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Scientific Reports|May 25, 2016
Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophiesT V Andreeva, T V Tyazhelova, V N Rykalina, et al.Genetika|December 12, 2007
[Polymorphism of the apolipoprotein E gene (APOE) in the populations of Russia and neighboring countries]S A Borinskaia, N R Kal'ina, E D Sanina, et al.Neurogenetics|November 21, 2001
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's diseaseM Nicolaou, Y Q Song, C A Sato, et al.Archives of Neurology|February 19, 2000
Association between angiotensin-converting enzyme and Alzheimer diseaseL A Farrer, T Sherbatich, S A Keryanov, et al.Human Molecular Genetics|July 1, 1996
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrantR Sherrington, S Froelich, S Sorbi, et al.Human Molecular Genetics|July 1, 1996
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatS Igarashi, Y Takiyama, G Cancel, et al.Neurology|November 1, 1993
Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's diseaseE I Rogaev, W J Lukiw, G Vaula, et al.Molekuliarnaia Biologiia|September 29, 2010
[Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer's disease patients and in normal cohorts from Russian populations]S A Golenkina, A Iu Gol'tsov, I L Kuznetsova, et al.Nature|June 29, 1995
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's diseaseR Sherrington, E I Rogaev, Y Liang, et al.Pageof 9