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A DNA Variant within the MYO7A Promoter Regulates YY1 Transcription Factor Binding and Gene Expression Serving as a Potential Dominant DFNA11 Auditory Genetic Modifier

The Journal of biological chemistry, 2011-04, Vol.286 (17), p.15278-15286

2011

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Resistance to Noise-Induced Hearing Loss in 129S6 and MOLF Mice: Identification of Independent, Overlapping, and Interacting Chromosomal Regions

Journal of the Association for Research in Otolaryngology, 2014-10, Vol.15 (5), p.721-738

2014

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A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunction

American journal of medical genetics. Part A, 2005-12, Vol.139A (2), p.86-95

2005

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A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings

BMC medical genetics, 2008-06, Vol.9 (1), p.48-48, Article 48

2008

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In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier

Otology & neurotology, 2008-09, Vol.29 (6), p.860-867

2008

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SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve

Annals of neurology, 2004-05, Vol.55 (5), p.713-720

2004

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Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating Neuropathies

American journal of human genetics, 2002-01, Vol.70 (1), p.244-250

2002

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The Type 1 Inositol 1,4,5-Trisphosphate Receptor Gene Is Altered in the opisthotonos Mouse

The Journal of neuroscience, 1997-01, Vol.17 (2), p.635-645

1997

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Vestibular function in families with inherited autosomal dominant hearing loss

Journal of vestibular research, 2008-01, Vol.18 (1), p.51-58

2008

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New gene for CMT

Journal of the peripheral nervous system, 2003-12, Vol.8 (4), p.206-206

2003

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Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

Nature genetics, 1998-08, Vol.19 (4), p.390-394

1998

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Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations

Genomics (San Diego, Calif.), 1995-09, Vol.29 (1), p.123-130

1995

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Searching the whole genome to identify genes contributing to noise resistance in inbred mouse strains

The Journal of the Acoustical Society of America, 2006-05, Vol.119 (5_Supplement), p.3267-3267

2006

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Searching for the Causes of Inherited Hearing Loss—How Is It Done?

Perspectives on hearing and hearing disorders. Research and diagnostics, 2004-11, Vol.8 (2), p.7

Street, Valerie A.

2004

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Mutations in a plasma membrane Ca 2+ -ATPase gene cause deafness in deafwaddler mice

Nature genetics, 1998-08, Vol.19 (4), p.390-394

1998

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Physical and Genetic Maps of thedeafwaddlerRegion on Distal Mouse Chr 6

Genomics (San Diego, Calif.), 1998-05, Vol.49 (3), p.371-377

1998

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Physical and Genetic Maps of the deafwaddlerRegion on Distal Mouse Chr 6

Genomics (San Diego, Calif.), 1998, Vol.49 (3), p.371-377

1998

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Physical Mapping of Potassium Channel Gene Clusters on Mouse Chromosomes Three and Six

Genomics (San Diego, Calif.), 1997-08, Vol.44 (1), p.110-117

1997

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Voltage-Gated Potassium Channel Genes Are Clustered in Paralogous Regions of the Mouse Genome

Genomics (San Diego, Calif.), 1994-04, Vol.20 (3), p.354-362

1994

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Physical and genetic maps of the deafwaddler region on distal mouse Chr 6

Genomics (San Diego, Calif.), 1998-05, Vol.49 (3), p.371-377

1998

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A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunction

American journal of medical genetics, 2005, Vol.139A (2), p.86-95

2005

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Assessing patients’ experiences with communication across the cancer care continuum

Patient education and counseling, 2016-08, Vol.99 (8), p.1343-1348

2016

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Molecular basis of differential adventitious rooting competence in poplar genotypes

Journal of experimental botany, 2022-06, Vol.73 (12), p.4046-4064

2022

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Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal

Muscle & nerve, 2016-08, Vol.54 (2), p.186-191

2016

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Gender differences in marital and military predictors of service member career satisfaction

Family relations, 2022-10, Vol.71 (4), p.1515-1537

2022

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A DNA Variant within the MYO7A Promoter Regulates YY1 Transcription Factor Binding and Gene Expression Serving as a Potential Dominant DFNA11 Auditory Genetic Modifier

Resistance to Noise-Induced Hearing Loss in 129S6 and MOLF Mice: Identification of Independent, Overlapping, and Interacting Chromosomal Regions

A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunction

A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings

In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier

SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve

Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating Neuropathies

The Type 1 Inositol 1,4,5-Trisphosphate Receptor Gene Is Altered in the opisthotonos Mouse

Vestibular function in families with inherited autosomal dominant hearing loss

New gene for CMT

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations

Searching the whole genome to identify genes contributing to noise resistance in inbred mouse strains

Searching for the Causes of Inherited Hearing Loss—How Is It Done?

Mutations in a plasma membrane Ca 2+ -ATPase gene cause deafness in deafwaddler mice

Physical and Genetic Maps of thedeafwaddlerRegion on Distal Mouse Chr 6

Physical and Genetic Maps of the deafwaddlerRegion on Distal Mouse Chr 6

Physical Mapping of Potassium Channel Gene Clusters on Mouse Chromosomes Three and Six

Voltage-Gated Potassium Channel Genes Are Clustered in Paralogous Regions of the Mouse Genome

Physical and genetic maps of the deafwaddler region on distal mouse Chr 6

A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunction

Assessing patients’ experiences with communication across the cancer care continuum

Molecular basis of differential adventitious rooting competence in poplar genotypes

Clinical Follow-Up for Duchenne Muscular Dystrophy Newborn Screening: A Proposal

Gender differences in marital and military predictors of service member career satisfaction

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