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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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grown oocytes of the frog (\u003Cjats:italic>Rana pipiens\u003C\u002Fjats:italic>) undergo cytoplasmic and nuclear maturation when treated with progesterone after the follicular envelopes have been removed. The mechanism of this maturation was investigated by injection of cytoplasm from progesterone‐treated oocytes at various stages of maturation into fully grown but immature oocytes. The injected cytoplasm becomes effective in inducing maturation by 12 hours after progesterone administration, reaches a maximum effectiveness around 20 hours, and then declines after the donor oocytes complete maturation. However, even cytoplasm from early embryos retains some capacity to induce oocyte maturation. The frequency with which maturation is induced is proportional to the volume of the injected cytoplasm. Progesterone itself is not directly responsible for the maturation‐producing effect of injected cytoplasm since injected progesterone does not promote maturation. However, externally applied progesterone does induce the completion of the first meiotic division, presumably by releasing a cytoplasmic “maturation promoting factor.” The production of this cytoplasmic factor was not affected by removal of the nucleus.\u003C\u002Fjats:p>\u003Cjats:p>After completion of the first meiotic division, oocytes cease further development at the metaphase of the second meiotic division, where they remain until fertilized or activated to develop. Cytoplasm from such secondary oocytes when injected into one of the blastomeres at the two‐cell stage of development suppresses mitosis as well as cleavage. Mitosis is usually arrested at metaphase. No such inhibition was brought about by injection of cytoplasm from cleaving blastomeres. Thus, the arrest of mitosis and cleavage can be attributed to a specific “cytostatic factor” in the cytoplasm of the secondary oocyte. Activation of donor secondary oocytes by insemination or pricking with a glass needle soon destroys the cytostatic factor. Likewise, addition of cortical cytoplasm to endoplasm from the secondary oocyte rapidly destroys the cytostatic capacity. This result implies that cortical material is involved in the process of removing the cytostatic factor at the time of normal activation or fertilization. Enucleation of oocytes demonstrated that production and removal of the cytostatic factor is independent of the nucleus.\u003C\u002Fjats:p>",{"EN":935},"Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes",{"VOID":937},"5106340",{"VOID":939},"10.1002\u002Fjez.1401770202","PUBLICATION","2024-09-04T17:50:37.360+00:00","Auto Verify",[31],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1401770202",[946,963],{"id":947,"sortIndex":32,"researcher":28,"roles":948,"affiliations":949,"properties":958},"19c218ee-fba8-420f-94e2-8db9f92a9c4f",[],[950],{"id":951,"sortIndex":32,"affiliation":952,"properties":28},"6d0f55a4-c25a-4005-9a4f-3f22ab0cff37",{"id":951,"createTime":28,"updateTime":28,"relativeEntities":953,"slug":28,"properties":954,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":957,"statistic":28},[],{"title":955},{"VI":956},"Department of Biology, Yale University, New Haven, Connecticut 06520.",[],{"title":959,"openalex":961},{"EN":960},"Yoshio Masui",{"VOID":962},"A5015403794",{"id":964,"sortIndex":40,"researcher":28,"roles":965,"affiliations":966,"properties":973},"844d9141-b87a-49ed-abe3-29bfda1f5827",[],[967],{"id":951,"sortIndex":32,"affiliation":968,"properties":28},{"id":951,"createTime":28,"updateTime":28,"relativeEntities":969,"slug":28,"properties":970,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":972,"statistic":28},[],{"title":971},{"VI":956},[],{"title":974,"openalex":976},{"EN":975},"Clement L. 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Zool. exp. gén. (Ser 3), 9, 284",{},{"id":28,"text":1035,"url":28,"identifiers":1036},"10.1016\u002F0014-4827(60)90345-1",{"doi":1035},{"id":28,"text":1038,"url":28,"identifiers":1039},"10.1073\u002Fpnas.57.3.607",{"doi":1038},{"id":28,"text":1041,"url":28,"identifiers":1042},"Detlaff T. A., 1966, Action of actinomycin and puromycin upon frog oöcyte maturation, J. Embryol. exp. Morphol., 16, 183",{},{"id":28,"text":1044,"url":28,"identifiers":1045},"Detlaff T. A., 1964, The role of the germinal vesicle in oöcyte Saturation in anurans as revealed by the removal and transplantation of nuclei, J. Embryol. exp. Morph., 12, 851",{},{"id":28,"text":1047,"url":28,"identifiers":1048},"Drury H. F., 1941, Amylacetate as a clearing agent for embryonic material, Stain Tech., 6, 21, 