TBX22 Missense Mutations Found in Patients with X-Linked Cleft Palate Affect DNA Binding, Sumoylation, and Transcriptional Repression
- 1 October 2007
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 81 (4), 700-712
- https://doi.org/10.1086/521033
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- SUMO1 Haploinsufficiency Leads to Cleft Lip and PalateScience, 2006
- Modification of Msx1 by SUMO-1Biochemical and Biophysical Research Communications, 2006
- SATB2 Is a Multifunctional Determinant of Craniofacial Patterning and Osteoblast DifferentiationCell, 2006
- T-Box Genes in Vertebrate DevelopmentAnnual Review of Genetics, 2005
- TBX5 nuclear localization is mediated by dual cooperative intramolecular signalsJournal of Molecular and Cellular Cardiology, 2003
- Functional Analysis of TBX5 Missense Mutations Associated with Holt-Oram SyndromePublished by Elsevier BV ,2003
- Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndromeHuman Molecular Genetics, 2001
- Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndromeNature Genetics, 1997
- Mutations in human cause limb and cardiac malformation in Holt-Oram syndromeNature Genetics, 1997
- Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyNature Genetics, 1997