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Human Molecular Genetics|February 3, 2000
Huntingtin is required for normal hematopoiesisM Metzler, C D Helgason, I Dragatsis, et al.Human Genetics|December 1, 1993
South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch populationJ C Defesche, D E van Diermen, P J Lansberg, et al.American Journal of Medical Genetics|September 1, 1993
Diagnosis of Huntington disease: a model for the stages of psychological response based on experience of a predictive testing programM Bloch, S Adam, A Fuller, et al.Gene|September 7, 2000
Human huntingtin-associated protein (HAP-1) gene: genomic organisation and an intragenic polymorphismJ Nasir, M J Lafuente, K Duan, et al.Neuroscience|June 11, 1999
Forskolin and dopamine D1 receptor activation increase huntingtin's association with endosomes in immortalized neuronal cells of striatal originM Kim, J Velier, K Chase, et al.Journal of Lipid Research|December 1, 1993
Recurrent pancreatitis and chylomicronemia in an extended Dutch kindred is caused by a Gly154-->Ser substitution in lipoprotein lipaseT Bruin, S Tuzgöl, D E van Diermen, et al.Human Molecular Genetics|October 1, 1993
Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expressionB Lin, J M Rommens, R K Graham, et al.Gut|October 22, 2008
Enhanced susceptibility to pancreatitis in severe hypertriglyceridaemic lipoprotein lipase-deficient mice and agonist-like function of pancreatic lipase in pancreatic cellsY Wang, L Sternfeld, F Yang, et al.Clinical Pharmacology and Therapeutics|April 17, 2013
HLA-A 31:01 and HLA-B 15:02 as genetic markers for carbamazepine hypersensitivity in childrenU Amstutz, C J D Ross, L I Castro-Pastrana, et al.Atherosclerosis|January 16, 1998
Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 alleleL O Abdel-Wareth, S N Pimstone, J P Lagarde, et al.Pageof 34