| Year |
Citation |
Score |
| 2020 |
Hasle N, Cooke A, Srivatsan S, Huang H, Stephany JJ, Krieger Z, Jackson D, Tang W, Pendyala S, Monnat RJ, Trapnell C, Hatch EM, Fowler DM. High-throughput, microscope-based sorting to dissect cellular heterogeneity. Molecular Systems Biology. 16: e9442. PMID 32500953 DOI: 10.15252/Msb.20209442 |
0.338 |
|
| 2020 |
Carbone M, Arron ST, Beutler B, Bononi A, Cavenee W, Cleaver JE, Croce CM, D'Andrea A, Foulkes WD, Gaudino G, Groden JL, Henske EP, Hickson ID, Hwang PM, Kolodner RD, ... ... Monnat RJ, et al. Tumour predisposition and cancer syndromes as models to study gene-environment interactions. Nature Reviews. Cancer. PMID 32472073 DOI: 10.1038/S41568-020-0265-Y |
0.402 |
|
| 2019 |
Pellenz S, Phelps M, Tang W, Hovde BT, Sinit RB, Fu W, Li H, Chen E, Monnat RJ. New human chromosomal sites with 'safe harbor' potential for targeted transgene insertion. Human Gene Therapy. PMID 30793977 DOI: 10.1089/Hum.2018.169 |
0.382 |
|
| 2018 |
Juarez E, Chambwe N, Tang W, Mitchell AD, Owen N, Kumari A, Monnat RJ, McCullough AK. An RNAi screen in human cell lines reveals conserved DNA damage repair pathways that mitigate formaldehyde sensitivity. Dna Repair. PMID 30389308 DOI: 10.1016/J.Dnarep.2018.10.002 |
0.426 |
|
| 2018 |
Knijnenburg TA, Wang L, Zimmermann MT, Chambwe N, Gao GF, Cherniack AD, Fan H, Shen H, Way GP, Greene CS, Liu Y, Akbani R, Feng B, Donehower LA, Miller C, ... ... Monnat RJ, et al. Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas. Cell Reports. 23: 239-254.e6. PMID 29617664 DOI: 10.1016/J.Celrep.2018.03.076 |
0.366 |
|
| 2018 |
Mabrey FL, Chien SS, Martins TS, Annis J, Sekizaki TS, Dai J, Beckman RA, Loeb LA, Carson A, Patay B, Blau CA, Oehler VG, Celik SS, Lee S, Monnat RJ, et al. High Throughput Drug Screening of Leukemia Stem Cells Reveals Resistance to Standard Therapies and Sensitivity to Other Agents in Acute Myeloid Leukemia Blood. 132: 180-180. DOI: 10.1182/Blood-2018-180 |
0.311 |
|
| 2017 |
Lebel M, Monnat RJ. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases. Ageing Research Reviews. 41: 82-97. PMID 29146545 DOI: 10.1016/J.Arr.2017.11.003 |
0.398 |
|
| 2017 |
Kamath-Loeb AS, Zavala-van Rankin DG, Flores-Morales J, Emond MJ, Sidorova JM, Carnevale A, Cárdenas-Cortés MD, Norwood TH, Monnat RJ, Loeb LA, Mercado-Celis GE. Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype. Scientific Reports. 7: 44081. PMID 28276523 DOI: 10.1038/Srep44081 |
0.396 |
|
| 2016 |
Fu W, Ligabue A, Rogers KJ, Akey JM, Monnat RJ. Human RECQ Helicase Pathogenic Variants, Population Variation and 'Missing' Diseases. Human Mutation. PMID 27859906 DOI: 10.1002/Humu.23148 |
0.353 |
|
| 2016 |
Kehrli K, Phelps M, Lazarchuk P, Chen E, Monnat R, Sidorova JM. Class I Histone Deacetylase HDAC1 and WRN RECQ Helicase Contribute Additively to Protect Replication Forks upon Hydroxyurea-induced Arrest Journal of Biological Chemistry. 291: 24487-24503. PMID 27672210 DOI: 10.1074/Jbc.M115.708594 |
0.328 |
|
| 2016 |
Tokita M, Kennedy SR, Risques RA, Chun SG, Pritchard C, Oshima J, Liu Y, Bryant-Greenwood PK, Welcsh P, Monnat RJ. Werner syndrome through the lens of tissue and tumour genomics. Scientific Reports. 6: 32038. PMID 27559010 DOI: 10.1038/Srep32038 |
0.301 |
|
| 2016 |
Oshima J, Sidorova JM, Monnat RJ. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions. Ageing Research Reviews. PMID 26993153 DOI: 10.1016/J.Arr.2016.03.002 |
