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Results: 1-24 |
Results: 24

Authors: Chitnis, S Monteiro, J Glass, D Apatoff, B Salmon, J Concannon, P Gregersen, PK
Citation: S. Chitnis et al., The role of X-chromosome inactivation in female predisposition to autoimmunity (vol 2, pg 399, 2000), ARTHRITIS R, 3(3), 2001, pp. 399-399

Authors: Argentaro, A Wapelhorst, B Concannon, P Harley, VR
Citation: A. Argentaro et al., Linkage studies of SOX13, the ICA12 autoantigen gene, in families with type 1 diabetes, MOL GEN MET, 72(4), 2001, pp. 356-359

Authors: Concannon, P Gisoldi, E Phillips, S Grossman, R
Citation: P. Concannon et al., Diaper dermatitis: A therapeutic dilemma. Results of a double-blind placebo controlled trial of miconazole nitrate 0.25%, PEDIAT DERM, 18(2), 2001, pp. 149-155

Authors: Concannon, P Levac, K Rawson, R Tennant, B Bensadoun, A
Citation: P. Concannon et al., Seasonal changes in serum leptin, food intake, and body weight in photoentrained woodchucks, AM J P-REG, 281(3), 2001, pp. R951-R959

Authors: Desai-Mehta, A Cerosaletti, KM Concannon, P
Citation: A. Desai-mehta et al., Distinct functional domains of nibrin mediate Mre11 binding, focus formation, and nuclear localization, MOL CELL B, 21(6), 2001, pp. 2184-2191

Authors: Buscemi, G Savio, C Zannini, L Micciche, F Masnada, D Nakanishi, M Tauchi, H Komatsu, K Mizutani, S Khanna, K Chen, P Concannon, P Chessa, L Delia, D
Citation: G. Buscemi et al., Chk2 activation dependence on Nbs1 after DNA damage, MOL CELL B, 21(15), 2001, pp. 5214-5222

Authors: Teraoka, SN Malone, KE Doody, DR Suter, NM Ostrander, EA Daling, JR Concannon, P
Citation: Sn. Teraoka et al., Increased frequency of ATM mutations in breast carcinoma patients with early onset disease and positive family history, CANCER, 92(3), 2001, pp. 479-487

Authors: Cox, NJ Wapelhorst, B Morrison, VA Johnson, L Pinchuk, L Spielman, RS Todd, JA Concannon, P
Citation: Nj. Cox et al., Seven regions of the genome show evidence of linkage to type 1 diabetes ina consensus analysis of 767 multiplex families, AM J HU GEN, 69(4), 2001, pp. 820-830

Authors: Chitnis, S Monteiro, J Glass, D Apatoff, B Salmon, J Concannon, P Gregersen, PK
Citation: S. Chitnis et al., The role of X-chromosome inactivation in female predisposition to autoimmunity, ARTHRITIS R, 2(5), 2000, pp. 399-406

Authors: Horikawa, Y Oda, N Cox, NJ Li, XQ Orho-Melander, M Hara, M Hinokio, Y Lindner, TH Mashima, H Schwarz, PEH del Bosque-Plata, L Horikawa, Y Oda, Y Yoshiuchi, I Colilla, S Polonsky, KS Wei, S Concannon, P Iwasaki, N Schulze, T Baier, LJ Bogardus, C Groop, L Boerwinkle, E Hanis, CL Bell, GI
Citation: Y. Horikawa et al., Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus, NAT GENET, 26(2), 2000, pp. 163-175

Authors: Gatei, M Young, D Cerosaletti, KM Desai-Mehta, A Spring, K Kozlov, S Lavin, MF Gatti, RA Concannon, P Khanna, K
Citation: M. Gatei et al., ATM-dependent phosphorylation of nibrin in response to radiation exposure, NAT GENET, 25(1), 2000, pp. 115-119

Authors: Godbole, A Concannon, P Glasson, M
Citation: A. Godbole et al., Intussusception presenting as profound lethargy, J PAEDIAT C, 36(4), 2000, pp. 392-394

