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Results: 1-15 |
Results: 15
Genome evolution at the genus level: Comparison of three complete genomes of hyperthermophilic Archaea
Authors: Lecompte, O Ripp, R Puzos-Barbe, V Duprat, S Heilig, R Dietrich, J Thierry, JC Poch, O
Citation: O. Lecompte et al., Genome evolution at the genus level: Comparison of three complete genomes of hyperthermophilic Archaea, GENOME RES, 11(6), 2001, pp. 981-993
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 new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia
Authors: Bernard, OA Busson-LeConiat, M Ballerini, P Mauchauffe, M Della Valle, V Monni, R Khac, FN Mercher, T Penard-Lacronique, V Pasturaud, P Gressin, L Heilig, R Daniel, MT Lessard, M Berger, R
Citation: Oa. Bernard et al., A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia, LEUKEMIA, 15(10), 2001, pp. 1495-1504
Initial view of the human genomic sequence
Authors: Heilig, R Bruls, T
Citation: R. Heilig et T. Bruls, Initial view of the human genomic sequence, M S-MED SCI, 17(3), 2001, pp. 299-308
The complete genome sequence of the murine respiratory pathogen Mycoplasmapulmonis
Authors: Chambaud, I Heilig, R Ferris, S Barbe, V Samson, D Galisson, F Moszer, I Dybvig, K Wroblewski, H Viari, A Rocha, EPC Blanchard, A
Citation: I. Chambaud et al., The complete genome sequence of the murine respiratory pathogen Mycoplasmapulmonis, NUCL ACID R, 29(10), 2001, pp. 2145-2153
Initial sequencing and analysis of the human genome
Authors: Lander, ES Linton, LM Birren, B Nusbaum, C Zody, MC Baldwin, J Devon, K Dewar, K Doyle, M FitzHugh, W Funke, R Gage, D Harris, K Heaford, A Howland, J Kann, L Lehoczky, J LeVine, R McEwan, P McKernan, K Meldrim, J Mesirov, JP Miranda, C Morris, W Naylor, J Raymond, C Rosetti, M Santos, R Sheridan, A Sougnez, C Stange-Thomann, N Stojanovic, N Subramanian, A Wyman, D Rogers, J Sulston, J Ainscough, R Beck, S Bentley, D Burton, J Clee, C Carter, N Coulson, A Deadman, R Deloukas, P Dunham, A Dunham, I Durbin, R French, L Grafham, D Gregory, S Hubbard, T Humphray, S Hunt, A Jones, M Lloyd, C McMurray, A Matthews, L Mercer, S Milne, S Mullikin, JC Mungall, A Plumb, R Ross, M Shownkeen, R Sims, S Waterston, RH Wilson, RK Hillier, LW McPherson, JD Marra, MA Mardis, ER Fulton, LA Chinwalla, AT Pepin, KH Gish, WR Chissoe, SL Wendl, MC Delehaunty, KD Miner, TL Delehaunty, A Kramer, JB Cook, LL Fulton, RS Johnson, DL Minx, PJ Clifton, SW Hawkins, T Branscomb, E Predki, P Richardson, P Wenning, S Slezak, T Doggett, N Cheng, JF Olsen, A Lucas, S Elkin, C Uberbacher, E Frazier, M Gibbs, RA Muzny, DM Scherer, SE Bouck, JB Sodergren, EJ Worley, KC Rives, CM Gorrell, JH Metzker, ML Naylor, SL Kucherlapati, RS Nelson, DL Weinstock, GM Sakaki, Y Fujiyama, A Hattori, M Yada, T Toyoda, A Itoh, T Kawagoe, C Watanabe, H Totoki, Y Taylor, T Weissenbach, J Heilig, R Saurin, W Artiguenave, F Brottier, P Bruls, T Pelletier, E Robert, C Wincker, P Rosenthal, A Platzer, M Nyakatura, G Taudien, S Rump, A Yang, HM Yu, J Wang, J Huang, GY Gu, J Hood, L Rowen, L Madan, A Qin, SZ Davis, RW Federspiel, NA Abola, AP Proctor, MJ Myers, RM Schmutz, J Dickson, M Grimwood, J Cox, DR Olson, MV Kaul, R Raymond, C Shimizu, N Kawasaki, K Minoshima, S Evans, GA Athanasiou, M Schultz, R Roe, BA Chen, F Pan, HQ Ramser, J Lehrach, H Reinhardt, R McCombie, WR de la Bastide, M Dedhia, N Blocker, H Hornischer, K Nordsiek, G Agarwala, R Aravind, L Bailey, JA Bateman, A Batzoglou, S Birney, E Bork, P Brown, DG Burge, CB Cerutti, L Chen, HC Church, D Clamp, M Copley, RR Doerks, T Eddy, SR Eichler, EE Furey, TS Galagan, J Gilbert, JGR Harmon, C Hayashizaki, Y Haussler, D Hermjakob, H Hokamp, K Jang, WH Johnson, LS Jones, TA Kasif, S Kaspryzk, A Kennedy, S Kent, WJ Kitts, P Koonin, EV Korf, I Kulp, D Lancet, D Lowe, TM McLysaght, A Mikkelsen, T Moran, JV Mulder, N Pollara, VJ Ponting, CP Schuler, G Schultz, JR Slater, G Smit, AFA Stupka, E Szustakowki, J Thierry-Mieg, D Thierry-Mieg, J Wagner, L Wallis, J Wheeler, R Williams, A Wolf, YI Wolfe, KH Yang, SP Yeh, RF Collins, F Guyer, MS Peterson, J Felsenfeld, A Wetterstrand, KA Patrinos, A Morgan, MJ
Citation: Es. Lander et al., Initial sequencing and analysis of the human genome, NATURE, 409(6822), 2001, pp. 860-921
