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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. 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ESTIMATION OF PEPSIN, TRYPSIN, PAPAIN, AND CATHEPSIN WITH HEMOGLOBIN",{"VOID":891},"19873094",{"VOID":893},"10.1085\u002Fjgp.22.1.79",[102],"https:\u002F\u002Frupress.org\u002Fjgp\u002Farticle\u002F22\u002F1\u002F79\u002F11764\u002FTHE-ESTIMATION-OF-PEPSIN-TRYPSIN-PAPAIN-AND",[897],{"id":898,"sortIndex":36,"researcher":26,"roles":899,"affiliations":900,"properties":912},"de6a46e1-2106-4217-9576-674869293dc6",[],[901],{"id":902,"sortIndex":36,"affiliation":903,"properties":26},"ed8fd1a5-cc74-41b7-9dc2-f95889bdb4d7",{"id":904,"createTime":905,"updateTime":906,"relativeEntities":907,"slug":908,"properties":909,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"31f6dba9-faec-4274-a686-28143d785281","2024-10-02T01:29:31.739+00:00","2024-10-10T06:14:05.019+00:00",[],"From-the-Laboratories-of-The-Rockefeller-Institute-for-Medical-Research-Princeton-New-Jersey",{"title":910},{"EN":911},"From the Laboratories of The Rockefeller Institute for Medical Research, Princeton, New Jersey",{"openalex":913,"title":915},{"VOID":914},"A5023340745",{"EN":916},"M. 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Impedance changes were determined as functions of current and of the composition of the environmental solutions. It was shown that rectification is present in asymmetrical systems and that it increases with the membrane potential. The behavior in pairs of solutions of the same salt at different concentrations has formed the basis for the studies although a few experiments with different salts at the same concentrations gave results consistent with the conclusions drawn.\u003C\u002Fjats:p>\n               \u003Cjats:p>A theoretical picture has been presented based on the use of the general kinetic equations for ion motion under the influence of diffusion and electrical forces and on a consideration of possible membrane structures. The equations have been solved for two very simple cases; one based on the assumption of microscopic electroneutrality, and the other on the assumption of a constant electric field. The latter was found to give better results than the former in interpreting the data on potentials and rectification, showing agreement, however, of the right order of magnitude only. Although the indications are that a careful treatment of boundary conditions may result in better agreement with experiment, no attempt has been made to carry this through since the data now available are not sufficiently complete or reproducible. Applications of the second theoretical case to the squid giant axon have been made showing qualitative agreement with the rectification properties and very good agreement with the membrane potential data.\u003C\u002Fjats:p>",{"EN":975},"POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES",{"VOID":977},"19873371",{"VOID":979},"10.1085\u002Fjgp.27.1.37",[102],"https:\u002F\u002Frupress.org\u002Fjgp\u002Farticle\u002F27\u002F1\u002F37\u002F12030\u002FPOTENTIAL-IMPEDANCE-AND-RECTIFICATION-IN-MEMBRANES",[983],{"id":984,"sortIndex":36,"researcher":26,"roles":985,"affiliations":986,"properties":998},"238b8b62-612b-4802-b8de-09930b80f6bf",[],[987],{"id":988,"sortIndex":36,"affiliation":989,"properties":26},"ea708f03-dcd7-400a-adaa-fad690ab1397",{"id":990,"createTime":991,"updateTime":992,"relativeEntities":993,"slug":994,"properties":995,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"21594818-b880-4420-bb03-439e18055736","2024-01-15T02:27:00.633+00:00","2024-12-10T11:06:55.860+00:00",[],"From-the-Department-of-Physiology-College-of-Physicians-and-Surgeons-Columbia-University-New-York",{"title":996},{"VI":997},"From the Department of Physiology, College of Physicians and Surgeons, Columbia University, New York",{"openalex":999,"title":1001},{"VOID":1000},"A5106261506",{"EN":1002},"David E. 