相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Genetic etiology of hearing loss in Iran
Mojgan Babanejad et al.
HUMAN GENETICS (2022)
The STRING database in 2021: customizable protein-protein networks, and functional characterization of user-uploaded gene/measurement sets
Damian Szklarczyk et al.
NUCLEIC ACIDS RESEARCH (2021)
Expression profiling and functional characterization of the duplicated Oxr1b gene in zebrafish
Hao Xu et al.
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY D-GENOMICS & PROTEOMICS (2021)
Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges
Sedigheh Delmaghani et al.
JOURNAL OF CLINICAL MEDICINE (2020)
THOC1deficiency leads to late-onset nonsyndromic hearing loss throughp53-mediated hair cell apoptosis
Luping Zhang et al.
PLOS GENETICS (2020)
Combined whole-mount fluorescence in situ hybridization and antibody staining in zebrafish embryos and larvae
Jianbo He et al.
NATURE PROTOCOLS (2020)
Zebrafish Oxr1a Knockout Reveals Its Role in Regulating Antioxidant Defenses and Aging
Hao Xu et al.
GENES (2020)
Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction
Julia Wang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
Atoh1 and other related key regulators in the development of auditory sensory epithelium in the mammalian inner ear: function and interplay
Chao Zhong et al.
DEVELOPMENTAL BIOLOGY (2019)
Anatomical map of the cranial vasculature and sensory ganglia
Laura Taberner et al.
JOURNAL OF ANATOMY (2018)
Preventing neurodegeneration by adrenergic astroglial excitation
Robert Zorec et al.
FEBS JOURNAL (2018)
TLDc proteins: new players in the oxidative stress response and neurological disease
Mattea J. Finelli et al.
MAMMALIAN GENOME (2017)
Anatomical and physiological development of the human inner ear
Rebecca Lim et al.
HEARING RESEARCH (2016)
Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss
Christina M. Sloan-Heggen et al.
HUMAN GENETICS (2016)
Neurocognitive factors in sensory restoration of early deafness: a connectome model
Andrej Kral et al.
LANCET NEUROLOGY (2016)
Mapping the H+ (V)-ATPase interactome: identification of proteins involved in trafficking, folding, assembly and phosphorylation
Maria Merkulova et al.
SCIENTIFIC REPORTS (2015)
Whole-exome sequencing and its impact in hereditary hearing loss
Tahir Atik et al.
GENETICS RESEARCH (2015)
Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86
Atteeq U. Rehman et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
Human OXR1 maintains mitochondrial DNA integrity and counteracts hydrogen peroxide-induced oxidative stress by regulating antioxidant pathways involving p21
Mingyi Yang et al.
FREE RADICAL BIOLOGY AND MEDICINE (2014)
TBC1D24 Mutation Causes Autosomal-Dominant Nonsyndromic Hearing Loss
Hela Azaiez et al.
HUMAN MUTATION (2014)
The genetic basis of DOORS syndrome: an exome-sequencing study
Philippe M. Campeau et al.
LANCET NEUROLOGY (2014)
The embryonic expression patterns of zebrafish genes encoding LysM-domains
R. J. F. Laroche et al.
GENE EXPRESSION PATTERNS (2013)
Structural/functional analysis of the human OXR1 protein: identification of exon 8 as the anti-oxidant encoding function
Kenan C. Murphy et al.
BMC MOLECULAR BIOLOGY (2012)
Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss
Oscar Diaz-Horta et al.
PLOS ONE (2012)
A Spatial and Temporal Gradient of Fgf Differentially Regulates Distinct Stages of Neural Development in the Zebrafish Inner Ear
Shruti Vemaraju et al.
PLOS GENETICS (2012)
Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration
Peter L. Oliver et al.
PLOS GENETICS (2011)
Hearing loss: a common disorder caused by many rare alleles
Dorith Raviv et al.
YEAR IN HUMAN AND MEDICAL GENETICS: NEW TRENDS IN MENDELIAN GENETICS (2010)
Smad2/3 activities are required for induction and patterning of the neuroectoderm in zebrafish
Shunji Jia et al.
DEVELOPMENTAL BIOLOGY (2009)
Inner ear pathology and loss of hearing in estrogen receptor-beta deficient mice
Rusana Simonoska et al.
JOURNAL OF ENDOCRINOLOGY (2009)
Regulation of cell fate in the sensory epithelia of the inner ear
Matthew W. Kelley
NATURE REVIEWS NEUROSCIENCE (2006)
Stress induction and mitochondrial localization of Oxr1 proteins in yeast and humans
NA Elliott et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Deafness genes and their diagnostic applications
K Cryns et al.
AUDIOLOGY AND NEURO-OTOLOGY (2004)
Neurogenin1 defines zebrafish cranial sensory ganglia precursors
P Andermann et al.
DEVELOPMENTAL BIOLOGY (2002)
Functional genomics reveals a family of eukaryotic oxidation protection genes
MR Volkert et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)