10.3109\u002F10520294109106190",{"doi":1049},"10.3109\u002F10520294109106190",{"id":28,"text":1051,"url":28,"identifiers":1052},"10.1016\u002F0014-4827(61)90347-0",{"doi":1051},{"id":28,"text":1054,"url":28,"identifiers":1055},"Goldstein L., 1967, The Control of Nuclear Activity, 3",{},{"id":28,"text":1057,"url":28,"identifiers":1058},"Graham C. F., 1966, The regulation of DNA synthesis and mitosis in multinucleate frog eggs, J. Cell. Sci., 1, 363, 10.1242\u002Fjcs.1.3.363",{"doi":1059},"10.1242\u002Fjcs.1.3.363",{"id":28,"text":1061,"url":28,"identifiers":1062},"10.1016\u002F0012-1606(66)90020-0",{"doi":1061},{"id":28,"text":1064,"url":28,"identifiers":1065},"10.1073\u002Fpnas.58.2.545",{"doi":1064},{"id":28,"text":1067,"url":28,"identifiers":1068},"Gurdon J. B., 1968, Changes in somatic cell nuclei inserted into growing and maturing amphibian oöcytes, J. Embryol. exp. Morphol., 20, 401",{},{"id":28,"text":1070,"url":28,"identifiers":1071},"10.1111\u002Fj.1469-185X.1968.tb00960.x",{"doi":1070},{"id":28,"text":1073,"url":28,"identifiers":1074},"Harris H., 1967, The reactivation of the red cell nucleus, J. Cell Sci., 2, 23, 10.1242\u002Fjcs.2.1.23",{"doi":1075},"10.1242\u002Fjcs.2.1.23",{"id":28,"text":1077,"url":28,"identifiers":1078},"10.2307\u002F1538709",{"doi":1077},{"id":28,"text":1080,"url":28,"identifiers":1081},"10.1086\u002Fphyszool.12.2.30151487",{"doi":1080},{"id":28,"text":1083,"url":28,"identifiers":1084},"Herlant M., 1913, Etude sur les bases cytologiques du mécanisme de la parthenogénèse expérimentale chez les Amphibiens, Arch. Biol., 28, 505",{},{"id":28,"text":1086,"url":28,"identifiers":1087},"10.1002\u002Fjez.1400930205",{"doi":1086},{"id":28,"text":1089,"url":28,"identifiers":1090},"Katagiri C., 1959, Cortical change at fertilization in the egg of the grass frog, Rana temporaria, J. Fac. Sci. Hokkaido Univ., 14, 166",{},{"id":28,"text":1092,"url":28,"identifiers":1093},"10.1083\u002Fjcb.34.1.111",{"doi":1092},{"id":28,"text":1095,"url":28,"identifiers":1096},"10.1002\u002Fjez.1401570308",{"doi":1095},{"id":28,"text":1098,"url":28,"identifiers":1099},"10.1016\u002F0022-2836(69)90282-4",{"doi":1098},{"id":28,"text":1101,"url":28,"identifiers":1102},"10.1002\u002Fjez.1401660309",{"doi":1101},{"id":28,"text":1104,"url":28,"identifiers":1105},"10.1016\u002F0012-1606(65)90032-1",{"doi":1104},{"id":28,"text":1107,"url":28,"identifiers":1108},"10.1002\u002Fjez.1401640304",{"doi":1107},{"id":28,"text":1110,"url":28,"identifiers":1111},"Merriam R. W., 1969, Movement of cytoplasmic proteins into nuclei induced to enlarge and initiate DNA or RNA synthesis, J. Cell Sci., 5, 333, 10.1242\u002Fjcs.5.2.333",{"doi":1112},"10.1242\u002Fjcs.5.2.333",{"id":28,"text":1114,"url":28,"identifiers":1115},"Monroy A., 1965, The Biochemistry of Animal Development 1, 73",{},{"id":28,"text":1117,"url":28,"identifiers":1118},"10.1073\u002Fpnas.54.1.107",{"doi":1117},{"id":28,"text":1120,"url":28,"identifiers":1121},"Moore B., 1940, Chromosomes of frog eggs and embryos stained by Feulgen method to avoid excessive staining of yolk granules, Anat. Rec., 78",{},{"id":28,"text":1123,"url":28,"identifiers":1124},"Osanai K., 1967, Inhibition of development with the extract from the unfertilized eggs of the Japanese Palolo, Sci. Rep. Tohoku Unic. Ser. IV (Biol.), 33, 129",{},{"id":28,"text":1126,"url":28,"identifiers":1127},"10.3181\u002F00379727-124-31993",{"doi":1126},{"id":28,"text":1129,"url":28,"identifiers":1130},"10.1002\u002Fjez.1401660307",{"doi":1129},{"id":28,"text":1132,"url":28,"identifiers":1133},"10.1002\u002Fjmor.1050230106",{"doi":1132},{"id":28,"text":1135,"url":28,"identifiers":1136},"10.1016\u002F0012-1606(66)90019-4",{"doi":1135},{"id":28,"text":1138,"url":28,"identifiers":1139},"10.1016\u002F0012-1606(69)90065-7",{"doi":1138},{"id":28,"text":1141,"url":28,"identifiers":1142},"10.1016\u002F0012-1606(70)90172-7",{"doi":1141},{"id":28,"text":1144,"url":28,"identifiers":1145},"10.1016\u002F0012-1606(68)90010-9",{"doi":1144},{"id":28,"text":1147,"url":28,"identifiers":1148},"10.1016\u002F0014-4827(69)90472-8",{"doi":1147},{"id":28,"text":1150,"url":28,"identifiers":1151},"Tchou‐Su, 1942, Fertílízation of artificially ovulated premature eggs of Bufo, Sci. 