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The kinetics of the Na currents are governed by a composite of voltage- and time-dependent gating processes with voltage- and time-dependent block of channels by drug. Conventional measurements of steady-state sodium inactivation by use of 50-ms prepulses show a large negative voltage shift of the inactivation curve with neutral benzocaine and with some ionizable amines like lidocaine and tetracaine, but no shift is seen with quaternary OX-572. However, when the experiment is done with repetitive application of a prepulse-testpulse waveform, a shift with the quaternary cations (applied internally) is seen as well. 1-min hyperpolarizations of lidocaine- or tetracaine-treated fibers restore two to four times as many channels to the conducting pool as 50-ms hyperpolarizations. Raising the external Ca++ concentration also has a strong unblocking effect. These manipulations do not relieve block in fibers treated with internal quaternary drugs. The results are interpreted in terms of a single receptor in Na channels for the different drug types. Lipid-soluble drug forms are thought to come and go from the receptor via a hydrophobic region of the membrane, while charged and less lipid-soluble forms pass via a hydrophilic region (the inner channel mouth). The hydrophilic pathway is open only when the gates of the channel are open. Any drug form in the channel increases the probability of closing the inactivation gate which, in effect, is equivalent to a negative shift of the voltage dependence of inactivation.\u003C\u002Fjats:p>",{"EN":1057},"Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction.",{"VOID":1059},"300786",{"VOID":1061},"10.1085\u002Fjgp.69.4.497","Author affiliation is blank",[102],"https:\u002F\u002Frupress.org\u002Fjgp\u002Farticle\u002F69\u002F4\u002F497\u002F26804\u002FLocal-anesthetics-hydrophilic-and-hydrophobic",[1066],{"id":1067,"sortIndex":36,"researcher":26,"roles":1068,"affiliations":1069,"properties":1070},"f2b3c052-06c3-46de-8379-aad53d578148",[],[],{"openalex":1071,"orcid":1073,"title":1075},{"VOID":1072},"A5049507794",{"VOID":1074},"https:\u002F\u002Forcid.org\u002F0000-0002-7266-1671",{"EN":1076},"Bertil Hille",{"url":26,"publisher":1078,"properties":1103},{"id":659,"createTime":660,"updateTime":661,"relativeEntities":1079,"slug":663,"properties":1080,"entityType":24,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"subjectFields":1086,"manageAffiliations":1087,"indexDatabases":1088,"url":744,"thumbnailPath":26,"statistic":26,"gsStatistic":26,"type":26,"analyzePriority":26},[],{"country":1081,"issn":1082,"introduce":1083,"eissn":1084,"title":1085},{"VOID":666},{"VOID":668},{"EN":670},{"VOID":672},{"EN":674},[],[],[1089,1096],{"id":707,"indexDatabase":1090,"url":720,"indexYears":721,"academicFieldIds":1095,"indexDatabaseRanking":724},{"id":709,"createTime":710,"updateTime":711,"relativeEntities":1091,"label":1092,"description":1093,"key":717,"publicationTags":1094,"standard":26},[],{"EN":714,"VI":714},{"EN":714,"VI":716},[719],[723],{"id":726,"indexDatabase":1097,"url":741,"indexYears":26,"academicFieldIds":1102,"indexDatabaseRanking":26},{"id":728,"createTime":729,"updateTime":730,"relativeEntities":1098,"label":1099,"description":1100,"key":737,"publicationTags":1101,"standard":26},[],{"EN":733,"VI":733},{"VI":735,"EN":736},[739,740],[743],{"volume":1104,"pages":1106,"issue":1108},{"VOID":1105},"69",{"VOID":1107},"497-515",{"VOID":1109},"4",1728,{"total":1110,"publishYear":26,"statisticByYear":1112},{"2012":125,"2013":287,"2014":396,"2015":285,"2016":240,"2017":260,"2018":396,"2019":244,"2020":240,"2021":238,"2022":159,"2023":241,"2024":52},"1977-04-01",1977,[],{"id":1117,"createTime":1118,"updateTime":1118,"relativeEntities":1119,"slug":1120,"properties":1121,"entityType":769,"verifyStatus":25,"verifyTime":1118,"verifyNote":770,"syncStatus":28,"languages":1137,"translateLanguages":26,"viewCount":36,"primaryUrl":1138,"fullTextUrl":26,"authors":1139,"publicationType":823,"publisherRelationship":1174,"citationCount":1206,"citationInfo":1207,"publishDate":1209,"publishYear":1210,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":1211,"isForceReanalyzing":873},"a36a5758-9979-443f-9ff7-3bfcc5c715a0","2024-12-06T12:08:14.931+00:00",[],"INDEPENDENT-FUNCTIONS-OF-VIRAL-PROTEIN-AND-NUCLEIC-ACID-IN-GROWTH-OF-BACTERIOPHAGE",{"mag":1122,"keywords":1124,"pmc":1125,"openalex":1127,"abstract":1129,"title":1131,"pm":1133,"doi":1135},{"VOID":1123},"1988037647",{},{"VOID":1126},"2147348",{"VOID":1128},"W1988037647",{"EN":1130},"\u003Cjats:p>1. Osmotic