(Q28513818)

25 January 2017

title

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw) (English)

1 reference

25 January 2017

mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw) (English)

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Cadherin 23 (otocadherin)

18 November 2024

main subject

1 reference

ATPase, Ca transporting, plasma membrane 2

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

1 reference

K. Noben-Trauth

1

1 reference

25 January 2017

Q. Y. Zheng

2

1 reference

25 January 2017

K. R. Johnson

3

1 reference

25 January 2017

P. M. Nishina

4

1 reference

25 January 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9325047

18 November 2024

publication date

15 September 1997

1 reference

full work available at URL

25 January 2017

https://api.elsevier.com/content/article/PII:S0888754397948692?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

https://api.elsevier.com/content/article/PII:S0888754397948692?httpAccept=text/plain

18 November 2024

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

18 November 2024

1 reference

25 January 2017

volume

44

1 reference

25 January 2017

issue

3

1 reference

25 January 2017

page(s)

266–272

1 reference

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

25 January 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

18 November 2024

2

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

18 November 2024

3

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

18 November 2024

4

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse

18 November 2024

5

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins

18 November 2024

6

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains

18 November 2024

7

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

A type VII myosin encoded by the mouse deafness gene shaker-1

18 November 2024

8

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

18 November 2024

9

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

A Macintosh program for storage and analysis of experimental genetic mapping data

18 November 2024

11

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

A candidate gene for the mouse mutation tubby

18 November 2024

13

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Inherited hearing defects in mice

18 November 2024

14

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations

18 November 2024

15

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10.

18 November 2024

16

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

Defective myosin VIIA gene responsible for Usher syndrome type 1B

18 November 2024

17

1 reference

https://api.crossref.org/works/10.1006/GENO.1997.4869

18 November 2024

Identifiers

0 references

1 reference