Levecque C - Search Results

1

Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.

Levecque C, Elbaz A, Clavel J, Richard F, Vidal JS, Amouyel P, Tzourio C, Alpérovitch A, Chartier-Harlin MC. Levecque C, et al. Hum Mol Genet. 2003 Jan 1;12(1):79-86. doi: 10.1093/hmg/ddg009. Hum Mol Genet. 2003. PMID: 12490535

2

S18Y polymorphism in the UCH-L1 gene and Parkinson's disease: evidence for an age-dependent relationship.

Elbaz A, Levecque C, Clavel J, Vidal JS, Richard F, Corrèze JR, Delemotte B, Amouyel P, Alpérovitch A, Chartier-Harlin MC, Tzourio C. Elbaz A, et al. Among authors: levecque c. Mov Disord. 2003 Feb;18(2):130-7. doi: 10.1002/mds.10326. Mov Disord. 2003. PMID: 12539205

3

CYP2D6 polymorphism, pesticide exposure, and Parkinson's disease.

Elbaz A, Levecque C, Clavel J, Vidal JS, Richard F, Amouyel P, Alpérovitch A, Chartier-Harlin MC, Tzourio C. Elbaz A, et al. Among authors: levecque c. Ann Neurol. 2004 Mar;55(3):430-4. doi: 10.1002/ana.20051. Ann Neurol. 2004. PMID: 14991823

4

Association of polymorphisms in the Tau and Saitohin genes with Parkinson's disease.

Levecque C, Elbaz A, Clavel J, Vidal JS, Amouyel P, Alpérovitch A, Tzourio C, Chartier-Harlin MC. Levecque C, et al. J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):478-80. doi: 10.1136/jnnp.2003.015750. J Neurol Neurosurg Psychiatry. 2004. PMID: 14966169 Free PMC article.

5

No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease.

Levecque C, Destée A, Mouroux V, Becquet E, Defebvre L, Amouyel P, Chartier-Harlin MC. Levecque C, et al. J Neural Transm (Vienna). 2001;108(8-9):979-84. doi: 10.1007/s007020170017. J Neural Transm (Vienna). 2001. PMID: 11716150

6

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease.

Chartier-Harlin MC, Kachergus J, Roumier C, Mouroux V, Douay X, Lincoln S, Levecque C, Larvor L, Andrieux J, Hulihan M, Waucquier N, Defebvre L, Amouyel P, Farrer M, Destée A. Chartier-Harlin MC, et al. Among authors: levecque c. Lancet. 2004 Sep 25-Oct 1;364(9440):1167-9. doi: 10.1016/S0140-6736(04)17103-1. Lancet. 2004. PMID: 15451224

7

Assessment of Nurr1 nucleotide variations in familial Parkinson's disease.

Levecque C, Destée A, Mouroux V, Amouyel P, Chartier-Harlin MC. Levecque C, et al. Neurosci Lett. 2004 Aug 12;366(2):135-8. doi: 10.1016/j.neulet.2004.05.028. Neurosci Lett. 2004. PMID: 15276233

8

Genetic analysis of synphilin-1 in familial Parkinson's disease.

Farrer M, Destée A, Levecque C, Singleton A, Engelender S, Becquet E, Mouroux V, Richard F, Defebvre L, Crook R, Hernandez D, Ross CA, Hardy J, Amouyel P, Chartier-Harlin MC. Farrer M, et al. Among authors: levecque c. Neurobiol Dis. 2001 Apr;8(2):317-23. doi: 10.1006/nbdi.2000.0326. Neurobiol Dis. 2001. PMID: 11300726

9

Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2-, AP-1-, and Rab22-dependent steps.

Holloway ZG, Velayos-Baeza A, Howell GJ, Levecque C, Ponnambalam S, Sztul E, Monaco AP. Holloway ZG, et al. Among authors: levecque c. Mol Biol Cell. 2013 Jun;24(11):1735-48, S1-8. doi: 10.1091/mbc.E12-08-0625. Epub 2013 Apr 17. Mol Biol Cell. 2013. PMID: 23596324 Free PMC article.

10

The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.

Velayos-Baeza A, Levecque C, Kobayashi K, Holloway ZG, Monaco AP. Velayos-Baeza A, et al. Among authors: levecque c. J Biol Chem. 2010 Dec 17;285(51):40148-62. doi: 10.1074/jbc.M110.145961. Epub 2010 Oct 13. J Biol Chem. 2010. PMID: 20943657 Free PMC article.

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