(Q50481967)

14 March 2018

title

Stereocilia: the long and the short of it (English)

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

29 March 2024

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

29 March 2024

1

Inna A Belyantseva

1 reference

14 March 2018

Thomas B. Friedman

5

object named as

Thomas B Friedman

1 reference

14 March 2018

Erich T Boger

3

object named as

Erich T Boger

1 reference

14 March 2018

author name string

Valentina Labay

2

1 reference

14 March 2018

Andrew J. Griffith

4

1 reference

PubMed ID

14604820

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14604820

29 March 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

PubMed ID

14604820

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14604820

29 March 2024

publication date

1 November 2003

1 reference

14 March 2018

full work available at URL

https://api.elsevier.com/content/article/PII:S1471491403002156?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

https://api.elsevier.com/content/article/PII:S1471491403002156?httpAccept=text/plain

29 March 2024

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Trends in Molecular Medicine

29 March 2024

published in

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14 March 2018

volume

9

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14 March 2018

issue

11

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14 March 2018

page(s)

458-461

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14 March 2018

Detection of Ca2+ entry through mechanosensitive channels localizes the site of mechanoelectrical transduction in hair cells

cites work

1

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Calcium imaging of single stereocilia in hair cells: localization of transduction channels at both ends of tip links

29 March 2024

2

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Cochlear mechanisms from a phylogenetic viewpoint

29 March 2024

3

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Genetic epidemiology of hearing impairment

29 March 2024

4

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

29 March 2024

5

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

PDZ domains and the organization of supramolecular complexes

29 March 2024

6

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Protein modules as organizers of membrane structure

29 March 2024

7

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

29 March 2024

8

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

29 March 2024

9

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions

29 March 2024

10

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

29 March 2024

11

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Defective myosin VIIA gene responsible for Usher syndrome type 1B

29 March 2024

12

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

29 March 2024

13

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

29 March 2024

14

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

29 March 2024

15

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

29 March 2024

16

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

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

29 March 2024

17

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Elongation of hair cell stereocilia is defective in the mouse mutant whirler

29 March 2024

19

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

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

29 March 2024

21

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2

29 March 2024

22

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

29 March 2024

23

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells

29 March 2024

24

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

Rapid renewal of auditory hair bundles

29 March 2024

25

1 reference

https://api.crossref.org/works/10.1016/J.MOLMED.2003.09.008

29 March 2024

Identifiers

1 reference

14 March 2018

PubMed ID

14604820

1 reference

14 March 2018