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Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
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scientific journal article
Attributes
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rdf:type
Item
description
article scientifique publié en 2005
(fr)
artículu científicu espublizáu en 2005
(ast)
vědecký článek publikovaný v roce 2005
(cs)
2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված
(hy)
2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
(hyw)
наукова стаття, опублікована в грудні 2005
(uk)
wetenschappelijk artikel (gepubliceerd op 2005/12/15)
(nl)
vedecký článok (publikovaný 2005/12/15)
(sk)
مقالة علمية (نشرت في 15-12-2005)
(ar)
scientific journal article
(en)
im Dezember 2005 veröffentlichter wissenschaftlicher Artikel
(de)
publication date
wds:Q28119203-C063C395-113E-4E4A-A0EE-DA851BE21B08
publication date
2005-12-15 00:00:00Z
(
xsd:dateTime
)
language of work or name
wds:Q28119203-D1425905-BFD0-4976-B221-BF8A4DADBC4C
language of work or name
English
author name string
wds:Q28119203-5389C663-F541-49C5-8626-6E2B41343CB8
wds:Q28119203-6789033A-AC7D-4BDC-8EB2-5DECF91534F1
wds:Q28119203-6C3FC536-2CFE-40F9-B22E-2E4E845BB8C8
wds:Q28119203-ED3B019A-19E9-4FCE-9F5B-DD07D2F96797
wds:Q28119203-F0F32D23-0F90-486E-9662-145FC3BAFD7C
OpenCitations bibliographic resource ID
wds:Q28119203-1DC54D4E-3440-42D0-A7FC-DC48242424AE
OpenCitations bibliographic resource ID
https://w3id.org/oc/corpus/br/2764234
author name string
Ulrike Zimmermann
Heleen te Brinke
Jan Reiners
Karin Jürgens
Nora Overlack
OpenCitations bibliographic resource ID
2764234
rdfs:label
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(en)
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(nl)
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(ast)
skos:prefLabel
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(en)
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(nl)
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(ast)
name
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(en)
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(nl)
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(ast)
author
wds:Q28119203-0796A7A4-F9CD-4DFA-8A93-10FA84155D32
wds:Q28119203-4F329F0D-D34C-4375-AFEF-42B80933B57D
wds:Q28119203-80047C92-113E-48E9-AD77-A2B4B3D2278E
wds:Q28119203-864EF5E8-61EA-4230-88E1-DAEBCAE112AF
wds:Q28119203-DEFFAABE-B54C-4094-9030-11F6522F4831
wds:Q28119203-FC0EB039-56E7-4DA3-8DF8-9FD23D64D7C5
author
Uwe Wolfrum
Tina Märker
Ronald Roepman
Erwin van Wijk
Marlies Knipper
Hannie Kremer
title
wds:Q28119203-15148B63-DA3C-42B5-B0F2-BBC9A37076C9
title
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2
(en)
page(s)
wds:Q28119203-4AD8EDE5-35F8-4ABA-974D-918CB79F3265
page(s)
3933–3943
instance of
wds:Q28119203-89CCB153-4490-47C3-96EA-488AF680F764
instance of
scholarly article
main subject
wds:Q28119203-0E8FC674-D68E-4DA7-A551-A3D592EE56F9
wds:Q28119203-3ABB9BF9-C374-4538-A8B3-4E195B6CBC62
wds:Q28119203-A2B51C54-07A4-4C8F-9674-85281691555D
wds:Q28119203-E12DF8FD-55C4-4902-967B-2272E9E41CA6
main subject
Usher syndrome
Protocadherin 15
Usher syndrome type 1
Sodium bicarbonate cotransporter 3
PubMed ID
wds:Q28119203-35B527BA-586A-4C37-A9F5-070706FDC8AD
PubMed ID
http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16301216
PubMed ID
16301216
published in
wds:Q28119203-CD56FF37-E247-4F1C-89B3-B4E069CDEF61
published in
Human Molecular Genetics
issue
wds:Q28119203-D9E290D7-852D-47EB-A957-562C1412727C
volume
wds:Q28119203-9B589C73-055B-471A-8DDA-6124AEF8C34A
issue
24
volume
14
DOI
wds:Q28119203-7691025E-E6AC-4A53-A2A6-C9823763BB85
DOI
http://dx.doi.org/10.1093/HMG/DDI417
DOI
10.1093/HMG/DDI417
ResearchGate publication ID
wds:Q28119203-CDCCC203-515C-4E5D-8387-C23C969A7ABE
ResearchGate publication ID
7467886
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q28119203
is
cites work
of
The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1
RpgrORF15 connects to the usher protein network through direct interactions with multiple whirlin isoforms
Function and expression pattern of nonsyndromic deafness genes
The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically
A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells
Retinitis pigmentosa
Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23
The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins
The proteome of the mouse photoreceptor sensory cilium complex
Predicting candidate genes for human deafness disorders: a bioinformatics approach
Sticky signaling--adhesion class G protein-coupled receptors take the stage
Quiet as a mouse: dissecting the molecular and genetic basis of hearing
The dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteins
Harmonin in the murine retina and the retinal phenotypes of Ush1c-mutant mice and human USH1C.
Genetics and pathological mechanisms of Usher syndrome
Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane.
Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa
The divergence, actions, roles, and relatives of sodium-coupled bicarbonate transporters
Neuronal expression of sodium/bicarbonate cotransporter NBCn1 (SLC4A7) and its response to chronic metabolic acidosis
Modular structure of sodium-coupled bicarbonate transporters
Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.
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