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Retinal degeneration mutants in the mouse
scientific article (publication date: February 2002)
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instance of
scholarly article
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review article
1 reference
stated in
Europe PubMed Central
title
Retinal degeneration mutants in the mouse
(English)
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main subject
retinal degeneration
1 reference
based on heuristic
inferred from title
author name string
B Chang
series ordinal
1
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N L Hawes
series ordinal
2
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R E Hurd
series ordinal
3
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M T Davisson
series ordinal
4
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S Nusinowitz
series ordinal
5
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J R Heckenlively
series ordinal
6
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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
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinal degeneration in the pcd cerebellar mutant mouse. II. Electron microscopic analysis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
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inferred from DOI database lookup
Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
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inferred from DOI database lookup
Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)
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reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
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7 January 2021
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inferred from DOI database lookup
Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New mouse primary retinal degeneration (rd-3)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
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inferred from DOI database lookup
Genetic and physical maps of the mouse rd3 locus; exclusion of the ortholog of USH2A.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
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7 January 2021
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inferred from DOI database lookup
Studies of visual function and its decay in mice with hereditary retinal degeneration.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
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inferred from DOI database lookup
Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
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7 January 2021
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inferred from DOI database lookup
Development and degeneration of retina in rds mutant mice: electron microscopy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
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inferred from DOI database lookup
Retinal Degeneration in the Mouse Is Rodless Retina
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
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inferred from DOI database lookup
The vit gene maps to the mi (microphthalmia) locus of the laboratory mouse
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinal degeneration in the pcd cerebellar mutant mouse. I. Light microscopic and autoradiographic analysis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
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inferred from DOI database lookup
Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominance in a late-onset motor neuron disease in the mouse
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Purkinje cell degeneration, a new neurological mutation in the mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two types of retinal degeneration in cerebellar mutant mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new H-2-linked mutation, rds, causing retinal degeneration in the mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A candidate gene for the mouse mutation tubby
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development and degeneration of retina in rds mutant mice: the electroretinogram
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development and degeneration of retina in rds mutant mice: light microscopy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of dark-rearing on the retinal degeneration of the C57BL/6-mivit/mivit mouse.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A medley of retinal dystrophies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0042-6989%2801%2900146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0042-6989(01)00146-8
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2672152
OpenCitations bibliographic resource ID
2672152
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2672152
PubMed ID
11853768
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2672152
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