0.426 |
|
| 2016 |
Tang W, Robles AI, Beyer RP, Gray LT, Nguyen GH, Oshima J, Maizels N, Harris CC, Monnat RJ. The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription. Human Molecular Genetics. PMID 26984941 DOI: 10.1093/Hmg/Ddw079 |
0.407 |
|
| 2015 |
Huang JC, Sidorova J, Chien S, Dai J, Logsdon B, Lee S, Monnat RJ, Becker PS. Mini-Chromosome Maintenance (MCM) DNA Helicase Genes Influence Acute Myeloid Leukemia (AML) Replication and Response to Chemotherapy-Induced DNA Damage Blood. 126: 3629-3629. DOI: 10.1182/Blood.V126.23.3629.3629 |
0.38 |
|
| 2014 |
Rogers KJ, Fu W, Akey JM, Monnat RJ. Global and disease-associated genetic variation in the human Fanconi anemia gene family. Human Molecular Genetics. 23: 6815-25. PMID 25104853 DOI: 10.1093/Hmg/Ddu400 |
0.344 |
|
| 2014 |
Nguyen GH, Tang W, Robles AI, Beyer RP, Gray LT, Welsh JA, Schetter AJ, Kumamoto K, Wang XW, Hickson ID, Maizels N, Monnat RJ, Harris CC. Regulation of gene expression by the BLM helicase correlates with the presence of G-quadruplex DNA motifs. Proceedings of the National Academy of Sciences of the United States of America. 111: 9905-10. PMID 24958861 DOI: 10.1073/Pnas.1404807111 |
0.342 |
|
| 2014 |
Pellenz S, Monnat RJ. Identification and analysis of genomic homing endonuclease target sites. Methods in Molecular Biology (Clifton, N.J.). 1123: 245-64. PMID 24510271 DOI: 10.1007/978-1-62703-968-0_16 |
0.385 |
|
| 2014 |
Li H, Monnat RJ. Homing endonuclease target site specificity defined by sequential enrichment and next-generation sequencing of highly complex target site libraries. Methods in Molecular Biology (Clifton, N.J.). 1123: 151-63. PMID 24510267 DOI: 10.1007/978-1-62703-968-0_12 |
0.369 |
|
| 2014 |
Friedman JI, Li H, Monnat RJ. Quantifying the information content of homing endonuclease target sites by single base pair profiling. Methods in Molecular Biology (Clifton, N.J.). 1123: 135-49. PMID 24510266 DOI: 10.1007/978-1-62703-968-0_11 |
0.372 |
|
| 2013 |
Lao VV, Welcsh P, Luo Y, Carter KT, Dzieciatkowski S, Dintzis S, Meza J, Sarvetnick NE, Monnat RJ, Loeb LA, Grady WM. Altered RECQ Helicase Expression in Sporadic Primary Colorectal Cancers. Translational Oncology. 6: 458-69. PMID 23908689 DOI: 10.1593/Tlo.13238 |
0.324 |
|
| 2013 |
Glukhova VA, Tomazela DM, Findlay GD, Monnat RJ, MacCoss MJ. Rapid assessment of RNAi-mediated protein depletion by selected reaction monitoring mass spectrometry. Journal of Proteome Research. 12: 3246-54. PMID 23713831 DOI: 10.1021/Pr400067K |
0.687 |
|
| 2013 |
Metzger MJ, Stoddard BL, Monnat RJ. PARP-mediated repair, homologous recombination, and back-up non-homologous end joining-like repair of single-strand nicks. Dna Repair. 12: 529-34. PMID 23684799 DOI: 10.1016/J.Dnarep.2013.04.004 |
0.367 |
|
| 2013 |
Hughes BT, Sidorova J, Swanger J, Monnat RJ, Clurman BE. Essential role for Cdk2 inhibitory phosphorylation during replication stress revealed by a human Cdk2 knockin mutation. Proceedings of the National Academy of Sciences of the United States of America. 110: 8954-9. PMID 23671119 DOI: 10.1073/Pnas.1302927110 |
0.328 |
|
| 2013 |
Berti M, Ray Chaudhuri A, Thangavel S, Gomathinayagam S, Kenig S, Vujanovic M, Odreman F, Glatter T, Graziano S, Mendoza-Maldonado R, Marino F, Lucic B, Biasin V, Gstaiger M, Aebersold R, ... ... Monnat RJ, et al. Human RECQ1 promotes restart of replication forks reversed by DNA topoisomerase I inhibition. Nature Structural & Molecular Biology. 20: 347-54. PMID 23396353 DOI: 10.1038/Nsmb.2501 |
