(Q35269713)

7 August 2017

1 reference

title

Doyne Lecture. Rhodopsin and autosomal dominant retinitis pigmentosa (English)

1 reference

7 August 2017

Dryja TP

1

1 reference

7 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1358680

18 September 2022

publication date

1 January 1992

1 reference

7 August 2017

1 reference

7 August 2017

volume

6 ( Pt 1)

1 reference

7 August 2017

page(s)

1-10

1 reference

Localization of Usher syndrome type II to chromosome 1q.

7 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Identification of the cystic fibrosis gene: chromosome walking and jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

A polymorphic DNA marker genetically linked to Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Isolation and nucleotide sequence of the gene encoding human rhodopsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Cloning of cDNAs encoding human interphotoreceptor retinoid-binding protein (IRBP) and comparison with bovine IRBP sequences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

The sequence of human retinal S-antigen reveals similarities with alpha-transducin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Alpha transducin is present in blue-, green-, and red-sensitive cone photoreceptors in the human retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Cyclic GMP phosphodiesterase from cattle retina. Amino acid sequence of the gamma-subunit and nucleotide sequence of the corresponding cDNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Gamma-subunit of mouse retinal cyclic-GMP phosphodiesterase: cDNA and corresponding amino acid sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Bgl II RFLP recognized by a human IRBP cDNA localized to chromosome 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Molecular genetics of inherited variation in human color vision

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Molecular biology of the visual pigments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Retinitis pigmentosa and mutations in rhodopsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Role of the intradiscal domain in rhodopsin assembly and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Membrane morphogenesis in retinal rod outer segments: inhibition by tunicamycin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Human photoreceptor topography

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa

21 January 2018

2 references

https://api.crossref.org/works/10.1038%2FEYE.1992.2

21 January 2018

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Regional Distribution of Retinal Degeneration in Patients with the Proline to Histidine Mutation in Codon 23 of the Rhodopsion Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

Prevalence of retinitis pigmentosa in Maine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Assignment of the rhodopsin gene to human chromosome three, region 3q21-3q24 by in situ hybridization studies

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Isolation and analysis of the mouse opsin gene

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

A structural model for ovine rhodopsin

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Rhodopsin content in the outer segment membranes of bovine and frog retinal rods

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Rhodopsin Thr58Arg Mutation in a Family with Autosomal Dominant Retinitis Pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Diagnosis of genetic disease by primer-specified restriction map modification, with application to cystic fibrosis and retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1992.2

7 January 2021

Identifiers

DOI

10.1038/EYE.1992.2

1 reference

7 August 2017

1 reference