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Results: 1-19 |
Results: 19
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
Authors: Magre, J Delepine, M Khallouf, E Gedde-Dahl, T Van Maldergem, L Sobel, E Papp, J Meier, M Megarbane, A Lathrop, M Capeau, J
Citation: J. Magre et al., Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13, NAT GENET, 28(4), 2001, pp. 365-370
Mutations in the gene encoding SLURP-1 in Mel de Meleda
Authors: Fischer, J Bouadjar, B Heilig, R Huber, M Lefevre, C Jobard, F Macari, F Bakija-Konsuo, A Ait-Belkacem, F Weissenbach, J Lathrop, M Hohl, D Prud'homme, JF
Citation: J. Fischer et al., Mutations in the gene encoding SLURP-1 in Mel de Meleda, HUM MOL GEN, 10(8), 2001, pp. 875-880
A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps
Authors: Bihoreau, MT Sebag-Montefiore, L Godfrey, RF Wallis, RH Brown, JH Danoy, PA Collins, SC Rouard, M Kaisaki, PJ Lathrop, M Gauguier, D
Citation: Mt. Bihoreau et al., A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps, GENOMICS, 75(1-3), 2001, pp. 57-69
Epidemiological study of the Genetics and Environment of Asthma, bronchialhyperresponsiveness and atopy (EGEA). Protocol and potential selection factors
Authors: Kauffmann, F Dizier, MH Annesi-Maesano, I Bousquet, J Charpin, D Demenais, F Ecochard, D Feingold, J Gormand, F Grimfeld, A Lathrop, M Matran, R Neukirch, F Paty, E Pison, C Scheinmann, P Vervloet, D Lockhart, A
Citation: F. Kauffmann et al., Epidemiological study of the Genetics and Environment of Asthma, bronchialhyperresponsiveness and atopy (EGEA). Protocol and potential selection factors, REV EPIDEM, 49(4), 2001, pp. 343-356
Genetic influences on the end-stage effector phase of arthritis
Authors: Ji, H Gauguier, D Ohmura, K Gonzalez, A Duchatelle, V Danoy, P Garchon, HJ Degott, C Lathrop, M Benoist, C Mathis, D
Citation: H. Ji et al., Genetic influences on the end-stage effector phase of arthritis, J EXP MED, 194(3), 2001, pp. 321-330
A genomewide scan for type 1-diabetes susceptibility in Scandinavian families: Identification of new loci with evidence of interactions
Authors: Holm, P Julier, C Kockum, I Senee, V Blanc, H Papp, J Akesson, K Bartsocas, C de Leiva, A Dahlquist, G Ronningen, KS Lathrop, M Luthman, H Pociot, F Nerup, J
Citation: P. Holm et al., A genomewide scan for type 1-diabetes susceptibility in Scandinavian families: Identification of new loci with evidence of interactions, AM J HU GEN, 69(6), 2001, pp. 1301-1313
Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome
Authors: Lefevre, C Jobard, F Caux, F Bouadjar, B Karaduman, A Heilig, R Lakhdar, H Wollenberg, A Verret, JL Weissenbach, J Ozguc, M Lathrop, M Prud'homme, JF Fischer, J
Citation: C. Lefevre et al., Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome, AM J HU GEN, 69(5), 2001, pp. 1002-1012
Genome screen for asthma and related phenotypes in the French EGEA study
Authors: Dizier, MH Besse-Schmittler, C Guilloud-Bataille, M Annesi-Maesano, I Boussaha, M Bousquet, J Charpin, D Degioanni, A Gormand, F Grimfeld, A Hochez, J Hyne, G Lockhart, A Luillier-Lacombe, M Matran, R Meunier, F Neukirch, F Pacheco, Y Parent, V Paty, E Pin, I Pison, C Scheinmann, P Thobie, N Vervloet, D Kauffmann, F Feingold, J Lathrop, M Demenais, F
Citation: Mh. Dizier et al., Genome screen for asthma and related phenotypes in the French EGEA study, AM J R CRIT, 162(5), 2000, pp. 1812-1818
Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene witha high G-C content
Authors: Escary, JL Cecillon, M Maciazek, J Lathrop, M Tournier-Lasserve, E Joutel, A
Citation: Jl. Escary et al., Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene witha high G-C content, HUM MUTAT, 16(6), 2000, pp. 518-526
Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis
Authors: Nandrot, E Dufour, EM Provost, AC Pequignot, MO Bonnel, S Gogat, K Marchant, D Rouillac, C de Conde, BS Bihoreau, MT Shaver, C Dufier, JL Marsac, C Lathrop, M Menasche, M Abitbol, MM