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B., 1941, Developmental patterns in simple slime molds, Growth (third Growth Symposium), 5, 41",{},{"id":28,"text":1579,"url":28,"identifiers":1580},"Rashevsky N.1938Mathematical Biophysics. Chicago.",{},{"id":28,"text":1582,"url":28,"identifiers":1583},"Runyon E. H., 1942, Aggregation of separate cells of Dictyostelium to form a multicellular body, Collecting Net, 17, 88",{},{"id":28,"text":1585,"url":28,"identifiers":1586},"von Schuckmann W., 1924, Zur Biologie von Dictyostelium mucoroides Bref, Centbl. Bakt. (etc.) (I), 91, 302",{},{"id":28,"text":1588,"url":28,"identifiers":1589},"von Schuckmann W., 1925, Zur Morphologie und Biologie von Dictyostelium mucoroides Bref, Arch. Protistenk., 51, 495",{},{"id":28,"text":1591,"url":28,"identifiers":1592},"10.1007\u002FBF02145237",{"doi":1591},{"id":28,"text":1594,"url":28,"identifiers":1595},"10.1002\u002Fjez.1400680304",{"doi":1594},{"id":28,"text":1396,"url":28,"identifiers":1597},{"doi":1396},{"id":1599,"createTime":1600,"updateTime":1600,"relativeEntities":1601,"slug":1602,"properties":1603,"entityType":940,"verifyStatus":26,"verifyTime":1616,"verifyNote":942,"languages":1617,"translateLanguages":28,"viewCount":32,"primaryUrl":1618,"fullTextUrl":28,"authors":1619,"publicationType":978,"publisherRelationship":1692,"citationCount":1720,"citationInfo":1721,"publishDate":1724,"publishYear":1722,"citationAnalyzeStatus":879,"lastCitationAnalyze":28,"indexDatabases":1725,"openAccess":28,"references":1726,"isForceReanalyzing":1161},"764b8940-cdfa-4727-9033-048d088c55cb","2024-11-26T14:56:43.232+00:00",[],"Mollusc-larval-shell-formation-amorphous-calcium-carbonate-is-a-precursor-phase-for-aragonite",{"openalex":1604,"mag":1606,"abstract":1608,"title":1610,"pm":1612,"doi":1614},{"VOID":1605},"W2125704002",{"VOID":1607},"2125704002",{"EN":1609},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>The larval shells of the marine bivalves \u003Cjats:italic>Mercenaria mercenaria\u003C\u002Fjats:italic> and \u003Cjats:italic>Crassostrea gigas\u003C\u002Fjats:italic> are investigated by polarized light microscopy, infrared spectroscopy, Raman imaging spectroscopy, and scanning electron microscopy. Both species contain similar shell ultrastructures. We show that larval shells contain amorphous calcium carbonate (ACC), in addition to aragonite. The aragonite is much less crystalline than nonbiogenic aragonite. We further show that the initially deposited mineral phase is predominantly ACC that subsequently partially transforms into aragonite. The postset juvenile shell, as well as the adult shell of \u003Cjats:italic>Mercenaria\u003C\u002Fjats:italic> also contains aragonite that is less crystalline than nonbiogenic aragonite. We conclude that ACC fulfills an important function in mollusc larval shell formation. It is conceivable that ACC may also be involved in adult shell formation. \u003Cjats:italic>J. Exp. Zool. 293:478–491, 2002\u003C\u002Fjats:italic>. © 2002 Wiley‐Liss, Inc.\u003C\u002Fjats:p>",{"EN":1611},"Mollusc larval shell formation: amorphous calcium carbonate is a precursor phase for aragonite",{"VOID":1613},"12486808",{"VOID":1615},"10.1002\u002Fjez.90004","2024-11-26T14:56:43.231+00:00",[31],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.90004",[1620,1639,1658,1675],{"id":1621,"sortIndex":32,"researcher":28,"roles":1622,"affiliations":1623,"properties":1632},"d943e851-5cf0-43bd-9cd2-3a7df7f45f46",[],[1624],{"id":1625,"sortIndex":32,"affiliation":1626,"properties":28},"0287918c-4426-4a18-89ae-53328237988e",{"id":1625,"createTime":28,"updateTime":28,"relativeEntities":1627,"slug":28,"properties":1628,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1631,"statistic":28},[],{"title":1629},{"VI":1630},"Department of Structural Biology, Weizmann Institute of Science, 76100, Rehovot, Israel",[],{"orcid":1633,"title":1635,"openalex":1637},{"VOID":1634},"https:\u002F\u002Forcid.org\u002F0000-0002-7345-341X",{"EN":1636},"Ingrid M. 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of 30 species of fish were examined for their content of LDH isozymes. One major isozyme system was found in all fish. In addition, two minor systems restricted to eyes and to gonads were found in many fish. Fish may be classified into four groups on the basis of their possession of one, two, three, or five major isozymes of LDH. The major isozyme patterns can be attributed to the polymers of two protein subunits under the control of two genes, as in mammals and birds, but the variety of heteropolymers produced varies in different species. The fluke and other flatfish are exceptional in that they synthesize only one kind of subunit which polymerizes to form a single variety of LDH. All other fish produced at least two major isozymes presumably the homopolymers of \u003Cjats:italic>A\u003C\u002Fjats:italic> and \u003Cjats:italic>B\u003C\u002Fjats:italic> subunits. The three‐isozyme fish produce, in addition, a single heteropolymer. A few fish produce three heteropolymers and two homopolymers to produce the characteristic pattern of five isozymes seen in mammals.\u003C\u002Fjats:p>\u003Cjats:p>In populations of the whiting, which has five major isozymes, two mutant alleles at the \u003Cjats:italic>B\u003C\u002Fjats:italic> locus were discovered. Each of these alleles produced polypeptides with characteristic electrophoretic mobilities. Consequently, heterozygous individuals contained more than 15 isozymes.