0.376 |
|
| 2013 |
Sidorova JM, Kehrli K, Mao F, Monnat R. Distinct functions of human RECQ helicases WRN and BLM in replication fork recovery and progression after hydroxyurea-induced stalling Dna Repair. 12: 128-139. PMID 23253856 DOI: 10.1016/J.Dnarep.2012.11.005 |
0.438 |
|
| 2012 |
Duxin JP, Moore HR, Sidorova J, Karanja K, Honaker Y, Dao B, Piwnica-Worms H, Campbell JL, Monnat RJ, Stewart SA. Okazaki fragment processing-independent role for human Dna2 enzyme during DNA replication. The Journal of Biological Chemistry. 287: 21980-91. PMID 22570476 DOI: 10.1074/Jbc.M112.359018 |
0.425 |
|
| 2012 |
Li H, Ulge UY, Hovde BT, Doyle LA, Monnat RJ. Comprehensive homing endonuclease target site specificity profiling reveals evolutionary constraints and enables genome engineering applications. Nucleic Acids Research. 40: 2587-98. PMID 22121229 DOI: 10.1093/Nar/Gkr1072 |
0.378 |
|
| 2011 |
Ulge UY, Baker DA, Monnat RJ. Comprehensive computational design of mCreI homing endonuclease cleavage specificity for genome engineering. Nucleic Acids Research. 39: 4330-9. PMID 21288879 DOI: 10.1093/Nar/Gkr022 |
0.345 |
|
| 2010 |
Monnat RJ. Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology. Seminars in Cancer Biology. 20: 329-39. PMID 20934517 DOI: 10.1016/J.Semcancer.2010.10.002 |
0.387 |
|
| 2010 |
Mao FJ, Sidorova JM, Lauper JM, Emond MJ, Monnat RJ. The human WRN and BLM RecQ helicases differentially regulate cell proliferation and survival after chemotherapeutic DNA damage. Cancer Research. 70: 6548-55. PMID 20663905 DOI: 10.1158/0008-5472.Can-10-0475 |
0.407 |
|
| 2010 |
Thangavel S, Mendoza-Maldonado R, Tissino E, Sidorova JM, Yin J, Wang W, Monnat RJ, Falaschi A, Vindigni A. Human RECQ1 and RECQ4 helicases play distinct roles in DNA replication initiation. Molecular and Cellular Biology. 30: 1382-96. PMID 20065033 DOI: 10.1128/Mcb.01290-09 |
0.398 |
|
| 2010 |
Dhillon KK, Sidorova JM, Albertson TM, Anderson JB, Ladiges WC, Rabinovitch PS, Preston BD, Monnat RJ. Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase. Dna Repair. 9: 11-22. PMID 19896421 DOI: 10.1016/J.Dnarep.2009.09.013 |
0.361 |
|
| 2009 |
Sidorova JM, Li N, Schwartz DC, Folch A, Monnat RJ. Microfluidic-assisted analysis of replicating DNA molecules. Nature Protocols. 4: 849-61. PMID 19444242 DOI: 10.1038/Nprot.2009.54 |
0.358 |
|
| 2009 |
Rey L, Sidorova JM, Puget N, Boudsocq F, Biard DS, Monnat RJ, Cazaux C, Hoffmann JS. Human DNA polymerase eta is required for common fragile site stability during unperturbed DNA replication. Molecular and Cellular Biology. 29: 3344-54. PMID 19380493 DOI: 10.1128/Mcb.00115-09 |
0.432 |
|
| 2009 |
McConnell Smith A, Takeuchi R, Pellenz S, Davis L, Maizels N, Monnat RJ, Stoddard BL. Generation of a nicking enzyme that stimulates site-specific gene conversion from the I-AniI LAGLIDADG homing endonuclease. Proceedings of the National Academy of Sciences of the United States of America. 106: 5099-104. PMID 19276110 DOI: 10.1073/Pnas.0810588106 |
0.414 |
|
| 2009 |
Li H, Pellenz S, Ulge U, Stoddard BL, Monnat RJ. Generation of single-chain LAGLIDADG homing endonucleases from native homodimeric precursor proteins. Nucleic Acids Research. 37: 1650-62. PMID 19153140 DOI: 10.1093/Nar/Gkp004 |
