(Q35566986)

8 August 2017

1 reference

title

The nature of dominant mutations of rhodopsin and implications for gene therapy (English)

1 reference

8 August 2017

0 references

Theodore G Wensel

2

0 references

author name string

John H Wilson

series ordinal

1

1 reference

8 August 2017

publication date

1 October 2003

1 reference

8 August 2017

published in

Molecular Neurobiology

1 reference

8 August 2017

volume

28

1 reference

8 August 2017

issue

2

1 reference

8 August 2017

page(s)

149-158

1 reference

https://scigraph.springernature.com/pub.10.1385/mn:28:2:149

8 August 2017

exact match

0 references

cites work

Supernormal vision and high-resolution retinal imaging through adaptive optics

1 reference

12 December 2020

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

1 reference

12 December 2020

The relationship between opsin overexpression and photoreceptor degeneration

1 reference

12 December 2020

Segmental genomic replacement in embryonic stem cells by double lox targeting

1 reference

12 December 2020

Mechanisms of rhodopsin inactivation in vivo as revealed by a COOH-terminal truncation mutant.

1 reference

12 December 2020

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Rhodopsin and phototransduction: a model system for G protein-linked receptors

1 reference

12 December 2020

Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene.

1 reference

12 December 2020

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutant rhodopsin transgene expression on a null background

1 reference

12 December 2020

Aggresomes, inclusion bodies and protein aggregation

1 reference

12 December 2020

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

1 reference

12 December 2020

Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa.

1 reference

12 December 2020

Molecular genetics of human retinal disease

1 reference

12 December 2020

Aggregates in neurodegenerative disease: crowds and power?

1 reference

12 December 2020

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

12 December 2020

Constitutively active mutants of rhodopsin

1 reference

12 December 2020

Morphological, physiological, and biochemical changes in rhodopsin knockout mice

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene

1 reference

12 December 2020

Ribozyme rescue of photoreceptor cells in P23H transgenic rats: long-term survival and late-stage therapy.

1 reference

12 December 2020

Management of inherited outer retinal dystrophies: present and future

1 reference

12 December 2020

A gene complex controlling segmentation in Drosophila

1 reference

12 December 2020

G-protein-coupled receptor dimerization: modulation of receptor function.

1 reference

12 December 2020

Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns.

1 reference

12 December 2020

Dominant-negative p53 mutations selected in yeast hit cancer hot spots

1 reference

12 December 2020

Targeting RAS signalling pathways in cancer therapy

1 reference

12 December 2020

Transient dichroism in photoreceptor membranes indicates that stable oligomers of rhodopsin do not form during excitation

1 reference

12 December 2020

Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Strategems in vitro for gene therapies directed to dominant mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

Specificity in intracellular protein aggregation and inclusion body formation

1 reference

12 December 2020

The arrangement of the three cone classes in the living human eye.

1 reference

12 December 2020

A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

1 reference

12 December 2020

Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures

1 reference

12 December 2020

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

1 reference

12 December 2020

Rhodopsin dimers in native disc membranes

1 reference

12 December 2020

On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention

1 reference

12 December 2020

Cotranslation of activated mutant p53 with wild type drives the wild-type p53 protein into the mutant conformation

1 reference

12 December 2020

Functional inactivation of genes by dominant negative mutations

1 reference

12 December 2020

Identifiers

DOI

10.1385/MN:28:2:149

1 reference

Dimensions Publication ID

8 August 2017

1043595616

0 references

1 reference