\u003C\u002Fjats:p>\u003Cjats:p>A variety of minor isozymes that appear on zymograms may represent modifications of the major isozymes. However, the minor isozyme systems of the gonad and the eye seem to be genetically distinct molecular systems, separate from and in addition to the major isozyme system.\u003C\u002Fjats:p>",{"EN":1851},"Lactate dehydrogenase isozyme patterns of fish",{"VOID":1853},"5894308",{"VOID":1855},"10.1002\u002Fjez.1401590304",[31],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1401590304",[1859,1882],{"id":1860,"sortIndex":32,"researcher":28,"roles":1861,"affiliations":1862,"properties":1879},"e782c97a-23c4-46b4-963f-cbeae7ffba7c",[],[1863,1871],{"id":1864,"sortIndex":32,"affiliation":1865,"properties":28},"c6df8998-afa6-4fb6-8668-a19397e4c9eb",{"id":1864,"createTime":28,"updateTime":28,"relativeEntities":1866,"slug":28,"properties":1867,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":1870,"statistic":28},[],{"title":1868},{"VI":1869},"Bermuda Biological Station, St. George's 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In freshwater (FW) teleost gill, the mechanism of NaCl uptake is more controversial and involves apical V‐type H\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase linked to an apical Na\u003Cjats:sup>+\u003C\u002Fjats:sup> channel, apical Cl\u003Cjats:sup>−\u003C\u002Fjats:sup>–HCO\u003Cjats:inline-graphic xmlns:xlink=\"http:\u002F\u002Fwww.w3.org\u002F1999\u002Fxlink\" xlink:href=\"graphic\u002Ftex2gif-stack-1.gif\" xlink:title=\"urn:x-wiley:0022104X:media:JEZ10127:tex2gif-stack-1\" \u002F> exchange and basolateral Na\u003Cjats:sup>+\u003C\u002Fjats:sup>,K\u003Cjats:sup>+\u003C\u002Fjats:sup>‐ATPase. Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> uptake (in FW and SW) is via Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> channels in the apical membrane and Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup>‐ATPase in the basolateral membrane. Mainly this transport occurs in mitochondria rich (MR) chloride cells, but there is a role for the pavement cells also. 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10.1242\u002Fjeb.200.6.1047",{"doi":2587},"10.1242\u002Fjeb.200.6.1047",{"id":28,"text":2589,"url":28,"identifiers":2590},"10.1016\u002FS1095-6433(97)00403-0",{"doi":2589},{"id":28,"text":2592,"url":28,"identifiers":2593},"10.1016\u002FS0734-9750(99)00035-X",{"doi":2592},{"id":28,"text":2595,"url":28,"identifiers":2596},"10.1074\u002Fjbc.M008209200",{"doi":2595},{"id":28,"text":2598,"url":28,"identifiers":2599},"10.1007\u002FBF00233449",{"doi":2598},{"id":2601,"createTime":2602,"updateTime":2602,"relativeEntities":2603,"slug":2604,"properties":2605,"entityType":940,"verifyStatus":26,"verifyTime":2602,"verifyNote":942,"languages":2618,"translateLanguages":28,"viewCount":32,"primaryUrl":2619,"fullTextUrl":28,"authors":2620,"publicationType":978,"publisherRelationship":2653,"citationCount":2680,"citationInfo":2681,"publishDate":2684,"publishYear":2682,"citationAnalyzeStatus":879,"lastCitationAnalyze":28,"indexDatabases":2685,"openAccess":28,"references":2686,"isForceReanalyzing":1161},"25b183c2-16b4-4f45-b706-44f7697cb0fd","2024-09-01T11:40:34.037+00:00",[],"A-triple-stain-technique-for-evaluating-normal-acrosome-reactions-of-human-sperm",{"openalex":2606,"mag":2608,"abstract":2610,"title":2612,"pm":2614,"doi":2616},{"VOID":2607},"W1980066996",{"VOID":2609},"1980066996",{"EN":2611},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>A triple‐stain technique has been developed to score normal acrosome‐reacted human sperm in fixed smears. Live and dead sperm are first differentiated using the vital stain trypan blue. Sperm are then fixed in glutar‐aldehyde, dried onto slides, and the postacrosomal region and acrosome are differentiated using Bismark brown and Rose Bengal. Slides are examined at 1,000 × with a bright‐field microscope and assessed for (1) the percentage of sperm that were alive at the time of fixation and (2) the percentage of sperm that had undergone normal acrosome reactions. Experiments are included that show that trypan blue is a reliable stain for dead sperm and that Rose Bengal stains only sperm having intact acrosomes. This technique may have applications in experimental and clinical studies on sperm capacitation, acrosome reactions, and fertilization in laboratory and domestic animals as well as in man.