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Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2007
A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 geneGiovanni Fabbrini, Massimo Pasquini, Cinzia Aurilia, et al.Circulation Research|May 13, 2006
ACE polymorphismsF A Sayed-Tabatabaei, B A Oostra, A Isaacs, et al.Gastroenterology|July 1, 1993
A mutation in bilirubin uridine 5'-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type IIP J Bosma, B Goldhoorn, R P Oude Elferink, et al.Human Molecular Genetics|June 1, 1996
FMRP is associated to the ribosomes via RNAF Tamanini, N Meijer, C Verheij, et al.Plos One|November 8, 2012
Dopaminergic neuronal loss and dopamine-dependent locomotor defects in Fbxo7-deficient zebrafishTianna Zhao, Herma Zondervan-van der Linde, Lies-Anne Severijnen, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 16, 1999
N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam studyB S Harhangi, B A Oostra, P Heutink, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotypeEsther Brusse, Inge de Koning, Anneke Maat-Kievit, et al.Human Molecular Genetics|August 1, 1997
Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testisF Tamanini, R Willemsen, L van Unen, et al.Human Molecular Genetics|May 6, 2006
Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteinsCorinne M Spencer, Ekaterina Serysheva, Lisa A Yuva-Paylor, et al.The Biochemical Journal|October 21, 1999
Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2PF Tamanini, L Van Unen, C Bakker, et al.Pageof 51