封底图片

IF 2.4 4区生物学 Q4 CELL BIOLOGY

Cytoskeleton Pub Date : 2024-10-22 DOI:10.1002/cm.21940

{"title":"封底图片","authors":"","doi":"10.1002/cm.21940","DOIUrl":null,"url":null,"abstract":"<p>ON THE BACK COVER: DA-Raf inhibits ERK activation, resulting in the suppression of collective cell migration and invasion of KRAS-mutant cancer cells. In human pancreatic carcinoma MIA PaCa-2 cells, phospho-ERK1/2 (magenta) is suppressed by the expression of EGFP-DA-Raf (green). EGFP-DA-Raf is concentrated on the plasma membrane.</p><p>Credit: Aoi Matsuda and Takeshi Endo (Chiba University, Japan)\n\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":55186,"journal":{"name":"Cytoskeleton","volume":"81 9-10","pages":"C4"},"PeriodicalIF":2.4000,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cm.21940","citationCount":"0","resultStr":"{\"title\":\"Back Cover Image\",\"authors\":\"\",\"doi\":\"10.1002/cm.21940\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>ON THE BACK COVER: DA-Raf inhibits ERK activation, resulting in the suppression of collective cell migration and invasion of KRAS-mutant cancer cells. In human pancreatic carcinoma MIA PaCa-2 cells, phospho-ERK1/2 (magenta) is suppressed by the expression of EGFP-DA-Raf (green). EGFP-DA-Raf is concentrated on the plasma membrane.</p><p>Credit: Aoi Matsuda and Takeshi Endo (Chiba University, Japan)\\n\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":55186,\"journal\":{\"name\":\"Cytoskeleton\",\"volume\":\"81 9-10\",\"pages\":\"C4\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cm.21940\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cytoskeleton\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cm.21940\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytoskeleton","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cm.21940","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}

引用次数: 0

摘要

封底：DA-Raf 可抑制 ERK 激活，从而抑制 KRAS 突变癌细胞的集体迁移和侵袭。在人类胰腺癌 MIA PaCa-2 细胞中，EGFP-DA-Raf（绿色）的表达抑制了磷酸ERK1/2（品红色）。EGFP-DA-Raf集中在质膜上。资料来源：Aoi Matsuda 和 Takeshi Endo（日本千叶大学）

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Back Cover Image

查看原文本刊更多论文

Back Cover Image

ON THE BACK COVER: DA-Raf inhibits ERK activation, resulting in the suppression of collective cell migration and invasion of KRAS-mutant cancer cells. In human pancreatic carcinoma MIA PaCa-2 cells, phospho-ERK1/2 (magenta) is suppressed by the expression of EGFP-DA-Raf (green). EGFP-DA-Raf is concentrated on the plasma membrane.

Credit: Aoi Matsuda and Takeshi Endo (Chiba University, Japan)

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Cytoskeleton CELL BIOLOGY-

CiteScore

5.50

自引率

3.40%

发文量

审稿时长

6-12 weeks

期刊介绍： Cytoskeleton focuses on all aspects of cytoskeletal research in healthy and diseased states, spanning genetic and cell biological observations, biochemical, biophysical and structural studies, mathematical modeling and theory. This includes, but is certainly not limited to, classic polymer systems of eukaryotic cells and their structural sites of attachment on membranes and organelles, as well as the bacterial cytoskeleton, the nucleoskeleton, and uncoventional polymer systems with structural/organizational roles. Cytoskeleton is published in 12 issues annually, and special issues will be dedicated to especially-active or newly-emerging areas of cytoskeletal research.