Knock-in human rhodopsin-GFP fusions as mouse models for human disease and targets for gene therapy (Q34836312)

4 August 2017

Knock-in human rhodopsin-GFP fusions as mouse models for human disease and targets for gene therapy (English)

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4 August 2017

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Fung Chan

1

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4 August 2017

Allan Bradley

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2

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4 August 2017

Theodore G Wensel

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3

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4 August 2017

John H Wilson

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4

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4 August 2017

language of work or name

English

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publication date

7 June 2004

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

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4 August 2017

101

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24

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4 August 2017

9109-9114

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describes a project that uses

4 August 2017

ImageQuant

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC428481/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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The role of tangential dispersion in retinal mosaic formation

8 July 2018

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8 July 2018

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Rhodopsin: structural basis of molecular physiology

8 July 2018

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Mutant rhodopsin transgene expression on a null background

8 July 2018

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Identification of an outer segment targeting signal in the COOH terminus of rhodopsin using transgenic Xenopus laevis

8 July 2018

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Blocking transcription of the human rhodopsin gene by triplex-mediated DNA photocrosslinking

8 July 2018

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Engineering mouse chromosomes with Cre-loxP: range, efficiency, and somatic applications

8 July 2018

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Segmental genomic replacement in embryonic stem cells by double lox targeting

8 July 2018

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Morphological, physiological, and biochemical changes in rhodopsin knockout mice

8 July 2018

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8 July 2018

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IgA class switch in I alpha exon-deficient mice. Role of germline transcription in class switch recombination

8 July 2018

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8 July 2018

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Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase

8 July 2018

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Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse

8 July 2018

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

8 July 2018

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8 July 2018

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Crossref

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A functional rhodopsin-green fluorescent protein fusion protein localizes correctly in transgenic Xenopus laevis retinal rods and is expressed in a time-dependent pattern

21 January 2018

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

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/15184660

12 December 2020

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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

PubMed

https://pubmed.ncbi.nlm.nih.gov/15184660

12 December 2020

inferred from PubMed ID database lookup

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15184660

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.0403149101

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4 August 2017

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4 August 2017

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