J.Bailey(Green. (2000):Dissecting the cell biology ofColletotrichuminfection processes. In: Prusky D. S. Freeman M. B. Dickman (eds) Colletotrichum Host Specificity Pathology and Host–pathogen Interaction pp. 57–77. APS Press St. Paul MN.",{},{"id":28,"text":1655,"url":28,"identifiers":1656},"10.1016\u002FS0048-4059(81)80056-2",{"doi":1655},{"id":28,"text":1658,"url":28,"identifiers":1659},"10.1104\u002Fpp.108.1.163",{"doi":1658},{"id":28,"text":1661,"url":28,"identifiers":1662},"10.1016\u002F0048-4059(78)90080-2",{"doi":1661},{"id":28,"text":1664,"url":28,"identifiers":1665},"10.1016\u002FS0885-5765(88)80023-7",{"doi":1664},{"id":28,"text":1667,"url":28,"identifiers":1668},"10.1111\u002Fj.1439-0434.1998.tb04681.x",{"doi":1667},{"id":28,"text":1670,"url":28,"identifiers":1671},"10.1016\u002F0048-4059(85)90050-5",{"doi":1670},{"id":28,"text":1673,"url":28,"identifiers":1674},"Scholes J. D., 1995, How do biotrophic pathogens affect the photosynthetic metabolism of their hosts?, Aspects Appl. Biol., 42, 91",{},{"id":28,"text":1676,"url":28,"identifiers":1677},"10.1094\u002FPhyto-82-760",{"doi":1676},{"id":28,"text":1679,"url":28,"identifiers":1680},"Smedegaard‐Petersen V.(1984):The role of respiration and energy generation in diseased and disease‐resistant plants. In: Wood R. K. S. J. G. Jellis (eds) Plant Diseases: Infection Damage and Loss pp. 73–85. Blackwell Scientific Oxford UK.",{},{"id":28,"text":1682,"url":28,"identifiers":1683},"Stangarlin J. R., 2000, Atividades de ribulose‐1,5‐bifosfato carboxilase‐oxigenase (rubisco), clorofilase, β‐1,3‐glucanase e quitinase e conteúdo de clorofila em cultivares de feijoeiro (Phaseolus vulgaris) infectados com Uromyces appendiculatus, Summa Phytopathologica, 26, 34",{},{"id":28,"text":1685,"url":28,"identifiers":1686},"Stangarlin J. R., 2000, Efeito de Phaeoisariopsis griseola na atividade de ribulose‐1,5‐bifosfato carboxilase‐oxigenase, clorofilase, β‐1,3‐glucanase e quitinase em cultivares de Phaseolus vulgaris, Fitopatologia Brasileira, 25, 59",{},{"id":28,"text":1688,"url":28,"identifiers":1689},"10.1094\u002FPhyto-74-77",{"doi":1688},{"id":28,"text":1691,"url":28,"identifiers":1692},"10.1111\u002Fj.1439-0434.1995.tb00214.x",{"doi":1691},{"id":28,"text":1694,"url":28,"identifiers":1695},"10.1016\u002F0885-5765(89)90067-2",{"doi":1694},{"id":28,"text":1697,"url":28,"identifiers":1698},"Wong P. Y. O., 1978, Effect of Colletotrichum lindemuthianum on photosynthesis and respiration of Vigna sesquipedalis, J. Plant Path., 92, 88",{},{"id":28,"text":1700,"url":28,"identifiers":1701},"Wong P. Y. O., 1978, Sugar metabolism and translocation in Vigna sesquipedalis infected by Colletotrichum lindemuthianum, J. Plant Path., 92, 102",{},{"id":28,"text":1703,"url":28,"identifiers":1704},"10.1006\u002Fpmpp.1995.1056",{"doi":1703},{"id":28,"text":1706,"url":28,"identifiers":1707},"Zaki A. I., 1965, The effect of bean rust on the translocation of photosynthetic products from diseased leaves, Phytopathology, 55, 528",{},{"id":1709,"createTime":1710,"updateTime":1711,"relativeEntities":1712,"slug":1713,"properties":1714,"entityType":990,"verifyStatus":26,"verifyTime":1710,"verifyNote":991,"languages":1728,"translateLanguages":1729,"viewCount":32,"primaryUrl":1730,"fullTextUrl":28,"authors":1731,"publicationType":1053,"publisherRelationship":1749,"citationCount":566,"citationInfo":1811,"publishDate":1814,"publishYear":1812,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":1815,"openAccess":28,"references":1816,"isForceReanalyzing":1419},"96461102-9ece-4893-af15-65089e4e4695","2024-09-24T21:13:54.075+00:00","2025-02-17T16:01:13.036+00:00",[],"The-Susceptibility-of-Monocotyledons-to-Agrobacterium-tumefaciens",{"openalex":1715,"mag":1717,"abstract":1719,"title":1722,"keywords":1725,"doi":1726},{"VOID":1716},"W2168012681",{"VOID":1718},"2168012681",{"EN":1720,"VI":1721},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The susceptibility of 257 monocotyledon species belonging to 139 genera and 27 families, has been tested and the literature on this subject reviewed. In contrast with dicotyledons and gymnosperms, monocotyledons are much less susceptible to \u003Cjats:italic>Agrobacterium tumefaciens\u003C\u002Fjats:italic>: only 3 % of the species of monocotyledons tested were host plants, whereas 60 % of the dicotyledons and gymnosperms were susceptible. Only the closely related monocotyledon orders \u003Cjats:italic>Liliales\u003C\u002Fjats:italic> (6 families) and Arales (1 family) contained species that were susceptible. These results are consistent with a proposed taxonomic relationship between the Liliales and the dicotyledons. A correlation between host biochemical capabilities and susceptibility to crown gall is suggested.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Độ nhạy cảm của 257 loài một lá mầm thuộc 139 chi và 27 họ đã được thử nghiệm và tài liệu về chủ đề này đã được xem xét. So với các loài hai lá mầm và thực vật hạt trần, các loài một lá mầm có độ nhạy cảm thấp hơn nhiều đối với \u003Cjats:italic>Agrobacterium tumefaciens\u003C\u002Fjats:italic>: chỉ có 3% các loài một lá mầm được thử nghiệm là cây ký chủ, trong khi đó 60% các loài hai lá mầm và thực vật hạt trần có độ nhạy cảm cao. Chỉ có các ngành một lá mầm có mối quan hệ gần gũi là \u003Cjats:italic>Liliales\u003C\u002Fjats:italic> (6 họ) và Arales (1 họ) chứa các loài nhạy cảm. Những kết quả này nhất quán với mối quan hệ hệ thống học được đề xuất giữa các loài \u003Cjats:italic>Liliales\u003C\u002Fjats:italic> và các loài hai lá mầm. Một mối tương quan giữa khả năng sinh hóa của cây ký chủ và độ nhạy cảm với khối u vương miện được gợi ý.