Inventaire - your friends and communities are your best library

Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis

Published in: American Journal of Human Genetics

Date of publication: October 1991

Language: English

Main subject: electrophoresis, retinitis pigmentosa

Cites articles 16

Date

Title

Authors

March 1, 1980

Population genetic studies of retinitis pigmentosa
October 1, 1983

Isolation, sequence analysis, and intron-exon arrangement of the gene encoding bovine rhodopsin
March 1, 1984

Prevalence of retinitis pigmentosa in Maine
May 1, 1985

Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis
April 1, 1985

Isolation and structure of a rhodopsin gene from D. melanogaster

,
1987

Detection and localization of single base changes by denaturing gradient gel electrophoresis
January 1, 1987

Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis
January 1, 1988

Isolation and sequence determination of the chicken rhodopsin gene
October 1, 1989

A simple and efficient non-organic procedure for the isolation of genomic DNA from blood
January 1, 1989

Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes
November 1, 1990

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
January 1, 1990

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
March 1, 1990

Rapid purification of PCR products for DNA sequencing using Sepharose CL-6B spin columns
January 1991

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa
January 1, 1991

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).
January 1, 1991

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin

Article -

Welcome to inventaire

The library of your friends and communities

You are offline