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Article

Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources.

Brain research - 26 May 2006

Parker Lisan L, Gao Jiangang, Zuo Jian

Abstract excerpt

Multiple mouse embryonic stem (ES) cell banks expand the capability to characterize functions of genes implicated in human disease and to develop mouse models for the further understanding of disease pathology. Genetic diseases that result in hearing loss can provide insight into causative molecu...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16630581
DOI: 10.1016/j.brainres.2006.03.032

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16630581-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources.PMID 16630581Read ↗

Generation and characterization of mice with Myh9 deficiency.Semantic proximity Read ↗

Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO miceSemantic proximity Read ↗

MYH9-siRNA and MYH9 mutant alleles: expression in cultured cell lines and their effects upon cell structure and function.Semantic proximity Read ↗

Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.Semantic proximity Read ↗

R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17.Semantic proximity Read ↗

Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A.Semantic proximity Read ↗

Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder.Semantic proximity Read ↗

Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9.Semantic proximity Read ↗

In vitro expression and characterization of MYH9 mutant alleles linked to hereditary hearing loss.Semantic proximity Read ↗

Zfp719 is a transcription factor important for maintenance of hearing in miceSemantic proximity Read ↗

Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains.Semantic proximity Read ↗

A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment.Semantic proximity Read ↗

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