\u003C\u002Fjats:p>",{"EN":1723,"VI":1724},"The Susceptibility of Monocotyledons to Agrobacterium tumefaciens","Độ nhạy cảm của các loài một lá mầm đối với Agrobacterium tumefaciens",{"VI":987},{"VOID":1727},"10.1111\u002Fj.1439-0434.1985.tb00829.x",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1439-0434.1985.tb00829.x",[1732],{"id":1733,"sortIndex":32,"researcher":28,"roles":1734,"affiliations":1735,"properties":1744,"displayName":1746,"givenName":28,"familyName":28},"3d126e94-70e1-4c1a-9f19-1b63a6d44f42",[],[1736],{"id":1737,"sortIndex":32,"affiliation":1738,"properties":28},"c8ec1613-5623-4966-b89a-b4a9a8d6255c",{"id":1737,"createTime":28,"updateTime":28,"relativeEntities":1739,"slug":28,"properties":1740,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1743,"statistic":28},[],{"title":1741},{"EN":1742},"Laboratorium voor Microbiologie en microbiële Genetica, Laboratorium voor Plantenfysiologie, Rijksuniversiteit te Gent, België",[],{"title":1745,"openalex":1747},{"EN":1746},"Marcel De Cleene",{"VOID":1748},"A5019146226",{"url":28,"publisher":1750,"properties":1805},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":1751,"slug":872,"properties":1752,"entityType":25,"verifyStatus":884,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":1757,"manageAffiliations":1774,"indexDatabases":1785,"url":957,"thumbnailPath":28,"statistic":1800,"gsStatistic":28,"type":28,"analyzePriority":28},[],{"country":1753,"eissn":1754,"issn":1755,"title":1756},{"VOID":875},{"VOID":877},{"VOID":879},{"EN":881},[1758,1762,1766,1770],{"id":887,"createTime":28,"updateTime":28,"relativeEntities":1759,"label":1760,"description":1761,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":890},{},{"id":893,"createTime":28,"updateTime":28,"relativeEntities":1763,"label":1764,"description":1765,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":896},{},{"id":899,"createTime":28,"updateTime":28,"relativeEntities":1767,"label":1768,"description":1769,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":902},{},{"id":905,"createTime":28,"updateTime":28,"relativeEntities":1771,"label":1772,"description":1773,"parentId":28,"standard":28,"scholarHubFieldId":28},[],{"EN":908},{},[1775,1780],{"id":912,"createTime":28,"updateTime":28,"relativeEntities":1776,"slug":28,"properties":1777,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1779,"statistic":28},[],{"title":1778},{"EN":916},[],{"id":919,"createTime":28,"updateTime":28,"relativeEntities":1781,"slug":28,"properties":1782,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1784,"statistic":28},[],{"title":1783},{"EN":923},[],[1786,1793],{"id":927,"indexDatabase":1787,"url":933,"indexYears":934,"academicFieldIds":1792,"indexDatabaseRanking":940},{"id":792,"createTime":28,"updateTime":28,"relativeEntities":1788,"label":1789,"description":1790,"key":798,"publicationTags":1791,"standard":28},[],{"EN":795,"VI":795},{"EN":795,"VI":797},[800],[936,937,938,939],{"id":942,"indexDatabase":1794,"url":954,"indexYears":28,"academicFieldIds":1799,"indexDatabaseRanking":28},{"id":944,"createTime":28,"updateTime":28,"relativeEntities":1795,"label":1796,"description":1797,"key":951,"publicationTags":1798,"standard":28},[],{"EN":947,"VI":947},{"EN":949,"VI":950},[953,785],[956],{"impactFactor":32,"impactFactorByYear":1801,"i10Index":126,"i10IndexLast5Year":32,"totalPublication":51,"totalPublicationByYear":1802,"totalCitation":961,"totalCitationByYear":1803,"totalCitationPerPublication":963,"totalCitationPerPublicationByYear":1804,"hindexLast5Year":47,"hindex":47},{},{"1964":40,"1966":40,"1968":40,"1979":40,"1980":40,"1982":40,"1984":40,"1985":40,"1986":40,"1995":40,"1999":40,"2000":40,"2003":40,"2008":123},{"1964":357,"1966":567,"1968":516,"1979":205,"1980":126,"1982":140,"1984":48,"1985":566,"1986":42,"1995":436,"1999":134,"2000":611,"2003":688,"2008":835},{"1964":357,"1966":567,"1968":516,"1979":205,"1980":126,"1982":140,"1984":48,"1985":566,"1986":42,"1995":436,"1999":134,"2000":611,"2003":688,"2008":611},{"issue":1806,"pages":1807,"volume":1809},{"VOID":1572},{"VOID":1808},"81-89",{"VOID":1810},"113",{"total":566,"publishYear":1812,"statisticByYear":1813},1985,{"2012":42,"2013":123,"2015":45,"2016":42,"2019":40,"2020":123,"2021":42},"1985-05-01",[940,953],[1817,1820,1823,1826,1829,1832,1835,1838,1841,1844,1847,1850,1853,1856,1859,1862,1865,1868,1871,1874,1877,1880,1883,1886,1889,1892,1895,1898,1901,1904,1907,1910,1913,1916,1919,1922,1925,1928,1931],{"id":28,"text":1818,"url":28,"identifiers":1819},"Amormino G., 1927, Richerche sull'azione del Bacterium tumefaciens negli animali, Boll. D. Soc. di Biol. Sper., 2",{},{"id":28,"text":1821,"url":28,"identifiers":1822},"Anonymous, 1976, The Staff of the University of the Liberty Hyde Bailey Hortorium",{},{"id":28,"text":1824,"url":28,"identifiers":1825},"Braun A. C., 1958, Morphology and