Authors:
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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
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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:
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:
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:
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
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
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
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:
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