0.429 |
|
| 2008 |
Loeb LA, Monnat RJ. DNA polymerases and human disease Nature Reviews Genetics. 9: 594-604. PMID 18626473 DOI: 10.1038/Nrg2345 |
0.404 |
|
| 2008 |
Berkovich E, Monnat RJ, Kastan MB. Assessment of protein dynamics and DNA repair following generation of DNA double-strand breaks at defined genomic sites. Nature Protocols. 3: 915-22. PMID 18451799 DOI: 10.1038/Nprot.2008.54 |
0.439 |
|
| 2008 |
Sidorova JM, Li N, Folch A, Monnat RJ. The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest. Cell Cycle (Georgetown, Tex.). 7: 796-807. PMID 18250621 DOI: 10.4161/Cc.7.6.5566 |
0.432 |
|
| 2007 |
Eklund JL, Ulge UY, Eastberg J, Monnat RJ. Altered target site specificity variants of the I-PpoI His-Cys box homing endonuclease. Nucleic Acids Research. 35: 5839-50. PMID 17720708 DOI: 10.1093/Nar/Gkm624 |
0.383 |
|
| 2007 |
Eastberg JH, Eklund J, Monnat R, Stoddard BL. Mutability of an HNH nuclease imidazole general base and exchange of a deprotonation mechanism. Biochemistry. 46: 7215-25. PMID 17516660 DOI: 10.1021/Bi700418D |
0.328 |
|
| 2007 |
Berkovich E, Monnat RJ, Kastan MB. Roles of ATM and NBS1 in chromatin structure modulation and DNA double-strand break repair. Nature Cell Biology. 9: 683-90. PMID 17486112 DOI: 10.1038/Ncb1599 |
0.417 |
|
| 2007 |
Kudlow BA, Kennedy BK, Monnat RJ. Werner and Hutchinson-Gilford progeria syndromes: mechanistic basis of human progeroid diseases. Nature Reviews. Molecular Cell Biology. 8: 394-404. PMID 17450177 DOI: 10.1038/Nrm2161 |
0.355 |
|
| 2007 |
Volná P, Jarjour J, Baxter S, Roffler SR, Monnat RJ, Stoddard BL, Scharenberg AM. Flow cytometric analysis of DNA binding and cleavage by cell surface-displayed homing endonucleases. Nucleic Acids Research. 35: 2748-58. PMID 17426121 DOI: 10.1093/Nar/Gkm182 |
0.395 |
|
| 2007 |
Dhillon KK, Sidorova J, Saintigny Y, Poot M, Gollahon K, Rabinovitch PS, Monnat RJ. Functional role of the Werner syndrome RecQ helicase in human fibroblasts. Aging Cell. 6: 53-61. PMID 17266675 DOI: 10.1111/J.1474-9726.2006.00260.X |
0.413 |
|
| 2006 |
Ashworth J, Havranek JJ, Duarte CM, Sussman D, Monnat RJ, Stoddard BL, Baker D. Computational redesign of endonuclease DNA binding and cleavage specificity. Nature. 441: 656-9. PMID 16738662 DOI: 10.1038/Nature04818 |
0.37 |
|
| 2005 |
Scharenberg AM, Rawlings DJ, Monnat RJ, Stoddard BL. 1048. Engineering and Development of I-AniI Homing Endonucleases for Gene Correction Applications Molecular Therapy. 11. DOI: 10.1016/J.Ymthe.2005.07.595 |
0.392 |
|
| 2004 |
Sussman D, Chadsey M, Fauce S, Engel A, Bruett A, Monnat R, Stoddard BL, Seligman LM. Isolation and characterization of new homing endonuclease specificities at individual target site positions. Journal of Molecular Biology. 342: 31-41. PMID 15313605 DOI: 10.1016/J.Jmb.2004.07.031 |
0.403 |
|
| 2004 |
Swanson C, Saintigny Y, Emond MJ, Monnat RJ. The Werner syndrome protein has separable recombination and survival functions. Dna Repair. 3: 475-82. PMID 15084309 DOI: 10.1016/J.Dnarep.2004.01.002 |
0.419 |
|
| 2004 |
Monnat RJ, Saintigny Y. Werner syndrome protein--unwinding function to explain disease. Science of Aging Knowledge Environment : Sage Ke. 2004: re3. PMID 15056797 DOI: 10.1126/Sageke.2004.13.Re3 |
0.385 |
|
| 2003 |
