找回密码
 To register

QQ登录

只需一步,快速开始

扫一扫,访问微社区

Titlebook: Discoidin Domain Receptors in Health and Disease; Rafael Fridman,Paul H. Huang Book 2016 Springer Science+Business Media New York 2016 can

[复制链接]
查看: 45417|回复: 57
发表于 2025-3-21 16:40:47 | 显示全部楼层 |阅读模式
书目名称Discoidin Domain Receptors in Health and Disease
编辑Rafael Fridman,Paul H. Huang
视频video
概述Provides critical reviews of an unexplored area of research focused on a unique set of RTKs that signal in response to collagen.Elucidates signaling networks in cancer cells activated by the extracell
图书封面Titlebook: Discoidin Domain Receptors in Health and Disease;  Rafael Fridman,Paul H. Huang Book 2016 Springer Science+Business Media New York 2016 can
描述The interactions of cells with their surrounding extracellular matrix (ECM) plays a pivotal role in driving normal cell behavior, from development to tissue differentiation and function. At the cellular level, organ homeostasis depends on a productive communication between cells and ECM, which eventually leads to the normal phenotypic repertoire that characterize each cell type in the organism.  A failure to establish these normal interactions and to interpret the cues emanating from the ECM is one of the major causes in abnormal development and the pathogenesis of multiple diseases. To recognize and act upon the biophysical signals that are generated by the cross talk between cells and ECM, the cells developed specific receptors, among them a unique set of receptor tyrosine kinases (RTKs), known as the Discoidin Domain Receptors (DDRs). The DDRs are the only RTKs that specifically bind to and are activated by collagen, a major protein component of the ECM. Hence, the DDRs are part of the signaling networks that translate information from the ECM, and thus they are key regulators of cell-matrix interactions. Under physiological conditions, DDRs control cell and tissue homeostasis b
出版日期Book 2016
关键词cancer migration; cell signaling; collagen; extracellular matrix; receptor tyrosine kinases
版次1
doihttps://doi.org/10.1007/978-1-4939-6383-6
isbn_softcover978-1-4939-8182-3
isbn_ebook978-1-4939-6383-6
copyrightSpringer Science+Business Media New York 2016
The information of publication is updating

书目名称Discoidin Domain Receptors in Health and Disease影响因子(影响力)




书目名称Discoidin Domain Receptors in Health and Disease影响因子(影响力)学科排名




书目名称Discoidin Domain Receptors in Health and Disease网络公开度




书目名称Discoidin Domain Receptors in Health and Disease网络公开度学科排名




书目名称Discoidin Domain Receptors in Health and Disease被引频次




书目名称Discoidin Domain Receptors in Health and Disease被引频次学科排名




书目名称Discoidin Domain Receptors in Health and Disease年度引用




书目名称Discoidin Domain Receptors in Health and Disease年度引用学科排名




书目名称Discoidin Domain Receptors in Health and Disease读者反馈




书目名称Discoidin Domain Receptors in Health and Disease读者反馈学科排名




单选投票, 共有 0 人参与投票
 

0票 0%

Perfect with Aesthetics

 

0票 0%

Better Implies Difficulty

 

0票 0%

Good and Satisfactory

 

0票 0%

Adverse Performance

 

0票 0%

Disdainful Garbage

您所在的用户组没有投票权限
发表于 2025-3-21 22:39:31 | 显示全部楼层
Staging and Performing Translationnd implantation, as well as wound healing and auditory sensation. In addition, genetically modified mice and DDR mutant mice highlight the role of DDRs in the enhancement or attenuation of diseases, including fibrosis, atherosclerosis, and osteoarthritis in various conditions..Studies on mouse model
发表于 2025-3-22 03:02:48 | 显示全部楼层
发表于 2025-3-22 06:05:59 | 显示全部楼层
发表于 2025-3-22 09:24:04 | 显示全部楼层
https://doi.org/10.1007/978-3-322-94744-4etastasis. The molecular mechanisms underlying how DDRs contribute to these and other pathologies need to be understood to find new markers and for development of therapeutic agents for treatment of disease. This is particularly the case for EOC in which mechanisms explaining the atypically high lev
发表于 2025-3-22 13:30:50 | 显示全部楼层
https://doi.org/10.1007/978-3-322-93990-6 we describe the key molecular interactions and signalling pathways elucidated by these studies and where appropriate highlight situations where signalling outcomes appear to be dependent on cellular context. We present an emerging molecular portrait of the DDRs and highlight areas where more intens
发表于 2025-3-22 20:15:20 | 显示全部楼层
https://doi.org/10.1007/978-3-322-93990-6llagen-independent cell–cell interactions. Collagen-activated DDR1 signals through NF-kB, PI3K/Akt and p38, JNK, and ERK1/2 MAPKs, while inactive DDR1 appears to interact with E-cadherin promoting cell–cell interactions. DDR1 interacts with several other receptors, including Notch1 and Frizzled5, an
发表于 2025-3-22 21:38:41 | 显示全部楼层
https://doi.org/10.1007/978-3-663-01602-1n osteoarthritic joint. If, as we suspect, DDR2 is one of the major contributors to progressive joint failure, then drugs that inhibit the kinase activity of DDR2 may be able to ameliorate osteoarthritis conditions.
发表于 2025-3-23 01:53:10 | 显示全部楼层
https://doi.org/10.1007/978-3-663-01602-1e pathways were not activated which resulted to an impressive preservation of renal function and structure. Further proof of evidence came from experiments with in vivo administration of antisense oligonucleotides against DDR1. The fact that this pharmacogenetic approach protected animals against th
发表于 2025-3-23 06:46:42 | 显示全部楼层
 关于派博传思  派博传思旗下网站  友情链接
派博传思介绍 公司地理位置 论文服务流程 影响因子官网 SITEMAP 大讲堂 北京大学 Oxford Uni. Harvard Uni.
发展历史沿革 期刊点评 投稿经验总结 SCIENCEGARD IMPACTFACTOR 派博系数 清华大学 Yale Uni. Stanford Uni.
|Archiver|手机版|小黑屋| 派博传思国际 ( 京公网安备110108008328) GMT+8, 2025-5-15 09:43
Copyright © 2001-2015 派博传思   京公网安备110108008328 版权所有 All rights reserved
快速回复 返回顶部 返回列表