Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndrome.
Open Access
- 7 March 2001
- journal article
- Published by Wiley in FEBS Letters
- Vol. 492 (1) , 112-118
- https://doi.org/10.1016/s0014-5793(01)02238-4
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Analysis of a Caenorhabditis elegans Twist homolog identifies conserved and divergent aspects of mesodermal patterningGenes & Development, 1998
- Twist-mediated Activation of the NK-4 Homeobox Gene in the Visceral Mesoderm of Drosophila Requires Two Distinct Clusters of E-box Regulatory ElementsPublished by Elsevier ,1997
- Mutations of the TWIST gene in the Saethre-Chotzene syndromeNature Genetics, 1997
- Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndromeNature Genetics, 1997
- The human H-twist gene is located at 7p21 and encodes a B-HLH protein that is 96% similar to its murine M-twist counterpartMammalian Genome, 1996
- Inhibition of Myogenic bHLH and MEF2 Transcription Factors by the bHLH Protein TwistScience, 1996
- twist is required in head mesenchyme for cranial neural tube morphogenesis.Genes & Development, 1995
- The M-twist gene of Mus is expressed in subsets of mesodermal cells and is closely related to the Xenopus X-twi and the Drosophila twist genesDevelopmental Biology, 1991
- A Xenopus mRNA related to Drosophila twist is expressed in response to induction in the mesoderm and the neural crestCell, 1989
- Thetwistgene: isolation of a Drosophila zygotle gene necessary for the establishment of dorsoventral patternNucleic Acids Research, 1987