Literature DB >> 18801787

Pure restrictive cardiomyopathy associated with cardiac troponin I gene mutation: mismatch between the lack of hypertrophy and the presence of disarray.

F I Gambarin1, M Tagliani, E Arbustini.   

Abstract

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Year:  2008        PMID： 18801787     DOI： 10.1136/hrt.2008.154203

Source DB:  PubMed          Journal:  Heart        ISSN： 1355-6037            Impact factor:   5.994


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  7 in total

Review 1.  Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all.

Authors:  Thomas E Callis; Brian C Jensen; Karen E Weck; Monte S Willis
Journal:  Expert Rev Mol Diagn       Date:  2010-04       Impact factor: 5.225

Review 2.  Genetic Insights into Primary Restrictive Cardiomyopathy.

Authors:  Andreas Brodehl; Brenda Gerull
Journal:  J Clin Med       Date:  2022-04-08       Impact factor: 4.964

Review 3.  Cardiac troponin mutations and restrictive cardiomyopathy.

Authors:  Michelle S Parvatiyar; Jose Renato Pinto; David Dweck; James D Potter
Journal:  J Biomed Biotechnol       Date:  2010-06-08

Review 4.  TNNI1, TNNI2 and TNNI3: Evolution, regulation, and protein structure-function relationships.

Authors:  Juan-Juan Sheng; Jian-Ping Jin
Journal:  Gene       Date:  2015-10-23       Impact factor: 3.688

5.  The evolutionarily conserved C-terminal peptide of troponin I is an independently configured regulatory structure to function as a myofilament Ca2+-desensitizer.

Authors:  Sienna Wong; Han-Zhong Feng; J-P Jin
Journal:  J Mol Cell Cardiol       Date:  2019-09-07       Impact factor: 5.000

6.  Insights into restrictive cardiomyopathy from clinical and animal studies.

Authors:  Pierre-Yves Jean-Charles; Yue-Jin Li; Chang-Long Nan; Xu-Pei Huang
Journal:  J Geriatr Cardiol       Date:  2011-09       Impact factor: 3.327

7.  Pediatric restrictive cardiomyopathy due to a heterozygous mutation of the TNNI3 gene.

Authors:  Yan Chen; Shiwei Yang; Jun Li; Gannan Wang; Yuming Qin; Daowu Wang; Kejiang Cao
Journal:  J Biomed Res       Date:  2013-04-20
  7 in total

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