Literature DB >> 10090775

Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function

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Abstract

Entities:  

Year:  1999        PMID: 10090775     DOI: 10.1021/bi9950701

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


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  13 in total

Review 1.  Nuclear tropomyosin and troponin in striated muscle: new roles in a new locale?

Authors:  P Bryant Chase; Mark P Szczypinski; Elliott P Soto
Journal:  J Muscle Res Cell Motil       Date:  2013-08-02       Impact factor: 2.698

2.  Functional effects of a tropomyosin mutation linked to FHC contribute to maladaptation during acidosis.

Authors:  Katherine A Sheehan; Grace M Arteaga; Aaron C Hinken; Fernando A Dias; Cibele Ribeiro; David F Wieczorek; R John Solaro; Beata M Wolska
Journal:  J Mol Cell Cardiol       Date:  2010-11-01       Impact factor: 5.000

Review 3.  Sarcomeric protein mutations in dilated cardiomyopathy.

Authors:  Audrey N Chang; James D Potter
Journal:  Heart Fail Rev       Date:  2005-09       Impact factor: 4.214

Review 4.  The myosin-activated thin filament regulatory state, M⁻-open: a link to hypertrophic cardiomyopathy (HCM).

Authors:  Sherwin S Lehrer; Michael A Geeves
Journal:  J Muscle Res Cell Motil       Date:  2014-04-17       Impact factor: 2.698

5.  Investigating the effects of tropomyosin mutations on its flexibility and interactions with filamentous actin using molecular dynamics simulation.

Authors:  Wenjun Zheng; Sarah E Hitchcock-DeGregori; Bipasha Barua
Journal:  J Muscle Res Cell Motil       Date:  2016-07-04       Impact factor: 2.698

Review 6.  Thin filament mutations: developing an integrative approach to a complex disorder.

Authors:  Jil C Tardiff
Journal:  Circ Res       Date:  2011-03-18       Impact factor: 17.367

7.  Role of cardiac troponin I carboxy terminal mobile domain and linker sequence in regulating cardiac contraction.

Authors:  Nancy L Meyer; P Bryant Chase
Journal:  Arch Biochem Biophys       Date:  2016-03-10       Impact factor: 4.013

8.  An internal domain of beta-tropomyosin increases myofilament Ca(2+) sensitivity.

Authors:  Ganapathy Jagatheesan; Sudarsan Rajan; Emily M Schulz; Rafeeq P H Ahmed; Natalia Petrashevskaya; Arnold Schwartz; Greg P Boivin; Grace M Arteaga; Tao Wang; Yi-Gang Wang; Muhammad Ashraf; Stephen B Liggett; John Lorenz; R John Solaro; David F Wieczorek
Journal:  Am J Physiol Heart Circ Physiol       Date:  2009-05-08       Impact factor: 4.733

9.  Structural destabilization of tropomyosin induced by the cardiomyopathy-linked mutation R21H.

Authors:  Thu Ly; Inna Krieger; Dmitri Tolkatchev; Cheyenna Krone; Timothy Moural; Fadel A Samatey; ChulHee Kang; Alla S Kostyukova
Journal:  Protein Sci       Date:  2017-11-21       Impact factor: 6.725

10.  Familial hypertrophic cardiomyopathy related E180G mutation increases flexibility of human cardiac α-tropomyosin.

Authors:  Campion K P Loong; Huan-Xiang Zhou; P Bryant Chase
Journal:  FEBS Lett       Date:  2012-08-14       Impact factor: 4.124

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