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D C Rubinsztein

Showing results (51-60 of 125) with videos related to

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Human Molecular Genetics|November 1, 1994
Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populationsD C Rubinsztein, J Leggo, W Amos, et al.
Journal of Medical Genetics|July 7, 2000
The ACE I allele is associated with increased risk for ruptured intracranial aneurysmsM Keramatipour, R S McConnell, P Kirkpatrick, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Biochimica Et Biophysica Acta|August 4, 1993
Identification of two new LDL-receptor mutations causing homozygous familial hypercholesterolemia in a South African of Indian originD C Rubinsztein, I Jialal, E Leitersdorf, et al.
Psychopharmacology|September 16, 2005
Stop signal response inhibition is not modulated by tryptophan depletion or the serotonin transporter polymorphism in healthy volunteers: implications for the 5-HT theory of impulsivityL Clark, J P Roiser, R Cools, et al.
Journal of Medical Genetics|November 14, 1997
Instability of normal (CTG)n alleles in the DM kinase geneD J Dow, D C Rubinsztein, J R Yates, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2000
Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's diseaseA Wyttenbach, J Carmichael, J Swartz, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|May 1, 1995
Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and IndiansD C Rubinsztein, G A Coetzee, D R van der Westhuyzen, et al.
American Journal of Medical Genetics|May 29, 1998
No association of the tryptophan hydroxylase gene with bipolar affective disorder, unipolar affective disorder, or suicidal behaviour in major affective disorderR A Furlong, L Ho, J S Rubinsztein, et al.
American Journal of Medical Genetics|July 14, 1999
Analysis of the monoamine oxidase A (MAOA) gene in bipolar affective disorder by association studies, meta-analyses, and sequencing of the promoterR A Furlong, L Ho, J S Rubinsztein, et al.
Pageof 13

Showing results (51-60 of 125) with videos related to

Sort By:
Pageof 13
Human Molecular Genetics|November 1, 1994
Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populationsD C Rubinsztein, J Leggo, W Amos, et al.
Journal of Medical Genetics|July 7, 2000
The ACE I allele is associated with increased risk for ruptured intracranial aneurysmsM Keramatipour, R S McConnell, P Kirkpatrick, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 15, 1997
Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington diseaseD C Rubinsztein, J Leggo, M Chiano, et al.
Biochimica Et Biophysica Acta|August 4, 1993
Identification of two new LDL-receptor mutations causing homozygous familial hypercholesterolemia in a South African of Indian originD C Rubinsztein, I Jialal, E Leitersdorf, et al.
Psychopharmacology|September 16, 2005
Stop signal response inhibition is not modulated by tryptophan depletion or the serotonin transporter polymorphism in healthy volunteers: implications for the 5-HT theory of impulsivityL Clark, J P Roiser, R Cools, et al.
Journal of Medical Genetics|November 14, 1997
Instability of normal (CTG)n alleles in the DM kinase geneD J Dow, D C Rubinsztein, J R Yates, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2000
Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's diseaseA Wyttenbach, J Carmichael, J Swartz, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|May 1, 1995
Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and IndiansD C Rubinsztein, G A Coetzee, D R van der Westhuyzen, et al.
American Journal of Medical Genetics|May 29, 1998
No association of the tryptophan hydroxylase gene with bipolar affective disorder, unipolar affective disorder, or suicidal behaviour in major affective disorderR A Furlong, L Ho, J S Rubinsztein, et al.
American Journal of Medical Genetics|July 14, 1999
Analysis of the monoamine oxidase A (MAOA) gene in bipolar affective disorder by association studies, meta-analyses, and sequencing of the promoterR A Furlong, L Ho, J S Rubinsztein, et al.
Pageof 13