(Q28156114)

English

Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis

scientific article (publication date: September 2003)

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scholarly article

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Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis (English)

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transmembrane protein

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epidermodysplasia verruciformis

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inferred from title

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author name string

Kiyoto Kurima

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Yandan Yang

2

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Katherine Sorber

3

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Andrew J Griffith

4

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language of work or name

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publication date

September 2003

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82

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3

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300-8

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Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

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7 January 2021

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Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

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7 January 2021

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The nature of inherited deafness in deafness mice.

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7 January 2021

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Inner ear pathology in the deafness mutant mouse.

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7 January 2021

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Evaluation of methods for the prediction of membrane spanning regions

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7 January 2021

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Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis

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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900154-X

7 January 2021

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Guidelines for human gene nomenclature

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Diverse trafficking patterns due to multiple traffic motifs in G protein-activated inwardly rectifying potassium channels from brain and heart

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900154-X

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Antigen presentation and T-cell activation in epidermodysplasia verruciformis

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7 January 2021

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Natural cell-mediated cytotoxicity against various target cells in patients with epidermodysplasia verruciformis

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Calcium signaling mechanisms in T lymphocytes

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A store-operated nonselective cation channel in lymphocytes is activated directly by Ca(2+) influx factor and diacylglycerol

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Human papillomavirus is a necessary cause of invasive cervical cancer worldwide

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Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD1 maps to 20p13

1 reference

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7 January 2021

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Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

1 reference

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Genetic Control of Neuroadapted Sindbis Virus Replication in Female Mice Maps to Chromosome 2 and Associates with Paralysis and Mortality

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Identification of a new locus for medullary cystic disease, on chromosome 16p12.

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The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16. The European Polycystic Kidney Disease Consortium

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PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

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7 January 2021

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Polycystin-2 is an intracellular calcium release channel

1 reference

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7 January 2021

based on heuristic

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Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

1 reference

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7 January 2021

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The molecules of mechanosensation.

1 reference

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7 January 2021

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A locus for primary ciliary dyskinesia maps to chromosome 19q

1 reference

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7 January 2021

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The ion channel polycystin-2 is required for left-right axis determination in mice

1 reference

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7 January 2021

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The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

1 reference

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

1 reference

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7 January 2021

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Identifiers

10.1016/S0888-7543(03)00154-X

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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