(Q45889604)

17 December 2017

review article

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title

Animal models of human retinal dystrophies (English)

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17 December 2017

author name string

Petersen-Jones SM

series ordinal

1

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17 December 2017

publication date

1 January 1998

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17 December 2017

published in

Eye

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17 December 2017

volume

12 ( Pt 3b)

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17 December 2017

page(s)

566-570

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17 December 2017

https://scigraph.springernature.com/pub.10.1038/eye.1998.146

exact match

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Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases

21 January 2018

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A review of research to elucidate the causes of the generalized progressive retinal atrophies

21 January 2018

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Selective absence of cone outer segment beta 3-transducin immunoreactivity in hereditary cone degeneration (cd).

21 January 2018

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Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness

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Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness

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

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

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Cyclic guanosine monophosphate: elevation in degenerating photoreceptor cells of the C3H mouse retina

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Isolation of a candidate cDNA for the gene causing retinal degeneration in the rd mouse

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

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

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Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase

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Retinal degeneration is rescued in transgenic rd mice by expression of the cGMP phosphodiesterase beta subunit

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

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Rod-Cone Dysplasia in Irish Setters: A Defect in Cyclic GMP Metabolism in Visual Cells

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Involvement of cyclic GMP phosphodiesterase activator in an hereditary retinal degeneration

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Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene

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Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

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Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa

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Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degeneration

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

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

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Cloning and characterization of the cDNA and gene encoding the gamma-subunit of cGMP-phosphodiesterase in canine retinal rod photoreceptor cells

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Complete rescue of photoreceptor dysplasia and degeneration in transgenic retinal degeneration slow (rds) mice

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7 January 2021

Identifiers

DOI

10.1038/EYE.1998.146

1 reference

17 December 2017

Dimensions Publication ID

1039664439

0 references

1 reference

17 December 2017