(Q24290185)

GOA release 2020-03-11

equilibrioception

1 reference

GOA release 2020-03-11

Usher syndrome

1 reference

inferred from title

Usher syndrome type 1C

1 reference

C Petit

12

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Rima Slim

object named as

R Slim

11

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Bronya J. B. Keats

10

object named as

B J Keats

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author name string

E Verpy

1

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M Leibovici

2

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I Zwaenepoel

3

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X Z Liu

4

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A Gal

5

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N Salem

6

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A Mansour

7

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S Blanchard

8

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I Kobayashi

Defective myosin VIIA gene responsible for Usher syndrome type 1B

9

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language of work or name

English

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publication date

September 2000

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published in

Nature Genetics

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volume

26

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issue

1

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page(s)

51-5

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cites work

1 reference

7 January 2021

Localization of two genes for Usher syndrome type I to chromosome 11.

1 reference

7 January 2021

The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region.

1 reference

7 January 2021

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

1 reference

7 January 2021

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells

1 reference

7 January 2021

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

1 reference

7 January 2021

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

1 reference

7 January 2021

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

7 January 2021

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

1 reference

7 January 2021

Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals

1 reference

7 January 2021

Characterization of human colon cancer antigens recognized by autologous antibodies

1 reference

7 January 2021

Isoforms of the human PDZ-73 protein exhibit differential tissue expression

1 reference

7 January 2021

Identification of an autoimmune enteropathy-related 75-kilodalton antigen

1 reference

7 January 2021

PDZ domains: targeting signalling molecules to sub-membranous sites

1 reference

7 January 2021

Protein modules as organizers of membrane structure

1 reference

7 January 2021

Contig Maps and Genomic Sequencing Identify Candidate Genes in the Usher 1C Locus

1 reference

7 January 2021

Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene

1 reference

7 January 2021

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

7 January 2021

The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure

1 reference

7 January 2021

From Src Homology domains to other signaling modules: proposal of the 'protein recognition code'.

1 reference

7 January 2021

A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.

1 reference

7 January 2021

Targeted disruption of otog results in deafness and severe imbalance

1 reference

7 January 2021

Unconventional myosins in inner-ear sensory epithelia

1 reference

7 January 2021

Expression of myosin VIIA during mouse embryogenesis.

1 reference

7 January 2021

Inherited hearing defects in mice

1 reference

7 January 2021

Identifying differences in mRNA expression by representational difference analysis of cDNA

1 reference

7 January 2021

The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system

1 reference

7 January 2021

A comprehensive set of sequence analysis programs for the VAX

1 reference

7 January 2021

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

1 reference

7 January 2021