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D C Rubinsztein

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Neuroscience Letters|January 7, 2000
A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder casesR A Furlong, L W Ho, J S Rubinsztein, et al.
The Journal of Clinical Investigation|October 1, 1990
Chylomicron remnant clearance from the plasma is normal in familial hypercholesterolemic homozygotes with defined receptor defectsD C Rubinsztein, J C Cohen, G M Berger, et al.
Journal of Lipid Research|November 1, 1992
Identification and properties of the proline664-leucine mutant LDL receptor in South Africans of Indian originD C Rubinsztein, G A Coetzee, A D Marais, et al.
American Journal of Medical Genetics|October 1, 1998
No association of a functional polymorphism in the dopamine D2 receptor promoter region with bipolar or unipolar affective disordersR A Furlong, T A Coleman, L Ho, et al.
American Journal of Human Genetics|March 7, 1998
A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer diseaseC Tysoe, J Whittaker, J Xuereb, et al.
American Journal of Human Genetics|July 27, 1999
Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorderR Kirk, R A Furlong, W Amos, et al.
Cell Death and Differentiation|July 19, 2014
Inhibition of autophagy, lysosome and VCP function impairs stress granule assemblyS J Seguin, F F Morelli, J Vinet, et al.
Journal of Medical Genetics|May 23, 2001
Autosomal dominant polycystic kidney disease unlinked to the PKD1 and PKD2 loci presenting as familial cerebral aneurysmR S McConnell, D C Rubinsztein, T F Fannin, et al.
Atherosclerosis|August 23, 1996
Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygoteE Langenhoven, L Warnich, R Thiart, et al.
Neuroscience Letters|January 24, 1997
Presenilin-1 intron 8 polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's diseaseC Tysoe, J Whittaker, N J Cairns, et al.
Pageof 13

Showing results (71-80 of 125) with videos related to

Sort By:
Pageof 13
Neuroscience Letters|January 7, 2000
A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder casesR A Furlong, L W Ho, J S Rubinsztein, et al.
The Journal of Clinical Investigation|October 1, 1990
Chylomicron remnant clearance from the plasma is normal in familial hypercholesterolemic homozygotes with defined receptor defectsD C Rubinsztein, J C Cohen, G M Berger, et al.
Journal of Lipid Research|November 1, 1992
Identification and properties of the proline664-leucine mutant LDL receptor in South Africans of Indian originD C Rubinsztein, G A Coetzee, A D Marais, et al.
American Journal of Medical Genetics|October 1, 1998
No association of a functional polymorphism in the dopamine D2 receptor promoter region with bipolar or unipolar affective disordersR A Furlong, T A Coleman, L Ho, et al.
American Journal of Human Genetics|March 7, 1998
A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer diseaseC Tysoe, J Whittaker, J Xuereb, et al.
American Journal of Human Genetics|July 27, 1999
Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorderR Kirk, R A Furlong, W Amos, et al.
Cell Death and Differentiation|July 19, 2014
Inhibition of autophagy, lysosome and VCP function impairs stress granule assemblyS J Seguin, F F Morelli, J Vinet, et al.
Journal of Medical Genetics|May 23, 2001
Autosomal dominant polycystic kidney disease unlinked to the PKD1 and PKD2 loci presenting as familial cerebral aneurysmR S McConnell, D C Rubinsztein, T F Fannin, et al.
Atherosclerosis|August 23, 1996
Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygoteE Langenhoven, L Warnich, R Thiart, et al.
Neuroscience Letters|January 24, 1997
Presenilin-1 intron 8 polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's diseaseC Tysoe, J Whittaker, N J Cairns, et al.
Pageof 13