Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness (Q28116173)

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

GOA release 2020-03-11

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V. R. Rao

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4 January 2017

G. B. Cohen

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2

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4 January 2017

D. D. Oprian

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3

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4 January 2017

language of work or name

English

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publication date

17 February 1994

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4 January 2017

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367

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639–642

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6464

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4 January 2017

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7 January 2021

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

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7 January 2021

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

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7 January 2021

On the molecular genetics of retinitis pigmentosa

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7 January 2021

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

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7 January 2021

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

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7 January 2021

Constitutively active mutants of rhodopsin

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7 January 2021

Mechanism of activation and inactivation of opsin: role of Glu113 and Lys296

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7 January 2021

Constitutive activation of opsin: influence of charge at position 134 and size at position 296.

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7 January 2021

Studies on rhodopsin. 9. pH and the hydrolysis of indicator yellow

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7 January 2021

TAUTOMERIC FORMS OF METARHODOPSIN.

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7 January 2021

Complex formation between metarhodopsin II and GTP-binding protein in bovine photoreceptor membranes leads to a shift of the photoproduct equilibrium

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Projection structure of rhodopsin

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7 January 2021

The probable arrangement of the helices in G protein-coupled receptors.

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7 January 2021

Transducin activation by rhodopsin without a covalent bond to the 11-cis-retinal chromophore

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7 January 2021

The structure of rhodopsin and the rod outer segment disk membrane

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7 January 2021

The photocurrent, noise and spectral sensitivity of rods of the monkey Macaca fascicularis

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7 January 2021

Possible mechanisms of photoreceptor damage by light in mammalian eyes

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7 January 2021

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

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7 January 2021

Arrestin function in inactivation of G protein-coupled receptor rhodopsin in vivo.

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7 January 2021

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

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7 January 2021

A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty

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7 January 2021

Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function.

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7 January 2021

Total synthesis of a gene for bovine rhodopsin

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7 January 2021

Expression of a synthetic bovine rhodopsin gene in monkey kidney cells

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7 January 2021