shock disrupts particles of phage T2 into material containing nearly all the phage sulfur in a form precipitable by antiphage serum, and capable of specific adsorption to bacteria. It releases into solution nearly all the phage DNA in a form not precipitable by antiserum and not adsorbable to bacteria. The sulfur-containing protein of the phage particle evidently makes up a membrane that protects the phage DNA from DNase, comprises the sole or principal antigenic material, and is responsible for attachment of the virus to bacteria.\u003C\u002Fjats:p>\n               \u003Cjats:p>2. Adsorption of T2 to heat-killed bacteria, and heating or alternate freezing and thawing of infected cells, sensitize the DNA of the adsorbed phage to DNase. These treatments have little or no sensitizing effect on unadsorbed phage. Neither heating nor freezing and thawing releases the phage DNA from infected cells, although other cell constituents can be extracted by these methods. These facts suggest that the phage DNA forms part of an organized intracellular structure throughout the period of phage growth.\u003C\u002Fjats:p>\n               \u003Cjats:p>3. Adsorption of phage T2 to bacterial debris causes part of the phage DNA to appear in solution, leaving the phage sulfur attached to the debris. Another part of the phage DNA, corresponding roughly to the remaining half of the DNA of the inactivated phage, remains attached to the debris but can be separated from it by DNase. Phage T4 behaves similarly, although the two phages can be shown to attach to different combining sites. The inactivation of phage by bacterial debris is evidently accompanied by the rupture of the viral membrane.\u003C\u002Fjats:p>\n               \u003Cjats:p>4. Suspensions of infected cells agitated in a Waring blendor release 75 per cent of the phage sulfur and only 15 per cent of the phage phosphorus to the solution as a result of the applied shearing force. The cells remain capable of yielding phage progeny.\u003C\u002Fjats:p>\n               \u003Cjats:p>5. The facts stated show that most of the phage sulfur remains at the cell surface and most of the phage DNA enters the cell on infection. Whether sulfur-free material other than DNA enters the cell has not been determined. The properties of the sulfur-containing residue identify it as essentially unchanged membranes of the phage particles. All types of evidence show that the passage of phage DNA into the cell occurs in non-nutrient medium under conditions in which other known steps in viral growth do not occur.\u003C\u002Fjats:p>\n               \u003Cjats:p>6. The phage progeny yielded by bacteria infected with phage labeled with radioactive sulfur contain less than 1 per cent of the parental radioactivity. The progeny of phage particles labeled with radioactive phosphorus contain 30 per cent or more of the parental phosphorus.\u003C\u002Fjats:p>\n               \u003Cjats:p>7. Phage inactivated by dilute formaldehyde is capable of adsorbing to bacteria, but does not release its DNA to the cell. This shows that the interaction between phage and bacterium resulting in release of the phage DNA from its protective membrane depends on labile components of the phage particle. By contrast, the components of the bacterium essential to this interaction are remarkably stable. The nature of the interaction is otherwise unknown.\u003C\u002Fjats:p>\n               \u003Cjats:p>8. The sulfur-containing protein of resting phage particles is confined to a protective coat that is responsible for the adsorption to bacteria, and functions as an instrument for the injection of the phage DNA into the cell. This protein probably has no function in the growth of intracellular phage. The DNA has some function. Further chemical inferences should not be drawn from the experiments presented.