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Molecular Pharmacology|July 27, 1999
Selective killing of cancer cells based on loss of heterozygosity and normal variation in the human genome: a new paradigm for anticancer drug therapyJ P Basilion, A R Schievella, E Burns, et al.Journal of Medical Genetics|October 5, 2006
Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindredsJ M Andresen, J Gayán, S S Cherny, et al.Biological Psychiatry|April 9, 1998
Identification of sequence variants and analysis of the role of the catechol-O-methyl-transferase gene in schizophrenia susceptibilityM Karayiorgou, J A Gogos, B L Galke, et al.Human Molecular Genetics|June 1, 1993
A gene from chromosome 4p16.3 with similarity to a superfamily of transporter proteinsM P Duyao, S A Taylor, A J Buckler, et al.Proceedings of the National Academy of Sciences of the United States of America|May 24, 2000
The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcriptionJ S Steffan, A Kazantsev, O Spasic-Boskovic, et al.Journal of Human Hypertension|February 6, 2009
Association between arterial stiffness and variations in oestrogen-related genesI Peter, A Kelley-Hedgepeth, G S Huggins, et al.The Journal of Experimental Medicine|April 1, 1990
Clustering of cytokine genes on mouse chromosome 11S D Wilson, P R Billings, P D'Eustachio, et al.The New England Journal of Medicine|May 25, 1989
Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1pS J Bale, N C Dracopoli, M A Tucker, et al.Nature Genetics|June 11, 1992
The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1AL J Valentijn, P A Bolhuis, I Zorn, et al.Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
A Rap guanine nucleotide exchange factor enriched highly in the basal gangliaH Kawasaki, G M Springett, S Toki, et al.Pageof 15