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Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2
scientific journal article
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scholarly article
1 reference
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PubMed
PubMed ID
10767548
retrieved
4 January 2017
title
Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2
(English)
1 reference
stated in
PubMed
PubMed ID
10767548
retrieved
4 January 2017
main subject
Cell migration inducing hyaluronidase 2
1 reference
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GOA release 2020-03-11
deafness
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inferred from title
author
Richard J Smith
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ORCID Public Data File 2021
Bronya J. B. Keats
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10
object named as
B. J. Keats
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PubMed
PubMed ID
10767548
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4 January 2017
author name string
D. A. Scott
series ordinal
1
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PubMed
PubMed ID
10767548
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4 January 2017
S. Drury
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2
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PubMed
PubMed ID
10767548
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4 January 2017
R. A. Sundstrom
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3
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PubMed
PubMed ID
10767548
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4 January 2017
J. Bishop
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4
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PubMed
PubMed ID
10767548
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4 January 2017
R. E. Swiderski
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5
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PubMed
PubMed ID
10767548
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R. Carmi
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PubMed
PubMed ID
10767548
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A. Ramesh
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PubMed
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10767548
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K. Elbedour
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PubMed
PubMed ID
10767548
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C. R. Srikumari Srisailapathy
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PubMed
PubMed ID
10767548
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4 January 2017
V. C. Sheffield
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11
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PubMed
PubMed ID
10767548
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R. J. Smith
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12
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PubMed
PubMed ID
10767548
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4 January 2017
language of work or name
English
0 references
publication date
4 April 2000
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PubMed
PubMed ID
10767548
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4 January 2017
published in
Gene
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PubMed
PubMed ID
10767548
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4 January 2017
volume
246
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PubMed
PubMed ID
10767548
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4 January 2017
page(s)
265–274
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PubMed
PubMed ID
10767548
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4 January 2017
issue
1-2
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PubMed
PubMed ID
10767548
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4 January 2017
cites work
Inner ear pathology in the deafness mutant mouse.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
retrieved
7 January 2021
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inferred from DOI database lookup
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
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inferred from DOI database lookup
A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
The deafness locus (dn) maps to mouse chromosome 19.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
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inferred from DOI database lookup
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Interpreting cDNA sequences: some insights from studies on translation
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
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inferred from DOI database lookup
A mutation in PDS causes non-syndromic recessive deafness
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
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inferred from DOI database lookup
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
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Genetic epidemiological studies of early-onset deafness in the U.S. school-age population
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
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inferred from DOI database lookup
Genetic epidemiology of hearing impairment
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
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inferred from DOI database lookup
Neonatal hearing screening
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early degeneration of sensory and ganglion cells in the inner ear of mice with uncomplicated genetic deafness (dn): preliminary observations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic deafness
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
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7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse deafness locus (dn) is associated with an inversion on chromosome 19
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0378-1119(00)00090-1
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4800226
OpenCitations bibliographic resource ID
4800226
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4800226
PubMed ID
10767548
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4800226
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