Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
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Autosomal recessive nonsyndromic deafness genes: a reviewGenetics of Nonsyndromic Congenital Hearing LossThe Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani PopulationsTMHS is an integral component of the mechanotransduction machinery of cochlear hair cellsTargeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutationFinding new genes for non-syndromic hearing loss through an in silico prioritization studyThe physiology of mechanoelectrical transduction channels in hearing.Rapid positional cloning of zebrafish mutations by linkage and homozygosity mapping using whole-genome sequencing.Unique transgenic animal model for hereditary hearing lossThe micromachinery of mechanotransduction in hair cells.Subunit determination of the conductance of hair-cell mechanotransducer channelsDeafness mutation mining using regular expression based pattern matching.A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12.Multiple loci influencing hippocampal degeneration identified by genome scanNovel function of LHFPL2 in female and male distal reproductive tract developmentRecessive mutations of TMC1 associated with moderate to severe hearing loss.USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.Non-syndromic hereditary sensorineural hearing loss: review of the genes involved.The how and why of identifying the hair cell mechano-electrical transduction channelNew treatment options for hearing loss.Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.The molecules that mediate sensory transduction in the mammalian inner ear.Functional Analysis of the Transmembrane and Cytoplasmic Domains of Pcdh15a in Zebrafish Hair Cells.TMIE is an essential component of the mechanotransduction machinery of cochlear hair cells.Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99.Research of genetic bases of hereditary non-syndromic hearing loss.The genetic dissection of Myo7a gene expression in the retinas of BXD mice.Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.The collagen receptor DDR1 co-localizes with the non-muscle myosin IIA in mice inner ear and contributes to the cytoarchitecture and stability of motile cells.Gene Therapy in Mouse Models of Deafness and Balance Dysfunction
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P2860
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
@en
type
label
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
@en
prefLabel
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
@en
P2093
P2860
P356
P1476
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
@en
P2093
A M Waryah
I A Belyantseva
M I Shabbir
Saima Riazuddin
Sheikh Riazuddin
P2860
P304
P356
10.1136/JMG.2005.039834
P407
P577
2006-02-03T00:00:00Z