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Molecular Biology of the Cell|June 26, 2009
{alpha}-synuclein and its A30P mutant affect actin cytoskeletal structure and dynamicsVítor L Sousa, Serena Bellani, Maila Giannandrea, et al.
Neuroscience and Biobehavioral Reviews|January 14, 2014
RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functionsPatrizia D'Adamo, Michela Masetti, Veronica Bianchi, et al.
Traffic (Copenhagen, Denmark)|August 17, 2006
Human cytomegalovirus DNA polymerase catalytic subunit pUL54 possesses independently acting nuclear localization and ppUL44 binding motifsGualtiero Alvisi, Alessandro Ripalti, Apollinaire Ngankeu, et al.
Plos One|July 3, 2013
Nonsense-mediated mRNA decay and loss-of-function of the protein underlie the X-linked epilepsy associated with the W356× mutation in synapsin IMaila Giannandrea, Fabrizia C Guarnieri, Niels H Gehring, et al.
Journal of Cell Science|November 3, 2011
Effects of phosphorylation and neuronal activity on the control of synapse formation by synapsin ILaura E Perlini, Francesca Botti, Eugenio F Fornasiero, et al.
Journal of Neurodevelopmental Disorders|July 23, 2014
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorderElena Bacchelli, Fabiola Ceroni, Dalila Pinto, et al.
Human Mutation|December 21, 2013
Increased dosage of RAB39B affects neuronal development and could explain the cognitive impairment in male patients with distal Xq28 copy number gainsLieselot Vanmarsenille, Maila Giannandrea, Nathalie Fieremans, et al.
Nature Communications|March 19, 2015
The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR compositionMaria Lidia Mignogna, Maila Giannandrea, Antonia Gurgone, et al.
American Journal of Human Genetics|February 18, 2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephalyMaila Giannandrea, Veronica Bianchi, Maria Lidia Mignogna, et al.
American Journal of Human Genetics|December 1, 2014
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyGabrielle R Wilson, Joe C H Sim, Catriona McLean, et al.
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