Literature DB >> 19174318

Estimate of the abundance of cardiomyopathic mutations in the β-myosin gene.

Micah Hamady, Massimo Buvoli, Leslie A Leinwand, Rob Knight.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2009        PMID： 19174318      PMCID： PMC2982777          DOI： 10.1016/j.ijcard.2008.12.199

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN： 0167-5273            Impact factor:   4.164


× No keyword cloud information.
  12 in total

1.  Detection of known mutations in hypertrophic cardiomyopathy using oligonucleotide microarrays assisted by improved base stacking hybridization.

Authors:  Dong Wang; Yan Li; Rui Zhang; Di Jiang; Xuemei Ma; Yuxiang Zhou; Jing Cheng
Journal:  Biotechnol Lett       Date:  2003-10       Impact factor: 2.461

2.  Mutations profile in Chinese patients with hypertrophic cardiomyopathy.

Authors:  Lei Song; Yubao Zou; Jizheng Wang; Zhimin Wang; Yisong Zhen; Kejia Lou; Qian Zhang; Xiaojian Wang; Hu Wang; Jia Li; Rutai Hui
Journal:  Clin Chim Acta       Date:  2005-01       Impact factor: 3.786

3.  Ethical authorship and publishing.

Authors:  Andrew J S Coats
Journal:  Int J Cardiol       Date:  2008-11-28       Impact factor: 4.164

Review 4.  Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes.

Authors:  Jil C Tardiff
Journal:  Heart Fail Rev       Date:  2005-09       Impact factor: 4.214

5.  Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.

Authors:  Pascale Richard; Philippe Charron; Lucie Carrier; Céline Ledeuil; Theary Cheav; Claire Pichereau; Abdelaziz Benaiche; Richard Isnard; Olivier Dubourg; Marc Burban; Jean-Pierre Gueffet; Alain Millaire; Michel Desnos; Ketty Schwartz; Bernard Hainque; Michel Komajda
Journal:  Circulation       Date:  2003-04-21       Impact factor: 29.690

6.  Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.

Authors:  Andreas Perrot; Hajo Schmidt-Traub; Bernard Hoffmann; Matthias Prager; Nana Bit-Avragim; Raisa I Rudenko; Dinara A Usupbaeva; Zhyldyz Kabaeva; Bakytbek Imanov; Mirsaid M Mirrakhimov; Rainer Dietz; Anna Wycisk; Michal Tendera; Reinhard Gessner; Karl Josef Osterziel
Journal:  J Mol Med (Berl)       Date:  2005-04-22       Impact factor: 4.599

7.  Low-density DNA microarrays are versatile tools to screen for known mutations in hypertrophic cardiomyopathy.

Authors:  Stephan Waldmüller; Petra Freund; Simon Mauch; Roland Toder; Hans-Peter Vosberg
Journal:  Hum Mutat       Date:  2002-05       Impact factor: 4.878

8.  [Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].

Authors:  Rafael Laredo; Lorenzo Monserrat; Manuel Hermida-Prieto; Xusto Fernández; Isabel Rodríguez; Laura Cazón; Inés Alvariño; Carlos Dumont; Pablo Piñón; Jesús Peteiro; Beatriz Bouzas; Alfonso Castro-Beiras
Journal:  Rev Esp Cardiol       Date:  2006-10       Impact factor: 4.753

9.  Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.

Authors:  Sara L Van Driest; Michele A Jaeger; Steve R Ommen; Melissa L Will; Bernard J Gersh; A Jamil Tajik; Michael J Ackerman
Journal:  J Am Coll Cardiol       Date:  2004-08-04       Impact factor: 24.094

10.  Shared genetic causes of cardiac hypertrophy in children and adults.

Authors:  Hiroyuki Morita; Heidi L Rehm; Andres Menesses; Barbara McDonough; Amy E Roberts; Raju Kucherlapati; Jeffrey A Towbin; J G Seidman; Christine E Seidman
Journal:  N Engl J Med       Date:  2008-04-09       Impact factor: 91.245
View more
  3 in total

1.  Population-based variation in cardiomyopathy genes.

Authors:  Jessica R Golbus; Megan J Puckelwartz; John P Fahrenbach; Lisa M Dellefave-Castillo; Don Wolfgeher; Elizabeth M McNally
Journal:  Circ Cardiovasc Genet       Date:  2012-07-04

2.  Myosin motor domains carrying mutations implicated in early or late onset hypertrophic cardiomyopathy have similar properties.

Authors:  Carlos D Vera; Chloe A Johnson; Jonathan Walklate; Arjun Adhikari; Marina Svicevic; Srboljub M Mijailovich; Ariana C Combs; Stephen J Langer; Kathleen M Ruppel; James A Spudich; Michael A Geeves; Leslie A Leinwand
Journal:  J Biol Chem       Date:  2019-10-03       Impact factor: 5.157

3.  The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects.

Authors:  Jonathan Walklate; Carlos Vera; Marieke J Bloemink; Michael A Geeves; Leslie Leinwand
Journal:  J Biol Chem       Date:  2016-03-04       Impact factor: 5.157
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.