AAAAAA
Results:
1-23
|
Results: 23
Authors:
Verpillat, P
Bouley, S
Campion, D
Hannequin, D
Dubois, B
Belliard, S
Puel, M
Thomas-Anterion, C
Agid, Y
Brice, A
Clerget-Darpoux, F
Citation: P. Verpillat et al., Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population, EUR J HUM G, 9(6), 2001, pp. 464-468
Authors:
Dugan, JP
Fetzer, GJ
Bowden, J
Farruggia, GJ
Williams, JZ
Piotrowski, CC
Vierra, K
Campion, D
Sitter, DN
Citation: Jp. Dugan et al., Airborne optical system for remote sensing of ocean waves, J ATMOSP OC, 18(7), 2001, pp. 1267-1276
Authors:
de Chaldee, M
Corbex, M
Campion, D
Jay, M
Samolyk, D
Petit, M
Thibaut, F
Laurent, C
Mallet, J
Citation: M. De Chaldee et al., No evidence for linkage between COMT and schizophrenia in a French population, PSYCHIAT R, 102(1), 2001, pp. 87-90
Authors:
Hannequin, D
Campion, D
Citation: D. Hannequin et D. Campion, Dominant forms of Alzheimer's disease: from genotype to phenotype., REV NEUROL, 157(4), 2001, pp. 384-392
Authors:
Pratschke, KM
Bellenger, CR
McAllister, H
Campion, D
Citation: Km. Pratschke et al., Barrier pressure at the gastroesophageal junction in anesthetized dogs, AM J VET RE, 62(7), 2001, pp. 1068-1072
Authors:
Zurutuza, L
Verpillat, P
Raux, G
Hannequin, D
Puel, M
Belliard, S
Michon, A
Pothin, Y
Camuzat, A
Penet, C
Martin, C
Brice, A
Campion, D
Clerget-Darpoux, F
Frebourg, T
Citation: L. Zurutuza et al., APOE promoter polymorphisms do not confer independent risk for Alzheimer'sdisease in a French population, EUR J HUM G, 8(9), 2000, pp. 713-716
Authors:
Verpillat, P
Bouley, S
Hannequin, D
Belliard, S
Puel, M
Thomas-Anterion, C
Dubois, B
Agid, Y
Campion, D
Clerget-Darpoux, F
Brice, A
Citation: P. Verpillat et al., alpha 2-macroglobulin gene and Alzheimer's disease: Confirmation of association by haplotypes analyses, ANN NEUROL, 48(3), 2000, pp. 400-402
Authors:
Camuzat, A
Verpillat, P
Dubois, B
Penet, C
Agid, CPY
Brice, A
Clerget-Darpoux, F
Moreaud, O
Puel, M
Kinter, J
Kozlov, S
Berger, P
Sonderegger, P
Raux, G
Campion, D
Hannequin, D
Frebourg, T
Citation: A. Camuzat et al., Mutations in the neuroserpin gene are rare in familial dementia, ANN NEUROL, 47(5), 2000, pp. 688-688
Authors:
Gantier, R
Gilbert, D
Dumanchin, C
Campion, D
Davoust, D
Toma, F
Frebourg, T
Citation: R. Gantier et al., The pathogenic L392V mutation of presenilin 1 decreases the affinity to glycogen synthase kinase-3 beta, NEUROSCI L, 283(3), 2000, pp. 217-220
Authors:
Campion, D
Citation: D. Campion, MLA millennial questionnaire on university issues - Reply, PMLA, 115(7), 2000, pp. 1996-1996
Authors:
Raux, G
Gantier, R
Thomas-Anterion, C
Boulliat, J
Verpillat, P
Hannequin, D
Brice, A
Frebourg, T
Campion, D
Citation: G. Raux et al., Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation, NEUROLOGY, 55(10), 2000, pp. 1577-1578
Authors:
Campion, D
Citation: D. Campion, The 'Scavenger', MIDWEST Q, 41(2), 2000, pp. 160-160
Authors:
Lopez-Perez, E
Dumanchin, C
Czech, C
Campion, D
Goud, B
Pradier, L
Frebourg, T
Checler, F
Citation: E. Lopez-perez et al., Overexpression of Rab11 or constitutively active Rab11 does not affect sAPP alpha and A beta secretions by wild-type and Swedish mutated beta APP-expressing HEK293 cells, BIOC BIOP R, 275(3), 2000, pp. 910-915
Authors:
Bonnet-Brilhault, F
Laurent, C
Campion, D
Thibaut, F
Lafargue, C
Charbonnier, F
Deleuze, JF
Menard, JF
Jay, M
Petit, M
Frebourg, T
Mallet, J
Citation: F. Bonnet-brilhault et al., No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia, EUR J HUM G, 7(2), 1999, pp. 247-250
Authors:
Dumanchin, C
Czech, C
Campion, D
Cuif, MH
Poyot, T
Martin, C
Charbonnier, F
Goud, B
Pradier, L
Frebourg, T
Citation: C. Dumanchin et al., Presenilins interact with Rab11, a small GTPase involved in the regulationof vesicular transport, HUM MOL GEN, 8(7), 1999, pp. 1263-1269
Authors:
Gantier, R
Dumanchin, C
Campion, D
Loutelier, C
Lange, C
Gagnon, J
Davoust, D
Frebourg, T
Toma, F
Citation: R. Gantier et al., The L392V mutation of presenilin 1 associated with autosomal dominant early-onset Alzheimer's disease alters the secondary structure of the hydrophilic loop, NEUROREPORT, 10(14), 1999, pp. 3071-3074
Authors:
Thibaut, F
Van der Elst, A
Campion, D
Martin, C
Coron, B
Dollfus, S
Frebourg, TH
Petit, M
Citation: F. Thibaut et al., Apolipoprotein E-epsilon(4) frequency in deficit schizophrenia, EUR PSYCHIA, 14(3), 1999, pp. 148-151
Authors:
de Chaldee, M
Laurent, C
Thibaut, F
Martinez, M
Samolyk, D
Petit, M
Campion, D
Mallet, J
Citation: M. De Chaldee et al., Linkage disequilibrium on the COMT gene in French schizophrenics and controls, AM J MED G, 88(5), 1999, pp. 452-457
Authors:
Campion, D
Citation: D. Campion, 'Hokusai in Iowa', POETRY, 174(5), 1999, pp. 278-278
Authors:
Ancolio, K
Dumanchin, C
Barelli, H
Warter, JM
Brice, A
Campion, D
Frebourg, T
Checler, F
Citation: K. Ancolio et al., Unusual phenotypic alteration of beta amyloid precursor protein (beta APP)maturation by a new Val-715 -> Met beta APP-770 mutation responsible for probable early-onset Alzheimer's disease, P NAS US, 96(7), 1999, pp. 4119-4124
Authors:
Campion, D
Citation: D. Campion, 'Old Men Fishing', MIDWEST Q, 40(4), 1999, pp. 377-378
Authors:
Campion, D
Citation: D. Campion, The 'Krater', COLL ENGL, 61(3), 1999, pp. 337-337
Authors:
Campion, D
Dumanchin, C
Hannequin, D
Dubois, B
Belliard, S
Puel, M
Thomas-Anterion, C
Michon, A
Martin, C
Charbonnier, F
Raux, G
Camuzat, A
Penet, C
Mesnage, V
Martinez, M
Clerget-Darpoux, F
Brice, A
Frebourg, T
Citation: D. Campion et al., Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum, AM J HU GEN, 65(3), 1999, pp. 664-670
Risultati:
1-23
|