2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4 - Test2 - elhamkhani - TriplyDB

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

http://www.wikidata.org/entity/Q24603242

about

Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes Actin dynamics in platelets Mutations in KPTN cause macrocephaly, neurodevelopmental delay, and seizures Positive selection, relaxation, and acceleration in the evolution of the human and chimp genome.New structural and functional contexts of the Dx[DN]xDG linear motif: insights into evolution of calcium-binding proteins Cochlin in the eye: functional implications.Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4.Auditory and vestibular hair cell stereocilia: relationship between functionality and inner ear disease.Cytoglobin inhibits migration through PI3K/AKT/mTOR pathway in fibroblast cells.

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P2860

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

http://www.wikidata.org/entity/Q24603242

description

2000 nî lūn-bûn

@nan

2000 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի մայիսին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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name

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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J.1469-1809.2000.6430189.X

P1433

Annals of Human Genetics

P1476

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4

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P2093

A F Chen

http://www.w3.org/2001/XMLSchema#string

A H Chen

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C L Jackson

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E L Bearer

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H F Mark

http://www.w3.org/2001/XMLSchema#string

R J Smith

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Z Li

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P2860

2E4 (kaptin): a novel actin-associated protein from human blood platelets found in lamellipodia and the tips of the stereocilia of the inner ear

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

An actin-associated protein present in the microtubule organizing center and the growth cones of PC-12 cells

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene

The 1993-94 Généthon human genetic linkage map

Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome.

Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

Actin filaments, stereocilia, and hair cells: how cells count and measure.

The actin filament content of hair cells of the bird cochlea is nearly constant even though the length, width, and number of stereocilia vary depending on the hair cell location.

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189-96

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scholarly article

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10.1046/J.1469-1809.2000.6430189.X

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P433

Pt 3

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64

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2000-05-01T00:00:00Z

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231932839

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11409409

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3376086

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