(Q36847786)

16 August 2017

title

Canine rod transducin alpha-1: cloning of the cDNA and evaluation of the gene as a candidate for progressive retinal atrophy (English)

1 reference

16 August 2017

K Ray

1

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16 August 2017

V J Baldwin

2

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16 August 2017

C Zeiss

3

1 reference

16 August 2017

G M Acland

4

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16 August 2017

G D Aguirre

5

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16 August 2017

publication date

1 January 1997

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16 August 2017

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16 August 2017

volume

16

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16 August 2017

issue

1

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16 August 2017

page(s)

71-77

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Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase

16 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

On the lod score method in linkage analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Nucleotide sequence for a cDNA encoding the alpha subunit of retinal transducin (GNAT1) isolated from the human eye

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Characterization of the human rod transducin alpha-subunit gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

The beta subunit of cyclic GMP phosphodiesterase mRNA is deficient in canine rod-cone dysplasia 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Retinal degeneration in mice lacking the gamma subunit of the rod cGMP phosphodiesterase

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Variation in retinal degeneration phenotype inherited at the prcd locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

Non-allelism of three genes (rcd1, rcd2 and erd) for early-onset hereditary retinal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

XLPRA: a canine retinal degeneration inherited as an X-linked trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.1.71.5122

10.1076/CEYR.16.1.71.5122

21 January 2018

Identifiers

DOI

1 reference

16 August 2017

1 reference