\u003C\u002Fjats:p>",{"EN":2613},"A triple‐stain technique for evaluating normal acrosome reactions of human sperm",{"VOID":2615},"6168732",{"VOID":2617},"10.1002\u002Fjez.1402150210",[31],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1402150210",[2621,2638],{"id":2622,"sortIndex":32,"researcher":28,"roles":2623,"affiliations":2624,"properties":2633},"d055b0b3-c3a4-43e1-8945-4cab30d1258c",[],[2625],{"id":2626,"sortIndex":32,"affiliation":2627,"properties":28},"0f0035fd-dbe5-4e10-85e1-68f2f1fc8094",{"id":2626,"createTime":28,"updateTime":28,"relativeEntities":2628,"slug":28,"properties":2629,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2632,"statistic":28},[],{"title":2630},{"VI":2631},"Department of Biology, University of California, Riverside, CA, 92521",[],{"title":2634,"openalex":2636},{"EN":2635},"Prudence Talbot",{"VOID":2637},"A5030472282",{"id":2639,"sortIndex":40,"researcher":28,"roles":2640,"affiliations":2641,"properties":2648},"333de84f-dbf4-413e-9499-4f8a9db8c9c2",[],[2642],{"id":2626,"sortIndex":32,"affiliation":2643,"properties":28},{"id":2626,"createTime":28,"updateTime":28,"relativeEntities":2644,"slug":28,"properties":2645,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2647,"statistic":28},[],{"title":2646},{"VI":2631},[],{"title":2649,"openalex":2651},{"EN":2650},"R. 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E., 1970, The acrosomal region and acrosome reaction in sperm of the golden hamster, Biol. Reprod., 3, 180, 10.1093\u002Fbiolreprod\u002F3.2.180",{"doi":2705},"10.1093\u002Fbiolreprod\u002F3.2.180",{"id":28,"text":2707,"url":28,"identifiers":2708},"Meizel S.(1978)The mammalian sperm acrosome rection: A biochemical approach. In Development in Mammals M. H. Johnson ed. Vol. 3 pp.1–64.",{},{"id":28,"text":2710,"url":28,"identifiers":2711},"Phillips H. J., 1973, Tissue Culture: Methods and Applications, 406, 10.1016\u002FB978-0-12-427150-0.50101-7",{"doi":2712},"10.1016\u002FB978-0-12-427150-0.50101-7",{"id":28,"text":2714,"url":28,"identifiers":2715},"Sokal R. R., 1976, Biometry: The principles and practice of statistics in biological research, 247",{},{"id":28,"text":2717,"url":28,"identifiers":2718},"10.1002\u002Fjez.1401980312",{"doi":2717},{"id":28,"text":2720,"url":28,"identifiers":2721},"10.1002\u002Fmrd.1120030303",{"doi":2720},{"id":28,"text":2723,"url":28,"identifiers":2724},"Yanagimachi R.(1978)Sperm‐egg association in mammals. In Current Topics in Developmental Biology. A. A. Moscona and Alberto Monroy eds. Vol. 12 pp.83–105.",{"doi":2725},"10.1016\u002FS0070-2153(08)60594-3",{"id":2727,"createTime":2728,"updateTime":2728,"relativeEntities":2729,"slug":2730,"properties":2731,"entityType":940,"verifyStatus":26,"verifyTime":2728,"verifyNote":942,"languages":2744,"translateLanguages":28,"viewCount":32,"primaryUrl":2745,"fullTextUrl":28,"authors":2746,"publicationType":978,"publisherRelationship":2793,"citationCount":2819,"citationInfo":2820,"publishDate":2097,"publishYear":1722,"citationAnalyzeStatus":879,"lastCitationAnalyze":28,"indexDatabases":2822,"openAccess":28,"references":2823,"isForceReanalyzing":1161},"4ee10ff9-35e5-4050-98b2-304eedd6302c","2024-09-28T23:04:12.412+00:00",[],"Fish-gill-morphology-inside-out",{"openalex":2732,"mag":2734,"abstract":2736,"title":2738,"pm":2740,"doi":2742},{"VOID":2733},"W1974051447",{"VOID":2735},"1974051447",{"EN":2737},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>In this short review of fish gill morphology we cover some basic gross anatomy as well as in some more detail the microscopic anatomy of the branchial epithelia from representatives of the major extant groups of fishes (Agnathans, Elasmobranchs, and Teleosts). The agnathan hagfishes have primitive gill pouches, while the lampreys have arch‐like gills similar to the higher fishes. In the lampreys and elasmobranchs, the gill filaments are supported by a complete interbranchial septum and water exits via external branchial slits or pores. In contrast, the teleost interbranchial septum is much reduced, leaving the ends of the filaments unattached, and the multiple gill openings are replaced by the single caudal opening of the operculum. The basic functional unit of the gill is the filament, which supports rows of plate‐like lamellae. The lamellae are designed for gas exchange with a large surface area and a thin epithelium surrounding a well‐vascularized core of pillar cell capillaries. The lamellae are positioned for the blood flow to be counter‐current to the water flow over the gills. Despite marked differences in the gross anatomy of the gill among the various groups, the cellular constituents of the epithelium are remarkably similar. The lamellar gas‐exchange surface is covered by squamous pavement cells, while large, mitochondria‐rich, ionocytes and mucocytes are found in greatest frequency in the filament epithelium. Demands for ionoregulation can often upset this balance. There has been much study of the structure and function of the branchial mitochondria‐rich cells. These cells are generally characterized by a high mitochondrial density and an amplification of the basolateral membrane through folding or the presence of an intracellular tubular system. Morphological subtypes of MRCs as well as some methods of MRC detection are discussed. © 2002 Wiley‐Liss, Inc.