Loss of Tgif Function Causes Holoprosencephaly by Disrupting the Shh Signaling Pathway
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Loss of Tgif Function Causes Holoprosencephaly by Disrupting the Shh Signaling Pathway
Authors
Keywords
-
Journal
PLoS Genetics
Volume 8, Issue 2, Pages e1002524
Publisher
Public Library of Science (PLoS)
Online
2012-02-24
DOI
10.1371/journal.pgen.1002524
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Analysis of genotype-phenotype correlations in human holoprosencephaly
- (2010) Benjamin D. Solomon et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Tgif1 represses apolipoprotein gene expression in liver
- (2010) Tiffany A. Melhuish et al. JOURNAL OF CELLULAR BIOCHEMISTRY
- Zebrafish zic2a patterns the forebrain through modulation of Hedgehog-activated gene expression
- (2009) N. A. Sanek et al. DEVELOPMENT
- Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation
- (2009) Shannon E. Powers et al. DEVELOPMENT
- Pathogenesis of holoprosencephaly
- (2009) Xin Geng et al. JOURNAL OF CLINICAL INVESTIGATION
- Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly
- (2008) Erich Roessler et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: Searching for population variations
- (2008) Emanuele Leoncini et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Gli3 coordinates three-dimensional patterning and growth of the tectum and cerebellum by integrating Shh and Fgf8 signaling
- (2008) S. Blaess et al. DEVELOPMENT
- Maternal Tgif is required for vascularization of the embryonic placenta
- (2008) Laurent Bartholin et al. DEVELOPMENTAL BIOLOGY
- Mouse Shh is required for prechordal plate maintenance during brain and craniofacial morphogenesis
- (2008) Kazushi Aoto et al. DEVELOPMENTAL BIOLOGY
- Haploinsufficiency of Six3 Fails to Activate Sonic hedgehog Expression in the Ventral Forebrain and Causes Holoprosencephaly
- (2008) Xin Geng et al. DEVELOPMENTAL CELL
- Genome-Wide Identification of Smad/Foxh1 Targets Reveals a Role for Foxh1 in Retinoic Acid Regulation and Forebrain Development
- (2008) Cristoforo Silvestri et al. DEVELOPMENTAL CELL
- Zic2 -associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation
- (2008) Nicholas Warr et al. HUMAN MOLECULAR GENETICS
- Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein
- (2008) Yongsu Jeong et al. NATURE GENETICS
- The genetics of early telencephalon patterning: some assembly required
- (2008) Jean M. Hébert et al. NATURE REVIEWS NEUROSCIENCE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now