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Publications by S H Lefevre
A T to C Mutation in the Polypyrimidine Tract of the Exon 9 Splicing Site of the RB1 Gene Responsible for Low Penetrance Hereditary Retinoblastoma
Journal of Medical Genetics
Genetics
Related publications
Low-Penetrance of RB-1 Gene Mutation in Familial Retinoblastoma 135
Pediatric Research
Child Health
Pediatrics
Perinatology
The Polypyrimidine Tract Binding Protein Binds Upstream of Neural Cell-Specific C-SRC Exon N1 to Repress the Splicing of the Intron Downstream.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Molecular Basis of Low-Penetrance Retinoblastoma
Archives of Ophthalmology
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
The Polypyrimidine Tract Binding Protein (PTB) Represses Splicing of Exon 6B From the -Tropomyosin Pre-mRNA by Directly Interfering With the Binding of the U2AF65 Subunit
Molecular and Cellular Biology
Cell Biology
Molecular Biology
An Intronic Splicing Silencer Causes Skipping of the IIIb Exon of Fibroblast Growth Factor Receptor 2 Through Involvement of Polypyrimidine Tract Binding Protein
Molecular and Cellular Biology
Cell Biology
Molecular Biology
A Novel Splice-Site Mutation on the MLC1 Gene Leading to Exon 9 Skipping and Megalencephalic Leukoencephalopathy With Subcortical Cysts in a Turkish Patient
Balkan Journal of Medical Genetics
Genetics
A Brain-Enriched Polypyrimidine Tract-Binding Protein Antagonizes the Ability of Nova to Regulate Neuron-Specific Alternative Splicing
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Novel Splicing Site Mutation of the GPR143 Gene in a Chinese X-Linked Ocular Albinism Pedigree
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
