Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1
- 1 March 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (3), 627-641
- https://doi.org/10.1086/318792
Abstract
No abstract availableKeywords
Funding Information
- Canadian Institutes of Health Research
- Alberta Heritage Foundation for Medical Research
This publication has 38 references indexed in Scilit:
- A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the EyeAmerican Journal of Human Genetics, 2001
- Chromosomal Duplication Involving the Forkhead Transcription Factor GeneFOXC1Causes Iris Hypoplasia and GlaucomaAmerican Journal of Human Genetics, 2000
- Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25European Journal of Human Genetics, 2000
- Expression of theMf1 gene in developing mouse hearts: Implication in the development of human congenital heart defectsDevelopmental Dynamics, 1999
- Dynamic DNA Contacts Observed in the NMR Structure of Winged Helix Protein-DNA ComplexJournal of Molecular Biology, 1999
- Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeNature Genetics, 1996
- Target of the Transcriptional Activation Function of Phage λ cl ProteinScience, 1994
- New Programs for Protein Tertiary Structure PredictionNature Biotechnology, 1993
- A single amino acid exchange transfers VP16-induced positive control from the Oct-1 to the Oct-2 homeo domain.Genes & Development, 1992
- The effect of a lambda repressor mutation on the activation of transcription initiation from the lambda PRM promoterCell, 1983