(Q44045954)

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

scientific article published on 28 June 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

ubiquitin-proteasome system

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retinitis pigmentosa

1 reference

based on heuristic

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author name string

Michelle E Illing

1

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Rahul S Rajan

2

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Neil F Bence

3

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Ron R Kopito

4

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

language of work or name

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publication date

28 June 2002

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Europe PubMed Central

PubMed publication ID

29 November 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

29 November 2017

277

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

37

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

34150-34160

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Apoptotic cell death in retinal degenerations.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

bcl-2 overexpression reduces apoptotic photoreceptor cell death in three different retinal degenerations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Morphological, physiological, and biochemical changes in rhodopsin knockout mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Rhodopsin's carboxy-terminal cytoplasmic tail acts as a membrane receptor for cytoplasmic dynein by binding to the dynein light chain Tctex-1

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Unfolding retinal dystrophies: a role for molecular chaperones?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Conformational disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Protein misfolding and disease; protein refolding and therapy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Ubiquitin is a common factor in intermediate filament inclusion bodies of diverse type in man, including those of Parkinson's disease, Pick's disease, and Alzheimer's disease, as well as Rosenthal fibres in cerebellar astrocytomas, cytoplasmic bodie

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Aggresomes, inclusion bodies and protein aggregation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Impairment of the ubiquitin-proteasome system by protein aggregation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Specificity in intracellular protein aggregation and inclusion body formation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

A new technique for the assay of infectivity of human adenovirus 5 DNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Aggresomes: a cellular response to misfolded proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

The role of multiubiquitination in dislocation and degradation of the alpha subunit of the T cell antigen receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

A multiubiquitin chain is confined to specific lysine in a targeted short-lived protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Recognition of the polyubiquitin proteolytic signal

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Identification of genes that modify ataxin-1-induced neurodegeneration.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

The ubiquitin pathway in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Protein aggregation: folding aggregates, inclusion bodies and amyloid

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Expression of centrin isoforms in the mammalian retina

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Centrin in the photoreceptor cells of mammalian retinae

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Degeneration of photoreceptors in rhodopsin mutants of Drosophila

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Retinal degeneration caused by dominant rhodopsin mutations in Drosophila.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Ubiquitin-mediated proteolysis: biological regulation via destruction

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M204955200

21 January 2018

Identifiers

10.1074/JBC.M204955200

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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