Grandori C, Wu KJ, Fernandez P, Ngouenet C, Grim J, Clurman BE, Moser MJ, Oshima J, Russell DW, Swisshelm K, Frank S, Amati B, Dalla-Favera R, Monnat RJ. Werner syndrome protein limits MYC-induced cellular senescence Genes and Development. 17: 1569-1574. PMID 12842909 DOI: 10.1101/Gad.1100303 |
0.377 |
|
| 2003 |
Chevalier B, Turmel M, Lemieux C, Monnat RJ, Stoddard BL. Flexible DNA target site recognition by divergent homing endonuclease isoschizomers I-CreI and I-MsoI. Journal of Molecular Biology. 329: 253-69. PMID 12758074 DOI: 10.1016/S0022-2836(03)00447-9 |
0.418 |
|
| 2002 |
Chevalier BS, Kortemme T, Chadsey MS, Baker D, Monnat RJ, Stoddard BL. Design, activity, and structure of a highly specific artificial endonuclease. Molecular Cell. 10: 895-905. PMID 12419232 DOI: 10.1016/S1097-2765(02)00690-1 |
0.391 |
|
| 2002 |
Saintigny Y, Makienko K, Swanson C, Emond MJ, Monnat RJ. Homologous recombination resolution defect in werner syndrome. Molecular and Cellular Biology. 22: 6971-8. PMID 12242278 DOI: 10.1128/Mcb.22.20.6971-6978.2002 |
0.449 |
|
| 2002 |
Colgin LM, Hackmann AF, Emond MJ, Monnat RJ. The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage. Proceedings of the National Academy of Sciences of the United States of America. 99: 1437-42. PMID 11818556 DOI: 10.1073/Pnas.032655699 |
0.346 |
|
| 2001 |
Prince PR, Emond MJ, Monnat RJ. Loss of Werner syndrome protein function promotes aberrant mitotic recombination. Genes & Development. 15: 933-8. PMID 11316787 DOI: 10.1101/Gad.877001 |
0.332 |
|
| 2001 |
Chevalier BS, Monnat RJ, Stoddard BL. The homing endonuclease I-CreI uses three metals, one of which is shared between the two active sites. Nature Structural Biology. 8: 312-6. PMID 11276249 DOI: 10.1038/86181 |
0.333 |
|
| 2000 |
Galburt EA, Chadsey MS, Jurica MS, Chevalier BS, Erho D, Tang W, Monnat RJ, Stoddard BL. Conformational changes and cleavage by the homing endonuclease I-PpoI: a critical role for a leucine residue in the active site. Journal of Molecular Biology. 300: 877-87. PMID 10891275 DOI: 10.1006/Jmbi.2000.3874 |
0.412 |
|
| 2000 |
Moser MJ, Kamath-Loeb AS, Jacob JE, Bennett SE, Oshima J, Monnat RJ. WRN helicase expression in Werner syndrome cell lines Nucleic Acids Research. 28: 648-654. PMID 10606667 DOI: 10.1093/Nar/28.2.648 |
0.391 |
|
| 1999 |
Prince PR, Ogburn CE, Moser MJ, Emond MJ, Martin GM, Monnat RJ. Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines. Human Genetics. 105: 132-8. PMID 10480367 DOI: 10.1007/S004399900078 |
0.346 |
|
| 1999 |
Colgin LM, Hackmann AF, Monnat RJ. Different somatic and germline HPRT1 mutations promote use of a common, cryptic intron 1 splice site. Mutations in brief no. 246. Online Human Mutation. 13: 504-505. PMID 10408785 DOI: 10.1002/(Sici)1098-1004(1999)13:6<504::Aid-Humu15>3.0.Co;2-6 |
0.336 |
|
| 1999 |
Moser MJ, Oshima J, Monnat RJ. WRN mutations in Werner syndrome Human Mutation. 13: 271-279. PMID 10220139 DOI: 10.1002/(Sici)1098-1004(1999)13:4<271::Aid-Humu2>3.0.Co;2-Q |
0.343 |
|
| 1999 |
Monnat RJ, Hackmann AFM, Cantrell MA. Generation of highly site-specific DNA double-strand breaks in human cells by the homing endonucleases I-PpoI and I-CreI Biochemical and Biophysical Research Communications. 255: 88-93. PMID 10082660 DOI: 10.1006/Bbrc.1999.0152 |
0.437 |
|
| 1998 |
Jurica MS, Monnat RJ, Stoddard BL. DNA recognition and cleavage by the LAGLIDADG homing endonuclease I-Crel Molecular Cell. 2: 469-476. PMID 9809068 DOI: 10.1016/S1097-2765(00)80146-X |
