(Q28589272)

31 January 2017

title

Vestibular dysgenesis in mice lacking Abr and Bcr Cdc42/RacGAPs (English)

1 reference

BCR activator of RhoGEF and GTPase

31 January 2017

main subject

1 reference

GOA release 2020-03-11

Active BCR-related gene

1 reference

GOA release 2020-03-11

author

Vesa Kaartinen

1

0 references

author name string

Andre Nagy

2

1 reference

31 January 2017

Ignacio Gonzalez-Gomez

3

1 reference

31 January 2017

John Groffen

4

1 reference

31 January 2017

Nora Heisterkamp

5

1 reference

31 January 2017

publication date

1 April 2002

1 reference

31 January 2017

published in

Developmental Dynamics

1 reference

31 January 2017

volume

223

1 reference

31 January 2017

issue

4

1 reference

31 January 2017

page(s)

517–525

1 reference

Abr and Bcr are multifunctional regulators of the Rho GTP-binding protein family.

31 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

Who does the hair cell's 'do? Rho GTPases and hair-bundle morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

The development of the vertebrate inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

Rho GTPases and signaling networks

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.10071

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

1 reference

31 January 2017

1 reference