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Anti-apoptotic factor z-Val-Ala-Asp-fluoromethylketone promotes the survival of cochlear hair cells in a mouse model for human deafness

Neuroscience, 2010-07, Vol.168 (3), p.851-857

2010

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A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

Journal of medical genetics, 2005-07, Vol.42 (7), p.588-594

2005

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Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III

Journal of medical genetics, 2003-10, Vol.40 (10), p.767-772

2003

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Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India

Journal of medical genetics, 2003-05, Vol.40 (5), p.e68-68

2003

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Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans

Science (American Association for the Advancement of Science), 1998-03, Vol.279 (5358), p.1950-1954

1998

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The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

Human genetics, 2000-01, Vol.106 (1), p.50-57

2000

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Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84

Journal of medical genetics, 2010-09, Vol.47 (9), p.643-645

2010

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Transgenic Mice with Increased Cu/Zn-Superoxide Dismutase Activity: Animal Model of Dosage Effects in Down Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1987-11, Vol.84 (22), p.8044-8048

1987

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From Flies' Eyes to Our Ears: Mutations in a Human Class III Myosin Cause Progressive Nonsyndromic Hearing Loss DFNB30

Proceedings of the National Academy of Sciences - PNAS, 2002-05, Vol.99 (11), p.7518-7523

2002

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Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally

Immunity (Cambridge, Mass.), 1998-08, Vol.9 (2), p.267-276

1998

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Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss

American journal of human genetics, 2006-01, Vol.78 (1), p.144-152

2006

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Characterization of Unconventional MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell's Waltzer Mice

Human molecular genetics, 1997-08, Vol.6 (8), p.1225-1231

1997

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MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

American journal of human genetics, 2001-09, Vol.69 (3), p.635-640

2001

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Otoancorin, An Inner Ear Protein Restricted to the Interface between the Apical Surface of Sensory Epithelia and Their Overlying Acellular Gels, Is Defective in Autosomal Recessive Deafness DFNB22

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (9), p.6240-6245

2002

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Role of Myosin VI in the Differentiation of Cochlear Hair Cells

Developmental biology, 1999-10, Vol.214 (2), p.331-341

1999

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Myosin VI is required for structural integrity of the apical surface of sensory hair cells in zebrafish

Developmental biology, 2004-08, Vol.272 (2), p.328-338

2004

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Hearing loss: mechanisms revealed by genetics and cell biology

Annual review of genetics, 2009-12, Vol.43 (1), p.411-437

2009

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The Notch Ligand Jagged1 is Required for Inner Ear Sensory Development

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (7), p.3873-3878

2001

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Hear come more genes

Nature medicine, 1998-11, Vol.4 (11), p.1238-1239

Avraham, Karen B

1998

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Multiple Mutations of MYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss

American journal of human genetics, 2003-06, Vol.72 (6), p.1571-1577

2003

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Modifying with mitochondria

Nature genetics, 2001-02, Vol.27 (2), p.136-137

Avraham, Karen B

2001

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The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

Nature genetics, 1995-12, Vol.11 (4), p.369-375

1995

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Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East

Human genetics, 2002-03, Vol.110 (3), p.284-289

2002

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Mapping of Unconventional Myosins in Mouse and Human

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.431-439

1996

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Down's syndrome: Abnormal neuromuscular junction in tongue of transgenic mice with elevated levels of human Cu/Zn-superoxide dismutase

Cell, 1988-09, Vol.54 (6), p.823-829

1988

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Anti-apoptotic factor z-Val-Ala-Asp-fluoromethylketone promotes the survival of cochlear hair cells in a mouse model for human deafness

A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III

Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India

Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84

Transgenic Mice with Increased Cu/Zn-Superoxide Dismutase Activity: Animal Model of Dosage Effects in Down Syndrome

From Flies' Eyes to Our Ears: Mutations in a Human Class III Myosin Cause Progressive Nonsyndromic Hearing Loss DFNB30

Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally

Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss

Characterization of Unconventional MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell's Waltzer Mice

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Otoancorin, An Inner Ear Protein Restricted to the Interface between the Apical Surface of Sensory Epithelia and Their Overlying Acellular Gels, Is Defective in Autosomal Recessive Deafness DFNB22

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

Myosin VI is required for structural integrity of the apical surface of sensory hair cells in zebrafish

Hearing loss: mechanisms revealed by genetics and cell biology

The Notch Ligand Jagged1 is Required for Inner Ear Sensory Development

Hear come more genes

Multiple Mutations of MYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss

Modifying with mitochondria

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East

Mapping of Unconventional Myosins in Mouse and Human

Down's syndrome: Abnormal neuromuscular junction in tongue of transgenic mice with elevated levels of human Cu/Zn-superoxide dismutase

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