Authors: Wilda, M Demuth, I Concannon, P Sperling, K Hameister, H
Citation: M. Wilda et al., Expression pattern of the Nijmegen breakage syndrome gene, Nbs1, during murine development, HUM MOL GEN, 9(12), 2000, pp. 1739-1744

Authors: Cerosaletti, KM Desai-Mehta, A Yeo, TC Kraakman-van der Zwet, M Zdzienicka, MZ Concannon, P
Citation: Km. Cerosaletti et al., Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation, MUTAGENESIS, 15(3), 2000, pp. 281-286

Authors: Yeo, TC Xia, D Hassouneh, S Yang, XO Sabath, DE Sperling, K Gatti, RA Concannon, P Willerford, DM
Citation: Tc. Yeo et al., V(D)J rearrangement in Nijmegen breakage syndrome, MOL IMMUNOL, 37(18), 2000, pp. 1131-1139

Authors: Vanasse, GJ Concannon, P Willerford, DM
Citation: Gj. Vanasse et al., Somatic versus germline origin of ATM mutations in T-PLL - Response, BLOOD, 96(1), 2000, pp. 376-376

Authors: Hiel, JA Weemaes, CM van den Heuvel, LP van Engelen, BG Gabreels, FJ Smeets, DF van der Burgt, I Chrzanovska, KH Bernatowska, E Krajewska-Walasek, M Bialecka, M Abramczuk, D Gregorek, H Michalkiewicz, I Perek, D Midro, AT Seemanova, E Belohradsky, BH Solder, B Barbi, G Wegner, RD Sperling, K Dixon, J Maraschio, P Marseglia, GL Green, A Taylor, AM Der Kaloustian, VM Komatsu, K Matsuura, S Conley, ME Concannon, P Gatti, RA
Citation: Ja. Hiel et al., Nijmegen breakage syndrome, ARCH DIS CH, 82(5), 2000, pp. 400-406

Authors: Gatti, RA Tward, A Concannon, P
Citation: Ra. Gatti et al., Cancer risk in ATM heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations, MOL GEN MET, 68(4), 1999, pp. 419-423

Authors: Cox, NJ Frigge, M Nicolae, DL Concannon, P Hanis, CL Bell, GI Kong, A
Citation: Nj. Cox et al., Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans, NAT GENET, 21(2), 1999, pp. 213-215

Authors: Vissinga, CS Yeo, TC Woessner, J Massa, HF Wilson, RK Trask, BJ Concannon, P
Citation: Cs. Vissinga et al., Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome, CYTOG C GEN, 87(1-2), 1999, pp. 80-84

Authors: Udar, NS Xu, SB Bay, JO Dandekar, SS Patel, N Chan, XG Liang, TY Uhrhammer, N Klisak, I Shizuya, H Yang, HM Samara, G Nelissen, J Sawicki, M Concannon, P Gatti, RA
Citation: Ns. Udar et al., Physical map of the region surrounding the Ataxia-Telangiectasia gene on human chromosome 11q22-23, NEUROPEDIAT, 30(4), 1999, pp. 176-180

Authors: Brawley, JV Concannon, P
Citation: Jv. Brawley et P. Concannon, Systematic mutagenesis of TCR complementarity-determining region 3 residues: A single conservative substitution dramatically improves response to both multiple HLA-DR alleles and peptide variants, J IMMUNOL, 163(9), 1999, pp. 4946-4952

Authors: Vanasse, GJ Concannon, P Willerford, DM
Citation: Gj. Vanasse et al., Regulated genomic instability and neoplasia in the lymphoid lineage, BLOOD, 94(12), 1999, pp. 3997-4010

Authors: Teraoka, SN Telatar, M Becker-Catania, S Liang, T Onengut, S Tolun, A Chessa, L Sanal, O Bernatowska, E Gatti, RA Concannon, P
Citation: Sn. Teraoka et al., Splicing defects in the ataxia-telangiectasia gene, ATM: Underlying mutations and consequences, AM J HU GEN, 64(6), 1999, pp. 1617-1631
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