physiology of plant tumors. Protoplasmatologia X, Pathologie des protoplasmas, 5, 1",{},{"id":28,"text":1827,"url":28,"identifiers":1828},"Brown N. A., 1937, Crown gall of the fasciated type on Asparagus sprengeri, Plant Disease Reporter, 21, 31",{},{"id":28,"text":1830,"url":28,"identifiers":1831},"10.1038\u002F2141029a0",{"doi":1830},{"id":28,"text":1833,"url":28,"identifiers":1834},"Chamberlain C. J., 1935, Methods in plant histology",{},{"id":28,"text":1836,"url":28,"identifiers":1837},"10.1139\u002Fcjr50c-015",{"doi":1836},{"id":28,"text":1839,"url":28,"identifiers":1840},"DeCleene M. 1975:Bijdragen tot de waardplanten de inductie en de karyologie van crown gall.Doctoral thesis Rijksuniversiteit Gent (Belgium).",{},{"id":28,"text":1842,"url":28,"identifiers":1843},"Cleene M., 1973, Het voorkomen van Agrobacterium kanker (crown gall) bij economisch belangrijke plantegeslachten, De Belg. Tuinbouw, 54, 196",{},{"id":28,"text":1845,"url":28,"identifiers":1846},"10.1007\u002FBF02860827",{"doi":1845},{"id":28,"text":1848,"url":28,"identifiers":1849},"10.1007\u002FBF02868853",{"doi":1848},{"id":28,"text":1851,"url":28,"identifiers":1852},"Ley J., 1972, Proc. 3rd Int. Conf. Pl. Path. Bacteria, 251",{},{"id":28,"text":1854,"url":28,"identifiers":1855},"Elliott C., 1930, Manual of bacterial plant pathogens",{},{"id":28,"text":1857,"url":28,"identifiers":1858},"Englfr A., 1964, H. Melchior und E. Werdermann",{},{"id":28,"text":1860,"url":28,"identifiers":1861},"Gadgil V. N., 1961, Studies on crown gall tumour. I Host susceptibility of the causal organism, Agrobacterium tumefaciens, strain B‐23, Trans. Bose Res. Inst., 24, 141",{},{"id":28,"text":1863,"url":28,"identifiers":1864},"Gal L, 1963, Über die Wirkung von Monokotyledonen‐Extrakten auf Agrobacterium tumefaciens, Zentralbl. Bakt., 116, 246",{},{"id":28,"text":1866,"url":28,"identifiers":1867},"10.1007\u002FBF01185602",{"doi":1866},{"id":28,"text":1869,"url":28,"identifiers":1870},"10.1002\u002Fj.1460-2075.1984.tb02254.x",{"doi":1869},{"id":28,"text":1872,"url":28,"identifiers":1873},"Hoerner G. R., 1945, Crown gall of hops, Plant Disease Reporter, 29, 98",{},{"id":28,"text":1875,"url":28,"identifiers":1876},"INDEX KEWENSIS",{},{"id":28,"text":1878,"url":28,"identifiers":1879},"Jakowsra S., 1949, Effects of Bacterium tumefaciens on Allium cepa, Phytopathology, 39, 683",{},{"id":28,"text":1881,"url":28,"identifiers":1882},"Johansen D. A., 1940, Plant microtechniques",{},{"id":28,"text":1884,"url":28,"identifiers":1885},"10.1086\u002F400904",{"doi":1884},{"id":28,"text":1887,"url":28,"identifiers":1888},"Kupila S., 1963, Crown gall as an anatomical and cytological problem, a review. Cancer Res., 23, 497",{},{"id":28,"text":1890,"url":28,"identifiers":1891},"10.1016\u002FB978-1-4831-9954-2.50006-9",{"doi":1890},{"id":28,"text":1893,"url":28,"identifiers":1894},"Lopatin M. I., 1936, The susceptibility of plants to Bacterium tumefaciens, the causative agent of the root‐cancer of plants, Mikrobiologia (Moskwa, 5, 716",{},{"id":28,"text":1896,"url":28,"identifiers":1897},"McLean R. C., 1962, Textbook of theoretical Botany",{},{"id":28,"text":1899,"url":28,"identifiers":1900},"Montemartini L., 1938, II. Bacterium tumefaciens, Boll. Ist. Sieroter. Milanese, 17, 551",{},{"id":28,"text":1902,"url":28,"identifiers":1903},"10.2307\u002F2437836",{"doi":1902},{"id":28,"text":1905,"url":28,"identifiers":1906},"10.1038\u002Fnbt0483-175",{"doi":1905},{"id":28,"text":1908,"url":28,"identifiers":1909},"Smith E. F., 1911, Crown gall of plants: its cause and remedy. U.S. Dept. Agric., Bur, Plant Industr. Bull., 213, 13",{},{"id":28,"text":1911,"url":28,"identifiers":1912},"Smith E. F., 1926, A Begonia immune to crown gall: with observations on other immune or semi‐immune plants, Phytopathology, 16, 491",{},{"id":28,"text":1914,"url":28,"identifiers":1915},"Stapp C., 1938, Der Pflanzenkrebs und sein Erreger Pseudomonas tumefaciens. VI. Asparagus sprengeri Rgl. und Phaseolus vulgaris L. als Wirtspflanzen, Zentralbl. Bakt., Abt, 116",{},{"id":28,"text":1917,"url":28,"identifiers":1918},"Strauss J., 1954, Maize endosperm tissue grown in vitro, Amer. J. Bot., 41, 487",{},{"id":28,"text":1920,"url":28,"identifiers":1921},"Takhtajan A., 1969, Origin and dispersal",{},{"id":28,"text":1923,"url":28,"identifiers":1924},"10.1007\u002FBF02861558",{"doi":1923},{"id":28,"text":1926,"url":28,"identifiers":1927},"10.2307\u002F2440606",{"doi":1926},{"id":28,"text":1929,"url":28,"identifiers":1930},"10.1038\u002F2121472a0",{"doi":1929},{"id":28,"text":1932,"url":28,"identifiers":1933},"Zander R., 1979, Handwörterbuch der Pflanzennamen",{},{"id":1935,"createTime":1936,"updateTime":1937,"relativeEntities":1938,"slug":1939,"properties":1940,"entityType":990,"verifyStatus":26,"verifyTime":1936,"verifyNote":991,"languages":1954,"translateLanguages":1955,"viewCount":32,"primaryUrl":1956,"fullTextUrl":28,"authors":1957,"publicationType":1053,"publisherRelationship":2105,"citationCount":611,"citationInfo":2168,"publishDate":2171,"publishYear":2169,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":2172,"openAccess":28,"references":2173,"isForceReanalyzing":1419},"cf4d4b74-9021-4b4b-8dd8-7479f02e4492","2024-10-02T05:28:36.233+00:00","2025-02-17T16:02:11.109+00:00",[],"Antifungal-Activity-of-a-Bowman-Birk-type-Trypsin-Inhibitor-from-Wheat-Kernel",{"openalex":1941,"mag":1943,"abstract":1945,"title":1948,"keywords":1951,"doi":1952},{"VOID":1942},"W2092726102",{"VOID":1944},"2092726102",{"EN":1946,"VI":1947},"\u003Cjats:p>A