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Neuroscience Letters|August 29, 2006
Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigraNilgün Akbas, Helmine Hochstrasser, Joelle Deplazes, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 10, 2005
Functional relevance of ceruloplasmin mutations in Parkinson's diseaseHelmine Hochstrasser, Jürgen Tomiuk, Uwe Walter, et al.The Journal of Molecular Diagnostics : JMD|April 12, 2008
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's diseaseChristopher Schroeder, Michael Walter, Daniela Berg, et al.Neurobiology of Disease|August 25, 2009
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeatsJana Boy, Thorsten Schmidt, Ulrike Schumann, et al.Neurobiology of Disease|January 19, 2010
Polyglutamine-induced neurodegeneration in SCA3 is not mitigated by non-expanded ataxin-3: conclusions from double-transgenic mouse modelsJeannette Hübener, Olaf RiessNeuroimage|August 26, 2006
Expression mapping of tetracycline-responsive prion protein promoter: digital atlasing for generating cell-specific disease modelsJana Boy, Trygve B Leergaard, Thorsten Schmidt, et al.Neuroscience Letters|November 15, 2003
Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigraBettina Felletschin, Peter Bauer, Uwe Walter, et al.Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|August 24, 2006
Spectrin mutations in spinocerebellar ataxia (SCA)Peter Bauer, Ludger Schöls, Olaf RiessProceedings of the National Academy of Sciences of the United States of America|April 6, 2004
Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's diseaseEsti Liani, Allon Eyal, Eyal Avraham, et al.Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.Pageof 83