(Q35947581)

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Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments

scientific article

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scholarly article

1 reference

Europe PubMed Central

11 August 2017

Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments (English)

1 reference

Europe PubMed Central

11 August 2017

author name string

T Li

1

1 reference

Europe PubMed Central

11 August 2017

W K Snyder

2

1 reference

Europe PubMed Central

11 August 2017

J E Olsson

3

1 reference

Europe PubMed Central

11 August 2017

T P Dryja

4

1 reference

Europe PubMed Central

11 August 2017

language of work or name

0 references

publication date

1 November 1996

1 reference

Europe PubMed Central

11 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

11 August 2017

93

1 reference

Europe PubMed Central

11 August 2017

14176-14181

1 reference

Europe PubMed Central

11 August 2017

24

1 reference

Europe PubMed Central

11 August 2017

Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Isolation and nucleotide sequence of the gene encoding human rhodopsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Changes in the localization and content of opsin during retinal development in the rds mutant mouse: immunocytochemistry and immunoassay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

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

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

https://api.crossref.org/works/10.1073%2FPNAS.93.24.14176

21 January 2018

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Polarized sorting of rhodopsin on post-Golgi membranes in frog retinal photoreceptor cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Constitutively active mutants of rhodopsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

2 October 2017

Photoreceptor degeneration in vitamin A deprivation and retinitis pigmentosa: the equivalent light hypothesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

27 July 2018

Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

27 July 2018

Retinal degeneration caused by dominant rhodopsin mutations in Drosophila.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

24 September 2018

Immunocytochemical localization of opsin in rod photoreceptors during periods of rapid disc assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

24 September 2018

Support for the equivalent light hypothesis for RP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

24 September 2018

Retinal degeneration in the pcd cerebellar mutant mouse. II. Electron microscopic analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

24 September 2018

Differential distribution of opsin in the plasma membrane of frog photoreceptors: an immunocytochemical study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19513

24 September 2018

Rod phototransduction in transgenic mice expressing a mutant opsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Membrane assembly in retinal photoreceptors. II. Immunocytochemical analysis of freeze-fractured rod photoreceptor membranes using anti-opsin antibodies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vesicular transport of newly synthesized opsin from the Golgi apparatus toward the rod outer segment. Ultrastructural immunocytochemical and autoradiographic evidence in Xenopus retinas

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antigen-antibody interaction. Synthetic peptides define linear antigenic determinants recognized by monoclonal antibodies directed to the cytoplasmic carboxyl terminus of rhodopsin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered cAMP levels in retinas from transgenic mice expressing a rhodopsin mutant

1 reference

https://pubmed.ncbi.nlm.nih.gov/8943080

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.93.24.14176

1 reference

Europe PubMed Central

11 August 2017

1996PNAS...9314176L

0 references

1 reference

Europe PubMed Central

11 August 2017

1 reference

Europe PubMed Central

11 August 2017

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0 references

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