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M R Hayden

Showing results (161-170 of 292) with videos related to

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Journal of Medical Genetics|December 1, 1993
Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic casesY P Goldberg, S E Andrew, J Theilmann, et al.
American Journal of Human Genetics|January 3, 2001
Wild-type huntingtin reduces the cellular toxicity of mutant huntingtin in vivoB R Leavitt, J A Guttman, J G Hodgson, et al.
Journal of Lipid Research|March 1, 1994
A compound heterozygote for lipoprotein lipase deficiency, Val69-->Leu and Gly188-->Glu: correlation between in vitro LPL activity and clinical expressionT Bruin, S Tuzgöl, W J Mulder, et al.
Nucleic Acids Research|November 25, 1991
Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3B Weber, O Riess, G Hutchinson, et al.
Acta Physiologica (Oxford, England)|November 6, 2008
The role of free fatty acids, pancreatic lipase and Ca+ signalling in injury of isolated acinar cells and pancreatitis model in lipoprotein lipase-deficient miceF Yang, Y Wang, L Sternfeld, et al.
Genomics|January 15, 1994
Precise mapping of the brain alpha 2-adrenergic receptor gene within chromosome 4p16O Riess, U Thies, I Siedlaczck, et al.
American Journal of Medical Genetics|August 26, 1998
Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo eventH E Henderson, S M Bijvoet, M A Mannens, et al.
Journal of Medical Genetics|August 1, 1997
Assessment of French patients with LPL deficiency for French Canadian mutationsL Foubert, J L De Gennes, J P Lagarde, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Neuroscience|April 2, 2016
Enhanced immune response to MMP3 stimulation in microglia expressing mutant huntingtinC Connolly, A Magnusson-Lind, G Lu, et al.
Pageof 30

Showing results (161-170 of 292) with videos related to

Sort By:
Pageof 30
Journal of Medical Genetics|December 1, 1993
Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic casesY P Goldberg, S E Andrew, J Theilmann, et al.
American Journal of Human Genetics|January 3, 2001
Wild-type huntingtin reduces the cellular toxicity of mutant huntingtin in vivoB R Leavitt, J A Guttman, J G Hodgson, et al.
Journal of Lipid Research|March 1, 1994
A compound heterozygote for lipoprotein lipase deficiency, Val69-->Leu and Gly188-->Glu: correlation between in vitro LPL activity and clinical expressionT Bruin, S Tuzgöl, W J Mulder, et al.
Nucleic Acids Research|November 25, 1991
Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3B Weber, O Riess, G Hutchinson, et al.
Acta Physiologica (Oxford, England)|November 6, 2008
The role of free fatty acids, pancreatic lipase and Ca+ signalling in injury of isolated acinar cells and pancreatitis model in lipoprotein lipase-deficient miceF Yang, Y Wang, L Sternfeld, et al.
Genomics|January 15, 1994
Precise mapping of the brain alpha 2-adrenergic receptor gene within chromosome 4p16O Riess, U Thies, I Siedlaczck, et al.
American Journal of Medical Genetics|August 26, 1998
Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo eventH E Henderson, S M Bijvoet, M A Mannens, et al.
Journal of Medical Genetics|August 1, 1997
Assessment of French patients with LPL deficiency for French Canadian mutationsL Foubert, J L De Gennes, J P Lagarde, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Neuroscience|April 2, 2016
Enhanced immune response to MMP3 stimulation in microglia expressing mutant huntingtinC Connolly, A Magnusson-Lind, G Lu, et al.
Pageof 30