\u003C\u002Fjats:p>",{"EN":2739},"Fish gill morphology: inside out",{"VOID":2741},"12115897",{"VOID":2743},"10.1002\u002Fjez.10124",[31],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.10124",[2747,2766],{"id":2748,"sortIndex":32,"researcher":28,"roles":2749,"affiliations":2750,"properties":2759},"b7617326-a573-4c9d-81e3-1779767c03e6",[],[2751],{"id":2752,"sortIndex":32,"affiliation":2753,"properties":28},"060921ed-42fe-48ab-8f0a-0f96630d79a9",{"id":2752,"createTime":28,"updateTime":28,"relativeEntities":2754,"slug":28,"properties":2755,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":2758,"statistic":28},[],{"title":2756},{"EN":2757},"Centro Interdisciplinar de Investigação Marinha e Ambiental (CIIMAR), 4150‐180 Porto, Portugal",[],{"orcid":2760,"title":2762,"openalex":2764},{"VOID":2761},"https:\u002F\u002Forcid.org\u002F0000-0003-3681-1166",{"EN":2763},"Jonathan M. 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R199",{},{"id":28,"text":2915,"url":28,"identifiers":2916},"10.1016\u002FS0022-5320(72)80011-X",{"doi":2915},{"id":28,"text":2918,"url":28,"identifiers":2919},"10.1016\u002FS1546-5098(08)60317-9",{"doi":2918},{"id":28,"text":2300,"url":28,"identifiers":2921},{"doi":2300},{"id":28,"text":2923,"url":28,"identifiers":2924},"10.1007\u002FBF00179758",{"doi":2923},{"id":28,"text":2321,"url":28,"identifiers":2926},{},{"id":28,"text":2318,"url":28,"identifiers":2928},{"doi":2318},{"id":28,"text":2930,"url":28,"identifiers":2931},"Karnovsky MJ, 1965, A formaldehyde–glutaraldehyde fixative of high osmolality for use in electron microscopy, J Cell Biol, 27, 137A",{},{"id":28,"text":2933,"url":28,"identifiers":2934},"Kawahara T, 1982, Intercellular junctions in chloride and pavement cells of Oplegnethus fasciatus, J Electron Microsc, 31, 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Horizon of new research, 203",{},{"id":28,"text":3067,"url":28,"identifiers":3068},"Sabóia SMT, 1996, Mucous cell types in the branchial epithelium of the euryhaline fish Poecilia vivipara, J Fish Biol, 49, 545",{},{"id":28,"text":3070,"url":28,"identifiers":3071},"10.1023\u002FA:1007732715334",{"doi":3070},{"id":28,"text":2503,"url":28,"identifiers":3073},{"doi":2503},{"id":28,"text":3075,"url":28,"identifiers":3076},"10.1016\u002F0309-1651(77)90074-1",{"doi":3075},{"id":28,"text":2522,"url":28,"identifiers":3078},{"doi":2522},{"id":28,"text":3080,"url":28,"identifiers":3081},"10.1007\u002FBF00337316",{"doi":3080},{"id":28,"text":3083,"url":28,"identifiers":3084},"Stetson DL, 1985, α and β types of carbonic anhydrase‐rich cells in turtle bladder, Am J Physiol, 249, F553",{},{"id":28,"text":3086,"url":28,"identifiers":3087},"10.1007\u002Fs004410000341",{"doi":3086},{"id":28,"text":3089,"url":28,"identifiers":3090},"Tsai J‐C, 1998, Effects of wheat germ agglutinin and colchicine on microtubules of the mitochondria‐rich cells and Ca2+ uptake in tilapia (Oreochromis mossambicus) larvae, J Exp Biol, 201, 2263, 10.1242\u002Fjeb.201.15.2263",{"doi":3091},"10.1242\u002Fjeb.201.15.2263",{"id":28,"text":3093,"url":28,"identifiers":3094},"10.2108\u002Fzsj.17.149",{"doi":3093},{"id":28,"text":3096,"url":28,"identifiers":3097},"10.2108\u002Fzsj.13.219",{"doi":3096},{"id":28,"text":3099,"url":28,"identifiers":3100},"10.1007\u002Fs004410051339",{"doi":3099},{"id":28,"text":3102,"url":28,"identifiers":3103},"van der Heijden AJH, 1997, Mitochondria‐rich cells in gills of tilapia (Oreochromis mossambicus) adapted to fresh water or sea water: Quantification by confocal laser scanning microscopy, J Exp Biol, 200, 55, 10.1242\u002Fjeb.200.1.55",{"doi":3104},"10.1242\u002Fjeb.200.1.55",{"id":28,"text":3106,"url":28,"identifiers":3107},"10.1002\u002F(SICI)1097-010X(19961001)276:2\u003C95::AID-JEZ2>3.0.CO;2-8",{"doi":3106},{"id":28,"text":3109,"url":28,"identifiers":3110},"10.1007\u002FBF00229086",{"doi":3109},{"id":28,"text":3112,"url":28,"identifiers":3113},"10.1007\u002Fs004419900101",{"doi":3112},{"id":28,"text":2573,"url":28,"identifiers":3115},{"doi":2573},{"id":28,"text":3117,"url":28,"identifiers":3118},"Wilson JM, 2000, Immunolocalization of ion‐transport proteins to branchial epithelium mitochondria‐rich cells in the mudskipper (Periophthalmodon schlosseri), J Exp Biol, 203, 2297, 10.1242\u002Fjeb.203.15.2297",{"doi":2577},{"id":28,"text":3120,"url":28,"identifiers":3121},"Wilson JM, 1996, Physiology of tropical fishes, 