首页/数据集/Overview of all PTPRQ mutations identified to date.

Overview of all PTPRQ mutations identified to date.

Figshare2015-12-03 更新2026-04-29 收录

遗传性耳聋

PTPRQ基因功能研究

数据链接：

https://figshare.com/articles/dataset/_Overview_of_all_PTPRQ_mutations_identified_to_date_/1396688 数据链接链接失效反馈

官方服务：

资源简介：

AR, Autosomal RecessiveOverview of all PTPRQ mutations identified to date.

应用场景：

创建时间：

2015-12-03

听觉转录组学

遗传性耳聋

The goal of this study was to isolate individual cochlear hair cells and supporting cells from wild type animals in order to characterize the transcriptome of functionally mature auditory hair cells i

NIAID Data Ecosystem170

Homo Sapiens Exome

外显子测序

遗传性耳聋

This study is to identify novel variants causing late-onset, non-syndromic hearing loss and vestibular dysfunction

NIAID Data Ecosystem60

Supplementary Material for: Audiovestibular Phenotypes and Advanced Magnetic Resonance Imaging Features of Cochlin Gene Mutation Carriers

遗传性耳聋

DFNA9病理机制

Objective: To describe clinical and imaging findings in a group of patients affected by nonsyndromic deafness A9 (DFNA9), using advanced magnetic resonance imaging (MRI) with 3-dimensional (3D) fluid-

NIAID Data Ecosystem30

GJB2 mutants and their hearing levels in this study.

遗传性耳聋

GJB2基因突变

(*average of 500, 1000, and 2000 Hz) (†average of 250, 500, 1000 Hz) GJB2 mutants and their hearing levels in this study.

NIAID Data Ecosystem60

Transcription profiling of mouse mutant for microRNA-96 vs. wildtype mice to identify potential targets

microRNA靶标

遗传性耳聋

The Diminuendo mouse mutant strain displays progressive deafness and carries a mutation in the gene mmu-mir-96, a microRNA. We carried out a microarray analysis using RNA extracted from the organ of C

Alliance of Genome Resources50

Overview of all PTPRQ mutations identified to date.

资源简介：

相关数据集