A Novel Human Gene,WSTF,Is Deleted in Williams Syndrome
- 1 December 1998
- journal article
- Published by Elsevier BV in Genomics
- Vol. 54 (2), 241-249
- https://doi.org/10.1006/geno.1998.5578
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- Repression of GCN5 Histone Acetyltransferase Activity via Bromodomain-Mediated Binding and Phosphorylation by the Ku–DNA-Dependent Protein Kinase ComplexMolecular and Cellular Biology, 1998
- KAP-1, a novel corepressor for the highly conserved KRAB repression domain.Genes & Development, 1996
- LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive CognitionCell, 1996
- Tetrahymena Histone Acetyltransferase A: A Homolog to Yeast Gcn5p Linking Histone Acetylation to Gene ActivationCell, 1996
- The PROSITE database, its status in 1995Nucleic Acids Research, 1996
- The PHD finger: Implications for chromatin-mediated transcriptional regulationTrends in Biochemical Sciences, 1995
- Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene.JCI Insight, 1994
- Hemizygosity at the elastin locus in a developmental disorder, Williams syndromeNature Genetics, 1993
- The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosisCell, 1993
- Basic local alignment search toolJournal of Molecular Biology, 1990