Literature DB >> 22257684

Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation.

Yi-Qing Yang, Xin-Hua Wang, Hong-Wei Tan, Wei-Feng Jiang, Wei-Yi Fang, Xu Liu.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2012        PMID： 22257684     DOI： 10.1016/j.ijcard.2011.12.091

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


× No keyword cloud information.
  15 in total

Review 1.  Emerging directions in the genetics of atrial fibrillation.

Authors:  Nathan R Tucker; Patrick T Ellinor
Journal:  Circ Res       Date:  2014-04-25       Impact factor: 17.367

Review 2.  Genetics of atrial fibrillation: from families to genomes.

Authors:  Ingrid E Christophersen; Patrick T Ellinor
Journal:  J Hum Genet       Date:  2015-05-21       Impact factor: 3.172

3.  Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.

Authors:  Juan Wang; Xue-Jiao Luo; Yuan-Feng Xin; Yi Liu; Zhong-Min Liu; Qian Wang; Ruo-Gu Li; Wei-Yi Fang; Xiao-Zhou Wang; Yi-Qing Yang
Journal:  DNA Cell Biol       Date:  2012-09-28       Impact factor: 3.311

Review 4.  Atrial fibrillation: the role of common and rare genetic variants.

Authors:  Morten S Olesen; Morten W Nielsen; Stig Haunsø; Jesper H Svendsen
Journal:  Eur J Hum Genet       Date:  2013-07-10       Impact factor: 4.246

5.  Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation.

Authors:  Jian-Yun Gu; Jia-Hong Xu; Hong Yu; Yi-Qing Yang
Journal:  Clinics (Sao Paulo)       Date:  2012-12       Impact factor: 2.365

Review 6.  GATA-dependent transcriptional and epigenetic control of cardiac lineage specification and differentiation.

Authors:  Sonia Stefanovic; Vincent M Christoffels
Journal:  Cell Mol Life Sci       Date:  2015-07-01       Impact factor: 9.261

Review 7.  Atrial fibrillation-a complex polygenetic disease.

Authors:  Julie H Andersen; Laura Andreasen; Morten S Olesen
Journal:  Eur J Hum Genet       Date:  2020-12-05       Impact factor: 4.246

8.  GATA5 loss-of-function mutations underlie tetralogy of fallot.

Authors:  Dong Wei; Han Bao; Xing-Yuan Liu; Ning Zhou; Qian Wang; Ruo-Gu Li; Ying-Jia Xu; Yi-Qing Yang
Journal:  Int J Med Sci       Date:  2012-12-10       Impact factor: 3.738

9.  Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.

Authors:  Wen-Hui Xie; Cheng Chang; Ying-Jia Xu; Ruo-Gu Li; Xin-Kai Qu; Wei-Yi Fang; Xu Liu; Yi-Qing Yang
Journal:  Clinics (Sao Paulo)       Date:  2013-06       Impact factor: 2.365

10.  PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation.

Authors:  Xing-Biao Qiu; Ying-Jia Xu; Ruo-Gu Li; Lei Xu; Xu Liu; Wei-Yi Fang; Yi-Qing Yang; Xin-Kai Qu
Journal:  Clinics (Sao Paulo)       Date:  2014-01       Impact factor: 2.365
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.