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N Ahituv

Showing results (1-10 of 10) with videos related to

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The Journal of the Operational Research Society|October 7, 1987
Devising a cooperation policy for emergency networksN Ahituv, O Berman
Journal of Basic and Clinical Physiology and Pharmacology|October 21, 2000
Auditory and vestibular mouse mutants: models for human deafnessN Ahituv, K B Avraham
Gene|February 13, 2001
Genomic structure of the human unconventional myosin VI geneN Ahituv, T Sobe, N G Robertson, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2001
The Notch ligand Jagged1 is required for inner ear sensory developmentA E Kiernan, N Ahituv, H Fuchs, et al.
Translational Psychiatry|September 3, 2014
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genesN Oksenberg, G D E Haliburton, W L Eckalbar, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfootW Lu, C A Bacino, B S Richards, et al.
American Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.
Molecular Psychiatry|February 3, 2016
Prenatal β-catenin/Brn2/Tbr2 transcriptional cascade regulates adult social and stereotypic behaviorsH Belinson, J Nakatani, B A Babineau, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
Clinical Pharmacology and Therapeutics|March 4, 2011
Functional characterization of liver enhancers that regulate drug-associated transportersM J Kim, P Skewes-Cox, H Fukushima, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
The Journal of the Operational Research Society|October 7, 1987
Devising a cooperation policy for emergency networksN Ahituv, O Berman
Journal of Basic and Clinical Physiology and Pharmacology|October 21, 2000
Auditory and vestibular mouse mutants: models for human deafnessN Ahituv, K B Avraham
Gene|February 13, 2001
Genomic structure of the human unconventional myosin VI geneN Ahituv, T Sobe, N G Robertson, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2001
The Notch ligand Jagged1 is required for inner ear sensory developmentA E Kiernan, N Ahituv, H Fuchs, et al.
Translational Psychiatry|September 3, 2014
Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genesN Oksenberg, G D E Haliburton, W L Eckalbar, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfootW Lu, C A Bacino, B S Richards, et al.
American Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.
Molecular Psychiatry|February 3, 2016
Prenatal β-catenin/Brn2/Tbr2 transcriptional cascade regulates adult social and stereotypic behaviorsH Belinson, J Nakatani, B A Babineau, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
Clinical Pharmacology and Therapeutics|March 4, 2011
Functional characterization of liver enhancers that regulate drug-associated transportersM J Kim, P Skewes-Cox, H Fukushima, et al.
Pageof 1