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R Hayden

Showing results (361-370 of 1,032) with videos related to

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American Journal of Human Genetics|May 1, 1987
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasM R Hayden, H Kirk, C Clark, et al.
Neurology|September 1, 1987
The combined use of positron emission tomography and DNA polymorphisms for preclinical detection of Huntington's diseaseM R Hayden, J Hewitt, A J Stoessl, et al.
Journal of the Cardiometabolic Syndrome|August 8, 2007
Myocardial myocyte remodeling and fibrosis in the cardiometabolic syndromeMelvin R Hayden, Nazif Chowdhury, Guru Govindarajan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 17, 2013
High frequency of intermediate alleles on Huntington disease-associated haplotypes in British Columbia's general populationAlicia Semaka, Chris Kay, Crystal N Doty, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 14, 2018
Identification of a novel caspase cleavage site in huntingtin that regulates mutant huntingtin clearanceDale D O Martin, Mandi E Schmidt, Yen T Nguyen, et al.
Pharmaceuticals (Basel, Switzerland)|December 31, 2025
Pridopidine, a Potent and Selective Therapeutic Sigma-1 Receptor (S1R) Agonist for Treating Neurodegenerative DiseasesNoga Gershoni Emek, Andrew M Tan, Michal Geva, et al.
Frontiers in Synaptic Neuroscience|March 9, 2019
Altered Regulation of Striatal Neuronal <i>N</i>-Methyl-D-Aspartate Receptor Trafficking by Palmitoylation in Huntington Disease Mouse ModelRujun Kang, Liang Wang, Shaun S Sanders, et al.
Human Molecular Genetics|November 10, 2005
Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington diseaseJeremy M Van Raamsdonk, Zoe Murphy, Elizabeth J Slow, et al.
American Journal of Human Genetics|February 1, 1992
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 24, 2003
Efflux and atherosclerosis: the clinical and biochemical impact of variations in the ABCA1 geneRoshni R Singaraja, Liam R Brunham, Henk Visscher, et al.
Pageof 104

Showing results (361-370 of 1,032) with videos related to

Sort By:
Pageof 104
American Journal of Human Genetics|May 1, 1987
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasM R Hayden, H Kirk, C Clark, et al.
Neurology|September 1, 1987
The combined use of positron emission tomography and DNA polymorphisms for preclinical detection of Huntington's diseaseM R Hayden, J Hewitt, A J Stoessl, et al.
Journal of the Cardiometabolic Syndrome|August 8, 2007
Myocardial myocyte remodeling and fibrosis in the cardiometabolic syndromeMelvin R Hayden, Nazif Chowdhury, Guru Govindarajan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 17, 2013
High frequency of intermediate alleles on Huntington disease-associated haplotypes in British Columbia's general populationAlicia Semaka, Chris Kay, Crystal N Doty, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 14, 2018
Identification of a novel caspase cleavage site in huntingtin that regulates mutant huntingtin clearanceDale D O Martin, Mandi E Schmidt, Yen T Nguyen, et al.
Pharmaceuticals (Basel, Switzerland)|December 31, 2025
Pridopidine, a Potent and Selective Therapeutic Sigma-1 Receptor (S1R) Agonist for Treating Neurodegenerative DiseasesNoga Gershoni Emek, Andrew M Tan, Michal Geva, et al.
Frontiers in Synaptic Neuroscience|March 9, 2019
Altered Regulation of Striatal Neuronal <i>N</i>-Methyl-D-Aspartate Receptor Trafficking by Palmitoylation in Huntington Disease Mouse ModelRujun Kang, Liang Wang, Shaun S Sanders, et al.
Human Molecular Genetics|November 10, 2005
Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington diseaseJeremy M Van Raamsdonk, Zoe Murphy, Elizabeth J Slow, et al.
American Journal of Human Genetics|February 1, 1992
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 24, 2003
Efflux and atherosclerosis: the clinical and biochemical impact of variations in the ABCA1 geneRoshni R Singaraja, Liam R Brunham, Henk Visscher, et al.
Pageof 104