trypsin inhibitor from wheat kernel (WTI) was found to have a strong antifungal activity against a number of pathogenic fungi and to inhibit fungal trypsin‐like activity. WTI inhibited \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> spore germination and hyphal growth of pathogens, with protein concentration required for 50% growth inhibition (IC\u003Cjats:sub>50\u003C\u002Fjats:sub>) values ranging from 111.7 to above 500 μg\u002Fml. As observed by electron microscopy, WTI determined morphological alterations represented by hyphal growth inhibition and branching. One of the fungal species tested, \u003Cjats:italic>Botrytis cinerea\u003C\u002Fjats:italic> produced a trypsin‐like protease, which was inhibited by the trypsin inhibitor. WTI, as well as other seed defence proteins, appear to be an important resistance factor in wheat kernels during rest and early germination when plants are particularly exposed to attack by potential soil‐borne pathogens.\u003C\u002Fjats:p>","\u003Cjats:p>Chất ức chế trypsin từ hạt lúa mạch (WTI) được phát hiện có hoạt tính chống nấm mạnh đối với một số loại nấm gây bệnh và ức chế hoạt động men trypsin‐giống của nấm. WTI ức chế \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> sự nảy mầm bào tử và sự phát triển sợi của các mầm bệnh, với nồng độ protein cần thiết để ức chế 50% sự phát triển (IC\u003Cjats:sub>50\u003C\u002Fjats:sub>) dao động từ 111,7 đến trên 500 μg\u002Fml. Như được quan sát bởi kính hiển vi điện tử, WTI đã tạo ra các thay đổi hình thái thể hiện bằng sự ức chế phát triển sợi và nhánh. Một trong các loài nấm được thử nghiệm, \u003Cjats:italic>Botrytis cinerea\u003C\u002Fjats:italic>, đã sản xuất một protease giống như trypsin, và đã bị ức chế bởi chất ức chế trypsin. WTI, cũng như các protein phòng thủ hạt khác, có vẻ là một yếu tố kháng quan trọng trong các hạt lúa mạch trong thời kỳ nghỉ và nảy mầm sớm khi thực vật đặc biệt dễ bị tấn công bởi các mầm bệnh tiềm tàng từ đất.\u003C\u002Fjats:p>",{"EN":1949,"VI":1950},"Antifungal Activity of a Bowman–Birk‐type Trypsin Inhibitor from Wheat Kernel","Hoạt Động Chống Nấm Của Một Chất Ức Chế Trypsin Kiểu Bowman–Birk Từ Hạt Lúa Mạch",{"VI":987},{"VOID":1953},"10.1046\u002Fj.1439-0434.2000.00527.x",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1046\u002Fj.1439-0434.2000.00527.x",[1958,1977,1994,2011,2028,2045,2060,2075,2090],{"id":1959,"sortIndex":32,"researcher":28,"roles":1960,"affiliations":1961,"properties":1970,"displayName":1974,"givenName":28,"familyName":28},"6d4630f4-8366-4b28-ab22-cf60bbc2af4f",[],[1962],{"id":1963,"sortIndex":32,"affiliation":1964,"properties":28},"f0a7fb4e-339b-4dc4-be0b-e06bcee66661",{"id":1963,"createTime":28,"updateTime":28,"relativeEntities":1965,"slug":28,"properties":1966,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1969,"statistic":28},[],{"title":1967},{"EN":1968},"Authors' addresses: )",[],{"orcid":1971,"title":1973,"openalex":1975},{"VOID":1972},"https:\u002F\u002Forcid.org\u002F0000-0002-8525-9980",{"EN":1974},"G. 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J.B. E., 1993, Chitin Enzymology, 15",{},{"id":28,"text":2178,"url":28,"identifiers":2179},"10.1146\u002Fannurev.bi.59.070190.004301",{"doi":2178},{"id":28,"text":2181,"url":28,"identifiers":2182},"10.1111\u002Fj.1439-0434.1983.tb00049.x",{"doi":2181},{"id":28,"text":2184,"url":28,"identifiers":2185},"10.1007\u002FBF01886809",{"doi":2184},{"id":28,"text":2187,"url":28,"identifiers":2188},"10.1016\u002FS0168-9452(98)00199-X",{"doi":2187},{"id":28,"text":2190,"url":28,"identifiers":2191},"10.1094\u002FPHYTO.1998.88.4.276",{"doi":2190},{"id":28,"text":2193,"url":28,"identifiers":2194},"10.1139\u002Fm97-031",{"doi":2193},{"id":28,"text":2196,"url":28,"identifiers":2197},"10.1016\u002F0014-5793(93)81451-5",{"doi":2196},{"id":28,"text":2199,"url":28,"identifiers":2200},"10.1094\u002FPhyto-72-151",{"doi":2199},{"id":28,"text":2202,"url":28,"identifiers":2203},"Garcia‐Olmedo F., 1987, Plant proteinaceous inhibitors of proteinases and α‐amylases, Oxf. Surv. Plant Mol. 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V., 1976, The biological significance of proteinase inhibitors in plants, Plant Sci. Lett., 7, 77, 10.1016\u002F0304-4211(76)90074-2",{"doi":2228},"10.1016\u002F0304-4211(76)90074-2",{"id":28,"text":2230,"url":28,"identifiers":2231},"10.1094\u002FMPMI-4-284",{"doi":2230},{"id":28,"text":2233,"url":28,"identifiers":2234},"Peng J. H., 1976, Increased proteinase inhibitor activity in response to infection of resistant tomato plants by Phytophthora infestans, Phytopathology, 66, 958",{},{"id":28,"text":2236,"url":28,"identifiers":2237},"Plunkett G., 1981, Proteinase inhibitors I and II from leaves of wounded tomato plants: purification and properties, Arch. Biochem. Biophys., 213, 463, 