The audiological phenotype of patients with a variant in non-muscle myosin genes

NIAID Data Ecosystem2026-05-02 收录

遗传性听力障碍

听觉表型分析

数据链接：

https://www.ncbi.nlm.nih.gov/sra/SRP581993 数据链接链接失效反馈

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资源简介：

Study about the audiological phenotype of patients with a variant in non-muscle myosin genes

创建时间：

2025-05-01

Hearing Loss in a Mouse Model of 22q11.2 Deletion Syndrome

遗传性听力障碍

中耳炎病理模型

22q11.2 Deletion Syndrome (22q11DS) arises from an interstitial chromosomal microdeletion encompassing at least 30 genes. This disorder is one of the most significant known cytogenetic risk factors fo

NIAID Data Ecosystem70

Genomic risk loci for hearing aid use.

遗传性听力障碍

全基因组关联分析

Loci were defined by the set of all SNPs in LD (r2 > 0.6, 1000 Genomes Phase 3 European samples) with an independently significant SNP (p < 5e-8) at that locus. Start and end refer to the left- and ri

NIAID Data Ecosystem50

RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM® genes for hereditary disorders of hearing and balance. Xenopus laevis

遗传性听力障碍

比较转录组分析

Purpose: To identify orthologous genes in Xenopus that are implicated in deafness and vestibular disorders in humans and to compare RNA-Seq and microarray to determine the advantages of each technolog

NIAID Data Ecosystem40

Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis

耳发育分子机制

遗传性听力障碍

Cellular heterogeneity hinders the extraction of functionally significant results and inference of regulatory networks from wide-scale expression profiles of complex mammalian organs. The mammalian in

Figshare2016-01-18 更新60

GO Term enrichment of hearing difficulty risk loci.

基因本体富集分析

遗传性听力障碍

For each GO Term, the number of genes, the regression coefficient of the gene set, standard error, the p-value, and the adjusted p-value are reported. (XLSX)

Figshare2020-09-28 更新50

The audiological phenotype of patients with a variant in non-muscle myosin genes

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