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Results: 1-14 |
Results: 14

Authors: Chevalier, BS Monnat, RJ Stoddard, BL
Citation: Bs. Chevalier et al., The LAGLIDADG homing endonuclease I-CreI shares three metals between two active sites (vol 8, pg 312, 2001), NAT ST BIOL, 8(5), 2001, pp. 473-473

Authors: Chevalier, BS Monnat, RJ Stoddard, BL
Citation: Bs. Chevalier et al., The homing endonuclease I-CreI uses three metals, one of which ss shared between the two active sites, NAT ST BIOL, 8(4), 2001, pp. 312-316

Authors: Prince, PR Emond, MJ Monnat, RJ
Citation: Pr. Prince et al., Loss of Werner syndrome protein function promotes aberrant mitotic recombination, GENE DEV, 15(8), 2001, pp. 933-938

Authors: Monnat, RJ
Citation: Rj. Monnat, Cancer pathogenesis in the human RecQ helicase deficiency syndromes, GANN MG CAN, (49), 2001, pp. 83-94

Authors: Moser, MJ Kamath-Loeb, AS Jacob, JE Bennett, SE Oshima, J Monnat, RJ
Citation: Mj. Moser et al., WRN helicase expression in Werner syndrome cell lines, NUCL ACID R, 28(2), 2000, pp. 648-654

Authors: Flory, MR Moser, MJ Monnat, RJ Davis, TN
Citation: Mr. Flory et al., Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin, P NAS US, 97(11), 2000, pp. 5919-5923

Authors: Galburt, EA Chadsey, MS Jurica, MS Chevalier, BS Erho, D Tang, WL Monnat, RJ Stoddard, BL
Citation: Ea. Galburt et al., Conformational changes and cleavage by the homing endonuclease I-Ppol: A critical role for a leucine residue in the active site, J MOL BIOL, 300(4), 2000, pp. 877-887

Authors: Moser, MJ Bigbee, WL Grant, SG Emond, MJ Langlois, RG Jensen, RH Oshima, J Monnat, RJ
Citation: Mj. Moser et al., Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes, CANCER RES, 60(9), 2000, pp. 2492-2496

Authors: Galburt, EA Chevalier, B Tang, WL Jurica, MS Flick, KE Monnat, RJ Stoddard, BL
Citation: Ea. Galburt et al., A novel endonuclease mechanism directly visualized for I-Ppol, NAT ST BIOL, 6(12), 1999, pp. 1096-1099

Authors: Moser, MJ Oshima, J Monnat, RJ
Citation: Mj. Moser et al., WRN mutations in Werner syndrome (vol 13, pg 271, 1998), HUM MUTAT, 14(1), 1999, pp. 84-85

Authors: Moser, MJ Oshima, J Monnat, RJ
Citation: Mj. Moser et al., WRN mutations in Werner syndrome, HUM MUTAT, 13(4), 1999, pp. 271-279

Authors: Prince, PR Ogburn, CE Moser, MJ Emond, MJ Martin, GM Monnat, RJ
Citation: Pr. Prince et al., Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines, HUM GENET, 105(1-2), 1999, pp. 132-138

Authors: Monnat, RJ
Citation: Rj. Monnat, Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race, CANCER, 86(4), 1999, pp. 728-729

Authors: Monnat, RJ Hackmann, AFM Cantrell, MA
Citation: Rj. Monnat et al., Generation of highly site-specific DNA double-strand breaks in human cellsby the homing endonucleases I-PpoI and I-CreI, BIOC BIOP R, 255(1), 1999, pp. 88-93
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