Literature DB >> 20033147

Genetic origins of pediatric heart disease.

D Woodrow Benson1.   

Abstract

Pediatric heart disease comprises many forms of cardiovascular disease in the young including cardiovascular malformations (CVM), cardiomyopathies, vasculopathies, e.g., Marfan syndrome, and cardiac arrhythmias. CVM are an important component of pediatric heart disease and constitute a major portion of clinically significant birth defects. In the past decade, the complementary nature of genetic, developmental, and biochemical approaches have contributed to extraordinary advances in understanding the origins of pediatric heart disease. Results of the studies of the cardiac transcription factor, NKX2.5, illustrate these accomplishments and at the same time provide a forecast of the nature of future genetic studies to better understand the origins of pediatric heart disease.

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Year:  2009        PMID: 20033147     DOI: 10.1007/s00246-009-9607-y

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  48 in total

1.  Preimplantation genetic diagnosis for Marfan syndrome.

Authors:  Claudia Spits; Martine De Rycke; Willem Verpoest; Willy Lissens; Andre Van Steirteghem; Inge Liebaers; Karen Sermon
Journal:  Fertil Steril       Date:  2006-06-06       Impact factor: 7.329

2.  Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.

Authors:  Kayoko Hirayama-Yamada; Mitsuhiro Kamisago; Kaoru Akimoto; Hiroyuki Aotsuka; Yoshihide Nakamura; Hideshi Tomita; Michiko Furutani; Shin-ichiro Imamura; Atsuyoshi Takao; Makoto Nakazawa; Rumiko Matsuoka
Journal:  Am J Med Genet A       Date:  2005-05-15       Impact factor: 2.802

3.  Drosophila NK-homeobox genes.

Authors:  Y Kim; M Nirenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

Review 4.  Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction.

Authors:  J J Nora
Journal:  Circulation       Date:  1968-09       Impact factor: 29.690

Review 5.  Incidence of congenital heart disease: II. Prenatal incidence.

Authors:  J I Hoffman
Journal:  Pediatr Cardiol       Date:  1995 Jul-Aug       Impact factor: 1.655

6.  Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5.

Authors:  C Biben; R Weber; S Kesteven; E Stanley; L McDonald; D A Elliott; L Barnett; F Köentgen; L Robb; M Feneley; R P Harvey
Journal:  Circ Res       Date:  2000-11-10       Impact factor: 17.367

7.  Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects.

Authors:  Laura E Briggs; Morihiko Takeda; Adolfo E Cuadra; Hiroko Wakimoto; Melissa H Marks; Alexandra J Walker; Tsugio Seki; Suk P Oh; Jonathan T Lu; Colin Sumners; Mohan K Raizada; Nobuo Horikoshi; Ellen O Weinberg; Kenji Yasui; Yasuhiro Ikeda; Kenneth R Chien; Hideko Kasahara
Journal:  Circ Res       Date:  2008-08-08       Impact factor: 17.367

Review 8.  Transcription factors and congenital heart defects.

Authors:  Krista L Clark; Katherine E Yutzey; D Woodrow Benson
Journal:  Annu Rev Physiol       Date:  2006       Impact factor: 19.318

9.  Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies.

Authors:  Hideko Kasahara; D Woodrow Benson
Journal:  Cardiovasc Res       Date:  2004-10-01       Impact factor: 10.787

10.  The gene tinman is required for specification of the heart and visceral muscles in Drosophila.

Authors:  R Bodmer
Journal:  Development       Date:  1993-07       Impact factor: 6.868

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  17 in total

1.  Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation.

Authors:  Julia B Winston; Claire E Schulkey; Iuan-Bor D Chen; Suk D Regmi; Maria Efimova; Jonathan M Erlich; Courtney A Green; Ashley Aluko; Patrick Y Jay
Journal:  Circ Cardiovasc Genet       Date:  2012-04-24

2.  Placental Nkx2-5 and target gene expression in early-onset and severe preeclampsia.

Authors:  Elena R Rivers; Anthony J Horton; Angela F Hawk; Elizabeth G Favre; Katherine M Senf; Paul J Nietert; Eugene Y Chang; Ann C Foley; Christopher J Robinson; Kyu-Ho Lee
Journal:  Hypertens Pregnancy       Date:  2014-07-02       Impact factor: 2.108

Review 3.  Transcription factor pathways and congenital heart disease.

Authors:  David J McCulley; Brian L Black
Journal:  Curr Top Dev Biol       Date:  2012       Impact factor: 4.897

4.  Evolutionary conservation of Nkx2.5 autoregulation in the second heart field.

Authors:  Christopher D Clark; Boding Zhang; Benjamin Lee; Samuel I Evans; Andrew B Lassar; Kyu-Ho Lee
Journal:  Dev Biol       Date:  2012-11-17       Impact factor: 3.582

5.  A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.

Authors:  Hassan Ashraf; Lagnajeet Pradhan; Eileen I Chang; Ryota Terada; Nicole J Ryan; Laura E Briggs; Rajib Chowdhury; Miguel A Zárate; Yukiko Sugi; Hyun-Joo Nam; D Woodrow Benson; Robert H Anderson; Hideko Kasahara
Journal:  Circ Cardiovasc Genet       Date:  2014-07-15

6.  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

7.  A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.

Authors:  Yi-Qing Yang; Li Li; Juan Wang; Xing-Yuan Liu; Xiao-Zhong Chen; Wei Zhang; Xiao-Zhou Wang; Jin-Qi Jiang; Xu Liu; Wei-Yi Fang
Journal:  Pediatr Cardiol       Date:  2011-11-20       Impact factor: 1.655

8.  A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects.

Authors:  Ming Li; Jingyun Li; Changshuai Wei; Qing Lu; Xinyu Tang; Stephen W Erickson; Stewart L MacLeod; Charlotte A Hobbs
Journal:  Ann Hum Genet       Date:  2015-11-27       Impact factor: 1.670

9.  GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect.

Authors:  Dong Wei; Han Bao; Ning Zhou; Gui-Fen Zheng; Xing-Yuan Liu; Yi-Qing Yang
Journal:  Pediatr Cardiol       Date:  2012-09-09       Impact factor: 1.655

10.  Associations of NKX2-5 Genetic Polymorphisms with the Risk of Congenital Heart Disease: A Meta-analysis.

Authors:  Xiaochuan Xie; Xiaohan Shi; Xiaoshuang Xun; Li Rao
Journal:  Pediatr Cardiol       Date:  2016-03-31       Impact factor: 1.655

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