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European Journal of Human Genetics : EJHG|June 1, 2006
New mutations in the NHS gene in Nance-Horan Syndrome families from the NetherlandsRalph J Florijn, Willem Loves, Liesbeth J J M Maillette de Buy Wenniger-Prick, et al.
Open Biology|November 28, 2019
Loss of CRMP2 O-GlcNAcylation leads to reduced novel object recognition performance in miceVillo Muha, Ritchie Williamson, Rachel Hills, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2010
Age-dependent maintenance of motor control and corticostriatal innervation by death receptor 3Jason Peter Twohig, Malcolm I Roberts, Nuria Gavalda, et al.
Human Molecular Genetics|May 6, 2009
X-linked cataract and Nance-Horan syndrome are allelic disordersMargherita Coccia, Simon P Brooks, Tom R Webb, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 28, 2025
Endogenous LRRK2 and PINK1 function in a convergent neuroprotective ciliogenesis pathway in the brainEnrico Bagnoli, Yu-En Lin, Sophie Burel, et al.
Scientific Reports|February 9, 2017
Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's diseaseRobert M Bragg, Sydney R Coffey, Rory M Weston, et al.
Histopathology|March 21, 2013
Another look at follicular lymphoma: immunophenotypic and molecular analyses identify distinct follicular lymphoma subgroupsTeresa Marafioti, Christiane Copie-Bergman, Maria Calaminici, et al.
Open Biology|November 9, 2018
Phosphorylation of Parkin at serine 65 is essential for its activation in vivoThomas G McWilliams, Erica Barini, Risto Pohjolan-Pirhonen, et al.
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