Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2-, AP-1-, and Rab22-dependent steps.
Holloway ZG. et al, (2013), Mol biol cell, 24, 1735 - S8
The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
Velayos-Baeza A. et al, (2010), J biol chem, 285, 40148 - 40162
The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway.
Levecque C. et al, (2009), Am j physiol cell physiol, 297, C160 - C168
Functional characterization of VPS13 proteins
Velayos-Baeza A. et al, (2007), Movement disorders, 22, I - I
Potential interaction partners of VPS13 proteins
Levecque C. et al, (2005), Movement disorders, 20, 1683 - 1683
α-synuclein locus duplication as a cause of familial Parkinson's disease
Chartier-Harlin MC. et al, (2004), Lancet, 364, 1167 - 1169
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease.
Chartier-Harlin M-C. et al, (2004), Lancet, 364, 1167 - 1169
Assessment of Nurr1 nucleotide variations in familial Parkinson's disease.
Levecque C. et al, (2004), Neurosci lett, 366, 135 - 138
Association of polymorphisms in the Tau and Saitohin genes with Parkinson's disease.
Levecque C. et al, (2004), J neurol neurosurg psychiatry, 75, 478 - 480
CYP2D6 polymorphism, pesticide exposure, and Parkinson's disease.
Elbaz A. et al, (2004), Ann neurol, 55, 430 - 434
S18Y polymorphism in the UCH-L1 gene and Parkinson's disease: evidence for an age-dependent relationship.
Elbaz A. et al, (2003), Mov disord, 18, 130 - 137
Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.
Levecque C. et al, (2003), Hum mol genet, 12, 79 - 86
The relation between Parkinson's disease and the S18Y polymorphism in the UCH-L1 gene is modified by age at onset
Elbaz A. et al, (2002), Neurology, 58, A110 - A111
No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease
Levecque C. et al, (2001), Journal of neurology, 248, 979 - 984
Genetic analysis of synphilin-1 in familial Parkinson's disease.
Farrer M. et al, (2001), Neurobiol dis, 8, 317 - 323
No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease.
Levecque C. et al, (2001), J neural transm (vienna), 108, 979 - 984