\u003C\u002Fjats:p>",{"EN":1132},"INDEPENDENT FUNCTIONS OF VIRAL PROTEIN AND NUCLEIC ACID IN GROWTH OF BACTERIOPHAGE",{"VOID":1134},"12981234",{"VOID":1136},"10.1085\u002Fjgp.36.1.39",[102],"https:\u002F\u002Frupress.org\u002Fjgp\u002Farticle\u002F36\u002F1\u002F39\u002F30168\u002FINDEPENDENT-FUNCTIONS-OF-VIRAL-PROTEIN-AND-NUCLEIC",[1140,1159],{"id":1141,"sortIndex":115,"researcher":26,"roles":1142,"affiliations":1143,"properties":1154},"65a76b95-4767-4390-85bf-45f19e005a83",[],[1144],{"id":1145,"sortIndex":36,"affiliation":1146,"properties":26},"dce0be18-7a99-49c5-8c68-82c1e4004ece",{"id":1147,"createTime":1148,"updateTime":1148,"relativeEntities":1149,"slug":1150,"properties":1151,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"c28c16f3-9ba8-45e0-8ece-2fe74deb07d2","2024-12-06T12:08:14.937+00:00",[],"From-the-Department-of-Genetics-Carnegie-Institution-of-Washington-Cold-Spring-Harbor-Long-Island",{"title":1152},{"EN":1153},"From the Department of Genetics, Carnegie Institution of Washington, Cold Spring Harbor, Long Island",{"openalex":1155,"title":1157},{"VOID":1156},"A5006754312",{"EN":1158},"Martha Chase",{"id":1160,"sortIndex":36,"researcher":26,"roles":1161,"affiliations":1162,"properties":1169},"e663d72a-8cf4-47ac-b541-deef9e900d66",[],[1163],{"id":1164,"sortIndex":36,"affiliation":1165,"properties":26},"9c19bb5f-e626-4709-9c51-bc91377b2be7",{"id":1147,"createTime":1148,"updateTime":1148,"relativeEntities":1166,"slug":1150,"properties":1167,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},[],{"title":1168},{"EN":1153},{"openalex":1170,"title":1172},{"VOID":1171},"A5037196391",{"EN":1173},"A. 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In most of these ions a quaternary nitrogen is surrounded by three ethyl groups and a fourth group that is very hydrophobic. Several of the ions cause inactivation of gK, a type of ionic gating that is not normally seen in squid axon; i.e., after depolarization gK increases and then spontaneously decreases to a small fraction of its peak value even though the depolarization is maintained. Observations on the mechanism of this gating show that (a) QA (quaternary ammonium) ions only enter K+ channels that have open activation gates (the normal permeability gates). (b) The activation gates of QA-occluded channels do not close readily. (c) Hyperpolarization helps to clear QA ions from the channels. (d) Raising the external K+ concentration also helps to clear QA ions from the channels. Observations (c) and (d) strongly suggest that K+ ions traverse the membrane by way of pores, and they cannot be explained by the usual type of carrier model. The data suggest that a K+ pore has two distinct parts: a wide inner mouth that can accept a hydrated K+ ion or a TEA+-like ion, and a narrower portion that can accept a dehydrated or partially dehydrated K+ ion, but not TEA+.\u003C\u002Fjats:p>",{"EN":1228},"Interaction of Tetraethylammonium Ion Derivatives with the Potassium Channels of Giant Axons",{"VOID":1230},"5112659",{"VOID":1232},"10.1085\u002Fjgp.58.4.413",[102],"https:\u002F\u002Frupress.org\u002Fjgp\u002Farticle\u002F58\u002F4\u002F413\u002F12987\u002FInteraction-of-Tetraethylammonium-Ion-Derivatives",[1236],{"id":1237,"sortIndex":36,"researcher":26,"roles":1238,"affiliations":1239,"properties":1250},"3aa7d4fc-9e20-4d74-9fe4-66c84a374d0a",[],[1240],{"id":1241,"sortIndex":36,"affiliation":1242,"properties":26},"337b9283-8040-4348-b7b1-75908ca532ed",{"id":1243,"createTime":1244,"updateTime":1244,"relativeEntities":1245,"slug":1246,"properties":1247,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"f0b0ff97-8bcb-479b-a912-f04480813c8b","2024-09-12T04:01:19.727+00:00",[],"From-the-Department-of-Physiology-University-of-Rochester-School-of-Medicine-and-Dentistry-Rochester-New-York-14620-and-the-Laboratorio-de-Fisiologia-Celular-Montemar-Chile",{"title":1248},{"EN":1249},"From the Department of Physiology, University of