10.1016\u002F0003-9861(82)90572-0",{"doi":2238},"10.1016\u002F0003-9861(82)90572-0",{"id":28,"text":2240,"url":28,"identifiers":2241},"10.1007\u002FBF01891977",{"doi":2240},{"id":28,"text":2243,"url":28,"identifiers":2244},"10.1016\u002FS0031-9422(00)97736-7",{"doi":2243},{"id":28,"text":2246,"url":28,"identifiers":2247},"10.1104\u002Fpp.90.3.1065",{"doi":2246},{"id":28,"text":2249,"url":28,"identifiers":2250},"10.1016\u002F0885-5765(87)90024-5",{"doi":2249},{"id":28,"text":2252,"url":28,"identifiers":2253},"Ryan C. A., 1990, Protease inhibitors in plants: genes for improving defences against insects and pathogens, Ann. Rev. Phytopathol., 28, 425, 10.1146\u002Fannurev.py.28.090190.002233",{"doi":2254},"10.1146\u002Fannurev.py.28.090190.002233",{"id":28,"text":2256,"url":28,"identifiers":2257},"Senser F., 1974, Suggestion of a protective function of proteinase inhibitors in potatoes: inhibition of proteolytic activity of micro‐organisms isolated from spoiled potato tubers, Z. Lebensm. Unters.-Forsch., 155, 100, 10.1007\u002FBF01460342",{"doi":2258},"10.1007\u002FBF01460342",{"id":28,"text":2260,"url":28,"identifiers":2261},"10.1104\u002Fpp.103.4.1311",{"doi":2260},{"id":28,"text":2263,"url":28,"identifiers":2264},"10.1007\u002FBF00197797",{"doi":2263},{"id":2266,"createTime":2267,"updateTime":2268,"relativeEntities":2269,"slug":2270,"properties":2271,"entityType":990,"verifyStatus":26,"verifyTime":2267,"verifyNote":991,"languages":2285,"translateLanguages":2286,"viewCount":32,"primaryUrl":2287,"fullTextUrl":28,"authors":2288,"publicationType":1053,"publisherRelationship":2342,"citationCount":159,"citationInfo":2405,"publishDate":2408,"publishYear":2406,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":2409,"openAccess":28,"references":2410,"isForceReanalyzing":1419},"02b05ff9-bbc9-4f9d-9773-c893bbb303a6","2024-10-11T00:04:47.249+00:00","2025-01-19T20:50:30.746+00:00",[],"Resistance-to-Pyrimethanil-and-other-Fungicides-in-i-Botrytis-cinerea-i-Populations-Collected-on-Vegetable-Crops-in-Spain",{"openalex":2272,"mag":2274,"abstract":2276,"title":2279,"keywords":2282,"doi":2283},{"VOID":2273},"W2054162127",{"VOID":2275},"2054162127",{"EN":2277,"VI":2278},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Forty‐seven greenhouses of vegetable crops were surveyed in south‐eastern Spain at the beginning of the epidemic (January 2000) to compare sensitivity of \u003Cjats:italic>Botrytis cinerea\u003C\u002Fjats:italic> populations to pyrimethanil (an anilinopyrimidine fungicide) after 4 years of treatment with an unexposed population from a 1992 collection. A standard method to test the sensitivity of \u003Cjats:italic>B. cinerea\u003C\u002Fjats:italic> to pyrimethanil in a defined minimal medium (1.75 g\u002Fl of KH\u003Cjats:sub>2\u003C\u002Fjats:sub>PO\u003Cjats:sub>4\u003C\u002Fjats:sub>, 0.75 g\u002Fl of MgSO\u003Cjats:sub>4\u003C\u002Fjats:sub>, 4 g\u002Fl of glucose and 4 g\u002Fl of gelatine) was used to establish frequency distributions of pyrimethanil sensitivity in both populations. Two different distributions for sensitive and resistant isolates were obtained. ED\u003Cjats:sub>50\u003C\u002Fjats:sub> of sensitive isolates in 1992 ranged from 0.05 to 0.5 mg a.i.\u002Fl (mean ± SE, 0.23 ± 0.02), and 0.04–0.4 mg a.i.\u002Fl in 2000 (0.11 ± 0.01). ED\u003Cjats:sub>50\u003C\u002Fjats:sub> for resistant isolates ranged from 1 to 10 mg a.i.\u002Fl in both surveys (5 ± 2.64 and 4.25 ± 2.14, in 1992 and 2000, respectively). No resistance build‐up to pyrimethanil was developed in \u003Cjats:italic>B. cinerea\u003C\u002Fjats:italic> populations after exposition of 4 years to the fungicide. An \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> monitoring procedure was developed based on testing on one single discriminatory dose of pyrimethanil (established at 0.7 mg a.i.\u002Fl). Isolates resistant to pyrimethanil in the \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> assay caused visible lesions on cucumber leaf discs treated with the fungicide. No significant differences in fitness (growth or sporulation) between resistant and sensitive isolates were obtained. The 307 isolates collected in January 2000 were tested \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> using discriminatory doses to estimate the frequencies of resistance of \u003Cjats:italic>B. cinerea\u003C\u002Fjats:italic> to benzimidazoles (carbendazim), dicarboximides (procymidone), \u003Cjats:italic>N\u003C\u002Fjats:italic>‐phenylcarbamates (diethofencarb), and anilinopyrimidines (pyrimethanil). Of the 307 isolates collected, 90% were resistant to benzimidazoles, 77% to dicarboximides, 23% to \u003Cjats:italic>N\u003C\u002Fjats:italic>‐phenylcarbamates and 12% to anilinopyrimidines (in this case of 165 isolates). Dicarboximide and benzimidazole cross‐resistant isolates were found in each of the surveyed greenhouses and accounted for 65.8%. Fourteen percentage of the population were resistant to dicarboximides, benzimidazoles and \u003Cjats:italic>N\u003C\u002Fjats:italic>‐phenylcarbamates, and 3% were also resistant to anilinopyrimidines.