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Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.
Genes, Brain, and Behavior|January 20, 2012
The effect of an mGluR5 inhibitor on procedural memory and avoidance discrimination impairments in Fmr1 KO miceM F Vinueza Veloz, R A M Buijsen, R Willemsen, et al.
Human Reproduction (Oxford, England)|November 6, 2015
Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiencyR A M Buijsen, J A Visser, P Kramer, et al.
Journal of Medical Genetics|December 1, 1996
Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X familyB B de Vries, C C Jansen, A A Duits, et al.
Biomacromolecules|September 2, 2008
Poly(ethylene glycol)-containing hydrogel surfaces for antifouling applications in marine and freshwater environmentsTobias Ekblad, Gunnar Bergström, Thomas Ederth, et al.
Biofouling|October 16, 2008
The potential of nano-structured silicon oxide type coatings deposited by PACVD for control of aquatic biofoulingLaurent Akesso, Michala E Pettitt, James A Callow, et al.
Human Molecular Genetics|June 13, 1998
L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patternsE Fransen, R D'Hooge, G Van Camp, et al.
Journal of Medical Genetics|June 1, 1996
Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotypeJ L Keulemans, A J Reuser, M A Kroos, et al.
ACS Applied Materials & Interfaces|September 16, 2011
Resistance of galactoside-terminated alkanethiol self-assembled monolayers to marine fouling organismsThomas Ederth, Tobias Ekblad, Michala E Pettitt, et al.
Neuron|August 2, 2005
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndromeS K E Koekkoek, K Yamaguchi, B A Milojkovic, et al.
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