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M R Hayden

Showing results (121-130 of 342) with videos related to

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American Journal of Human Genetics|February 28, 2001
Measurement of mutational flow implies both a high new-mutation rate for Huntington disease and substantial underascertainment of late-onset casesD Falush, E W Almqvist, R R Brinkmann, et al.
Cardiorenal Medicine|November 19, 2011
Phosphate Metabolism in Cardiorenal Metabolic DiseaseDeepashree Gupta, Stephen Brietzke, M R Hayden, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|March 1, 1991
The FDG/PET methodology for early detection of disease onset: a statistical modelC M Clark, W Ammann, W R Martin, et al.
Human Genetics|October 1, 1991
Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneityL J Greenberg, R W Martell, J Theilman, et al.
Cell Death and Differentiation|August 4, 2012
Intrinsic cleavage of receptor-interacting protein kinase-1 by caspase-6B J van Raam, D E Ehrnhoefer, M R Hayden, et al.
American Journal of Human Genetics|May 1, 1997
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG sizeR R Brinkman, M M Mezei, J Theilmann, et al.
Journal of Medical Genetics|October 1, 1996
Adverse psychological events occurring in the first year after predictive testing for Huntington's disease. The Canadian Collaborative Study Predictive TestingK Lawson, S Wiggins, T Green, et al.
Biochemical Society Transactions|May 1, 1993
Phenotypic variation of mutations in the human lipoprotein-lipase geneM R Hayden, J J Kastelein, H Funke, et al.
Genomics|July 1, 1992
The human beta-subunit of rod photoreceptor cGMP phosphodiesterase: complete retinal cDNA sequence and evidence for expression in brainC Collins, G Hutchinson, D Kowbel, et al.
Clinical Genetics|March 1, 1989
Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feetD Chitayat, E B Davis, B C McGillivray, et al.
Pageof 35

Showing results (121-130 of 342) with videos related to

Sort By:
Pageof 35
American Journal of Human Genetics|February 28, 2001
Measurement of mutational flow implies both a high new-mutation rate for Huntington disease and substantial underascertainment of late-onset casesD Falush, E W Almqvist, R R Brinkmann, et al.
Cardiorenal Medicine|November 19, 2011
Phosphate Metabolism in Cardiorenal Metabolic DiseaseDeepashree Gupta, Stephen Brietzke, M R Hayden, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|March 1, 1991
The FDG/PET methodology for early detection of disease onset: a statistical modelC M Clark, W Ammann, W R Martin, et al.
Human Genetics|October 1, 1991
Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneityL J Greenberg, R W Martell, J Theilman, et al.
Cell Death and Differentiation|August 4, 2012
Intrinsic cleavage of receptor-interacting protein kinase-1 by caspase-6B J van Raam, D E Ehrnhoefer, M R Hayden, et al.
American Journal of Human Genetics|May 1, 1997
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG sizeR R Brinkman, M M Mezei, J Theilmann, et al.
Journal of Medical Genetics|October 1, 1996
Adverse psychological events occurring in the first year after predictive testing for Huntington's disease. The Canadian Collaborative Study Predictive TestingK Lawson, S Wiggins, T Green, et al.
Biochemical Society Transactions|May 1, 1993
Phenotypic variation of mutations in the human lipoprotein-lipase geneM R Hayden, J J Kastelein, H Funke, et al.
Genomics|July 1, 1992
The human beta-subunit of rod photoreceptor cGMP phosphodiesterase: complete retinal cDNA sequence and evidence for expression in brainC Collins, G Hutchinson, D Kowbel, et al.
Clinical Genetics|March 1, 1989
Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feetD Chitayat, E B Davis, B C McGillivray, et al.
Pageof 35