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D C Rubinsztein

Showing results (31-40 of 125) with videos related to

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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 1, 1994
Monogenic primary hypercholesterolaemia in South AfricaD C Rubinsztein, D R van der Westhuyzen, G A Coetzee
Journal of Medical Genetics|July 4, 2001
Wild type Huntingtin reduces the cellular toxicity of mutant Huntingtin in mammalian cell models of Huntington's diseaseL W Ho, R Brown, M Maxwell, et al.
The Biochemical Journal|March 4, 2000
Alpha-synuclein overexpression promotes aggregation of mutant huntingtinR A Furlong, Y Narain, J Rankin, et al.
Nature Genetics|November 1, 1993
Site of (CCG) polymorphism in the HD geneD C Rubinsztein, J Leggo, D E Barton, et al.
Journal of Medical Genetics|October 21, 1999
A molecular investigation of true dominance in Huntington's diseaseY Narain, A Wyttenbach, J Rankin, et al.
Cell Death & Disease|August 26, 2011
The Parkinson's disease protein LRRK2 impairs proteasome substrate clearance without affecting proteasome catalytic activityM Lichtenberg, A Mansilla, V R Zecchini, et al.
Atherosclerosis|February 28, 1997
Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defectsF J Raal, G Pilcher, D C Rubinsztein, et al.
Neurology|November 24, 1999
Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneityE Reid, A M Dearlove, M L Whiteford, et al.
Human Molecular Genetics|October 1, 1993
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat numberD C Rubinsztein, D E Barton, B C Davison, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Markov chain Monte Carlo analysis of human Y-chromosome microsatellites provides evidence of biased mutationG Cooper, N J Burroughs, D A Rand, et al.
Pageof 13

Showing results (31-40 of 125) with videos related to

Sort By:
Pageof 13
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 1, 1994
Monogenic primary hypercholesterolaemia in South AfricaD C Rubinsztein, D R van der Westhuyzen, G A Coetzee
Journal of Medical Genetics|July 4, 2001
Wild type Huntingtin reduces the cellular toxicity of mutant Huntingtin in mammalian cell models of Huntington's diseaseL W Ho, R Brown, M Maxwell, et al.
The Biochemical Journal|March 4, 2000
Alpha-synuclein overexpression promotes aggregation of mutant huntingtinR A Furlong, Y Narain, J Rankin, et al.
Nature Genetics|November 1, 1993
Site of (CCG) polymorphism in the HD geneD C Rubinsztein, J Leggo, D E Barton, et al.
Journal of Medical Genetics|October 21, 1999
A molecular investigation of true dominance in Huntington's diseaseY Narain, A Wyttenbach, J Rankin, et al.
Cell Death & Disease|August 26, 2011
The Parkinson's disease protein LRRK2 impairs proteasome substrate clearance without affecting proteasome catalytic activityM Lichtenberg, A Mansilla, V R Zecchini, et al.
Atherosclerosis|February 28, 1997
Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defectsF J Raal, G Pilcher, D C Rubinsztein, et al.
Neurology|November 24, 1999
Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneityE Reid, A M Dearlove, M L Whiteford, et al.
Human Molecular Genetics|October 1, 1993
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat numberD C Rubinsztein, D E Barton, B C Davison, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Markov chain Monte Carlo analysis of human Y-chromosome microsatellites provides evidence of biased mutationG Cooper, N J Burroughs, D A Rand, et al.
Pageof 13