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  • 1-10 ل  28 نتائج ل ""CDH23 gene""

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Subject : cadherins
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Academic Journal

A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs.

  • Authors : Han F; Department of Otolaryngology-HNS, Case Western Reserve University, Cleveland, OH 44106, USA.; Yu H

Subjects: Point Mutation*; Amino Acid Chloromethyl Ketones/Amino Acid Chloromethyl Ketones/Amino Acid Chloromethyl Ketones/*therapeutic use ; Cadherins/Cadherins/Cadherins/*genetics

  • Source: The pharmacogenomics journal [Pharmacogenomics J] 2012 Feb; Vol. 12 (1), pp. 30-44. Date of Electronic Publication: 2010 Jul 20.Publisher: Nature Pub. Group Country of Publication: United States NLM ID: 101083949 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) mice

Subjects: Presbycusis; Genes, Recessive; Biology

  • Source: Gene. 499(2)

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Academic Journal

Alternative Splicing of Cdh23 Exon 68 Is Regulated by RBM24, RBM38, and PTBP1.

  • Authors : Li N; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong Province, China.; Du H

Subjects: Alternative Splicing*; Cadherins/Cadherins/Cadherins/*genetics ; Ear, Inner/Ear, Inner/Ear, Inner/*metabolism

  • Source: Neural plasticity [Neural Plast] 2020 Jul 25; Vol. 2020, pp. 8898811. Date of Electronic Publication: 2020 Jul 25 (Print Publication: 2020).Publisher: Hindawi Pub. Corp Country of Publication: United States NLM ID: 100883417 Publication Model: eCollection Cited Medium: Internet ISSN:

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Academic Journal

An Age-Related Hearing Protection Locus on Chromosome 16 of BXD Strain Mice.

  • Authors : Zheng QY; Department of Otolaryngology-Head and Neck Surgery, Case Western Reserve University, Cleveland, Ohio, USA.; Kui L

Subjects: Alleles* ; Chromosomes, Mammalian*; Auditory Threshold/Auditory Threshold/Auditory Threshold/*physiology

  • Source: Neural plasticity [Neural Plast] 2020 Jun 08; Vol. 2020, pp. 8889264. Date of Electronic Publication: 2020 Jun 08 (Print Publication: 2020).Publisher: Hindawi Pub. Corp Country of Publication: United States NLM ID: 100883417 Publication Model: eCollection Cited Medium: Internet ISSN:

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Academic Journal

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing.

Subjects: Exome* ; Mutation*; Asian People/Asian People/Asian People/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2014 Apr 28; Vol. 15, pp. 46. Date of Electronic Publication: 2014 Apr 28.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350

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Academic Journal

Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study.

  • Authors : Miyagawa M; Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto, Japan.; Nishio SY

Subjects: Mutation*; Cadherins/Cadherins/Cadherins/*genetics ; Hearing Loss/Hearing Loss/Hearing Loss/*epidemiology

  • Source: PloS one [PLoS One] 2012; Vol. 7 (8), pp. e40366. Date of Electronic Publication: 2012 Aug 10.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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Association between genetic polymorphisms of cadherin 23 and noise-induced hearing loss: a meta-analysis

Subjects: Aging; Polymorphism, Genetic; Asian People

  • Source: Annals of Human Biology. 49:41-53

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Alternative Splicing of Cdh23 Exon 68 Is Regulated by RBM24, RBM38, and PTBP1

Subjects: Article Subject; Neurosciences. Biological psychiatry. Neuropsychiatry; Biology

  • Source: Neural Plasticity, Vol 2020 (2020)Neural Plasticity

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Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss

Subjects: Hearing Loss, Sensorineural; Mutation; otorhinolaryngologic diseases

  • Source: Human Genetics. 141:903-914

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Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia

Subjects: Candidate gene; AcademicSubjects/MED00810; Quantitative Trait Loci

  • Source: Schizophrenia Bulletin

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  • 1-10 ل  28 نتائج ل ""CDH23 gene""