Rochester School of Medicine and Dentistry, Rochester, New York 14620, and the Laboratorio de Fisiologia Celular, Montemar, Chile",{"openalex":1251,"title":1253},{"VOID":1252},"A5069282218",{"EN":1254},"Clay M. Armstrong",{"url":26,"publisher":1256,"properties":1281},{"id":659,"createTime":660,"updateTime":661,"relativeEntities":1257,"slug":663,"properties":1258,"entityType":24,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"subjectFields":1264,"manageAffiliations":1265,"indexDatabases":1266,"url":744,"thumbnailPath":26,"statistic":26,"gsStatistic":26,"type":26,"analyzePriority":26},[],{"country":1259,"issn":1260,"introduce":1261,"eissn":1262,"title":1263},{"VOID":666},{"VOID":668},{"EN":670},{"VOID":672},{"EN":674},[],[],[1267,1274],{"id":707,"indexDatabase":1268,"url":720,"indexYears":721,"academicFieldIds":1273,"indexDatabaseRanking":724},{"id":709,"createTime":710,"updateTime":711,"relativeEntities":1269,"label":1270,"description":1271,"key":717,"publicationTags":1272,"standard":26},[],{"EN":714,"VI":714},{"EN":714,"VI":716},[719],[723],{"id":726,"indexDatabase":1275,"url":741,"indexYears":26,"academicFieldIds":1280,"indexDatabaseRanking":26},{"id":728,"createTime":729,"updateTime":730,"relativeEntities":1276,"label":1277,"description":1278,"key":737,"publicationTags":1279,"standard":26},[],{"EN":733,"VI":733},{"VI":735,"EN":736},[739,740],[743],{"volume":1282,"pages":1284,"issue":1286},{"VOID":1283},"58",{"VOID":1285},"413-437",{"VOID":1109},922,{"total":1287,"publishYear":26,"statisticByYear":1289},{"2012":244,"2013":124,"2014":103,"2015":124,"2016":103,"2017":124,"2018":103,"2019":52,"2020":298,"2021":52,"2022":116,"2023":158,"2024":114},"1971-10-01",1971,[],{"id":1294,"createTime":1295,"updateTime":1296,"relativeEntities":1297,"slug":1298,"properties":1299,"entityType":769,"verifyStatus":25,"verifyTime":1295,"verifyNote":770,"syncStatus":28,"languages":1317,"translateLanguages":26,"viewCount":36,"primaryUrl":1318,"fullTextUrl":26,"authors":1319,"publicationType":823,"publisherRelationship":1339,"citationCount":1372,"citationInfo":1373,"publishDate":1375,"publishYear":1376,"citationAnalyzeStatus":1377,"lastCitationAnalyze":1378,"indexDatabases":26,"openAccess":26,"references":1379,"isForceReanalyzing":873},"1bcfd51f-460e-4fe2-80b9-fe8a936e5e4c","2024-11-27T22:30:52.318+00:00","2026-02-11T07:31:38.064+00:00",[],"Time-and-calcium-dependence-of-activation-and-inactivation-of-calcium-induced-release-of-calcium-from-the-sarcoplasmic-reticulum-of-a-skinned-canine-cardiac-Purkinje-cell-",{"mag":1300,"keywords":1302,"pmc":1303,"openalex":1305,"abstract":1307,"title":1309,"pm":1311,"doi":1313,"gsPaper":1315},{"VOID":1301},"2011038097",{},{"VOID":1304},"2215800",{"VOID":1306},"W2011038097",{"EN":1308},"\u003Cjats:p>Microprocessor-controlled changes of [free Ca2+] at the outer surface of the sarcoplasmic reticulum (SR) wrapped around individual myofibrils of a skinned canine cardiac Purkinje cell and aequorin bioluminescence recording were used to study the mechanism of Ca2+-induced release of Ca2+ from the SR. This Ca2+ release is triggered by a rapid increase of [free Ca2+] at the outer surface of the SR of a previously quiescent skinned cell. Ca2+-induced release of Ca2+ occurred under conditions that prevented any synthesis of ATP from ADP, was affected differentially by interventions that depressed the SR Ca2+ pump about equally, and required ionic conditions incompatible with all known Ca2+-releasing, uncoupled, partial reactions of the Ca2+ pump. Increasing the [free Ca2+]trigger up to an optimum increased the amount of Ca2+ released. A supraoptimum increase of [free Ca2+] trigger inactivated Ca2+-induced release of Ca2+, but partial inactivation was also observed at [free Ca2+] below that necessary for its activation. The amplitude of the Ca2+ release induced by a given increase of [free Ca2+] decreased when the rate of this increase was diminished. These results suggest that Ca2+-induced release of Ca2+ is through a channel across the SR membrane with time- and Ca2+-dependent activation and inactivation. The inactivating binding site would have a higher affinity for Ca2+ but a lower rate constant than the activating site. Inactivation appeared to be a first-order kinetic reaction of Ca2+ binding to a single site at the outer face of the SR with a Q10 of 1.68. The removal of inactivation was the slowest step of the cycle, responsible for a highly temperature-dependent (Q10 approximately 4.00) refractory period.