(Q35562765)

8 August 2017

title

Molecular mechanisms of disease for mutations at Gly-90 in rhodopsin (English)

1 reference

8 August 2017

Arnau Cordomí

4

0 references

Michael E. Cheetham

object named as

Michael E Cheetham

7

0 references

Juan Jesús Pérez

object named as

Juan J Pérez

5

0 references

Pere Garriga Sole

1 reference

ORCID Public Data File 2021

author name string

Darwin Toledo

1

1 reference

8 August 2017

Eva Ramon

2

1 reference

8 August 2017

Mònica Aguilà

3

1 reference

8 August 2017

Hugo F Mendes

6

1 reference

8 August 2017

Pere Garriga

8

1 reference

8 August 2017

language of work or name

English

0 references

publication date

22 September 2011

1 reference

Journal of Biological Chemistry

8 August 2017

published in

1 reference

8 August 2017

volume

286

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8 August 2017

issue

46

1 reference

8 August 2017

page(s)

39993-40001

1 reference

1 rhodopsin mutations in congenital night blindness

8 August 2017

cites work

1 reference

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Covalent bond between ligand and receptor required for efficient activation in rhodopsin

12 July 2018

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The role of transmembrane segment II in 7TM receptor activation

12 July 2018

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A dual role for EDEM1 in the processing of rod opsin

12 July 2018

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Molecular mechanisms of rhodopsin retinitis pigmentosa and the efficacy of pharmacological rescue

12 July 2018

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12 July 2018

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Two protonation switches control rhodopsin activation in membranes

12 July 2018

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Night blindness and the mechanism of constitutive signaling of mutant G90D rhodopsin

12 July 2018

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12 July 2018

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Constitutive excitation by Gly90Asp rhodopsin rescues rods from degeneration caused by elevated production of cGMP in the dark.

12 July 2018

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12 July 2018

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Comparison of multiple Amber force fields and development of improved protein backbone parameters

12 July 2018

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12 July 2018

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12 July 2018

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Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

12 July 2018

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Isorhodopsin rather than rhodopsin mediates rod function in RPE65 knock-out mice

12 July 2018

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Retinal counterion switch in the photoactivation of the G protein-coupled receptor rhodopsin

12 July 2018

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Characterization of rhodopsin congenital night blindness mutant T94I.

12 July 2018

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The crystallographic model of rhodopsin and its use in studies of other G protein-coupled receptors

12 July 2018

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

12 July 2018

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The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formation.

12 July 2018

1 reference

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Structure and function in rhodopsin: Mass spectrometric identification of the abnormal intradiscal disulfide bond in misfolded retinitis pigmentosa mutants

12 July 2018

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12 July 2018

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Structure and function in rhodopsin: correct folding and misfolding in two point mutants in the intradiscal domain of rhodopsin identified in retinitis pigmentosa

12 July 2018

1 reference

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

12 July 2018

1 reference

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Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness

12 July 2018

1 reference

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

12 July 2018

1 reference

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

12 July 2018

1 reference

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Expression of a synthetic bovine rhodopsin gene in monkey kidney cells

12 July 2018

1 reference

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Effect of carboxylic acid side chains on the absorption maximum of visual pigments

12 July 2018

1 reference

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Glutamic acid-113 serves as the retinylidene Schiff base counterion in bovine rhodopsin

12 July 2018

1 reference

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Role of the intradiscal domain in rhodopsin assembly and function

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220564

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220564

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220564

Cell toxicity and conformational disease.

12 July 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Unusual thermal and conformational properties of the rhodopsin congenital night blindness mutant Thr-94 --> Ile.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Stability of dark state rhodopsin is mediated by a conserved ion pair in intradiscal loop E-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Altered functionality in rhodopsin point mutants associated with retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Modulating rhodopsin receptor activation by altering the pKa of the retinal Schiff base.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Opsin activation as a cause of congenital night blindness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Protein assistance in the photoisomerization of rhodopsin and 9-cis-rhodopsin--insights from experiment and theory.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Slow binding of retinal to rhodopsin mutants G90D and T94D.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.201517

Rhodopsin structure: some light into the shadows of retinal degenerations

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220564

Characterization of rhodopsin mis-sorting and constitutive activation in a transgenic rat model of retinitis pigmentosa.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3220564

Alterations in the photoactivation pathway of rhodopsin mutants associated with retinitis pigmentosa

26 September 2018

1 reference

12 December 2020

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

1 reference

12 December 2020

Structure and function in rhodopsin. Measurement of the rate of metarhodopsin II decay by fluorescence spectroscopy

1 reference

12 December 2020

Characterization of the mutant visual pigment responsible for congenital night blindness: a biochemical and Fourier-transform infrared spectroscopy study

1 reference

12 December 2020

Identifiers

DOI

10.1074/JBC.M110.201517

1 reference

8 August 2017

1 reference

8 August 2017

1 reference