Citation: E. Nandrot et al., Homozygous deletion in the coding sequence of the c-mer gene in RCS rats unravels general mechanisms of physiological cell adhesion and apoptosis, NEUROBIOL D, 7(6), 2000, pp. 586-599
Detailed comparative gene map of rat chromosome 1 with mouse and human genomes and physical mapping of an evolutionary chromosomal breakpoint
Authors: Kaisaki, PJ Rouard, M Danoy, PAC Wallis, RH Collins, SC Rice, M Levy, ER Lathrop, M Bihoreau, MT Gauguier, D
Citation: Pj. Kaisaki et al., Detailed comparative gene map of rat chromosome 1 with mouse and human genomes and physical mapping of an evolutionary chromosomal breakpoint, GENOMICS, 64(1), 2000, pp. 32-43
Genetic and environmental influences on left ventricular mass - A family study
Authors: Garner, C Lecomte, E Visvikis, S Abergel, E Lathrop, M Soubrier, F
Citation: C. Garner et al., Genetic and environmental influences on left ventricular mass - A family study, HYPERTENSIO, 36(5), 2000, pp. 740-746
Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls
Authors: Keavney, B McKenzie, C Parish, S Palmer, A Clark, S Youngman, L Delepine, M Lathrop, M Peto, R Collins, R
Citation: B. Keavney et al., Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls, LANCET, 355(9202), 2000, pp. 434-442
Human islets of Langerhans express the delta(c) isoform of calcium/calmodulin-dependent protein kinase II
Authors: Southam, L Ashfield, R Cox, R Lathrop, M Ashcroft, SJH
Citation: L. Southam et al., Human islets of Langerhans express the delta(c) isoform of calcium/calmodulin-dependent protein kinase II, DIABET M R, 15(4), 1999, pp. 243-246
EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy) - descriptive characteristics
Authors: Kauffmann, F Dizier, MH Annesi-Maesano, I Bousquet, J Charpin, D Demenais, F Ecochard, D Feingold, J Gormand, F Grimfeld, A Lathrop, M Matran, R Neukirch, F Paty, E Pin, I Pison, C Scheinmann, P Vervloet, D Lockhart, A
Citation: F. Kauffmann et al., EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy) - descriptive characteristics, CLIN EXP AL, 29, 1999, pp. 17-21
Linkage and physical mapping of rat microsatellites derived from minisatellite loci
Authors: Giraudeau, F Apiou, F Amarger, V Kaisaki, PJ Bihoreau, MT Lathrop, M Vergnaud, G Gauguier, D
Citation: F. Giraudeau et al., Linkage and physical mapping of rat microsatellites derived from minisatellite loci, MAMM GENOME, 10(4), 1999, pp. 405-409
Analysis of distribution in the human, pig, and rat genomes points toward a general subtelomeric origin of minisatellite structures (vol 52, pg 62, 1998).
Authors: Amarger, V Gauguier, D Yerle, M Apiou, F Pinton, P Giraudeau, F Monfouilloux, S Lathrop, M Dutrillaux, B Buard, J Vergnaud, G
Citation: V. Amarger et al., Analysis of distribution in the human, pig, and rat genomes points toward a general subtelomeric origin of minisatellite structures (vol 52, pg 62, 1998)., GENOMICS, 58(1), 1999, pp. 109-110
UKPDS 31: Hepatocyte nuclear factor-1alpha (the MODY3 gene) mutations in late onset Type II diabetic patients in the United Kingdom
Authors: Cox, RD Southam, L Hashim, Y Horton, V Mehta, Z Taghavi, J Lathrop, M Turner, R
Citation: Rd. Cox et al., UKPDS 31: Hepatocyte nuclear factor-1alpha (the MODY3 gene) mutations in late onset Type II diabetic patients in the United Kingdom, DIABETOLOG, 42(1), 1999, pp. 120-121
Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease
Authors: Andrew, LJ Brancolini, V de la Pena, LS Devoto, M Caeiro, F Marchegiani, R Reginato, A Gaucher, A Netter, P Gillet, P Loeuille, D Prockop, DJ Carr, A Wordsworth, BF Lathrop, M Butcher, S Considine, E Everts, K Nicod, A Walsh, S Williams, CJ
Citation: Lj. Andrew et al., Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease, AM J HU GEN, 64(1), 1999, pp. 136-145
Risultati: 1-19 |