Retinal degeneration mutants in the mouse (Q28202375)

Europe PubMed Central

title

Retinal degeneration mutants in the mouse (English)

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B Chang

1

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N L Hawes

2

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R E Hurd

3

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M T Davisson

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S Nusinowitz

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J R Heckenlively

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

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language of work or name

English

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publication date

February 2002

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published in

Vision Research

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volume

42

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issue

4

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page(s)

517-25

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cites work

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Retinal degeneration in the pcd cerebellar mutant mouse. II. Electron microscopic analysis

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9

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https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

New mouse primary retinal degeneration (rd-3)

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Genetic and physical maps of the mouse rd3 locus; exclusion of the ortholog of USH2A.

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Studies of visual function and its decay in mice with hereditary retinal degeneration

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https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Development and degeneration of retina in rds mutant mice: electron microscopy

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Retinal Degeneration in the Mouse Is Rodless Retina

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

The vit gene maps to the mi (microphthalmia) locus of the laboratory mouse

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Retinal degeneration in the pcd cerebellar mutant mouse. I. Light microscopic and autoradiographic analysis

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II.

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Autosomal dominance in a late-onset motor neuron disease in the mouse

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS)

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Purkinje cell degeneration, a new neurological mutation in the mouse

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Two types of retinal degeneration in cerebellar mutant mice

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

A new H-2-linked mutation, rds, causing retinal degeneration in the mouse

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

A candidate gene for the mouse mutation tubby

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Development and degeneration of retina in rds mutant mice: the electroretinogram

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse.

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Development and degeneration of retina in rds mutant mice: light microscopy

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Evidence of a difference in photoreceptor cell loss in the peripheral versus posterior regions of the vitiligo (C57BL/6J-mi(vit)/mi(vit)) mouse retina

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Effects of dark-rearing on the retinal degeneration of the C57BL/6-mivit/mivit mouse.

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

A medley of retinal dystrophies

1 reference

https://api.crossref.org/works/10.1016/S0042-6989(01)00146-8

7 January 2021

10.1016/S0042-6989(01)00146-8

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

11853768

1 reference

Consolidated OpenCitations Corpus – April 2017