0.383 |
|
| 1998 |
Argast GM, Stephens KM, Emond MJ, Monnat RJ. I-PpoI and I-CreI homing site sequence degeneracy determined by random mutagenesis and sequential in vitro enrichment. Journal of Molecular Biology. 280: 345-53. PMID 9665841 DOI: 10.1006/Jmbi.1998.1886 |
0.324 |
|
| 1998 |
Flick KE, Jurica MS, Monnat RJ, Stoddard BL. DNA binding and cleavage by the nuclear intron-encoded homing endonuclease I-Ppol Nature. 394: 96-101. PMID 9665136 DOI: 10.1038/27952 |
0.389 |
|
| 1997 |
Heath PJ, Stephens KM, Monnat RJ, Stoddard BL. The structure of I-CreI, a group I intron-encoded homing endonuclease Nature Structural Biology. 4: 468-476. PMID 9187655 DOI: 10.1038/Nsb0697-468 |
0.378 |
|
| 1997 |
Brooks-Wilson AR, Emond MJ, Monnat RJ. Unexpectedly low loss of heterozygosity in genetically unstable Werner syndrome cell lines. Genes, Chromosomes & Cancer. 18: 133-42. PMID 9115963 DOI: 10.1002/(Sici)1098-2264(199702)18:2<133::Aid-Gcc8>3.0.Co;2-3 |
0.333 |
|
| 1996 |
Martin GM, Ogburn CE, Colgin LM, Gown AM, Edland SD, Monnat RJ. Somatic mutations are frequent and increase with age in human kidney epithelial cells Human Molecular Genetics. 5: 215-221. PMID 8824877 DOI: 10.1093/Hmg/5.2.215 |
0.316 |
|
| 1993 |
Liu PK, Trujillo JM, Monnat RJ. Spectrum of spontaneous mutation in animal cells containing an aphidicolin-resistant DNA polymerase alpha. Mutation Research. 288: 229-36. PMID 7688082 DOI: 10.1016/0027-5107(93)90089-X |
0.352 |
|
| 1992 |
Monnat RJ, Chiaverotti TA, Hackmann AFM, Maresh GA. Molecular structure and genetic stability of human hypoxanthine phosphoribosyltransferase (HPRT) gene duplications Genomics. 13: 788-796. PMID 1639405 DOI: 10.1016/0888-7543(92)90154-K |
0.368 |
|
| 1992 |
Monnat RJ, Hackmann AFM, Chiaverotti TA. Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions Genomics. 13: 777-787. PMID 1639404 DOI: 10.1016/0888-7543(92)90153-J |
0.407 |
|
| 1991 |
Monnat RJ, Hackmann AFM, Chiaverotti TA, Maresh GA. Molecular analysis of human hprt gene deletions and duplications Advances in Experimental Medicine and Biology. 309: 113-120. PMID 1781354 DOI: 10.1007/978-1-4615-7703-4_25 |
0.353 |
|
| 1990 |
Fukuchi K, Tanaka K, Kumahara Y, Marumo K, Pride MB, Martin GM, Monnat RJ. Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients. Human Genetics. 84: 249-52. PMID 2303247 DOI: 10.1007/Bf00200569 |
0.311 |
|
| 1989 |
Fukuchi K, Martin GM, Monnat RJ. Mutator phenotype of Werner syndrome is characterized by extensive deletions Proceedings of the National Academy of Sciences of the United States of America. 86: 5893-5897. PMID 2762303 DOI: 10.1073/Pnas.86.15.5893 |
0.371 |
|
| 1988 |
Mita S, Monnat RJ, Loeb LA. Direct selection of mutations in the human mitochondrial tRNAThr gene: reversion of an 'uncloneable' phenotype Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 199: 183-190. PMID 3362158 DOI: 10.1016/0027-5107(88)90244-8 |
0.367 |
|
| 1986 |
Monnat RJ, Reay DT. Nucleotide sequence identity of mitochondrial DNA from different human tissues Gene. 43: 205-211. PMID 3744049 DOI: 10.1016/0378-1119(86)90208-8 |
0.329 |
|
| 1985 |
Monnat RJ, Loeb LA. Nucleotide sequence preservation of human mitochondrial DNA Proceedings of the National Academy of Sciences of the United States of America. 82: 2895-2899. PMID 2986144 DOI: 10.1073/Pnas.82.9.2895 |
0.362 |
|
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