Genetic and Functional Analyses ofZIC3Variants in Congenital Heart Disease
Published 2013 View Full Article
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Title
Genetic and Functional Analyses ofZIC3Variants in Congenital Heart Disease
Authors
Keywords
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Journal
HUMAN MUTATION
Volume 35, Issue 1, Pages 66-75
Publisher
Wiley
Online
2013-10-12
DOI
10.1002/humu.22457
References
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Related references
Note: Only part of the references are listed.- The phenotypic spectrum ofZIC3mutations includes isolated d-transposition of the great arteries and double outlet right ventricle
- (2013) Lisa C.A. D'Alessandro et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterning
- (2013) M. J. Sutherland et al. HUMAN MOLECULAR GENETICS
- An essential and highly conserved role for Zic3 in left–right patterning, gastrulation and convergent extension morphogenesis
- (2012) Ashley E. Cast et al. DEVELOPMENTAL BIOLOGY
- Zic3 is required in the extra-cardiac perinodal region of the lateral plate mesoderm for left–right patterning and heart development
- (2012) Zhengxin Jiang et al. HUMAN MOLECULAR GENETICS
- Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice
- (2012) Malgorzata E. Quinn et al. HUMAN MOLECULAR GENETICS
- From VACTERL-H to heterotaxy: Variable expressivity of ZIC3-related disorders
- (2011) Brian Chung et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies
- (2011) Lijiang Ma et al. CARDIOLOGY IN THE YOUNG
- Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease
- (2011) James E. J. Bedard et al. PLoS One
- Situs Inversus Totalis and a NovelZIC3Mutation in a Family with X-linked Heterotaxy
- (2011) Lisa C.A. D'Alessandro et al. Congenital Heart Disease
- Far from solved: A perspective on what we know about early mechanisms of left-right asymmetry
- (2010) Laura N. Vandenberg et al. DEVELOPMENTAL DYNAMICS
- Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?
- (2010) M. W. Wessels et al. JOURNAL OF MEDICAL GENETICS
- The Pluripotency Regulator Zic3 Is a Direct Activator of the Nanog Promoter in ESCs
- (2010) Linda Shushan Lim et al. STEM CELLS
- Disorders of left-right asymmetry: Heterotaxy and situs inversus
- (2009) Mardi J. Sutherland et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Familial transposition of the great arteries caused by multiple mutations in laterality genes
- (2009) A. De Luca et al. HEART
- Molecular mechanisms underlying polyalanine diseases
- (2009) C. Messaed et al. NEUROBIOLOGY OF DISEASE
- CD spectra show the relational style between Zic-, Gli-, Glis-zinc finger protein and DNA
- (2008) Kumiko Sakai-Kato et al. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS
- Functional and structural basis of the nuclear localization signal in the ZIC3 zinc finger domain
- (2008) Minoru Hatayama et al. HUMAN MOLECULAR GENETICS
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