Pradier L - Search Results

1

No replication of genetic association between candidate polymorphisms and Alzheimer's disease.

Cousin E, Macé S, Rocher C, Dib C, Muzard G, Hannequin D, Pradier L, Deleuze JF, Génin E, Brice A, Campion D. Cousin E, et al. Among authors: pradier l. Neurobiol Aging. 2011 Aug;32(8):1443-51. doi: 10.1016/j.neurobiolaging.2009.09.004. Epub 2009 Nov 3. Neurobiol Aging. 2011. PMID: 19889475

2

ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease.

Macé S, Cousin E, Ricard S, Génin E, Spanakis E, Lafargue-Soubigou C, Génin B, Fournel R, Roche S, Haussy G, Massey F, Soubigou S, Bréfort G, Benoit P, Brice A, Campion D, Hollis M, Pradier L, Benavides J, Deleuze JF. Macé S, et al. Among authors: pradier l. Neurobiol Dis. 2005 Feb;18(1):119-25. doi: 10.1016/j.nbd.2004.09.011. Neurobiol Dis. 2005. PMID: 15649702

3

No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease.

Cousin E, Hannequin D, Macé S, Dubois B, Ricard S, Génin E, Brun C, Chansac C, Pradier L, Frebourg T, Brice A, Campion D, Deleuze JF. Cousin E, et al. Among authors: pradier l. Neurosci Lett. 2003 Dec 19;353(2):153-5. doi: 10.1016/s0304-3940(03)01105-4. Neurosci Lett. 2003. PMID: 14664923

4

A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism.

Cousin E, Hannequin D, Ricard S, Macé S, Génin E, Chansac C, Brice A, Dubois B, Frebourg T, Mercken L, Benavides J, Pradier L, Campion D, Deleuze JF. Cousin E, et al. Among authors: pradier l. Neurosci Lett. 2003 May 15;342(1-2):5-8. doi: 10.1016/s0304-3940(03)00225-8. Neurosci Lett. 2003. PMID: 12727304

5

Is the saitohin gene involved in neurodegenerative diseases?

Verpillat P, Ricard S, Hannequin D, Dubois B, Bou J, Camuzat A, Pradier L, Frebourg T, Brice A, Clerget-Darpoux F, Deleuze JF, Campion D; French Study Group on Alzheimer's Disease and Frontotemporal Dementia. Verpillat P, et al. Among authors: pradier l. Ann Neurol. 2002 Dec;52(6):829-32. doi: 10.1002/ana.10384. Ann Neurol. 2002. PMID: 12447938

6

The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregates.

Gu WJ, Corti O, Araujo F, Hampe C, Jacquier S, Lücking CB, Abbas N, Duyckaerts C, Rooney T, Pradier L, Ruberg M, Brice A. Gu WJ, et al. Among authors: pradier l. Neurobiol Dis. 2003 Dec;14(3):357-64. doi: 10.1016/j.nbd.2003.08.011. Neurobiol Dis. 2003. PMID: 14678753

7

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse.

Itier JM, Ibanez P, Mena MA, Abbas N, Cohen-Salmon C, Bohme GA, Laville M, Pratt J, Corti O, Pradier L, Ret G, Joubert C, Periquet M, Araujo F, Negroni J, Casarejos MJ, Canals S, Solano R, Serrano A, Gallego E, Sanchez M, Denefle P, Benavides J, Tremp G, Rooney TA, Brice A, Garcia de Yebenes J. Itier JM, et al. Among authors: pradier l. Hum Mol Genet. 2003 Sep 15;12(18):2277-91. doi: 10.1093/hmg/ddg239. Epub 2003 Jul 22. Hum Mol Genet. 2003. PMID: 12915482

8

Presenilins and Alzheimer's disease: biological functions and pathogenic mechanisms.

Czech C, Tremp G, Pradier L. Czech C, et al. Among authors: pradier l. Prog Neurobiol. 2000 Mar;60(4):363-84. doi: 10.1016/s0301-0082(99)00033-7. Prog Neurobiol. 2000. PMID: 10670705 Review.

9

Unraveling substantia nigra sequential gene expression in a progressive MPTP-lesioned macaque model of Parkinson's disease.

Bassilana F, Mace N, Li Q, Stutzmann JM, Gross CE, Pradier L, Benavides J, Ménager J, Bezard E. Bassilana F, et al. Among authors: pradier l. Neurobiol Dis. 2005 Oct;20(1):93-103. doi: 10.1016/j.nbd.2005.02.005. Neurobiol Dis. 2005. PMID: 16137570

10

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

Abbas N, Lücking CB, Ricard S, Dürr A, Bonifati V, De Michele G, Bouley S, Vaughan JR, Gasser T, Marconi R, Broussolle E, Brefel-Courbon C, Harhangi BS, Oostra BA, Fabrizio E, Böhme GA, Pradier L, Wood NW, Filla A, Meco G, Denefle P, Agid Y, Brice A. Abbas N, et al. Among authors: pradier l. Hum Mol Genet. 1999 Apr;8(4):567-74. doi: 10.1093/hmg/8.4.567. Hum Mol Genet. 1999. PMID: 10072423

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