\u003C\u002Fjats:p>",{"EN":1310},"Time and calcium dependence of activation and inactivation of calcium-induced release of calcium from the sarcoplasmic reticulum of a skinned canine cardiac Purkinje 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Ionic currents under voltage-clamp conditions were measured in sodium-free solutions containing the test cation. The measured reversal potential and the Goldman equation were used to calculate relative permeabilities. The permeability sequence was: sodium ≈ hydroxylamine > hydrazine > ammonium ≈ formamidine ≈ guanidine ≈ hydroxyguanidine > aminoguanididine >> methylamine. The cations of the following compounds were not measurably permeant: N-methylhydroxylamine, methylhydrazine, methylamine, methylguanidine, acetamidine, dimethylamine, tetramethylammonium, tetraethylammonium, ethanolamine, choline, tris(hydroxymethyl)amino methane, imidazole, biguanide, and triaminoguanidine. Thus methyl and methylene groups render cations impermeant. The results can be explained on geometrical grounds by assuming that the sodium channel is an oxygen-lined pore about 3 A by 5 A in cross-section. One pair of oxygens is assumed to be an ionized carboxylic acid. Methyl and amino groups are wider than the 3 A width of the channel. Nevertheless, cations containing amino groups can slide through the channel by making hydrogen bonds to the oxygens. However, methyl groups, being unable to form hydrogen bonds, are too wide to pass through.\u003C\u002Fjats:p>",{"EN":1521},"The Permeability of the Sodium Channel to Organic Cations in Myelinated Nerve",{"VOID":1523},"5315827",{"VOID":1525},"10.1085\u002Fjgp.58.6.599",[102],"https:\u002F\u002Frupress.org\u002Fjgp\u002Farticle\u002F58\u002F6\u002F599\u002F31396\u002FThe-Permeability-of-the-Sodium-Channel-to-Organic",[1529],{"id":1530,"sortIndex":36,"researcher":26,"roles":1531,"affiliations":1532,"properties":1543},"eb1e36ef-3d22-4d04-8bec-ad8cbe3a82c8",[],[1533],{"id":1534,"sortIndex":36,"affiliation":1535,"properties":26},"eb432b31-d942-4f2c-83b3-881fa3b05543",{"id":1536,"createTime":1537,"updateTime":1537,"relativeEntities":1538,"slug":1539,"properties":1540,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"9d61d085-d3f6-449a-a216-54e23e74b398","2024-09-22T11:00:56.419+00:00",[],"From-the-Department-of-Physiology-and-Biophysics-University-of-Washington-School-of-Medicine-Seattle-Washington-98105",{"title":1541},{"EN":1542},"From the Department of Physiology and Biophysics, University of Washington School of Medicine, Seattle, Washington 98105",{"openalex":1544,"orcid":1545,"title":1546},{"VOID":1072},{"VOID":1074},{"EN":1076},{"url":26,"publisher":1548,"properties":1573},{"id":659,"createTime":660,"updateTime":661,"relativeEntities":1549,"slug":663,"properties":1550,"entityType":24,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36,"subjectFields":1556,"manageAffiliations":1557,"indexDatabases":1558,"url":744,"thumbnailPath":26,"statistic":26,"gsStatistic":26,"type":26,"analyzePriority":26},[],{"country":1551,"issn":1552,"introduce":1553,"eissn":1554,"title":1555},{"VOID":666},{"VOID":668},{"EN":670},{"VOID":672},{"EN":674},[],[],[1559,1566],{"id":707,"indexDatabase":1560,"url":720,"indexYears":721,"academicFieldIds":1565,"indexDatabaseRanking":724},{"id":709,"createTime":710,"updateTime":711,"relativeEntities":1561,"label":1562,"description":1563,"key":717,"publicationTags":1564,"standard":26},[],{"EN":714,"VI":714},{"EN":714,"VI":716},[719],[723],{"id":726,"indexDatabase":1567,"url":741,"indexYears":26,"academicFieldIds":1572,"indexDatabaseRanking":26},{"id":728,"createTime":729,"updateTime":730,"relativeEntities":1568,"label