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Results: 1-7 |
Results: 7
An alternative mode of translation permits production of a variant NBS1 protein from the common Nijmegen breakage syndrome allele
Authors: Maser, RS Zinkel, R Petrini, JHJ
Citation: Rs. Maser et al., An alternative mode of translation permits production of a variant NBS1 protein from the common Nijmegen breakage syndrome allele, NAT GENET, 27(4), 2001, pp. 417-421
Mre11 complex and DNA replication: Linkage to E2F and sites of DNA synthesist
Authors: Maser, RS Mirzoeva, OK Wells, J Olivares, H Williams, BR Zinkel, RA Farnham, PJ Petrini, JHJ
Citation: Rs. Maser et al., Mre11 complex and DNA replication: Linkage to E2F and sites of DNA synthesist, MOL CELL B, 21(17), 2001, pp. 6006-6016
Isolation of Bcl-2 binding proteins that exhibit homology with BAG-1 and suppressor of death domains protein
Authors: Antoku, K Maser, RS Scully, WJ Delach, SM Johnson, DE
Citation: K. Antoku et al., Isolation of Bcl-2 binding proteins that exhibit homology with BAG-1 and suppressor of death domains protein, BIOC BIOP R, 286(5), 2001, pp. 1003-1010
ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway
Authors: Lim, DS Kim, ST Xu, B Maser, RS Lin, JY Petrini, JHJ Kastan, MB
Citation: Ds. Lim et al., ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway, NATURE, 404(6778), 2000, pp. 613
Radiosensitivity in Nijmegen Breakage syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects
Authors: Girard, PM Foray, N Stumm, M Waugh, A Riballo, E Maser, RS Phillips, WP Petrini, J Arlett, CF Jeggo, PA
Citation: Pm. Girard et al., Radiosensitivity in Nijmegen Breakage syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects, CANCER RES, 60(17), 2000, pp. 4881-4888
Analysis of the role of conserved cysteine residues in the Bcl-2 oncoprotein
Authors: Maser, RS Antoku, K Scully, WJ Cho, RL Johnson, DE
Citation: Rs. Maser et al., Analysis of the role of conserved cysteine residues in the Bcl-2 oncoprotein, BIOC BIOP R, 277(1), 2000, pp. 171-178
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder
Authors: Stewart, GS Maser, RS Stankovic, T Bressan, DA Kaplan, MI Jaspers, NGJ Raams, A Byrd, PJ Petrini, JHJ Taylor, AMR
Citation: Gs. Stewart et al., The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder, CELL, 99(6), 1999, pp. 577-587
Risultati: 1-7 |