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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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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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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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Beethoven, a mouse model for dominant, progressive hearing loss DFNA36

Nature genetics, 2002-03, Vol.30 (3), p.257-258

2002

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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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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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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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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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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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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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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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The DFNA15 Deafness Mutation Affects POU4F3 Protein Stability, Localization, and Transcriptional Activity

Molecular and Cellular Biology, 2003-11, Vol.23 (22), p.7957-7964

2003

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Transgenic mice with expression of elevated levels of copper-zinc superoxide dismutase in the lungs are resistant to pulmonary oxygen toxicity

The Journal of clinical investigation, 1991-06, Vol.87 (6), p.2162-2168

1991

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A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein

Human molecular genetics, 2002-05, Vol.11 (11), p.1311-1316

2002

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Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity

Biochemical and biophysical research communications, 2004-11, Vol.324 (1), p.372-381

2004

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microRNA-224 regulates Pentraxin 3, a component of the humoral arm of innate immunity, in inner ear inflammation

Human molecular genetics, 2014-06, Vol.23 (12), p.3138-3146

2014

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Mouse models for human deafness: current tools for new fashions

Trends in Molecular Medicine, 2002-09, Vol.8 (9), p.447-451

2002

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Positional-candidate cloning of genes from mouse mutants

Methods in molecular biology (Clifton, N.J.), 2001, Vol.158, p.369

Avraham, K B

2001

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Diminished serotonin uptake in platelets of transgenic mice with increased Cu/Zn‐superoxide dismutase activity

The EMBO journal, 1989-05, Vol.8 (5), p.1385-1392

1989

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Molecular Diversity of the SCG10/Stathmin Gene Family in the Mouse

Genomics (San Diego, Calif.), 1993-11, Vol.18 (2), p.360-373

1993

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Cell damage by excess CuZnSOD and down's syndrome

Biomedicine & pharmacotherapy, 1994, Vol.48 (5), p.231,240-237,240

1994

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cDNA Cloning, Tissue Distribution, and Chromosomal Localization of Ocp2, a Gene Encoding a Putative Transcription-Associated Factor Predominantly Expressed in the Auditory Organs

Genomics (San Diego, Calif.), 1995-06, Vol.27 (3), p.389-398

1995

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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

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

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

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36

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

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

Hearing loss: mechanisms revealed by genetics and cell biology

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

The Notch Ligand Jagged1 is Required for Inner Ear Sensory Development

Modifying with mitochondria

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

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

The DFNA15 Deafness Mutation Affects POU4F3 Protein Stability, Localization, and Transcriptional Activity

Transgenic mice with expression of elevated levels of copper-zinc superoxide dismutase in the lungs are resistant to pulmonary oxygen toxicity

A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein

Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity

microRNA-224 regulates Pentraxin 3, a component of the humoral arm of innate immunity, in inner ear inflammation

Mouse models for human deafness: current tools for new fashions

Positional-candidate cloning of genes from mouse mutants

Diminished serotonin uptake in platelets of transgenic mice with increased Cu/Zn‐superoxide dismutase activity

Molecular Diversity of the SCG10/Stathmin Gene Family in the Mouse

Cell damage by excess CuZnSOD and down's syndrome

cDNA Cloning, Tissue Distribution, and Chromosomal Localization of Ocp2, a Gene Encoding a Putative Transcription-Associated Factor Predominantly Expressed in the Auditory Organs

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