123",{},{"id":28,"text":3123,"url":28,"identifiers":3124},"10.1016\u002FS1095-6433(02)00042-9",{"doi":3123},{"id":28,"text":3126,"url":28,"identifiers":3127},"10.1007\u002Fs004410050557",{"doi":3126},{"id":28,"text":3129,"url":28,"identifiers":3130},"10.1007\u002FBF00307376",{"doi":3129},{"id":28,"text":3132,"url":28,"identifiers":3133},"10.1002\u002Fjmor.1051490105",{"doi":3132},{"id":3135,"createTime":3136,"updateTime":3136,"relativeEntities":3137,"slug":3138,"properties":3139,"entityType":940,"verifyStatus":26,"verifyTime":3136,"verifyNote":942,"languages":3150,"translateLanguages":28,"viewCount":32,"primaryUrl":3151,"fullTextUrl":28,"authors":3152,"publicationType":978,"publisherRelationship":3189,"citationCount":3216,"citationInfo":3217,"publishDate":3220,"publishYear":3218,"citationAnalyzeStatus":879,"lastCitationAnalyze":28,"indexDatabases":3221,"openAccess":28,"references":3222,"isForceReanalyzing":1161},"7f9c15a7-529b-4398-9230-bb8ba9903d00","2024-09-03T21:32:35.756+00:00",[],"Temperature-dependent-sex-determination-in-crocodilians",{"openalex":3140,"mag":3142,"abstract":3144,"title":3146,"doi":3148},{"VOID":3141},"W1967116629",{"VOID":3143},"1967116629",{"EN":3145},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>Half of the 22 extant crocodilians show evidence of temperature‐dependent sex determination (TSD). We examine evidence for TSD in 11 species by reviewing reports on five and presenting new data for six. The female‐male pattern (FM; females at low temperature, males at high temperature) attributed to \u003Cjats:italic>Alligator mississippiensis\u003C\u002Fjats:italic> and \u003Cjats:italic>Caiman crocodilus\u003C\u002Fjats:italic> are here revised to be female‐male‐female (FMF; males at intermediate temperature, females at low and high temperatures). A similar pattern characterizes \u003Cjats:italic>Crocodylus palustris, C. moreletii, C. siamensis\u003C\u002Fjats:italic>, and \u003Cjats:italic>Gavialis gangeticus\u003C\u002Fjats:italic> based on new data; published accounts establish a FMF pattern in \u003Cjats:italic>Crocodylus porosus, C. johnstoni\u003C\u002Fjats:italic>, and \u003Cjats:italic>C. niloticus\u003C\u002Fjats:italic>. TSD apparently occurs in \u003Cjats:italic>Paleosuchus trigonatus\u003C\u002Fjats:italic> and \u003Cjats:italic>Alligator sinensis\u003C\u002Fjats:italic>, but patterns are not yet documented. In the well‐studied species, the incubation temperatures for FM transitions are congruent, but MF transition temperatures differ among species. In \u003Cjats:italic>A. mississippiensis\u003C\u002Fjats:italic>, 100% males are produced over a range of constant incubation temperatures, whereas in \u003Cjats:italic>C. johnstoni\u003C\u002Fjats:italic>, only low proportions of males are produced at any constant temperature.\u003C\u002Fjats:p>\u003Cjats:p>The thermosensitive period (TSP) for \u003Cjats:italic>A. mississippiensis\u003C\u002Fjats:italic> occurs during stages 21 to 24 (days 30–45 at intermediate temperatures) and coincides with gonadal differentiation. A similar scenario is suggested in other species. The TSP in \u003Cjats:italic>A. mississippiensis\u003C\u002Fjats:italic> (and possibly other crocodilians) encompasses the third quarter of development and occurs later than in turtles and a lizard. In \u003Cjats:italic>A. mississippiensis\u003C\u002Fjats:italic> as in turtles, the duration (cumulative effect) and\u002For the magnitude (potency effect) of incubation temperatures during the TSP predictably alter sex ratios. TSP chronologies and features which are shared among TSD reptiles suggest common, underlying mechanisms; \u003Cjats:italic>A. mississippiensis\u003C\u002Fjats:italic> is an appropriate model for further study. In crocodilians, clutch effects are a significant source of variation in TSD response. Hatchling sex ratios previously reported for \u003Cjats:italic>A. mississippiensis\u003C\u002Fjats:italic> are reconsidered in light of our new data. © 1994 Wiley‐Liss, Inc.\u003C\u002Fjats:p>",{"EN":3147},"Temperature‐dependent sex determination in crocodilians",{"VOID":3149},"10.1002\u002Fjez.1402700105",[31],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1002\u002Fjez.1402700105",[3153,3172],{"id":3154,"sortIndex":32,"researcher":28,"roles":3155,"affiliations":3156,"properties":3165},"322de633-2b2a-412a-9ed8-c6fa90fc9854",[],[3157],{"id":3158,"sortIndex":32,"affiliation":3159,"properties":28},"f9b14f27-3101-4de1-9222-691c897916f7",{"id":3158,"createTime":28,"updateTime":28,"relativeEntities":3160,"slug":28,"properties":3161,"entityType":28,"verifyStatus":28,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":28,"url":28,"parentIds":3164,"statistic":28},[],{"title":3162},{"EN":3163},"†Department of Biology, University of North Dakota, Grand Forks, North Dakota 58202",[],{"orcid":3166,"title":3168,"openalex":3170},{"VOID":3167},"https:\u002F\u002Forcid.org\u002F0000-0002-8001-0940",{"EN":3169},"Keith A. 