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Results: 1-25 | 26-31
Results: 1-25/31
Global linear gyrokinetic simulations in quasi-symmetric configurations
Authors: Jost, G Tran, TM Cooper, WA Villard, L Appert, K
Citation: G. Jost et al., Global linear gyrokinetic simulations in quasi-symmetric configurations, PHYS PLASMA, 8(7), 2001, pp. 3321-3333
Effect of E x B flows on global linear ion temperature gradient modes
Authors: Maccio, M Vaclavik, J Villard, L
Citation: M. Maccio et al., Effect of E x B flows on global linear ion temperature gradient modes, PHYS PLASMA, 8(3), 2001, pp. 895-906
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications forthe disease
Authors: Villard, L Levy, N Xiang, FQ Kpebe, A Labelle, V Chevillard, C Zhang, ZP Schwartz, CE Tardieu, M Chelly, J Anvret, M Fontes, M
Citation: L. Villard et al., Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications forthe disease, J MED GENET, 38(7), 2001, pp. 435-442
Applicability of the ballooning transform to trapped ion modes
Authors: Falchetto, GL Vaclavik, J Maccio, M Brunner, S Villard, L
Citation: Gl. Falchetto et al., Applicability of the ballooning transform to trapped ion modes, PHYS PLASMA, 7(4), 2000, pp. 1196-1203
Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28
Authors: Villard, L des Portes, V Levy, N Louboutin, JP Recan, D Coquet, M Chabrol, B Figarella-Branger, D Chelly, J Pellissier, JF Fontes, M
Citation: L. Villard et al., Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28, EUR J HUM G, 8(2), 2000, pp. 125-129
MECP2 mutations account for most cases of typical forms of Rett syndrome
Authors: Bienvenu, T Carrie, A de Roux, N Vinet, MC Jonveaux, P Couvert, P Villard, L Arzimanoglou, A Beldjord, C Fontes, M Tardieu, M Chelly, J
Citation: T. Bienvenu et al., MECP2 mutations account for most cases of typical forms of Rett syndrome, HUM MOL GEN, 9(9), 2000, pp. 1377-1384
Molecular characterization of a new human T-box gene (TBX22) located in Xq21.1 encoding a protein containing a truncated T-domain
Authors: Laugier-Anfossi, F Villard, L
Citation: F. Laugier-anfossi et L. Villard, Molecular characterization of a new human T-box gene (TBX22) located in Xq21.1 encoding a protein containing a truncated T-domain, GENE, 255(2), 2000, pp. 289-296
Ribotyping and rapid identification of Staphylococcus xylosus by 16-23S spacer amplification
Authors: Villard, L Kodjo, A Borges, E Maurin, F Richard, Y
Citation: L. Villard et al., Ribotyping and rapid identification of Staphylococcus xylosus by 16-23S spacer amplification, FEMS MICROB, 185(1), 2000, pp. 83-87
Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation
Authors: Friez, MJ Essop, FB Krause, A Castiglia, L Ragusa, A Sossey-Alaoui, K Nelson, RL May, MM Michaelis, RC Srivastava, AK Schwartz, CE Stevenson, RE Goldman, A Villard, L Longshore, JW
Citation: Mj. Friez et al., Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation, HUM GENET, 106(1), 2000, pp. 36-39
Detection of Escherichia coli O157 : H7 in heifers' faecal samples using an automated immunoconcentration system
Authors: Vernozy-Rozand, C Feng, P Montet, MP Ray-Gueniot, S Villard, L Bavai, C Meyrand, A Mazuy, C Atrache, V
Citation: C. Vernozy-rozand et al., Detection of Escherichia coli O157 : H7 in heifers' faecal samples using an automated immunoconcentration system, LETT APPL M, 30(3), 2000, pp. 217-222
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]?
