About: Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice

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rdf:type	Item
description	artículu científicu espublizáu en 2003 (ast) vědecký článek publikovaný v roce 2003 (cs) 2003 թվականի մարտին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в березні 2003 (uk) 2003 թուականի Մարտին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت في مارس 2003) (ar) vedecký článok (publikovaný 2003/03/01) (sk) wetenschappelijk artikel (gepubliceerd op 2003/03/01) (nl) im März 2003 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28592537-240FFC1E-FF84-4017-B70A-B88ED1D47D14
publication date	2003-03-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q28592537-05A36069-F024-4B63-B0F5-EC60BB3F4464 wds:Q28592537-298ED4C2-FA70-41C2-89DA-D888C3FE9B8B wds:Q28592537-3E45A5A7-3F1F-486B-8245-FD03AAF1ED37 wds:Q28592537-4B0B4A32-6DC0-4A95-A4D9-25FE76F7216D wds:Q28592537-4C6C1022-3E24-455D-ABAB-57135104AD36 wds:Q28592537-572495ED-2B50-448B-8F32-2288A2C96486 wds:Q28592537-6B5CB5A4-58CD-457B-971D-4942BDEA7C81 wds:Q28592537-8D5B7666-E951-4492-AC13-DC6CE8D550A3 wds:Q28592537-93B6B337-88BD-4406-869A-7F849E933A3B wds:Q28592537-94804C2F-09EE-4491-8646-4807DC376F71 wds:Q28592537-AF3F5B1C-63D6-4F3D-A760-FE692CE3736B wds:Q28592537-B5B0C5EF-B9C0-4B90-A3B7-825B9EEF0C07 wds:Q28592537-D43F615C-1D6E-4379-9411-F18797E76156 wds:Q28592537-D4699A4B-EBDE-453F-B0F7-990929EA6B9C wds:Q28592537-E14FDFDE-1241-4FF6-8363-A23405B256E5 wds:Q28592537-FE070CB1-FAAA-4B36-A9F1-217F672540B9
author name string	Choji Taya Hiromichi Yonekawa Ken Kitamura Toshihiko Shiroishi Hisashi Tokano Shigeharu Wakana Yasuhiro Yoshikawa Yoshiaki Kikkawa Kazusaku Kamiya Toyoyuki Takada Hiroshi Shitara Kunihiko Shimizu Ryo Kominami Yuichi Wakabayashi Mieko Okamoto Yuki Kohara
rdfs:label	Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (en) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (nl) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (ast)
skos:prefLabel	Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (en) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (nl) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (ast)
name	Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (en) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (nl) Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (ast)
title	wds:Q28592537-60899DEA-2734-49A7-B8A2-856B412ECD57
title	Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice (en)
page(s)	wds:Q28592537-DD97EF4E-791E-4F40-91D1-3C0D6CAFE3B6
page(s)	453–461
instance of	wds:Q28592537-6566B9C1-8E04-422F-9FAA-513E1D2FD447
instance of	scholarly article
main subject	wds:Q28592537-278B12FD-A28D-42B4-83CF-AC75B725F9AD wds:Q28592537-59FDEC12-ED63-46FC-9261-569F5EB5FB38
main subject	deafness USH1 protein network component sans
PubMed ID	wds:Q28592537-18F3DEEB-BB91-46E9-A476-EE79AACDD3E6
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12588793
PubMed ID	12588793
published in	wds:Q28592537-5D58BC33-9ADC-4517-8426-5525C219D7F6
published in	Human Molecular Genetics
issue	wds:Q28592537-0C026E74-482B-4610-B56D-BF1B41D4D5E4
volume	wds:Q28592537-907CCF0C-9BE7-4444-B16A-A1EAEF59223A
issue	5
volume	12
DOI	wds:Q28592537-DA64AAE8-7599-4B72-9089-15A4E70EC738
DOI	http://dx.doi.org/10.1093/HMG/12.5.453
DOI	10.1093/HMG/12.5.453
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28592537
is cites work of	A quantitative survey of gravity receptor function in mutant mouse strains Characterization of the transcriptome of nascent hair cells and identification of direct targets of the Atoh1 transcription factor Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia Genetics of hearing and deafness Human hereditary hearing impairment: mouse models can help to solve the puzzle A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans Primary cilia in planar cell polarity regulation of the inner ear The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear function Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26). Tankyrase polymerization is controlled by its sterile alpha motif and poly(ADP-ribose) polymerase domains Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses Genetics and pathological mechanisms of Usher syndrome Molecular epidemiology of Usher syndrome in Italy Tip links in hair cells: molecular composition and role in hearing loss Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells Review series: The cell biology of hearing Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray Characterization of the Drosophila ortholog of the human Usher Syndrome type 1G protein sans

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