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Results: 1-12 |
Results: 12
Rapid isolation of tissue-specific genes from rat kidney
Authors: Hu, ED Chen, ZX Fredrickson, TA Spurr, N Gentle, S Sims, M Zhu, Y Halsey, W Van Horn, S Mao, J Sathe, GM Brooks, DP
Citation: Ed. Hu et al., Rapid isolation of tissue-specific genes from rat kidney, EXP NEPHROL, 9(2), 2001, pp. 156-164
Identification of a novel kidney-specific gene downregulated in acute ischemic renal failure (vol 279, pg F426, 2000)
Authors: Hu, E Chen, Z Fredrickson, T Gellai, M Jugus, M Contino, L Spurr, N Sims, M Halsey, W Van Horn, S Mao, J Ganesh, S Brooks, D
Citation: E. Hu et al., Identification of a novel kidney-specific gene downregulated in acute ischemic renal failure (vol 279, pg F426, 2000), AM J P-REN, 280(6), 2001, pp. NIL_3-NIL_3
Making drug discovery a SN(i)P
Authors: Campbell, DA Valdes, A Spurr, N
Citation: Da. Campbell et al., Making drug discovery a SN(i)P, DRUG DISC T, 5(9), 2000, pp. 388-396
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
Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource
Authors: Nolan, PM Peters, J Vizor, L Strivens, M Washbourne, R Hough, T Wells, C Glenister, P Thornton, C Martin, J Fisher, E Rogers, D Hagan, J Reavill, C Gray, I Wood, J Spurr, N Browne, M Rastan, S Hunter, J Brown, SDM
Citation: Pm. Nolan et al., Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource, MAMM GENOME, 11(7), 2000, pp. 500-506
Identification of a novel kidney-specific gene downregulated in acute ischemic renal failure
Authors: Hu, E Chen, ZX Fredrickson, T Gellai, M Jugus, M Contino, L Spurr, N Sims, M Halsey, W Van Horn, S Mao, J Sathe, G Brooks, D
Citation: E. Hu et al., Identification of a novel kidney-specific gene downregulated in acute ischemic renal failure, AM J P-REN, 279(3), 2000, pp. F426-F439
Cloning and characterisation of ITGAV, the genomic sequence for human celladhesion protein (vitronectin) receptor alpha subunit, CD51
Authors: Sims, MA Field, SD Barnes, MR Shaikh, N Ellington, K Murphy, KE Spurr, N Campbell, DA
Citation: Ma. Sims et al., Cloning and characterisation of ITGAV, the genomic sequence for human celladhesion protein (vitronectin) receptor alpha subunit, CD51, CYTOG C GEN, 89(3-4), 2000, pp. 268-271
The Pro-115 -> Gln mutation in peroxisome-proliferator-activated receptor (PPAR) gamma 2 is extremely rare in a large cohort of US Caucasians
Authors: Terrett, J Chamberlain, J Rastan, S Marshall, R McGinnis, R Spurr, N O'Brien, E Evans, C Rut, A
Citation: J. Terrett et al., The Pro-115 -> Gln mutation in peroxisome-proliferator-activated receptor (PPAR) gamma 2 is extremely rare in a large cohort of US Caucasians, CLIN SCI, 99(1), 2000, pp. 89-90
Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study
Authors: Laake, K Launonen, V Niederacher, D Gudlaugsdottir, S Seitz, S Rio, P Champeme, MH Bieche, I Birnbaum, D White, G Sztan, M Sever, N Plummer, S Osorio, A Broeks, A Huusko, P Spurr, N Borg, A Cleton-Jansen, AM van't Veer, L Benitez, J Casey, G Peterlin, B Olah, E Varley, J Bignon, YJ Scherneck, S Sigurdardottir, V Lidereau, R Eyfjord, J Beckmann, MW Winqvist, R Skovlund, E Borresen-Dale, AL
Citation: K. Laake et al., Loss of heterozygosity at 11q23.1 and survival in breast cancer: Results of a large European study, GENE CHROM, 25(3), 1999, pp. 212-221
New technologies and DNA resources for high throughput biology
Authors: Spurr, N Darvasi, A Terrett, J Jazwinska, L
Citation: N. Spurr et al., New technologies and DNA resources for high throughput biology, BR MED B, 55(2), 1999, pp. 309-324
European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables
Authors: Launonen, V Laake, K Huusko, P Niederacher, D Beckmann, MW Barkardottir, RB Geirsdottir, EK Gudmundsson, J Rio, P Bignon, YJ Seitz, S Scherneck, S Bieche, I Champeme, MH Birnbaum, D White, G Varley, J Sztan, M Olah, E Osorio, A Benitez, J Spurr, N Velikonja, N Peterlin, B Borg, A Cleton-Jansen, AM Devilee, P Bloigu, R Lidereau, R Borresen-Dale, AL Winqvist, R
Citation: V. Launonen et al., European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables, BR J CANC, 80(5-6), 1999, pp. 879-882
Genetics and epidemiology of hereditary breast cancer
Authors: Devilee, P Barkardottir, RB Bevilacqua, G Bignon, YJ Bishop, T Borg, A Borresen-Dale, AL Chang-Claude, J Easton, D Eyfjord, J Feunteun, J Goldgar, D Haites, N Holm, N Kruse, T Larsson, C Lenoir, G Lidereau, R Nevanlinna, H Ponder, B Scherneck, S Schmitt, F Sobol, H Solomon, E Spurr, N Steel, M Stratton, M Varley, J Vasen, H Vassilaros, S Wagner, T Willems, P Winqvist, R
Citation: P. Devilee et al., Genetics and epidemiology of hereditary breast cancer, BIOM HLTH R, 24, 1998, pp. 339-346
Risultati: 1-12 |