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Mechanical forces drive ordered patterning of hair cells in the mammalian inner ear

Nature communications, 2020-10, Vol.11 (1), p.5137-5137, Article 5137

2020

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Genomic analysis of inherited hearing loss in the Palestinian population

Proceedings of the National Academy of Sciences - PNAS, 2020-08, Vol.117 (33), p.20070-20076

2020

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microRNAs: the art of silencing in the ear

EMBO molecular medicine, 2012-09, Vol.4 (9), p.849-859

2012

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MicroRNAs are essential for development and function of inner ear hair cells in vertebrates

Proceedings of the National Academy of Sciences - PNAS, 2009-05, Vol.106 (19), p.7915-7920

2009

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Hereditary hearing loss: From human mutation to mechanism

Hearing research, 2011-11, Vol.281 (1), p.3-10

2011

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DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory sensory epithelium

Scientific reports, 2018-11, Vol.8 (1), p.17348-15, Article 17348

2018

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SPIKE: a database of highly curated human signaling pathways

Nucleic acids research, 2011-01, Vol.39 (Database issue), p.D793

2011

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Ankrd6 is a mammalian functional homolog of Drosophila planar cell polarity gene diego and regulates coordinated cellular orientation in the mouse inner ear

Developmental biology, 2014-11, Vol.395 (1), p.62-72

2014

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Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation

The Journal of biological chemistry, 2010-07, Vol.285 (28), p.21724-21735

2010

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MicroRNAs in sensorineural diseases of the ear

Frontiers in molecular neuroscience, 2013-12, Vol.6, p.52-52

2013

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A "Tric" to tighten cell-cell junctions in the cochlea for hearing

The Journal of clinical investigation, 2013-09, Vol.123 (9), p.3712-3715

2013

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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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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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Gfi1 and Gfi1b act equivalently in haematopoiesis, but have distinct, non-overlapping functions in inner ear development

EMBO reports, 2006-03, Vol.7 (3), p.326-333

2006

Volltextzugriff (PDF)

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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Functional Characterization of Pendrin Mutations Found in the Israeli and Palestinian Populations

Cellular physiology and biochemistry, 2011-01, Vol.28 (3), p.477-484

2011

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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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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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Mouse Models for Deafness: Lessons for the Human Inner Ear and Hearing Loss

Ear and hearing, 2003-08, Vol.24 (4), p.332-341

Avraham, Karen B.

2003

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Transcription profiling of inner ears from Pou4f3ddl/ddl identifies Gfi1 as a target of the Pou4f3 deafness gene

Human molecular genetics, 2004-09, Vol.13 (18), p.2143-2153

2004

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Connexin-associated deafness and speech perception outcome of cochlear implantation

Archives of otolaryngology--head & neck surgery, 2006-05, Vol.132 (5), p.495

2006

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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 deafness: recent advances and clinical implications

Journal of basic and clinical physiology and pharmacology, 2002, Vol.13 (2), p.75

2002

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Multiple Mutations ofMYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss

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

2003

Volltextzugriff (PDF)

Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor

Archives of otolaryngology--head & neck surgery, 2000-05, Vol.126 (5), p.633

2000

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Mechanical forces drive ordered patterning of hair cells in the mammalian inner ear

Genomic analysis of inherited hearing loss in the Palestinian population

microRNAs: the art of silencing in the ear

MicroRNAs are essential for development and function of inner ear hair cells in vertebrates

Hereditary hearing loss: From human mutation to mechanism

DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory sensory epithelium

SPIKE: a database of highly curated human signaling pathways

Ankrd6 is a mammalian functional homolog of Drosophila planar cell polarity gene diego and regulates coordinated cellular orientation in the mouse inner ear

Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation

MicroRNAs in sensorineural diseases of the ear

A "Tric" to tighten cell-cell junctions in the cochlea for hearing

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

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

Gfi1 and Gfi1b act equivalently in haematopoiesis, but have distinct, non-overlapping functions in inner ear development

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

Functional Characterization of Pendrin Mutations Found in the Israeli and Palestinian Populations

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

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

Mouse Models for Deafness: Lessons for the Human Inner Ear and Hearing Loss

Transcription profiling of inner ears from Pou4f3ddl/ddl identifies Gfi1 as a target of the Pou4f3 deafness gene

Connexin-associated deafness and speech perception outcome of cochlear implantation

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

Genetics of deafness: recent advances and clinical implications

Multiple Mutations ofMYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss

Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor

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