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Một cuộc khảo sát đã được thực hiện trên 47 nhà kính trồng cây rau ở miền đông nam Tây Ban Nha vào đầu dịch bệnh (tháng 1 năm 2000) để so sánh độ nhạy cảm của các quần thể \u003Cjats:italic>Botrytis cinerea\u003C\u002Fjats:italic> đối với pyrimethanil (một loại thuốc trừ nấm anilinopyrimidine) sau 4 năm điều trị với một quần thể chưa tiếp xúc từ bộ sưu tập năm 1992. Một phương pháp chuẩn để kiểm tra độ nhạy cảm của \u003Cjats:italic>B. cinerea\u003C\u002Fjats:italic> đối với pyrimethanil trong một môi trường tối thiểu xác định (1.75 g\u002Fl KH\u003Cjats:sub>2\u003C\u002Fjats:sub>PO\u003Cjats:sub>4\u003C\u002Fjats:sub>, 0.75 g\u002Fl MgSO\u003Cjats:sub>4\u003C\u002Fjats:sub>, 4 g\u002Fl glucose và 4 g\u002Fl gelatin) đã được sử dụng để thiết lập các phân phối tần suất về độ nhạy cảm với pyrimethanil ở cả hai quần thể. Hai phân phối khác nhau cho các biến thể nhạy cảm và kháng đã được thu nhận. ED\u003Cjats:sub>50\u003C\u002Fjats:sub> của các biến thể nhạy cảm vào năm 1992 nằm trong khoảng từ 0.05 đến 0.5 mg a.i.\u002Fl (trung bình ± SE, 0.23 ± 0.02), và từ 0.04 đến 0.4 mg a.i.\u002Fl vào năm 2000 (0.11 ± 0.01). ED\u003Cjats:sub>50\u003C\u002Fjats:sub> cho các biến thể kháng nằm trong khoảng từ 1 đến 10 mg a.i.\u002Fl trong cả hai cuộc khảo sát (5 ± 2.64 và 4.25 ± 2.14, vào năm 1992 và 2000, tương ứng). Không có sự gia tăng khả năng kháng pyrimethanil nào được phát triển trong các quần thể \u003Cjats:italic>B. cinerea\u003C\u002Fjats:italic> sau 4 năm tiếp xúc với thuốc trừ nấm này. Một quy trình theo dõi \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> đã được phát triển dựa trên việc kiểm tra một liều phân biệt duy nhất của pyrimethanil (được thiết lập ở mức 0.7 mg a.i.\u002Fl). Các biến thể kháng pyrimethanil trong thử nghiệm \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> đã gây ra tổn thương rõ rệt trên các đĩa lá dưa chuột được xử lý bằng thuốc trừ nấm. Không có sự khác biệt đáng kể nào về độ thích nghi (tăng trưởng hoặc tạo bào tử) giữa các biến thể kháng và nhạy cảm. 307 biến thể được thu thập vào tháng 1 năm 2000 đã được kiểm tra \u003Cjats:italic>in vitro\u003C\u002Fjats:italic> bằng cách sử dụng các liều phân biệt để ước tính tỷ lệ kháng của \u003Cjats:italic>B. cinerea\u003C\u002Fjats:italic> đối với benzimidazoles (carbendazim), dicarboximides (procymidone), \u003Cjats:italic>N\u003C\u002Fjats:italic>-phenylcarbamates (diethofencarb), và anilinopyrimidines (pyrimethanil). Trong số 307 biến thể thu thập, 90% kháng lại benzimidazoles, 77% kháng dicarboximides, 23% kháng \u003Cjats:italic>N\u003C\u002Fjats:italic>-phenylcarbamates và 12% kháng anilinopyrimidines (trong số 165 biến thể này).  Các biến thể kháng chéo giữa dicarboximides và benzimidazoles đã được phát hiện ở mỗi nhà kính được khảo sát và chiếm 65,8%. Mười bốn phần trăm dân số kháng lại dicarboximides, benzimidazoles và \u003Cjats:italic>N\u003C\u002Fjats:italic>-phenylcarbamates, và 3% cũng kháng lại anilinopyrimidines.\u003C\u002Fjats:p>",{"EN":2280,"VI":2281},"Resistance to Pyrimethanil and other Fungicides in \u003Ci>Botrytis cinerea\u003C\u002Fi> Populations Collected on Vegetable Crops in Spain","Kháng thuốc Pyrimethanil và các thuốc trừ nấm khác trong quần thể \u003Ci>Botrytis cinerea\u003C\u002Fi> thu thập trên cây rau ở Tây Ban Nha",{"VI":987},{"VOID":2284},"10.1111\u002Fj.1439-0434.2004.00880.x",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1439-0434.2004.00880.x",[2289,2308,2325],{"id":2290,"sortIndex":32,"researcher":28,"roles":2291,"affiliations":2292,"properties":2301,"displayName":2305,"givenName":28,"familyName":28},"875b5365-9051-4127-80de-abec4ce2f572",[],[2293],{"id":2294,"sortIndex":32,"affiliation":2295,"properties":28},"698f74b4-6037-4971-b285-d0ebcff00048",{"id":2294,"createTime":28,"updateTime":28,"relativeEntities":2296,"slug":28,"properties":2297,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2300,"statistic":28},[],{"title":2298},{"EN":2299},"Authors' addresses: 1Department of Plant Protection, INIA, Ctra. De la Coruña km 7, 28040 Madrid, Spain",[],{"orcid":2302,"title":2304,"openalex":2306},{"VOID":2303},"https:\u002F\u002Forcid.org\u002F0000-0001-5277-2334",{"EN":2305},"C. 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J, 1988, Plant Disease Epidemiology, 185",{},{"id":28,"text":2415,"url":28,"identifiers":2416},"10.1094\u002FPDIS.2003.87.6.662",{"doi":2415},{"id":28,"text":2418,"url":28,"identifiers":2419},"Birchmore RJ, 1996, FRAC methods for monitoring the sensitivity of Botrytis cinerea to anilinopyrimidine fungicides developed by the anilinopyrimidine fungicide resistance committee of GIFAP, OILB Bull, 26, 181",{},{"id":28,"text":2421,"url":28,"identifiers":2422},"Birchmore RJ, 1996, A baseline for the sensitivity of Botrytis cinerea to pyrimethanil, Bright Crop Prot Conf Pests Dis, 1, 713",{},{"id":28,"text":2424,"url":28,"identifiers":2425},"10.1006\u002Fpest.1999.2414",{"doi":2424},{"id":28,"text":2427,"url":28,"identifiers":2428},"Delcán J, 1997, Sensitivity distribution of Botrytis cinerea from Spanish greenhouses to the mixture of carbendazim and diethofencarb, Phytopathol Med, 36, 123",{},{"id":28,"text":2430,"url":28,"identifiers":2431},"Faretra F, 1989, New natural variants of Botryotinia fuckeliana (Botrytis cinerea) coupling benzimidazole‐resistance to insensitivity toward the N‐phenylcarbamate diethofencarb, Phytopathol Med, 28, 98",{},{"id":28,"text":2433,"url":28,"identifiers":2434},"10.1016\u002F0261-2194(96)00021-X",{"doi":2433},{"id":28,"text":2436,"url":28,"identifiers":2437},"10.1111\u002Fj.1365-3059.1986.tb01984.x",{"doi":2436},{"id":28,"text":2439,"url":28,"identifiers":2440},"Gasztonyi