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R Hayden

Showing results (891-900 of 910) with videos related to

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Human Molecular Genetics|May 24, 2007
Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosageAlexandre Kuhn, Darlene R Goldstein, Angela Hodges, et al.
Clinical Genetics|June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000S Creighton, E W Almqvist, D MacGregor, et al.
Nature Genetics|August 4, 1999
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiencyA Brooks-Wilson, M Marcil, S M Clee, et al.
Clinical Genetics|May 2, 2007
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsY P Goldberg, J MacFarlane, M L MacDonald, et al.
The Journal of Clinical Investigation|September 15, 2022
Haploinsufficiency of CYP8B1 associates with increased insulin sensitivity in humansShiqi Zhong, Raphael Chèvre, David Castaño Mayan, et al.
The Journal of Cell Biology|December 23, 2009
IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosomeLeslie Michels Thompson, Charity T Aiken, Linda S Kaltenbach, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2017
ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol LevelsLaia Trigueros-Motos, Julian C van Capelleveen, Federico Torta, et al.
Circulation. Cardiovascular Genetics|December 18, 2012
The impact of partial and complete loss-of-function mutations in endothelial lipase on high-density lipoprotein levels and functionality in humansRoshni R Singaraja, Suthesh Sivapalaratnam, Kees Hovingh, et al.
Neurogenetics|March 19, 2004
Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16Luc Djoussé, Beth Knowlton, Michael R Hayden, et al.
Journal of Lipid Research|November 22, 2024
The bile acid chenodeoxycholic acid associates with reduced stroke in humans and miceVera F Monteiro-Cardoso, Xin Yi Yeo, Han-Gyu Bae, et al.
Pageof 91

Showing results (891-900 of 910) with videos related to

Sort By:
Pageof 91
Human Molecular Genetics|May 24, 2007
Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosageAlexandre Kuhn, Darlene R Goldstein, Angela Hodges, et al.
Clinical Genetics|June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000S Creighton, E W Almqvist, D MacGregor, et al.
Nature Genetics|August 4, 1999
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiencyA Brooks-Wilson, M Marcil, S M Clee, et al.
Clinical Genetics|May 2, 2007
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsY P Goldberg, J MacFarlane, M L MacDonald, et al.
The Journal of Clinical Investigation|September 15, 2022
Haploinsufficiency of CYP8B1 associates with increased insulin sensitivity in humansShiqi Zhong, Raphael Chèvre, David Castaño Mayan, et al.
The Journal of Cell Biology|December 23, 2009
IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosomeLeslie Michels Thompson, Charity T Aiken, Linda S Kaltenbach, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 9, 2017
ABCA8 Regulates Cholesterol Efflux and High-Density Lipoprotein Cholesterol LevelsLaia Trigueros-Motos, Julian C van Capelleveen, Federico Torta, et al.
Circulation. Cardiovascular Genetics|December 18, 2012
The impact of partial and complete loss-of-function mutations in endothelial lipase on high-density lipoprotein levels and functionality in humansRoshni R Singaraja, Suthesh Sivapalaratnam, Kees Hovingh, et al.
Neurogenetics|March 19, 2004
Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16Luc Djoussé, Beth Knowlton, Michael R Hayden, et al.
Journal of Lipid Research|November 22, 2024
The bile acid chenodeoxycholic acid associates with reduced stroke in humans and miceVera F Monteiro-Cardoso, Xin Yi Yeo, Han-Gyu Bae, et al.
Pageof 91