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Methods in Molecular Biology (Clifton, N.J.)|June 18, 2004
The CGG repeat and the FMR1 geneVioleta Stoyanova, Ben A OostraFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 21, 2004
Loss of FMR1 hypermethylation in somatic cell heterokaryonsVioleta Stoyanova, Stefano Rossetti, Leontine VAN Unen, et al.Biochimica Et Biophysica Acta|February 24, 2009
FMR1: a gene with three facesBen A Oostra, Rob WillemsenHuman Molecular Genetics|September 28, 2002
Gene finding in genetically isolated populationsPeter Heutink, Ben A OostraHuman Molecular Genetics|September 4, 2003
A fragile balance: FMR1 expression levelsBen A Oostra, Rob WillemsenAmerican Journal of Medical Genetics. Part A|October 12, 2013
Fragile X syndrome: From protein function to therapyClaudia Bagni, Ben A OostraMethods in Molecular Biology (Clifton, N.J.)|June 12, 2013
The CGG repeat and the FMR1 geneRenate K Hukema, Ben A OostraCurrent Opinion in Pediatrics|November 25, 2003
Understanding the biological underpinnings of fragile X syndromePietro Chiurazzi, Giovanni Neri, Ben A OostraJournal of Molecular Medicine (Berlin, Germany)|January 9, 2004
Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's diseaseVincenzo Bonifati, Ben A Oostra, Peter HeutinkCurrent Neurology and Neuroscience Reports|September 1, 2005
FXTAS: a progressive neurologic syndrome associated with Fragile X premutationRob Willemsen, Edwin Mientjes, Ben A OostraPageof 31