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R Hayden

Showing results (231-240 of 1,032) with videos related to

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American Journal of Medical Genetics|February 15, 1992
Predictive testing for Huntington disease in Canada: the experience of those receiving an increased riskM Bloch, S Adam, S Wiggins, et al.
Journal of Neurophysiology|July 9, 2004
Enhanced striatal NR2B-containing N-methyl-D-aspartate receptor-mediated synaptic currents in a mouse model of Huntington diseaseLijun Li, Timothy H Murphy, Michael R Hayden, et al.
Journal of Medical Genetics|February 1, 1992
The lipoprotein lipase Gly188----Glu mutation in South Africans of Indian descent: evidence suggesting common origins and an increased frequencyH E Henderson, F Hassan, G M Berger, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 2, 1980
The origin of Huntington's chorea in the Afrikaner population of South AfricaM R Hayden, H C Hopkins, M Macrea, et al.
The New England Journal of Medicine|October 30, 1986
Linkage of the G8 marker on chromosome 4 to Huntington's disease in a large American black familyT D Bird, J Hewitt, P M Conneally, et al.
Handbook of Clinical Neurology|September 24, 2008
Chapter 15 Juvenile amyotrophic lateral sclerosisPaul Orban, Rebecca S Devon, Michael R Hayden, et al.
Diabetes|July 17, 2014
Hepatic ABCA1 expression improves β-cell function and glucose toleranceWilleke de Haan, Joanna M Karasinska, Piers Ruddle, et al.
Neurology|August 16, 2013
De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotypeGunnar Houge, Ove Bruland, Inga Bjørnevoll, et al.
International Journal of Molecular Sciences|January 21, 2023
Ultrastructural Remodeling of the Blood-Brain Barrier and Neurovascular Unit by Lipopolysaccharide-Induced NeuroinflammationMichelle A Erickson, Tatyana Shulyatnikova, William A Banks, et al.
Clinical Genetics|March 21, 2014
Personalized gene silencing therapeutics for Huntington diseaseC Kay, N H Skotte, A L Southwell, et al.
Pageof 104

Showing results (231-240 of 1,032) with videos related to

Sort By:
Pageof 104
American Journal of Medical Genetics|February 15, 1992
Predictive testing for Huntington disease in Canada: the experience of those receiving an increased riskM Bloch, S Adam, S Wiggins, et al.
Journal of Neurophysiology|July 9, 2004
Enhanced striatal NR2B-containing N-methyl-D-aspartate receptor-mediated synaptic currents in a mouse model of Huntington diseaseLijun Li, Timothy H Murphy, Michael R Hayden, et al.
Journal of Medical Genetics|February 1, 1992
The lipoprotein lipase Gly188----Glu mutation in South Africans of Indian descent: evidence suggesting common origins and an increased frequencyH E Henderson, F Hassan, G M Berger, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 2, 1980
The origin of Huntington's chorea in the Afrikaner population of South AfricaM R Hayden, H C Hopkins, M Macrea, et al.
The New England Journal of Medicine|October 30, 1986
Linkage of the G8 marker on chromosome 4 to Huntington's disease in a large American black familyT D Bird, J Hewitt, P M Conneally, et al.
Handbook of Clinical Neurology|September 24, 2008
Chapter 15 Juvenile amyotrophic lateral sclerosisPaul Orban, Rebecca S Devon, Michael R Hayden, et al.
Diabetes|July 17, 2014
Hepatic ABCA1 expression improves β-cell function and glucose toleranceWilleke de Haan, Joanna M Karasinska, Piers Ruddle, et al.
Neurology|August 16, 2013
De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotypeGunnar Houge, Ove Bruland, Inga Bjørnevoll, et al.
International Journal of Molecular Sciences|January 21, 2023
Ultrastructural Remodeling of the Blood-Brain Barrier and Neurovascular Unit by Lipopolysaccharide-Induced NeuroinflammationMichelle A Erickson, Tatyana Shulyatnikova, William A Banks, et al.
Clinical Genetics|March 21, 2014
Personalized gene silencing therapeutics for Huntington diseaseC Kay, N H Skotte, A L Southwell, et al.
Pageof 104