(Q52535765)

2 May 2018

title

Disruption of a retinal guanylyl cyclase gene leads to cone-specific dystrophy and paradoxical rod behavior. (English)

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2 May 2018

author name string

Yang RB

1

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2 May 2018

Robinson SW

2

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2 May 2018

Xiong WH

3

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2 May 2018

Yau KW

4

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2 May 2018

Birch DG

5

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2 May 2018

Garbers DL

6

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2 May 2018

language of work or name

English

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publication date

1 July 1999

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2 May 2018

published in

Journal of Neuroscience

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2 May 2018

volume

19

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2 May 2018

issue

14

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2 May 2018

page(s)

5889-5897

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2 May 2018

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse

cites work

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Transduction mechanisms of vertebrate and invertebrate photoreceptors.

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Cloning, sequencing, and expression of a 24-kDa Ca(2+)-binding protein activating photoreceptor guanylyl cyclase.

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Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy.

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A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1

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Phototransduction mechanism in retinal rods and cones. The Friedenwald Lecture

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A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors

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GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy

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Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy

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Phospholipase C beta 4 is involved in modulating the visual response in mice

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Kinetics of recovery of the dark-adapted salamander rod photoresponse

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Gene targeting in embryonic stem cells

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A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype

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The membrane current of single rod outer segments

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A retGC-1 mutation in autosomal dominant cone-rod dystrophy.

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Constitutive activation of photoreceptor guanylate cyclase by Y99C mutant of GCAP-1. Possible role in causing human autosomal dominant cone degeneration

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Two membrane forms of guanylyl cyclase found in the eye

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A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

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The localization of guanylyl cyclase-activating proteins in the mammalian retina

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Hereditary retinal degeneration in the Rhode Island Red chicken. I. Histology and ERG

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Identification of components of a phosphoinositide signaling pathway in retinal rod outer segments

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Primary structure and differential gene expression of three membrane forms of guanylyl cyclase found in the eye of the teleost Oryzias latipes

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Functional characterization of a guanylyl cyclase-activating protein from vertebrate rods. Cloning, heterologous expression, and localization

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Molecular cloning of a retina-specific membrane guanylyl cyclase

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The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

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The bovine rod outer segment guanylate cyclase, ROS-GC, is present in both outer segment and synaptic layers of the retina

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Localization of guanylate cyclase-activating protein 2 in mammalian retinas

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12 December 2020

Molecular cloning and characterization of retinal photoreceptor guanylyl cyclase-activating protein

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12 December 2020

Two eye guanylyl cyclases are expressed in the same photoreceptor cells and form homomers in preference to heteromers

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Ultrastructural localization of retinal guanylate cyclase in human and monkey retinas

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Turned on by Ca2+! The physiology and pathology of Ca(2+)-binding proteins in the retina

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Specific binding of peanut lectin to a class of retinal photoreceptor cells. A species comparison.

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Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1.

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Gene array and expression of mouse retina guanylate cyclase activating proteins 1 and 2.

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Guanylyl cyclase receptors

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Chromosomal localization and genomic organization of genes encoding guanylyl cyclase receptors expressed in olfactory sensory neurons and retina.

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12 December 2020

10.1523/JNEUROSCI.19-14-05889.1999

Identifiers

DOI

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2 May 2018

PMC publication ID

6783089

0 references

1 reference

2 May 2018