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Methods in Molecular Biology (Clifton, N.J.)|June 12, 2013
The CGG repeat and the FMR1 geneRenate K Hukema, Ben A OostraJournal of Neurochemistry|November 19, 2008
CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndromeJudith R Brouwer, Karin Huizer, Lies-Anne Severijnen, et al.Learning & Memory (Cold Spring Harbor, N.Y.)|November 6, 2008
Gustatory plasticity in C. elegans involves integration of negative cues and NaCl taste mediated by serotonin, dopamine, and glutamateRenate K Hukema, Suzanne Rademakers, Gert JansenExpert Opinion on Therapeutic Targets|August 22, 2015
The quest for targeted therapy in fragile X syndromeShimriet Zeidler, Renate K Hukema, Rob WillemsenJournal of Neuropathology and Experimental Neurology|May 10, 2013
FBXO7 immunoreactivity in α-synuclein-containing inclusions in Parkinson disease and multiple system atrophyTianna Zhao, Lies-Anne Severijnen, Marcel van der Weiden, et al.Frontiers in Molecular Neuroscience|November 23, 2017
Combination Therapy in Fragile X Syndrome; Possibilities and Pitfalls Illustrated by Targeting the mGluR5 and GABA Pathway SimultaneouslyShimriet Zeidler, Helen de Boer, Renate K Hukema, et al.European Journal of Medical Genetics|December 11, 2017
Potential pathogenic mechanisms underlying Fragile X Tremor Ataxia Syndrome: RAN translation and/or RNA gain-of-function?Manon Boivin, Rob Willemsen, Renate K Hukema, et al.Frontiers in Molecular Biosciences|March 29, 2020
<i>In silico, in vitro</i>, and <i>in vivo</i> Approaches to Identify Molecular Players in Fragile X Tremor and Ataxia SyndromeSaif N Haify, Teresa Botta-Orfila, Renate K Hukema, 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 OostraPageof 31