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Results: 1-17 |
Results: 17
The frissonnant mutant mouse, a model of dopamino-sensitive, inherited motor syndrome
Authors: Callizot, N Guenet, JL Baillet, C Warter, JM Poindron, P
Citation: N. Callizot et al., The frissonnant mutant mouse, a model of dopamino-sensitive, inherited motor syndrome, NEUROBIOL D, 8(3), 2001, pp. 447-458
Genetic and physical delineation of the region overlapping the progressivemotor neuropathy (pmn) locus on mouse chromosome 13
Authors: Martin, N Jaubert, J Glaser, P Szatanik, M Guenet, JL
Citation: N. Martin et al., Genetic and physical delineation of the region overlapping the progressivemotor neuropathy (pmn) locus on mouse chromosome 13, GENOMICS, 75(1-3), 2001, pp. 9-16
Neurobiological effects of a null mutation depend on genetic context: Comparison between two hotfoot alleles of the delta-2 ionotropic glutamate receptor
Authors: Lalouette, A Lohof, A Sotelo, C Guenet, JL Mariani, J
Citation: A. Lalouette et al., Neurobiological effects of a null mutation depend on genetic context: Comparison between two hotfoot alleles of the delta-2 ionotropic glutamate receptor, NEUROSCIENC, 105(2), 2001, pp. 443-455
The CD4 T cell-deficient mouse mutation nackt (nkt) involves a deletion inthe cathepsin L (Ctsl) gene
Authors: Benavides, F Venables, A Klug, HP Glasscock, E Rudensky, A Gomez, M Palenzuela, NM Guenet, JL Richie, ER Conti, CJ
Citation: F. Benavides et al., The CD4 T cell-deficient mouse mutation nackt (nkt) involves a deletion inthe cathepsin L (Ctsl) gene, IMMUNOGENET, 53(3), 2001, pp. 233-242
Sequence interpretation - Functional annotation of mouse genome sequences
Authors: Nadeau, JH Balling, R Barsh, G Beier, D Brown, SDM Bucan, M Camper, S Carlson, G Copeland, N Eppig, J Fletcher, C Frankel, WN Ganten, D Goldowitz, D Goodnow, C Guenet, JL Hicks, G de Angelis, MH Jackson, I Jacob, HJ Jenkins, N Johnson, D Justice, M Kay, S Kingsley, D Lehrach, H Magnuson, T Meisler, M Poustka, AM Rinchik, EM Rossant, J Russell, LB Schimenti, J Shiroishi, T Skarnes, WC Soriano, P Stanford, W Takahashi, JS Wurst, W Zimmer, A
Citation: Jh. Nadeau et al., Sequence interpretation - Functional annotation of mouse genome sequences, SCIENCE, 291(5507), 2001, pp. 1251
Murine models for human diseases.
Authors: Benavides, F Guenet, JL
Citation: F. Benavides et Jl. Guenet, Murine models for human diseases., MEDICINA, 61(2), 2001, pp. 215-231
A systematic, genome-wide, phenotype-driven mutagenesis programme for genefunction studies in the mouse
Authors: Nolan, PM Peters, J Strivens, M Rogers, D Hagan, J Spurr, N Gray, IC Vizor, L Brooker, D Whitehill, E Washbourne, R Hough, T Greenaway, S Hewitt, M Liu, XH McCormack, S Pickford, K Selley, R Wells, C Tymowska-Lalanne, Z Roby, P Glenister, P Thornton, C Thaung, C Stevenson, JA Arkell, R Mburu, P Hardisty, R Kiernan, A Erven, H Steel, KP Voegeling, S Guenet, JL Nickols, C Sadri, R Naase, M Isaacs, A Davies, K Browne, M Fisher, EMC Martin, J Rastan, S Brown, SDM Hunter, J
Citation: Pm. Nolan et al., A systematic, genome-wide, phenotype-driven mutagenesis programme for genefunction studies in the mouse, NAT GENET, 25(4), 2000, pp. 440-443
Determination of the mouse homologous region for the rat dmy locus
Authors: Kitada, K Guenet, JL Serikawa, T
Citation: K. Kitada et al., Determination of the mouse homologous region for the rat dmy locus, J EXP ANIM, 41(1-2), 2000, pp. 40-43
Genomic organization, chromosomal assignment, and expression analysis of the mouse Suppressor of fused gene (Sufu) coding a Gli protein partner
Authors: Simon-Chazottes, D Paces-Fessy, M Lamour-Isnard, C Guenet, JL Blanchet-Tournier, MF
Citation: D. Simon-chazottes et al., Genomic organization, chromosomal assignment, and expression analysis of the mouse Suppressor of fused gene (Sufu) coding a Gli protein partner, MAMM GENOME, 11(8), 2000, pp. 614-621
The genes encoding mouse lysyl hydroxylase isoforms map to Chromosomes 4, 5, and 9
Authors: Sipila, L Szatanik, M Vainionpaa, H Ruotsalainen, H Myllyla, R Guenet, JL
Citation: L. Sipila et al., The genes encoding mouse lysyl hydroxylase isoforms map to Chromosomes 4, 5, and 9, MAMM GENOME, 11(12), 2000, pp. 1132-1134
Mouse chromosome 19
Authors: Poirier, C Elliott, R Guenet, JL
Citation: C. Poirier et al., Mouse chromosome 19, MAMM GENOME, 11(11), 2000, pp. 958-958
Genes encoding troponin I and troponin T are organized as three paralogouspairs in the mouse genome
Authors: Barton, PJR Mullen, AJ Cullen, ME Dhoot, GK Simon-Chazottes, D Guenet, JL
Citation: Pjr. Barton et al., Genes encoding troponin I and troponin T are organized as three paralogouspairs in the mouse genome, MAMM GENOME, 11(10), 2000, pp. 926-929
Phenotypic analysis of new deaf and vestibular mouse mutants
Authors: Erven, A Kiernan, AE de Angelis, MH Fuchs, H Balling, R Guenet, JL Avraham, KB Ben-David, O Vreugde, S Nolan, P Peters, J Cattanach, B Skynner, M Allen, N Brown, SDM Steel, KP
Citation: A. Erven et al., Phenotypic analysis of new deaf and vestibular mouse mutants, BR J AUDIOL, 34(2), 2000, pp. 85-85
Mouse Chromosome 19
Authors: Poirier, C Guenet, JL
Citation: C. Poirier et Jl. Guenet, Mouse Chromosome 19, MAMM GENOME, 10(10), 1999, pp. 960-960
Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency
Authors: Benavides, F Giordano, M Fiette, L Brunialti, ALB Palenzuela, NM Vanzulli, S Baldi, P Schmidt, R Pasqualini, CD Guenet, JL
Citation: F. Benavides et al., Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency, IMMUNOGENET, 49(5), 1999, pp. 413-419
Three new allelic mouse mutations that cause skeletal overgrowth involve the natriuretic peptide receptor C gene (Npr3)
Authors: Jaubert, J Jaubert, F Martin, N Washburn, LL Lee, BK Eicher, EM Guenet, JL
Citation: J. Jaubert et al., Three new allelic mouse mutations that cause skeletal overgrowth involve the natriuretic peptide receptor C gene (Npr3), P NAS US, 96(18), 1999, pp. 10278-10283
Wild mice as a source of genetic polymorphism.
Authors: Guenet, JL
Citation: Jl. Guenet, Wild mice as a source of genetic polymorphism., PATH BIOL, 46(9), 1998, pp. 685-688
Risultati: 1-17 |