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Publications

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

The function of chorein

Velayos-Baeza A. et al, (2008), 87 - +

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

Include forthcoming?