(Q21710681)

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

AAV-mediated delivery of ciliary neurotrophic factor prolongs photoreceptor survival in the rhodopsin knockout mouse

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Glial cell line derived neurotrophic factor delays photoreceptor degeneration in a transgenic rat model of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Constitutively active mutants of rhodopsin

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Constitutive opsin signaling: night blindness or retinal degeneration?

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Dark adaptation and the retinoid cycle of vision

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

A trip to the ER: coping with stress

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Altered functionality in rhodopsin point mutants associated with retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

The carboxyl-terminal domain is essential for rhodopsin transport in rod photoreceptors

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Ubiquitin, cellular inclusions and their role in neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Aggresomes, inclusion bodies and protein aggregation

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Phototransduction: crystal clear

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Unfolding retinal dystrophies: a role for molecular chaperones?

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Rhodopsin maturation antagonized by dominant rhodopsin mutants.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Rhodopsin arginine-135 mutants are phosphorylated by rhodopsin kinase and bind arrestin in the absence of 11-cis-retinal

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Accelerated transport and maturation of lysosomal α–galactosidase A in Fabry lymphoblasts by an enzyme inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Polyglutamine protein aggregates are dynamic

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Activation of mislocalized opsin kills rod cells: a novel mechanism for rod cell death in retinal disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Morphological, physiological, and biochemical changes in rhodopsin knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

The Chaperone Environment at the Cytoplasmic Face of the Endoplasmic Reticulum Can Modulate Rhodopsin Processing and Inclusion Formation

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Retinoids assist the cellular folding of the autosomal dominant retinitis pigmentosa opsin mutant P23H.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Prefibrillar amyloid protein aggregates share common features of cytotoxicity.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Suppression of wild-type rhodopsin maturation by mutants linked to autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

A naturally occurring mutation of the opsin gene (T4R) in dogs affects glycosylation and stability of the G protein-coupled receptor

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Rhodopsin and retinitis pigmentosa: shedding light on structure and function

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Interference of Crx-dependent transcription by ataxin-7 involves interaction between the glutamine regions and requires the ataxin-7 carboxy-terminal region for nuclear localization

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Progressive decrease in chaperone protein levels in a mouse model of Huntington's disease and induction of stress proteins as a therapeutic approach

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135-Trp). Disease phenotype in a Swedish family

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Prevention of transthyretin amyloid disease by changing protein misfolding energetics.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Crystal structure of rhodopsin: A G protein-coupled receptor

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Impairment of the ubiquitin-proteasome system by protein aggregation

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

A morphometric study of light-induced damage in transgenic rat models of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

The nature of dominant mutations of rhodopsin and implications for gene therapy

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

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://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Activation of caspase-3 in the retina of transgenic rats with the rhodopsin mutation s334ter during photoreceptor degeneration

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

Increased expression of brain-derived neurotrophic factor preserves retinal function and slows cell death from rhodopsin mutation or oxidative damage.

1 reference

https://api.crossref.org/works/10.1016%2FJ.MOLMED.2005.02.007

7 January 2021

10.1016/J.MOLMED.2005.02.007

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dt6pkyt4t5eqvh36iu6dylgpcm

30 July 2022

mapped directly with Wikidata item

Fatcat ID

release_dt6pkyt4t5eqvh36iu6dylgpcm

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dt6pkyt4t5eqvh36iu6dylgpcm

30 July 2022

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

1874972

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://api.fatcat.wiki/v0/release/dt6pkyt4t5eqvh36iu6dylgpcm

30 July 2022