Authors: Briault, S Villard, L Rogner, U Coy, J Odent, S Lucas, J Passage, E Zhu, DP Shrimpton, A Pembrey, M Till, M Guichet, A Dessay, S Fontes, M Poustka, A Moraine, C
Citation: S. Briault et al., Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]?, AM J MED G, 95(2), 2000, pp. 178-181
9th international workshop on fragile X syndrome and X-linked mental retardation
Authors: Fryns, JP Borghgraef, M Brown, TW Chelly, J Fisch, GS Hamel, B Hanauer, A Lacombe, D Luo, L MacPherson, JN Mandel, JL Moraine, C Mulley, J Nelson, D Oostra, B Partington, M Ramakers, GJA Ropers, HH Rousseau, F Schwartz, C Steinbach, P Stoll, C Tranebjaerg, L Turner, G Van Bokhoven, H Vianna-Morgante, A Villard, L Warren, ST
Citation: Jp. Fryns et al., 9th international workshop on fragile X syndrome and X-linked mental retardation, AM J MED G, 94(5), 2000, pp. 345-360
Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families
Authors: Lossi, AM Colleaux, L Chiaroni, P Fontes, M Villard, L Abidi, F Schwartz, C Briault, S Moraine, C
Citation: Am. Lossi et al., Exclusion of nine candidate genes for their involvement in X-linked FG syndrome (FGS1) in three families, AM J MED G, 94(5), 2000, pp. 386-388
Identification of a mutation in the XNP/ATR-X gene in a family reported asSmith-Fineman-Myers syndrome
Authors: Villard, L Fontes, M Ades, LC Gecz, J
Citation: L. Villard et al., Identification of a mutation in the XNP/ATR-X gene in a family reported asSmith-Fineman-Myers syndrome, AM J MED G, 91(1), 2000, pp. 83-85
Differentiation of Pasteurella haemolytica from other Pasteurella by amplification of the 16-23S intergenic region
Authors: Kodjo, A Villard, L Greenland, T Bizet, C Sanchis, R Martel, JL Richard, Y
Citation: A. Kodjo et al., Differentiation of Pasteurella haemolytica from other Pasteurella by amplification of the 16-23S intergenic region, REV MED VET, 151(3), 2000, pp. 217-220
Magnetic topology and guiding centre drift orbits in a reversed shear tokamak
Authors: Fischer, O Cooper, WA Villard, L
Citation: O. Fischer et al., Magnetic topology and guiding centre drift orbits in a reversed shear tokamak, NUCL FUSION, 40(8), 2000, pp. 1453-1462
Stability of Alfven eigenmodes in optimized tokamaks
Authors: Jaun, A Fasoli, A Vaclavik, J Villard, L
Citation: A. Jaun et al., Stability of Alfven eigenmodes in optimized tokamaks, NUCL FUSION, 40(7), 2000, pp. 1343-1348
Two affected boys in a Rett syndrome family - Clinical and molecular findings
Authors: Villard, L Kpebe, A Cardoso, C Chelly, J Tardieu, M Fontes, M
Citation: L. Villard et al., Two affected boys in a Rett syndrome family - Clinical and molecular findings, NEUROLOGY, 55(8), 2000, pp. 1188-1193
Magneto-hydro-dynamic limits in spherical tokamaks
Authors: Hender, TC Allfrey, SJ Akers, R Appel, LC Bevir, MK Buttery, RJ Gryaznevich, M Jenkins, I Kwon, OJ McClements, KG Martin, R Medvedev, S Nightingale, MPS Ribeiro, C Roach, CM Robinson, DC Sharapov, SE Sykes, A Villard, L Walsh, MJ
Citation: Tc. Hender et al., Magneto-hydro-dynamic limits in spherical tokamaks, PHYS PLASMA, 6(5), 1999, pp. 1958-1968
Characterization of xnp-1, a Caenorhabditis elegans gene similar to the human XNP/ATR-X gene
Authors: Villard, L Fontes, M Ewbank, JJ
Citation: L. Villard et al., Characterization of xnp-1, a Caenorhabditis elegans gene similar to the human XNP/ATR-X gene, GENE, 236(1), 1999, pp. 13-19
Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogene
Authors: Villard, L Belougne, J Lossi, AM Fontes, M Colleaux, L
Citation: L. Villard et al., Transcript map of the human chromosome Xq11-Xq21 region: localization of 33 novel genes and one pseudogene, GENE, 235(1-2), 1999, pp. 43-50
Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes
Authors: Tassone, F Villard, L Clancy, K Gardiner, K
Citation: F. Tassone et al., Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes, GENE, 226(2), 1999, pp. 211-223
Carpenter-Waziri syndrome results from a mutation in XNP
Authors: Abidi, F Schwartz, CE Carpenter, NJ Villard, L Fontes, M Curtis, M
Citation: F. Abidi et al., Carpenter-Waziri syndrome results from a mutation in XNP, AM J MED G, 85(3), 1999, pp. 249-251
Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997
Authors: Holden, JJA Percy, M Allingham-Hawkins, D Brown, WT Chiurazzi, P Fisch, G Gane, L Gunter, C Hagerman, R Jenkins, EC Kooy, RF Lubs, HA Murray, A Neri, G Schwartz, C Tranebjaerg, L Villard, L Willems, PJ
Citation: Jja. Holden et al., Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997, AM J MED G, 83(4), 1999, pp. 221-236
Pulsed-field gel electrophoresis is more efficient than ribotyping and random amplified polymorphic DNA analysis in discrimination of Pasteurella haemolytica strains
Authors: Kodjo, A Villard, L Bizet, C Martel, JL Sanchis, R Borges, E Gauthier, D Maurin, F Richard, Y
Citation: A. Kodjo et al., Pulsed-field gel electrophoresis is more efficient than ribotyping and random amplified polymorphic DNA analysis in discrimination of Pasteurella haemolytica strains, J CLIN MICR, 37(2), 1999, pp. 380-385
Risultati: 1-25 | 26-31