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Nature Genetics|August 31, 2001
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndromeA Zimprich, M Grabowski, F Asmus, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|December 29, 2004
The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodiesA Hofer, D Berg, F Asmus, et al.Journal of Medical Genetics|January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsM Sharma, J C Mueller, A Zimprich, et al.Biofabrication|July 23, 2014
Evaluation of the effect of expansion and shear stress on a self-assembled endothelium mimicking nanomatrix coating for drug eluting stents in vitro and in vivoAdinarayana Andukuri, IlJae Min, Patrick Hwang, et al.Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.Human Molecular Genetics|May 16, 1998
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)J R Vaughan, M J Farrer, Z K Wszolek, et al.Neurobiology of Disease|January 8, 2010
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystoniaM Walter, M Bonin, R Saunders Pullman, et al.Journal of Medical Genetics|December 14, 2004
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's diseaseM Martinez, A Brice, J R Vaughan, et al.Applied and Environmental Microbiology|November 23, 2006
Influence of dangling ends and surface-proximal tails of targets on probe-target duplex formation in 16S rRNA gene-based diagnostic arraysRobert D Stedtfeld, Lukas M Wick, Samuel W Baushke, et al.Neuroscience Letters|August 24, 1999
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, et al.Pageof 60