":1569,"description":1570,"key":737,"publicationTags":1571,"standard":26},[],{"EN":733,"VI":733},{"VI":735,"EN":736},[739,740],[743],{"volume":1574,"pages":1575,"issue":1577},{"VOID":1283},{"VOID":1576},"599-619",{"VOID":856},749,{"total":1578,"publishYear":26,"statisticByYear":1580},{"2012":356,"2013":50,"2014":173,"2015":51,"2016":53,"2017":103,"2018":53,"2019":116,"2020":158,"2021":158,"2022":111,"2023":135,"2024":111},"1971-12-01",[],{"id":1584,"createTime":1585,"updateTime":1585,"relativeEntities":1586,"slug":1587,"properties":1588,"entityType":769,"verifyStatus":25,"verifyTime":1604,"verifyNote":770,"syncStatus":28,"languages":1605,"translateLanguages":26,"viewCount":36,"primaryUrl":1606,"fullTextUrl":26,"authors":1607,"publicationType":823,"publisherRelationship":1645,"citationCount":1677,"citationInfo":1678,"publishDate":1680,"publishYear":1681,"citationAnalyzeStatus":28,"lastCitationAnalyze":26,"indexDatabases":26,"openAccess":26,"references":1682,"isForceReanalyzing":873},"8bd0fab4-af8e-4be7-81a1-2b99f1f0f3a1","2024-09-01T18:05:00.397+00:00",[],"A-Physical-Interpretation-of-the-Phenomenological-Coefficients-of-Membrane-Permeability",{"mag":1589,"keywords":1591,"pmc":1592,"openalex":1594,"abstract":1596,"title":1598,"pm":1600,"doi":1602},{"VOID":1590},"2115780849",{},{"VOID":1593},"2195155",{"VOID":1595},"W2115780849",{"EN":1597},"\u003Cjats:p>A \"translation\" of the phenomenological permeability coefficients into friction and distribution coefficients amenable to physical interpretation is presented. Expressions are obtained for the solute permeability coefficient ω and the reflection coefficient σ for both non-electrolytic and electrolytic permeants. An analysis of the coefficients is given for loose membranes as well as for dense natural membranes where transport may go through capillaries or by solution in the lipoid parts of the membrane. Water diffusion and filtration and the relation between these and capillary pore radius of the membrane are discussed. For the permeation of ions through the charged membranes equations are developed for the case of zero electrical current in the membrane. The correlation of σ with ω and Lp for electrolytes resembles that for non-electrolytes. In this case ω and σ depend markedly on ion concentration and on the charge density of the membrane. The reflection coefficient may assume negative values indicating anomalous osmosis. An analysis of the phenomena of anomalous osmosis was carried out for the model of Teorell and Meyer and Sievers and the results agree with the experimental data of Loeb and of Grim and Sollner. A set of equations and reference curves are presented for the evaluation of ω and σ in the transport of polyvalent ions through charged membranes.\u003C\u002Fjats:p>",{"EN":1599},"A Physical Interpretation of the Phenomenological Coefficients of Membrane Permeability",{"VOID":1601},"13752127",{"VOID":1603},"10.1085\u002Fjgp.45.1.143","2024-09-01T18:05:00.396+00:00",[102],"https:\u002F\u002Frupress.org\u002Fjgp\u002Farticle\u002F45\u002F1\u002F143\u002F30570\u002FA-Physical-Interpretation-of-the-Phenomenological",[1608,1630],{"id":1609,"sortIndex":36,"researcher":26,"roles":1610,"affiliations":1611,"properties":1623},"4476ffb3-8048-4805-9882-dd3bb26fbc92",[],[1612],{"id":1613,"sortIndex":36,"affiliation":1614,"properties":26},"a0ad487d-fdf2-47b2-baa7-8c4028f3538c",{"id":1615,"createTime":1616,"updateTime":1617,"relativeEntities":1618,"slug":1619,"properties":1620,"entityType":98,"verifyStatus":28,"verifyTime":26,"verifyNote":26,"syncStatus":28,"languages":26,"translateLanguages":26,"viewCount":36},"a646aab1-e549-4655-b7f7-81d714bd49d7","2023-12-17T13:50:32.379+00:00","2024-09-01T18:05:00.411+00:00",[],"From-The-Weizmann-Institute-of-Science-Rehovoth-Israel",{"title":1621},{"VI":1622},"From The Weizmann Institute of Science, Rehovoth, Israel",{"openalex":1624,"orcid":1626,"title":1628},{"VOID":1625},"A5041456564",{"VOID":1627},"https:\u002F\u002Forcid.org\u002F0000-0001-7757-8335",{"EN":1629},"O. 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