Campion D - Search Results

1

A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations.

Cassinari K, Quenez O, Joly-Hélas G, Beaussire L, Le Meur N, Castelain M, Goldenberg A, Guerrot AM, Brehin AC, Deleuze JF, Boland A, Rovelet-Lecrux A, Campion D, Saugier-Veber P, Gruchy N, Frebourg T, Nicolas G, Sarafan-Vasseur N, Chambon P. Cassinari K, et al. Among authors: campion d. Clin Chem. 2019 Sep;65(9):1153-1160. doi: 10.1373/clinchem.2019.304246. Epub 2019 Jul 10. Clin Chem. 2019. PMID: 31292136

2

The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease.

Campion D, Martin C, Heilig R, Charbonnier F, Moreau V, Flaman JM, Petit JL, Hannequin D, Brice A, Frebourg T. Campion D, et al. Genomics. 1995 Mar 20;26(2):254-7. doi: 10.1016/0888-7543(95)80208-4. Genomics. 1995. PMID: 7601450

3

No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia.

Bonnet-Brilhault F, Laurent C, Campion D, Thibaut F, Lafargue C, Charbonnier F, Deleuze JF, Ménard JF, Jay M, Petit M, Frebourg T, Mallet J. Bonnet-Brilhault F, et al. Among authors: campion d. Eur J Hum Genet. 1999 Feb-Mar;7(2):247-50. doi: 10.1038/sj.ejhg.5200278. Eur J Hum Genet. 1999. PMID: 10196711

4

The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene.

Jacquet H, Berthelot J, Bonnemains C, Simard G, Saugier-Veber P, Raux G, Campion D, Bonneau D, Frebourg T. Jacquet H, et al. Among authors: campion d. J Med Genet. 2003 Jan;40(1):e7. doi: 10.1136/jmg.40.1.e7. J Med Genet. 2003. PMID: 12525555 Free PMC article. No abstract available.

5

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: campion d. Neurosci Lett. 2003 Dec 19;353(2):153-5. doi: 10.1016/s0304-3940(03)01105-4. Neurosci Lett. 2003. PMID: 14664923

6

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.

Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D. Rovelet-Lecrux A, et al. Among authors: campion d. Nat Genet. 2006 Jan;38(1):24-6. doi: 10.1038/ng1718. Epub 2005 Dec 20. Nat Genet. 2006. PMID: 16369530

7

Hyperprolinemia is not associated with childhood onset schizophrenia.

Jacquet H, Rapoport JL, Hecketsweiler B, Bobb A, Thibaut F, Frébourg T, Campion D. Jacquet H, et al. Among authors: campion d. Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):192. doi: 10.1002/ajmg.b.30263. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16389584

8

Inhibition of proteasome and Shaggy/Glycogen synthase kinase-3beta kinase prevents clearance of phosphorylated tau in Drosophila.

Blard O, Frébourg T, Campion D, Lecourtois M. Blard O, et al. Among authors: campion d. J Neurosci Res. 2006 Oct;84(5):1107-15. doi: 10.1002/jnr.21006. J Neurosci Res. 2006. PMID: 16878320

9

Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques.

Dumanchin C, Tournier I, Martin C, Didic M, Belliard S, Carlander B, Rouhart F, Duyckaerts C, Pellissier JF, Latouche JB, Hannequin D, Frebourg T, Tosi M, Campion D. Dumanchin C, et al. Among authors: campion d. Hum Mutat. 2006 Oct;27(10):1063. doi: 10.1002/humu.9458. Hum Mutat. 2006. PMID: 16941492

10

Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila.

Blard O, Feuillette S, Bou J, Chaumette B, Frébourg T, Campion D, Lecourtois M. Blard O, et al. Among authors: campion d. Hum Mol Genet. 2007 Mar 1;16(5):555-66. doi: 10.1093/hmg/ddm011. Epub 2007 Feb 19. Hum Mol Genet. 2007. PMID: 17309878

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