Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation (Q28594919)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17876667%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation (English)

2 references

1 February 2017

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Lipoma HMGIC fusion partner-like 5

7 January 2020

main subject

1 reference

GOA release 2020-03-11

1 reference

3

1 reference

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7 January 2020

author name string

Chantal M Longo-Guess

series ordinal

1

1 reference

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7 January 2020

Leona H Gagnon

series ordinal

2

1 reference

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7 January 2020

Kenneth R Johnson

series ordinal

4

1 reference

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7 January 2020

publication date

18 September 2007

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7 January 2020

number of pages

11

1 reference

inferred from page(s)

2 references

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7 January 2020

volume

18

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7 January 2020

issue

9

2 references

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7 January 2020

page(s)

646-656

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00335-007-9049-x

7 January 2020

exact match

0 references

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A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

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17 March 2017

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17 March 2017

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

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17 March 2017

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Hair cells in the inner ear of the pirouette and shaker 2 mutant mice

17 March 2017

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NeuroD-null mice are deaf due to a severe loss of the inner ear sensory neurons during development

17 March 2017

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The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

17 March 2017

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

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Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

7 April 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.

27 November 2018

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27 November 2018

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27 November 2018

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27 November 2018

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27 November 2018

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12 December 2020

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12 December 2020

High-resolution scanning-electron microscopy of stereocilia using the osmium-thiocarbohydrazide coating technique

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12 December 2020

Differentiation and maturation of the sensory hair bundles in the fetal and postnatal vestibular receptors of the mouse: a scanning electron microscopy study

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10.1007/S00335-007-9049-X

Identifiers

DOI

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7 January 2020

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7 January 2020

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1 February 2017