Usherin expression is highly conserved in mouse and human tissues (Q24318463)

GOA release 2020-03-11

author name string

Nicole Pearsall

1

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Gautam Bhattacharya

2

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Jim Wisecarver

3

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Joe Adams

4

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Dominic Cosgrove

5

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William Kimberling

Biotin amplification of biotin and horseradish peroxidase signals in histochemical stains

6

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language of work or name

English

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publication date

December 2002

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published in

Hearing Research

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volume

174

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issue

1-2

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page(s)

55-63

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cites work

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Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

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Structure and function of laminin: anatomy of a multidomain glycoprotein

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Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome type IIa.

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Structure and distribution of modules in extracellular proteins

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Usher syndrome: definition and estimate of prevalence from two high-risk populations

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Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41

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A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.

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Seminiferous Tubule Basement Membrane

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Assembly of Type IV Collagen

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Localization of Usher syndrome type II to chromosome 1q.

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Genetic Studies of Usher Syndrome

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Differential expression of two basement membrane collagen genes, COL4A6 and COL4A5, demonstrated by immunofluorescence staining using peptide-specific monoclonal antibodies

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Usher syndrome: from genetics to pathogenesis.

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Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q

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The prevalence of Usher syndrome and other retinal dystrophy-hearing impairment associations.

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Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

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Role for transforming growth factor-beta1 in alport renal disease progression.

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

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Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa

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