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Results: 1-9 |
Results: 9

Authors: Testera, G Carraro, C Joffrain, W Lagomarsino, V Manuzio, D Manuzio, G Rouleau, G
Citation: G. Testera et al., Toward the production of antihydrogen at rest in ATHENA, NUCL INST A, 461(1-3), 2001, pp. 253-255

Authors: Ftouhi-Paquin, N Alda, M Grof, P Chretien, N Rouleau, G Turecki, G
Citation: N. Ftouhi-paquin et al., Identification of three polymorphisms in the translated region of PLC-gamma 1 and their investigation in lithium responsive bipolar disorder, AM J MED G, 105(3), 2001, pp. 301-305

Authors: Calado, A Tome, FMS Brais, B Rouleau, G Kuhn, U Wahle, E Carmo-Fonseca, M
Citation: A. Calado et al., Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA, HUM MOL GEN, 9(15), 2000, pp. 2321-2328

Authors: Ross, BM Eder, K Moszczynska, A Mamalias, N Lamarche, J Ang, L Pandolfo, M Rouleau, G Kirchgessner, M Kish, SJ
Citation: Bm. Ross et al., Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1, MOVEMENT D, 15(2), 2000, pp. 294-300

Authors: Joober, R Benkelfat, C Jannatipour, M Turecki, G Lal, S Mandel, JL Bloom, D Lalonde, P Lopes-Cendes, I Fortin, D Rouleau, G
Citation: R. Joober et al., Polyglutamine-containing proteins in schizophrenia, MOL PSYCHI, 4(1), 1999, pp. 53-57

Authors: Ames, F Audi, G Beck, D Bollen, G Simon, MD Jertz, R Kluge, HJ Kohl, A Konig, M Lunney, D Martel, I Moore, RB Otto, T Patyk, Z Raimbault-Hartmann, H Rouleau, G Savard, G Schark, E Schwarz, S Schweikhard, L Stolzenberg, H Szerypo, J
Citation: F. Ames et al., High-accuracy mass determination of unstable cesium and barium isotopes, NUCL PHYS A, 651(1), 1999, pp. 3-30

Authors: Dichgans, M Schols, L Herzog, J Stevanin, G Weirich-Schwaiger, H Rouleau, G Burk, K Klockgether, T Zuhlke, C Laccone, F Riess, O Gasser, T
Citation: M. Dichgans et al., Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families, NEUROLOGY, 52(4), 1999, pp. 849-851

Authors: Mackay, D Ionides, A Kibar, Z Rouleau, G Berry, V Moore, A Shiels, A Bhattacharya, S
Citation: D. Mackay et al., Connexin46 mutations in autosomal dominant congenital cataract, AM J HU GEN, 64(5), 1999, pp. 1357-1364

Authors: Al-Chalabi, A Andersen, PM Chioza, B Shaw, C Sham, PC Robberecht, W Matthijs, G Camu, V Marklund, SL Forsgren, L Rouleau, G Laing, NG Hurse, PV Siddique, T Leigh, PN Powell, JF
Citation: A. Al-chalabi et al., Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor, HUM MOL GEN, 7(13), 1998, pp. 2045-2050
Risultati: 1-9 |