Citation Impact
Citing Papers
Transcriptome Profile of Human Colorectal Adenomas
2007
Spatially resolved, highly multiplexed RNA profiling in single cells
2015 StandoutScience
KIAA1199, a deafness gene of unknown function, is a new hyaluronan binding protein involved in hyaluronan depolymerization
2013
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
2013 StandoutScience
Isothermal amplified detection of DNA and RNA
2014
Molecular epidemiology of DFNB1 deafness in France
2004
2D transition metal dichalcogenides
2017 Standout
Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association
2010
Mouse models to study inner ear development and hereditary hearing loss
2007
Sequence Variants in Host Cell Factor C1 Are Associated With Ménière's Disease
2008
Gene expression analysis of the murine model of amyotrophic lateral sclerosis: Studies of the Leu126delTT mutation in SOD1
2007
Pendred syndrome, DFNB4, andPDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations
2001
Photodynamic Therapy
1998 Standout
Epithelial Cell Stretching and Luminal Acidification Lead to a Retarded Development of Stria Vascularis and Deafness in Mice Lacking Pendrin
2011
Newborn Hearing Screening — A Silent Revolution
2006 Standout
Probing the Function of STAS Domains of the Arabidopsis Sulfate Transporters
2004
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Multigenic control of thyroid hormone functions in the nervous system
2008
Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear–mitochondrial interaction
2003
The NC2 Domain of Collagen IX Provides Chain Selection and Heterotrimerization
2010
Inflammaging and anti-inflammaging: A systemic perspective on aging and longevity emerged from studies in humans
2006 Standout
The single-cell transcriptional landscape of mammalian organogenesis
2019 StandoutNature
Identification and characterization of mouse otic sensory lineage genes
2015
Early detection of aging cartilage and osteoarthritis in mice and patient samples using atomic force microscopy
2009 Standout
Inflammation and Colon Cancer
2010 Standout
Sensorineural hearing loss in children
2005 Standout
Genomic Analysis of the Function of the Transcription Factor gata3 during Development of the Mammalian Inner Ear
2009
Trends in the search for bioactive microbial metabolites
1992 StandoutNobel
A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene
2006
Integrated system for the screening of the specificity of protein kinase inhibitors
1993
The Collagen Family
2010 Standout
A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment
2002
Discovery of a Novel, Potent, and Src Family-selective Tyrosine Kinase Inhibitor
1996 Standout
Genomic Analysis of Reactive Astrogliosis
2012 Standout
The clinical impact of glycobiology: targeting selectins, Siglecs and mammalian glycans
2021 StandoutNobel
Programmed Cell Senescence during Mammalian Embryonic Development
2013 Standout
Pressure Induced Superconductivity in Pristine1 T − TiSe 2
2009
Hyaluronan: A modulator of the tumor microenvironment
2016
树鼩——作为一种新颖的非人灵长类实验疾病动物模型
2017 Standout
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome
2001
DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21–12.1
2003
Transient Receptor Potential Cation Channels in Disease
2007 Standout
Pendred's Syndrome and Genetic Defects in Thyroid Hormone Synthesis
2000
Role of phosphatase and tensin homolog in the development of the mammalian auditory system
2010 StandoutNobel
Tyrosine protein kinase inhibition and cancer
1994
Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection
2016 StandoutNatureNobel
Neurosensory mechanotransduction
2008 StandoutNobel
Mitochondrial deafness
2007
The Discovery of Rolling Circle Amplification and Rolling Circle Transcription
2016 Standout
Advanced Thermoelectric Design: From Materials and Structures to Devices
2020 Standout
Physiological and Molecular Basis of Thyroid Hormone Action
2001 Standout
Sulfur Assimilation in Photosynthetic Organisms: Molecular Functions and Regulations of Transporters and Assimilatory Enzymes
2011 Standout
Plasma Membrane Channels Formed by Connexins: Their Regulation and Functions
2003
Thyroid Hormone Regulation of Metabolism
2014 Standout
Molecular Genetics of Hearing Loss
2001
More similar than you think: Frog metamorphosis as a model of human perinatal endocrinology
2015
Life cycle of connexins in health and disease
2006 Standout
Diagnostic criteria for Menière's disease
2015 Standout
Kondo-like phonon scattering in thermoelectric clathrates
2019
Disorders of balance and vestibular function in US adults: data from the National Health and Nutrition Examination Survey, 2001-2004.
2009 Standout
trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation
2001
Clinical Practice Guideline: Sudden Hearing Loss (Update)
2019 Standout
Growth Factors, Matrices, and Forces Combine and Control Stem Cells
2009 StandoutScience
[32] Use of erbstatin as protein-tyrosine kinase inhibitor
1991
Genetics of Sensory Mechanotransduction
2002 StandoutNobel
Works of Satoko Abe being referenced
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease
2003
Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation
2005
Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues**Nucleotide sequence data reported herein are available in the DDBJ/EMBL/GenBank databases; for details, see the Electronic-Database Information section of this article.
2003
Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss
2003
Type IX collagen is crucial for normal hearing
2005
Human Connexin 30 (GJB6), a Candidate Gene for Nonsyndromic Hearing Loss: Molecular Cloning, Tissue-Specific Expression, and Assignment to Chromosome 13q12
1999
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation
2003
The responsible genes in Japanese deafness patients and clinical application using Invader assay
2008
Induction of morphological change by tyrosine kinase inhibitors in Rous sarcoma virus‐transformed rat kidney cells
1991
Type IX collagen knock-out mouse shows progressive hearing loss
2005
Superconductivity mediated by a soft phonon mode: Specific heat, resistivity, thermal expansion, and magnetization ofY B 6
2006
Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the pendred gene
1999
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations
1999
Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the pendred gene
1999
Specific heat, magnetic susceptibility, resistivity and thermal expansion of the superconductorZr B 12
2005