A 30-Base-Pair Element in the First Intron of SOX9 Acts as an Enhancer in ATDC5
- 26 October 2001
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 288 (2) , 347-355
- https://doi.org/10.1006/bbrc.2001.5778
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralizationProceedings of the National Academy of Sciences, 2001
- Identification of an Enhancer Sequence within the First Intron Required for Cartilage-specific Transcription of the α2(XI) Collagen GeneJournal of Biological Chemistry, 2000
- Campomelic Dysplasia Translocation Breakpoints Are Scattered over 1 Mb Proximal to SOX9: Evidence for an Extended Control RegionAmerican Journal of Human Genetics, 1999
- Chondrocyte-specific Enhancer Elements in the Col11a2 Gene Resemble the Col2a1 Tissue-specific EnhancerJournal of Biological Chemistry, 1998
- Three High Mobility Group-like Sequences within a 48-Base Pair Enhancer of the Col2a1 Gene Are Required for Cartilage-specific Expression in VivoJournal of Biological Chemistry, 1998
- SOX9 directly regulates the type-ll collagen geneNature Genetics, 1997
- SOX9 Is a Potent Activator of the Chondrocyte-Specific Enhancer of the Proα1(II) Collagen GeneMolecular and Cellular Biology, 1997
- Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9Human Genetics, 1996
- Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related geneNature, 1994
- Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9Cell, 1994