Literature DB >> 15863664

GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart.

S M Reamon-Buettner1, J Borlak.   

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Year:  2005        PMID： 15863664      PMCID： PMC1736044          DOI： 10.1136/jmg.2004.025395

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  29 in total

1.  Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.

Authors:  Margaret J Wat; Tyler F Beck; Andrés Hernández-García; Zhiyin Yu; Danielle Veenma; Monica Garcia; Ashley M Holder; Jeanette J Wat; Yuqing Chen; Carrie A Mohila; Kevin P Lally; Mary Dickinson; Dick Tibboel; Annelies de Klein; Brendan Lee; Daryl A Scott
Journal:  Hum Mol Genet       Date:  2012-06-20       Impact factor: 6.150

2.  Somatic mutations in cardiac malformations.

Authors:  S M Reamon-Buettner; J Borlak
Journal:  J Med Genet       Date:  2006-08       Impact factor: 6.318

Review 3.  The pathogenesis of atrial and atrioventricular septal defects with special emphasis on the role of the dorsal mesenchymal protrusion.

Authors:  Laura E Briggs; Jayant Kakarla; Andy Wessels
Journal:  Differentiation       Date:  2012-06-17       Impact factor: 3.880

4.  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

Review 5.  Zinc and Zinc Transporters: Novel Regulators of Ventricular Myocardial Development.

Authors:  Wen Lin; Deqiang Li
Journal:  Pediatr Cardiol       Date:  2018-03-13       Impact factor: 1.655

6.  Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease.

Authors:  Ting Peng; Li Wang; Shu-Feng Zhou; Xiaotian Li
Journal:  Genetica       Date:  2010-11-26       Impact factor: 1.082

7.  Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population.

Authors:  Yang Liu; Bojian Li; Yuejuan Xu; Kun Sun
Journal:  Pediatr Cardiol       Date:  2017-02-04       Impact factor: 1.655

8.  Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.

Authors:  Margaret J Wat; Oleg A Shchelochkov; Ashley M Holder; Amy M Breman; Aditi Dagli; Carlos Bacino; Fernando Scaglia; Roberto T Zori; Sau Wai Cheung; Daryl A Scott; Sung-Hae Lee Kang
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

9.  8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families.

Authors:  John Ck Barber; Dave Bunyan; Merryl Curtis; Denise Robinson; Susanne Morlot; Anette Dermitzel; Thomas Liehr; Claudia Alves; Joana Trindade; Ana I Paramos; Clare Cooper; Kevin Ocraft; Emma-Jane Taylor; Viv K Maloney
Journal:  Mol Cytogenet       Date:  2010-02-18       Impact factor: 2.009

10.  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
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