M, 1995, Modern Selective Fungicide – Properties, Applications, and Mechanisms of Action, 389",{},{"id":28,"text":2442,"url":28,"identifiers":2443},"10.1094\u002FPDIS.1998.82.5.496",{"doi":2442},{"id":28,"text":2445,"url":28,"identifiers":2446},"10.1002\u002F(SICI)1096-9063(199607)47:3\u003C241::AID-PS410>3.0.CO;2-6",{"doi":2445},{"id":28,"text":2448,"url":28,"identifiers":2449},"10.1111\u002Fj.1365-3059.1992.tb02459.x",{"doi":2448},{"id":28,"text":2451,"url":28,"identifiers":2452},"10.1002\u002F(SICI)1096-9063(199606)47:2\u003C191::AID-PS415>3.0.CO;2-I",{"doi":2451},{"id":28,"text":2454,"url":28,"identifiers":2455},"Leroux P, 1994, Fungicide Resistance. Monograph. 60, 267",{},{"id":28,"text":2457,"url":28,"identifiers":2458},"10.1016\u002FS0261-2194(99)00074-5",{"doi":2457},{"id":28,"text":2460,"url":28,"identifiers":2461},"Leroux P, 1999, Modern Fungicides and Antifungal Compounds II, 297",{},{"id":28,"text":2463,"url":28,"identifiers":2464},"Löcher FJ, 1991, FRAC Methods for Monitoring Fungicide Resistance, 341",{},{"id":28,"text":2466,"url":28,"identifiers":2467},"10.1002\u002Fps.2780420304",{"doi":2466},{"id":28,"text":2469,"url":28,"identifiers":2470},"10.1002\u002Fps.2780450107",{"doi":2469},{"id":28,"text":2472,"url":28,"identifiers":2473},"10.1006\u002Fpest.1994.1023",{"doi":2472},{"id":28,"text":2475,"url":28,"identifiers":2476},"10.1094\u002FPD-76-0477",{"doi":2475},{"id":28,"text":2478,"url":28,"identifiers":2479},"Newman GL, 1992, Pyrimethanil: a new fungicide, Bright Crop Prot Conf Pests Dis, 1, 395",{},{"id":28,"text":2481,"url":28,"identifiers":2482},"10.1094\u002FPD-79-0294",{"doi":2481},{"id":28,"text":2484,"url":28,"identifiers":2485},"10.1046\u002Fj.1365-3059.1995.d01-140.x",{"doi":2484},{"id":28,"text":2487,"url":28,"identifiers":2488},"10.1094\u002FPHYTO.2000.90.11.1246",{"doi":2487},{"id":28,"text":2490,"url":28,"identifiers":2491},"10.1023\u002FA:1011250200724",{"doi":2490},{"id":28,"text":2493,"url":28,"identifiers":2494},"Smith CM, 1991, FRAC Methods for Monitoring Fungicide Resistance, 336",{},{"id":28,"text":2496,"url":28,"identifiers":2497},"Sokal RR, 1981, Biometry",{},{"id":28,"text":2499,"url":28,"identifiers":2500},"10.1146\u002Fannurev.py.29.090191.002225",{"doi":2499},{"id":2502,"createTime":2503,"updateTime":2504,"relativeEntities":2505,"slug":2506,"properties":2507,"entityType":990,"verifyStatus":26,"verifyTime":2521,"verifyNote":991,"languages":2522,"translateLanguages":2523,"viewCount":32,"primaryUrl":2524,"fullTextUrl":28,"authors":2525,"publicationType":1053,"publisherRelationship":2560,"citationCount":208,"citationInfo":2622,"publishDate":2625,"publishYear":2623,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":2626,"openAccess":28,"references":2627,"isForceReanalyzing":1419},"36f92bfe-6b0b-4d96-b2c2-bd45e2168b7d","2024-10-11T02:42:42.522+00:00","2025-01-19T20:49:30.272+00:00",[],"Scanning-Electron-Microscopy-of-i-Pseudomonas-syringae-i-pv-i-morsprunorum-i-on-Sweet-Cherry-Leaves",{"openalex":2508,"mag":2510,"abstract":2512,"title":2515,"keywords":2518,"doi":2519},{"VOID":2509},"W2012201422",{"VOID":2511},"2012201422",{"EN":2513,"VI":2514},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Scanning electron microscopy indicated that sub‐stomatal cavities on sweet cherry leaves are “protected sites” which shelter resident populations of \u003Cjats:italic>Pseudomonas syringae\u003C\u002Fjats:italic> pv. \u003Cjats:italic>morsprunorum\u003C\u002Fjats:italic>. Bacteria entered the stomata, multiplied in the cavities and emerged in a mass 6 days after inoculation. There were no visible symptoms, suggesting that the pathogen colonized the host in “sub‐clinical” numbers to generate populations which were then released onto the leaf surface under suitable conditions.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Kính hiển vi điện tử quét cho thấy các khoang phụ khí khổng trên lá anh đào ngọt là \"các vị trí được bảo vệ\" mà nơi trú ngụ của quần thể vi khuẩn \u003Cjats:italic>Pseudomonas syringae\u003C\u002Fjats:italic> pv. \u003Cjats:italic>morsprunorum\u003C\u002Fjats:italic>. Vi khuẩn xâm nhập vào khí khổng, phát triển trong các khoang và xuất hiện thành một khối vào ngày thứ 6 sau khi nhiễm. Không có triệu chứng rõ rệt, cho thấy rằng tác nhân gây bệnh đã thuộc địa hóa ký chủ với số lượng \"trong lâm sàng\" thấp để tạo ra những quần thể sau đó được phát tán ra bề mặt lá trong các điều kiện thích hợp.\u003C\u002Fjats:p>",{"EN":2516,"VI":2517},"Scanning Electron Microscopy of \u003Ci>Pseudomonas syringae\u003C\u002Fi> pv, \u003Ci>morsprunorum\u003C\u002Fi> on Sweet Cherry Leaves","Kính hiển vi điện tử quét về \u003Ci>Pseudomonas syringae\u003C\u002Fi> pv, \u003Ci>morsprunorum\u003C\u002Fi> trên lá anh đào ngọt",{"VI":987},{"VOID":2520},"10.1111\u002Fj.1439-0434.1983.tb00559.x","2024-10-11T02:42:42.521+00:00",[31],[30],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1439-0434.1983.tb00559.x",[2526,2543],{"id":2527,"sortIndex":32,"researcher":28,"roles":2528,"affiliations":2529,"properties":2538,"displayName":2540,"givenName":28,"familyName":28},"4e579a95-9d0e-46d6-8a04-e32201feca83",[],[2530],{"id":2531,"sortIndex":32,"affiliation":2532,"properties":28},"6c9dce49-e5bc-4bb0-9d9f-cc1be8a1f133",{"id":2531,"createTime":28,"updateTime":28,"relativeEntities":2533,"slug":28,"properties":2534,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2537,"statistic":28},[],{"title":2535},{"VI":2536},"Fruit and Fruit Technology Research Institute, Stellenbosch, South Africa",[],{"title":2539,"openalex":2541},{"EN":2540},"Isabel M. 