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Usherin expression is highly conserved in mouse and human tissues
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scholarly article
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title
Usherin expression is highly conserved in mouse and human tissues
(English)
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main subject
Usherin
1 reference
stated in
GOA release 2020-03-11
author name string
Nicole Pearsall
series ordinal
1
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Gautam Bhattacharya
series ordinal
2
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Jim Wisecarver
series ordinal
3
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Joe Adams
series ordinal
4
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Dominic Cosgrove
series ordinal
5
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William Kimberling
series ordinal
6
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language of work or name
English
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publication date
December 2002
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published in
Hearing Research
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volume
174
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issue
1-2
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page(s)
55-63
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cites work
Biotin amplification of biotin and horseradish peroxidase signals in histochemical stains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and function of laminin: anatomy of a multidomain glycoprotein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome type IIa.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and distribution of modules in extracellular proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Usher syndrome: definition and estimate of prevalence from two high-risk populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Seminiferous Tubule Basement Membrane
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assembly of Type IV Collagen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of Usher syndrome type II to chromosome 1q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic Studies of Usher Syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential expression of two basement membrane collagen genes, COL4A6 and COL4A5, demonstrated by immunofluorescence staining using peptide-specific monoclonal antibodies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Usher syndrome: from genetics to pathogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The prevalence of Usher syndrome and other retinal dystrophy-hearing impairment associations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role for transforming growth factor-beta1 in alport renal disease progression.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of two genes for Usher syndrome type I to chromosome 11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900635-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0378-5955(02)00635-4
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PubMed ID
12433396
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