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Andrews",{"VOID":3188},"A5066784305",{"url":28,"publisher":3190,"properties":3210},{"id":868,"createTime":869,"updateTime":870,"relativeEntities":3191,"slug":872,"properties":3192,"entityType":25,"verifyStatus":879,"verifyTime":28,"verifyNote":28,"languages":28,"translateLanguages":28,"viewCount":32,"subjectFields":3196,"manageAffiliations":3197,"indexDatabases":3198,"url":28,"thumbnailPath":28,"statistic":3205,"gsStatistic":28,"type":28,"analyzePriority":28},[],{"issn":3193,"title":3194,"eissn":3195},{"VOID":875},{"EN":872},{"VOID":878},[],[],[3199],{"id":884,"indexDatabase":3200,"url":890,"indexYears":891,"academicFieldIds":28,"indexDatabaseRanking":892},{"id":775,"createTime":28,"updateTime":28,"relativeEntities":3201,"label":3202,"description":3203,"key":781,"publicationTags":3204,"standard":28},[],{"EN":778,"VI":778},{"EN":778,"VI":780},[783],{"impactFactor":32,"impactFactorByYear":3206,"i10Index":202,"i10IndexLast5Year":32,"totalPublication":202,"totalPublicationByYear":3207,"totalCitation":896,"totalCitationByYear":3208,"totalCitationPerPublication":911,"totalCitationPerPublicationByYear":3209,"hindexLast5Year":69,"hindex":69},{},{"1942":40,"1947":40,"1955":40,"1958":123,"1961":40,"1963":40,"1964":40,"1971":40,"1972":40,"1973":40,"1974":40,"1976":40,"1977":40,"1980":40,"1981":123,"1982":123,"1983":40,"1984":40,"1987":40,"1991":123,"1992":123,"1993":40,"1994":42,"1995":40,"2001":40},{"1942":278,"1947":898,"1955":43,"1958":899,"1961":900,"1963":835,"1964":901,"1971":902,"1972":211,"1973":138,"1974":903,"1976":904,"1977":50,"1980":905,"1981":906,"1982":520,"1983":140,"1984":161,"1987":358,"1991":217,"1992":907,"1993":908,"1994":909,"1995":199,"2001":910},{"1942":278,"1947":898,"1955":43,"1958":913,"1961":900,"1963":835,"1964":901,"1971":902,"1972":211,"1973":138,"1974":903,"1976":904,"1977":50,"1980":905,"1981":914,"1982":915,"1983":140,"1984":161,"1987":358,"1991":916,"1992":206,"1993":908,"1994":917,"1995":199,"2001":910},{"issue":3211,"pages":3212,"volume":3214},{"VOID":1525},{"VOID":3213},"28-44",{"VOID":3215},"270",407,{"total":3216,"publishYear":3218,"statisticByYear":3219},1994,{"2012":145,"2013":47,"2014":147,"2015":129,"2016":128,"2017":357,"2018":127,"2019":51,"2020":129,"2021":127,"2022":126,"2023":134,"2024":46},"1994-09-15",[892],[3223,3226,3229,3232,3235,3238,3241,3244,3248,3251,3254,3257,3260,3263,3266,3269,3272,3275,3278,3281,3284,3287,3290,3293,3296,3299,3302,3305,3308,3311,3314,3317,3320,3323,3326,3329,3332,3335,3338,3341,3344,3347,3350,3353,3356,3359,3362,3365,3368,3371,3374,3377,3380,3383,3386,3389,3392,3395,3398,3401,3404,3407,3410,3413,3416,3419,3422,3425,3428,3431],{"id":28,"text":3224,"url":28,"identifiers":3225},"Allsteadt J.(1993)Incubation Temperature Affects Body Size Energy Reserves and Sex of Hatchling Alligators. 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J., 1985, Biology of the Reptilia, 329",{},{"id":28,"text":3300,"url":28,"identifiers":3301},"10.1038\u002F296850a0",{"doi":3300},{"id":28,"text":3303,"url":28,"identifiers":3304},"10.1111\u002Fj.1469-7998.1983.tb05781.x",{"doi":3303},{"id":28,"text":3306,"url":28,"identifiers":3307},"10.1016\u002FS0022-5193(05)80435-7",{"doi":3306},{"id":28,"text":3309,"url":28,"identifiers":3310},"Hines T. C., 1968, Alligator research in Florida: A progress report, Proc. Annual Conf. S. E. Assoc. Game and Fish Comm., 22, 166",{},{"id":28,"text":3312,"url":28,"identifiers":3313},"10.1111\u002Fj.1469-7998.1987.tb07458.x",{"doi":3312},{"id":28,"text":3315,"url":28,"identifiers":3316},"10.1093\u002Fgenetics\u002F131.1.155",{"doi":3315},{"id":28,"text":3318,"url":28,"identifiers":3319},"10.1111\u002Fj.1469-7998.1989.tb05009.x",{"doi":3318},{"id":28,"text":3321,"url":28,"identifiers":3322},"King F. 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One common pattern shows low temperatures yielding only males and high temperatures yielding only females. Another common pattern has low as well as high temperatures yielding only or mostly females and some intermediate temperatures yielding mostly males. Patterns tend to be associated with the direction of sexual dimorphism in adult size, especially for species with strong dimorphism.\u003C\u002Fjats:p>\u003Cjats:p>Pivotal temperatures (those yielding 1:1 sex ratios) within the best‐documented species and genera tend to increase with both latitude and longitude across central and southern North America. These geographic trends probably reflect factors that affect nest temperatures (duration of growing season, insolation, and prevailing amounts of shading by vegetation).\u003C\u002Fjats:p>\u003Cjats:p>Data from a population of the alligator snapping turtle \u003Cjats:italic>(Macroclemys temminckii)\u003C\u002Fjats:italic> suggest that some embryos are temperature‐independent females because these individuals become females even when they are shifted among male‐producing temperatures during development. These individuals are also more frequent in clutches of small eggs. 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