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Conidia of \u003Cjats:italic>P. oxalicum\u003C\u002Fjats:italic> can be dried by fluid bed drying and freeze drying maintaining 100% viability after both processes, but protective additives must be added for obtaining this viability in the case of freeze drying. The best viabilities were obtained after freeze drying with non‐fat skim milk (NFSM) + Tween 20, NFSM + peptone and NFSM + sucrose. However, NFSM + glycerol had only a 0.5% viability after freeze drying. Freeze‐dried \u003Cjats:italic>P. oxalicum\u003C\u002Fjats:italic> conidia with or without additives did not maintain viability over time at room temperature, while conidia dried in a fluidized bed drier had a 40–50% viability after 180 days of storage in these conditions. \u003Cjats:italic>Penicillium oxalicum\u003C\u002Fjats:italic> conidial viability after spray‐drying was lower than 20%. \u003Cjats:italic>Penicillium oxalicum\u003C\u002Fjats:italic> conidia dried by fluid bed drying were effective in reducing the incidence of \u003Cjats:italic>Fusarium\u003C\u002Fjats:italic> wilt of tomato under glasshouse and field conditions.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Ảnh hưởng của các phương pháp sấy đông khô, sấy phun, và sấy bằng giường khí tới khả năng sống sót của bào tử \u003Cjats:italic>Penicillium oxalicum\u003C\u002Fjats:italic> đã được so sánh. 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E., 1964, Phytopathology, 54, 576",{},{"id":3241,"createTime":3242,"updateTime":3243,"relativeEntities":3244,"slug":3245,"properties":3246,"entityType":990,"verifyStatus":26,"verifyTime":3242,"verifyNote":991,"languages":3260,"translateLanguages":3261,"viewCount":32,"primaryUrl":3262,"fullTextUrl":28,"authors":3263,"publicationType":1053,"publisherRelationship":3360,"citationCount":689,"citationInfo":3422,"publishDate":3424,"publishYear":2406,"citationAnalyzeStatus":884,"lastCitationAnalyze":28,"indexDatabases":3425,"openAccess":28,"references":3426,"isForceReanalyzing":1419},"58bb66d1-5847-42c5-8d4a-8dc49775d085","2025-01-01T22:49:49.389+00:00","2025-01-19T20:47:32.937+00:00",[],"Leaf-Symptoms-on-Plum-Coffee-and-Citrus-and-the-Relationship-with-the-Extent-of-Xylem-Vessels-Colonized-by-i-Xylella-fastidiosa-i-",{"openalex":3247,"mag":3249,"abstract":3251,"title":3254,"keywords":3257,"doi":3258},{"VOID":3248},"W2096577180",{"VOID":3250},"2096577180",{"EN":3252,"VI":3253},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Leaf petioles of plum, coffee and sweet orange were examined using scanning electron microscopy (SEM). The presence of \u003Cjats:italic>Xylella fastidiosa\u003C\u002Fjats:italic> in the samples was confirmed by polymerase chain reaction and gel electrophoresis. The number of vessels colonized by \u003Cjats:italic>X. fastidiosa\u003C\u002Fjats:italic> was determined by SEM in petiole areas that were transversally sectioned under liquid nitrogen. The percentage of colonized vessels in petioles of coffee was higher than in petioles of plum and citrus whether trees were exhibiting mild symptoms (MS) or severe symptoms (SS). The percentage of vessels colonized varied from 10.9 (MS) to 38.0% (SS), 26 (MS) to 51.6% (SS), and 8 (MS) to 11.8% (SS) for plum, coffee and citrus, respectively, and did not vary by position within the petiole. Severity of symptoms consistently reflected higher proportion of colonized vessels in coffee and plum, but not in citrus.\u003C\u002Fjats:p>","\u003Cjats:title>Tóm tắt\u003C\u002Fjats:title>\u003Cjats:p>Các cuống lá của mận, cà phê và quýt đã được khảo sát bằng kính hiển vi điện tử quét (SEM). Sự hiện diện của \u003Cjats:italic>Xylella fastidiosa\u003C\u002Fjats:italic> trong các mẫu đã được xác nhận bằng phản ứng chuỗi polymerase và điện di gel. Số lượng vô mạch bị xâm chiếm bởi \u003Cjats:italic>X. fastidiosa\u003C\u002Fjats:italic> đã được xác định bằng SEM tại các khu vực cuống lá được cắt ngang dưới nitơ lỏng. Tỷ lệ các vô mạch bị xâm chiếm ở cuống lá của cà phê cao hơn so với cuống lá của mận và quýt, bất kể cây thể hiện triệu chứng nhẹ (MS) hay triệu chứng nặng (SS). Tỷ lệ các vô mạch bị xâm chiếm biến đổi từ 10.9 (MS) đến 38.0% (SS), từ 26 (MS) đến 51.6% (SS), và từ 8 (MS) đến 11.8% (SS) cho mận, cà phê và quýt, tương ứng, và không có sự thay đổi theo vị trí trong cuống lá. Mức độ triệu chứng liên tục phản ánh tỷ lệ cao hơn của các vô mạch bị xâm chiếm ở cà phê và mận, nhưng không có ở quýt.\u003C\u002Fjats:p>",{"EN":3255,"VI":3256},"Leaf Symptoms on Plum, Coffee and Citrus and the Relationship with the Extent of Xylem Vessels Colonized by \u003Ci>Xylella fastidiosa\u003C\u002Fi>","Triệu Chứng Lá trên Mận, Cà Phê và Quýt và Mối Quan Hệ với Mức Độ Vòi Nhĩ Gỗ Bị Xâm Chiếm bởi \u003Ci>Xylella 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