Juan F. Rivelli, V. Santander, Sofía O. Peretti, N. E. Monesterolo, Ayelén D Nigra, Gabriela Previtali, M. R. Amaiden, C. Arce
{"title":"撤回声明","authors":"Juan F. Rivelli, V. Santander, Sofía O. Peretti, N. E. Monesterolo, Ayelén D Nigra, Gabriela Previtali, M. R. Amaiden, C. Arce","doi":"10.3109/10601333.2013.809988","DOIUrl":null,"url":null,"abstract":"Activation of Aldose Reductase by Interaction With Tubulin and Involvement of This Mechanism in Diabetic Cataract Formation. Diabetes. 10 April 2014 [Epub ahead of print]. DOI: 10.2337/db13-1265 DOI: 10.2337/db13-1265 Juan F. Rivelli, Verónica S. Santander, Sofía O. Peretti, Noelia E. Monesterolo, Ayelen D. Nigra, Gabriela Previtali, Marina R. Amaiden, Carlos A. Arce, Emiliano Primo, Angela T. Lisa, Juan Pie, and César H. Casale The corresponding author has formally requested to retract the above-titled paper, which was published ahead of print on 10 April 2014. The following image manipulations were included in the original version of the work: 1) Fig. 1A and B: Molecular weight markers from one blot were paired up with lanes from another blot. 2) Fig. 1A: Lanes 5 and 7 (aldose reductase revealed with anti-tubulin and tubulin revealed with anti–aldose reductase) were exchanged in from another immunoblot analysis. 3) Fig. 1D: Immunoblot images do not represent the original image as a portion of a doublet of the tubulin band (at elution volume 4). The original source image was erased to show a single band. 4) Fig. 2A: The molecular weight marker lane has been extracted from a different blot, and the tubulin band was spliced in from another source and digitally altered with the eraser tool to provide a better picture.","PeriodicalId":10446,"journal":{"name":"Clinical Research and Regulatory Affairs","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2013-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Statement of Retraction\",\"authors\":\"Juan F. Rivelli, V. Santander, Sofía O. Peretti, N. E. Monesterolo, Ayelén D Nigra, Gabriela Previtali, M. R. Amaiden, C. Arce\",\"doi\":\"10.3109/10601333.2013.809988\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Activation of Aldose Reductase by Interaction With Tubulin and Involvement of This Mechanism in Diabetic Cataract Formation. Diabetes. 10 April 2014 [Epub ahead of print]. DOI: 10.2337/db13-1265 DOI: 10.2337/db13-1265 Juan F. Rivelli, Verónica S. Santander, Sofía O. Peretti, Noelia E. Monesterolo, Ayelen D. Nigra, Gabriela Previtali, Marina R. Amaiden, Carlos A. Arce, Emiliano Primo, Angela T. Lisa, Juan Pie, and César H. Casale The corresponding author has formally requested to retract the above-titled paper, which was published ahead of print on 10 April 2014. The following image manipulations were included in the original version of the work: 1) Fig. 1A and B: Molecular weight markers from one blot were paired up with lanes from another blot. 2) Fig. 1A: Lanes 5 and 7 (aldose reductase revealed with anti-tubulin and tubulin revealed with anti–aldose reductase) were exchanged in from another immunoblot analysis. 3) Fig. 1D: Immunoblot images do not represent the original image as a portion of a doublet of the tubulin band (at elution volume 4). The original source image was erased to show a single band. 4) Fig. 2A: The molecular weight marker lane has been extracted from a different blot, and the tubulin band was spliced in from another source and digitally altered with the eraser tool to provide a better picture.\",\"PeriodicalId\":10446,\"journal\":{\"name\":\"Clinical Research and Regulatory Affairs\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Research and Regulatory Affairs\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3109/10601333.2013.809988\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Research and Regulatory Affairs","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10601333.2013.809988","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
醛糖还原酶与微管蛋白相互作用的激活及其参与糖尿病性白内障形成的机制。糖尿病。2014年4月10日[印刷前的Epub]。Juan F. Rivelli, Verónica S. Santander, Sofía O. Peretti, Noelia E. Monesterolo, Ayelen D. Nigra, Gabriela Previtali, Marina R. Amaiden, Carlos A. Arce, Emiliano Primo, Angela T. Lisa, Juan Pie和camesar H. Casale通讯作者已正式要求撤回上述标题的论文,该论文于2014年4月10日在印刷之前发表。以下图像处理包含在原始版本的工作中:1)图1A和B:来自一个印迹的分子量标记与来自另一个印迹的车道配对。2)图1A:通道5和通道7(醛糖还原酶与抗微管蛋白结合显示,微管蛋白与抗醛糖还原酶结合显示)从另一个免疫印迹分析中交换。3)图1D:免疫印迹图像不代表原始图像为微管蛋白带的一部分(洗脱体积为4)。原始源图像被擦除以显示单个带。4)图2A:从不同的印迹中提取分子量标记lane,从另一个来源拼接微管蛋白带,并使用橡皮擦工具进行数字修改,以提供更好的图像。
Activation of Aldose Reductase by Interaction With Tubulin and Involvement of This Mechanism in Diabetic Cataract Formation. Diabetes. 10 April 2014 [Epub ahead of print]. DOI: 10.2337/db13-1265 DOI: 10.2337/db13-1265 Juan F. Rivelli, Verónica S. Santander, Sofía O. Peretti, Noelia E. Monesterolo, Ayelen D. Nigra, Gabriela Previtali, Marina R. Amaiden, Carlos A. Arce, Emiliano Primo, Angela T. Lisa, Juan Pie, and César H. Casale The corresponding author has formally requested to retract the above-titled paper, which was published ahead of print on 10 April 2014. The following image manipulations were included in the original version of the work: 1) Fig. 1A and B: Molecular weight markers from one blot were paired up with lanes from another blot. 2) Fig. 1A: Lanes 5 and 7 (aldose reductase revealed with anti-tubulin and tubulin revealed with anti–aldose reductase) were exchanged in from another immunoblot analysis. 3) Fig. 1D: Immunoblot images do not represent the original image as a portion of a doublet of the tubulin band (at elution volume 4). The original source image was erased to show a single band. 4) Fig. 2A: The molecular weight marker lane has been extracted from a different blot, and the tubulin band was spliced in from another source and digitally altered with the eraser tool to provide a better picture.