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Publications by William Fairbrother
Linking C5 Deficiency to an Exonic Splicing Enhancer Mutation
Journal of Immunology
Allergy
Immunology
Related publications
A Nonsense Mutation in the Fibrillin-1 Gene of a Marfan Syndrome Patient Induces NMD and Disrupts an Exonic Splicing Enhancer
Genes and Development
Genetics
Developmental Biology
Evidence for the Function of an Exonic Splicing Enhancer After the First Catalytic Step of Pre-mRNA Splicing
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Selection of the Bovine Papillomavirus Type 1 Nucleotide 3225 3' Splice Site Is Regulated Through an Exonic Splicing Enhancer and Its Juxtaposed Exonic Splicing Suppressor.
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Multisite and Bidirectional Exonic Splicing Enhancer in CD44 Alternative Exon V3
RNA
Molecular Biology
Distinct Factor Requirements for Exonic Splicing Enhancer Function and Binding of U2AF to the Polypyrimidine Tract
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
A Synonymous Mutation in SPINK5 Exon 11 Causes Netherton Syndrome by Altering Exonic Splicing Regulatory Elements
Journal of Human Genetics
Genetics
Single Nucleotide Polymorphism–Based Validation of Exonic Splicing Enhancers
PLoS Biology
Immunology
Molecular Biology
Genetics
Biochemistry
Microbiology
Biological Sciences
Agricultural
Neuroscience
Binding of DAZAP1 and hnRNPA1/A2 to an Exonic Splicing Silencer in a Natural BRCA1 Exon 18 Mutant
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Janus Kinase 3 Deficiency Caused by a Homozygous Synonymous Exonic Mutation That Creates a Dominant Splice Site
Journal of Allergy and Clinical Immunology
Allergy
Immunology
