Literature DB >> 22878021

TGFβ3 mutations cause arrhythmogenic right ventricular dysplasia type 1 and open the door to understanding the biological role of TGFβ3 (where there's a will, there's a way).

Juan Tamargo.   

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Year:  2012        PMID： 22878021     DOI： 10.1093/cvr/cvs231

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN： 0008-6363            Impact factor:   10.787


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  4 in total

1.  Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans.

Authors:  Laurence Campens; Marjolijn Renard; Bram Trachet; Patrick Segers; Laura Muino Mosquera; Johan De Sutter; Lynn Sakai; Anne De Paepe; Julie De Backer
Journal:  Pediatr Res       Date:  2015-06-04       Impact factor: 3.756

2.  Transcriptomic and ChIP-seq Integrative Analysis Identifies KDM5A-Target Genes in Cardiac Fibroblasts.

Authors:  Yiyao Jiang; Xu Zhang; Ting Wei; Xianjie Qi; Isah Amir Abba; Nana Zhang; Yao Chen; Ran Wang; Chao Shi
Journal:  Front Cardiovasc Med       Date:  2022-07-01

Review 3.  Molecular mechanisms of arrhythmogenic cardiomyopathy.

Authors:  Karyn M Austin; Michael A Trembley; Stephanie F Chandler; Stephen P Sanders; Jeffrey E Saffitz; Dominic J Abrams; William T Pu
Journal:  Nat Rev Cardiol       Date:  2019-09       Impact factor: 32.419

Review 4.  Fibrosis in Arrhythmogenic Cardiomyopathy: The Phantom Thread in the Fibro-Adipose Tissue.

Authors:  Angela Serena Maione; Chiara Assunta Pilato; Michela Casella; Alessio Gasperetti; Ilaria Stadiotti; Giulio Pompilio; Elena Sommariva
Journal:  Front Physiol       Date:  2020-04-03       Impact factor: 4.566
  4 in total

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