A physical map of the human genome
Authors: McPherson, JD Marra, M Hillier, L Waterston, RH Chinwalla, A Wallis, J Sekhon, M Wylie, K Mardis, ER Wilson, RK Fulton, R Kucaba, TA Wagner-McPherson, C Barbazuk, WB Gregory, SG Humphray, SJ French, L Evans, RS Bethel, G Whittaker, A Holden, JL McCann, OT Dunham, A Soderlund, C Scott, CE Bentley, DR Schuler, G Chen, HC Jang, WH Green, ED Idol, JR Maduro, VVB Montgomery, KT Lee, E Miller, A Emerling, S Kucherlapati, R Gibbs, R Scherer, S Gorrell, JH Sodergren, E Clerc-Blankenburg, K Tabor, P Naylor, S Garcia, D de Jong, PJ Catanese, JJ Nowak, N Osoegawa, K Qin, SZ Rowen, L Madan, A Dors, M Hood, L Trask, B Friedman, C Massa, H Cheung, VG Kirsch, IR Reid, T Yonescu, R Weissenbach, J Bruls, T Heilig, R Branscomb, E Olsen, A Doggett, N Cheng, JF Hawkins, T Myers, RM Shang, J Ramirez, L Schmutz, J Velasquez, O Dixon, K Stone, NE Cox, DR Haussler, D Kent, WJ Furey, T Rogic, S Kennedy, S Jones, S Rosenthal, A Wen, GP Schilhabel, M Gloeckner, G Nyakatura, G Siebert, R Schlegelberger, B Korenburg, J Chen, XN Fujiyama, A Hattori, M Toyoda, A Yada, T Park, HS Sakaki, Y Shimizu, N Asakawa, S Kawasaki, K Sasaki, T Shintani, A Shimizu, A Shibuya, K Kudoh, J Minoshima, S Ramser, J Seranski, P Hoff, C Poustka, A Reinhardt, R Lehrach, H
Citation: Jd. Mcpherson et al., A physical map of the human genome, NATURE, 409(6822), 2001, pp. 934-941
A physical map of human chromosome 14
Authors: Bruls, T Gyapay, G Petit, JL Artiguenave, F Vico, V Qin, SZ Tin-Wollam, AM Da Silva, C Muselet, D Mavel, D Pelletier, E Levy, M Fujiyama, A Matsuda, F Wilson, R Rowen, L Hood, L Weissenbach, J Saurin, W Heilig, R
Citation: T. Bruls et al., A physical map of human chromosome 14, NATURE, 409(6822), 2001, pp. 947-948
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
Bacterial mode of replication with eukaryotic-like machinery in a hyperthermophilic archaeon
Authors: Myllykallio, H Lopez, P Lopez-Garcia, P Heilig, R Saurin, W Zivanovic, Y Philippe, H Forterre, P
Citation: H. Myllykallio et al., Bacterial mode of replication with eukaryotic-like machinery in a hyperthermophilic archaeon, SCIENCE, 288(5474), 2000, pp. 2212-2215
Characterization of the NPHP1 locus: Mutational mechanism involved in deletions in familial juvenile nephronophthisis
Authors: Saunier, S Calado, J Benessy, F Silbermann, F Heilig, R Weissenbach, J Antignac, C
Citation: S. Saunier et al., Characterization of the NPHP1 locus: Mutational mechanism involved in deletions in familial juvenile nephronophthisis, AM J HU GEN, 66(3), 2000, pp. 778-789
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
Authors: Hazan, J Fonknechten, N Mavel, D Paternotte, C Samson, D Artiguenave, F Davoine, CS Cruaud, C Durr, A Wincker, P Brottier, P Cattolico, L Barbe, V Burgunder, JM Prud'homme, JF Brice, A Fontaine, B Heilig, R Weissenbach, J
Citation: J. Hazan et al., Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia, NAT GENET, 23(3), 1999, pp. 296-303
A fine integrated map of the SPG4 locus excludes an expanded CAG repeat inchromosome 2p-linked autosomal dominant spastic paraplegia
Authors: Hazan, J Davoine, CS Mavel, D Fonknechten, N Paternotte, C Fizames, C Cruaud, C Samson, D Muselet, D Vega-Czarny, N Brice, A Gyapay, G Heilig, R Fontaine, B Weissenbach, J
Citation: J. Hazan et al., A fine integrated map of the SPG4 locus excludes an expanded CAG repeat inchromosome 2p-linked autosomal dominant spastic paraplegia, GENOMICS, 60(3), 1999, pp. 309-319
Construction of a highly annotated cosmid contig spanning 550 kb within the X-linked non-specific mental retardation candidate region at Xp21.3-22.1
Authors: Carrie, A Nepotes, V Billuart, P Beldjord, C Bienvenu, T Chelly, J Bruls, T Heilig, R Weissenbach, J Jun, L Marynen, P
Citation: A. Carrie et al., Construction of a highly annotated cosmid contig spanning 550 kb within the X-linked non-specific mental retardation candidate region at Xp21.3-22.1, AM J MED G, 85(3), 1999, pp. 252-254
Genetic linkage of Meleda disease to chromosome 8qter
Authors: Fischer, J Bouadjar, B Heilig, R Fizames, C Prud'homme, JF Weissenbach, J
Citation: J. Fischer et al., Genetic linkage of Meleda disease to chromosome 8qter, EUR J HUM G, 6(6), 1998, pp. 542-547
Risultati: 1-15 |