(Q48018820)

English

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.

scientific article published in July 1998

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5 December 2019

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 (English)

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5 December 2019

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Prescott Deininger

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5 December 2019

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5 December 2019

Richard J Smith

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5 December 2019

Val C. Sheffield

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5 December 2019

Bronya J. B. Keats

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B J Keats

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5 December 2019

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D A Scott

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5 December 2019

J H Greinwald

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5 December 2019

J R Marietta

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5 December 2019

S Drury

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5 December 2019

R E Swiderski

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5 December 2019

M M DeAngelis

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R Carmi

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A Ramesh

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5 December 2019

M L Kraft

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5 December 2019

K Elbedour

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5 December 2019

A B Skworak

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5 December 2019

R A Friedman

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5 December 2019

C R Srikumari Srisailapathy

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5 December 2019

K Verhoeven

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5 December 2019

G Van Gamp

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5 December 2019

M Lovett

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M A Batzer

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C C Morton

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5 December 2019

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publication date

1 July 1998

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5 December 2019

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5 December 2019

215

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5 December 2019

2

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5 December 2019

461-469

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5 December 2019

Isolation of cDNAs that are differentially expressed between androgen-dependent and androgen-independent prostate carcinoma cells using differential display PCR.

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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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7 January 2021

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A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900316-3

7 January 2021

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The deafness locus (dn) maps to mouse chromosome 19.

1 reference

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Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

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Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

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Genetic epidemiology of hearing impairment

1 reference

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Genes responsible for human hereditary deafness: symphony of a thousand

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Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening

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Alterations in gene expression associated with changes in the state of endothelial differentiation

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The mouse deafness locus (dn) is associated with an inversion on chromosome 19

1 reference

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7 January 2021

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The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

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Passage to India: the search for genes causing autosomal recessive nonsyndromic hearing loss.

1 reference

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Identifiers

10.1016/S0378-1119(98)00316-3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9758550%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9758550%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

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