Literature DB >> 8946132

New understandings in the genetics of congenital heart disease.

D W Benson1, C T Basson, C A MacRae.   

Abstract

In spite of the amazing success during the past half century in diagnosis and treatment of congenital heart disease, very little is known of its cause. However, a genetic cause has been clearly established for many forms of cardiovascular disease, and new understandings in the molecular genetics of congenital heart disease provide further insight. Progress has been quite impressive for some cardiovascular abnormalities, whereas in other areas the findings are more preliminary. For example, the molecular genetic cause of supravalvular aortic stenosis and the heart disease associated with Marfan syndrome has been clearly established. Impressive progress has been made in conotruncal defects, Holt-Oram syndrome, Alagille syndrome, and total anomalous pulmonary venous connection. In other areas, such as patent ductus arteriosus and atrioventricular septal defect, the findings are more preliminary. Taken as a whole, the prospect of understanding the genetic basis of congenital heart disease has never been better. Understanding the cause of congenital heart disease will provide new insights into both normal cardiac development and the pathophysiologic basis of congenital heart defects.

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Year:  1996        PMID: 8946132     DOI: 10.1097/00008480-199610000-00015

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  8 in total

Review 1.  Cardiovascular embryology.

Authors:  R Abdulla; G A Blew; M J Holterman
Journal:  Pediatr Cardiol       Date:  2004 May-Jun       Impact factor: 1.655

2.  TBX5 is required for embryonic cardiac cell cycle progression.

Authors:  Sarah C Goetz; Daniel D Brown; Frank L Conlon
Journal:  Development       Date:  2006-05-25       Impact factor: 6.868

Review 3.  Xenopus: An emerging model for studying congenital heart disease.

Authors:  Erin Kaltenbrun; Panna Tandon; Nirav M Amin; Lauren Waldron; Chris Showell; Frank L Conlon
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2011-04-28

4.  Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis.

Authors:  Daniel D Brown; Shauna N Martz; Olav Binder; Sarah C Goetz; Brenda M J Price; Jim C Smith; Frank L Conlon
Journal:  Development       Date:  2005-01-05       Impact factor: 6.868

5.  Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD.

Authors:  Paweł Stańczak; Joanna Witecka; Anna Szydło; Ewa Gutmajster; Małgorzata Lisik; Aleksandra Auguściak-Duma; Maciej Tarnowski; Tomasz Czekaj; Hanna Czekaj; Aleksander L Sieroń
Journal:  Eur J Hum Genet       Date:  2008-10-01       Impact factor: 4.246

6.  The Cardiac TBX5 Interactome Reveals a Chromatin Remodeling Network Essential for Cardiac Septation.

Authors:  Lauren Waldron; Jeffrey D Steimle; Todd M Greco; Nicholas C Gomez; Kerry M Dorr; Junghun Kweon; Brenda Temple; Xinan Holly Yang; Caralynn M Wilczewski; Ian J Davis; Ileana M Cristea; Ivan P Moskowitz; Frank L Conlon
Journal:  Dev Cell       Date:  2016-02-08       Impact factor: 12.270

7.  Quantitative proteomic analysis of serum from pregnant women carrying a fetus with conotruncal heart defect using isobaric tags for relative and absolute quantitation (iTRAQ) labeling.

Authors:  Ying Zhang; Yuan Kang; Qiongjie Zhou; Jizi Zhou; Huijun Wang; Hong Jin; Xiaohui Liu; Duan Ma; Xiaotian Li
Journal:  PLoS One       Date:  2014-11-13       Impact factor: 3.240

8.  GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.

Authors:  Kameel Kassab; Hadla Hariri; Lara Gharibeh; Akl C Fahed; Manal Zein; Inaam El-Rassy; Mona Nemer; Issam El-Rassi; Fadi Bitar; Georges Nemer
Journal:  Mol Genet Genomic Med       Date:  2015-12-20       Impact factor: 2.183

  8 in total

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