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Neurogenetics|August 5, 2003
Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2U Finckh, K van Hadeln, T Müller-Thomsen, et al.Alcoholism, Clinical and Experimental Research|September 1, 1996
Lack of allelic association of dopamine D1 and D2 (TaqIA) receptor gene polymorphisms with reduced dopaminergic sensitivity to alcoholismA Heinz, T Sander, H Harms, et al.Genomics|April 18, 1998
Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3U Finckh, S Xu, G Kumaramanickavel, et al.American Journal of Human Genetics|January 13, 2000
High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genesU Finckh, T Müller-Thomsen, U Mann, et al.Molecular Psychiatry|October 13, 2006
Plexin B3 is genetically associated with verbal performance and white matter volume in human brainD Rujescu, E M Meisenzahl, S Krejcova, et al.Alcoholism, Clinical and Experimental Research|June 8, 2001
Ethanol and gene expression in brainI Matsumoto, P A Wilce, T Buckley, et al.Annals of the New York Academy of Sciences|February 24, 2001
High frequency of mutations in four different disease genes in early-onset dementiaU Finckh, T Müller-Thomsen, U Mann, et al.Nature Genetics|November 5, 1997
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophyS M Gu, D A Thompson, C R Srikumari, et al.Pharmacogenetics|August 1, 1997
Influence of the dopamine D2 receptor (DRD2) genotype on neuroadaptive effects of alcohol and the clinical outcome of alcoholismU Finckh, H Rommelspacher, S Kuhn, et al.Human Molecular Genetics|November 13, 1998
Genetic association of an alpha2-macroglobulin (Val1000lle) polymorphism and Alzheimer's diseaseA Liao, R M Nitsch, S M Greenberg, et al.Pageof 5