(Q28118979)

4 January 2017

title

Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2 (English)

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Cell migration inducing hyaluronidase 2

4 January 2017

main subject

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ORCID Public Data File 2021

GOA release 2020-03-11

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1 reference

Bronya J. B. Keats

10

object named as

B. J. Keats

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4 January 2017

D. A. Scott

1

1 reference

4 January 2017

S. Drury

2

1 reference

4 January 2017

R. A. Sundstrom

3

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4 January 2017

J. Bishop

4

1 reference

4 January 2017

R. E. Swiderski

5

1 reference

4 January 2017

R. Carmi

6

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4 January 2017

A. Ramesh

7

1 reference

4 January 2017

K. Elbedour

8

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4 January 2017

C. R. Srikumari Srisailapathy

9

1 reference

4 January 2017

V. C. Sheffield

11

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4 January 2017

R. J. Smith

12

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4 January 2017

language of work or name

English

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publication date

4 April 2000

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4 January 2017

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4 January 2017

volume

246

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4 January 2017

issue

1-2

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4 January 2017

page(s)

265–274

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Inner ear pathology in the deafness mutant mouse.

4 January 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

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%2800%2900090-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Interpreting cDNA sequences: some insights from studies on translation

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Genetic epidemiology of hearing impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Neonatal hearing screening

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Early degeneration of sensory and ganglion cells in the inner ear of mice with uncomplicated genetic deafness (dn): preliminary observations

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2800%2900090-1

7 January 2021

10.1016/S0378-1119(00)00090-1

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017