Literature DB >> 16988728

Specific molecular targeting of renal injury in obstructive nephropathy.

R L Chevalier1.   

Abstract

Progression of most renal disease involves tubulointerstitial injury, characterized by tubular atrophy, inflammatory cell infiltration, and interstitial fibrosis. Transforming growth factor-beta1 is central in this process. As reported by Moon et al., molecular targeting of the transforming growth factor-beta1 signaling pathway can markedly suppress renal injury resulting from unilateral ureteral obstruction, an established model of obstructive nephropathy. Specific kinase inhibitors are promising therapeutic agents to slow or attenuate progressive renal fibrosis.

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Year:  2006        PMID: 16988728     DOI: 10.1038/sj.ki.5001815

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  4 in total

1.  Discoidin domain receptor 1 is a major mediator of inflammation and fibrosis in obstructive nephropathy.

Authors:  Dominique Guerrot; Monique Kerroch; Sandrine Placier; Sophie Vandermeersch; Claire Trivin; Mouna Mael-Ainin; Christos Chatziantoniou; Jean-Claude Dussaule
Journal:  Am J Pathol       Date:  2011-05-13       Impact factor: 4.307

2.  Puerarin attenuates renal fibrosis by reducing oxidative stress induced-epithelial cell apoptosis via MAPK signal pathways in vivo and in vitro.

Authors:  Xiangjun Zhou; Chen Bai; Xinbo Sun; Xiaoxin Gong; Yong Yang; Congbo Chen; Guang Shan; Qisheng Yao
Journal:  Ren Fail       Date:  2017-11       Impact factor: 2.606

3.  MiR-27b-3p inhibits the progression of renal fibrosis via suppressing STAT1.

Authors:  Lin Bai; Yongtao Lin; Juan Xie; Yiyuan Zhang; Hongwu Wang; Donghui Zheng
Journal:  Hum Cell       Date:  2021-01-17       Impact factor: 4.174

4.  The genetics of diabetic nephropathy.

Authors:  Eoin Brennan; Caitríona McEvoy; Denise Sadlier; Catherine Godson; Finian Martin
Journal:  Genes (Basel)       Date:  2013-11-05       Impact factor: 4.096

  4 in total

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