Year |
Citation |
Score |
2005 |
Tan E, Wong J, Nguyen D, Zhang Y, Erwin B, Van Ness LK, Baker SM, Galas DJ, Niemz A. Isothermal DNA amplification coupled with DNA nanosphere-based colorimetric detection. Analytical Chemistry. 77: 7984-92. PMID 16351146 DOI: 10.1021/Ac051364I |
0.307 |
|
2005 |
Baker SM, Brawley OW, Marks LS. Effects of untreated syphilis in the negro male, 1932 to 1972: a closure comes to the Tuskegee study, 2004. Urology. 65: 1259-62. PMID 15922414 DOI: 10.1016/j.urology.2004.10.023 |
0.328 |
|
2002 |
Qin J, Baker S, Te Riele H, Liskay RM, Arnheim N. Evidence for the lack of mismatch-repair directed antirecombination during mouse meiosis Journal of Heredity. 93: 201-205. PMID 12195036 DOI: 10.1093/Jhered/93.3.201 |
0.596 |
|
2000 |
Shoemaker AR, Haigis KM, Baker SM, Dudley S, Liskay RM, Dove WF. Mlh1 deficiency enhances several phenotypes of Apc(Min)/+ mice. Oncogene. 19: 2774-9. PMID 10851078 DOI: 10.1038/Sj.Onc.1203574 |
0.529 |
|
1999 |
Buermeyer AB, Deschênes SM, Baker SM, Liskay RM. Mammalian DNA mismatch repair. Annual Review of Genetics. 33: 533-64. PMID 10690417 DOI: 10.1146/Annurev.Genet.33.1.533 |
0.575 |
|
1999 |
Woods LM, Hodges CA, Baart E, Baker SM, Liskay M, Hunt PA. Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant mice. The Journal of Cell Biology. 145: 1395-406. PMID 10385520 DOI: 10.1083/Jcb.145.7.1395 |
0.453 |
|
1999 |
Yao X, Buermeyer AB, Narayanan L, Tran D, Baker SM, Prolla TA, Glazer PM, Liskay RM, Arnheim N. Different mutator phenotypes in Mlh1- versus Pms2-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 96: 6850-5. PMID 10359802 DOI: 10.1073/Pnas.96.12.6850 |
0.551 |
|
1999 |
Buermeyer AB, Wilson-Van Patten C, Baker SM, Liskay RM. The human MLH1 cDNA complements DNA mismatch repair defects in Mlh1-deficient mouse embryonic fibroblasts. Cancer Research. 59: 538-41. PMID 9973196 |
0.517 |
|
1998 |
Winter DB, Phung QH, Umar A, Baker SM, Tarone RE, Tanaka K, Liskay RM, Kunkel TA, Bohr VA, Gearhart PJ. Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2. Proceedings of the National Academy of Sciences of the United States of America. 95: 6953-8. PMID 9618520 DOI: 10.1073/Pnas.95.12.6953 |
0.6 |
|
1998 |
Baker SM, Harris AC, Tsao JL, Flath TJ, Bronner CE, Gordon M, Shibata D, Liskay RM. Enhanced intestinal adenomatous polyp formation in Pms2-/-;Min mice. Cancer Research. 58: 1087-9. PMID 9515784 |
0.504 |
|
1998 |
Prolla TA, Baker SM, Harris AC, Tsao JL, Yao X, Bronner CE, Zheng B, Gordon M, Reneker J, Arnheim N, Shibata D, Bradley A, Liskay RM. Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair. Nature Genetics. 18: 276-9. PMID 9500552 DOI: 10.1038/Ng0398-276 |
0.584 |
|
1997 |
Fritzell JA, Narayanan L, Baker SM, Bronner CE, Andrew SE, Prolla TA, Bradley A, Jirik FR, Liskay RM, Glazer PM. Role of DNA mismatch repair in the cytotoxicity of ionizing radiation. Cancer Research. 57: 5143-7. PMID 9371516 |
0.448 |
|
1997 |
Tsao JL, Davis SD, Baker SM, Liskay RM, Shibata D. Intestinal stem cell division and genetic diversity. A computer and experimental analysis. The American Journal of Pathology. 151: 573-9. PMID 9250170 |
0.387 |
|
1997 |
Narayanan L, Fritzell JA, Baker SM, Liskay RM, Glazer PM. Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2. Proceedings of the National Academy of Sciences of the United States of America. 94: 3122-7. PMID 9096356 DOI: 10.1073/Pnas.94.7.3122 |
0.605 |
|
1996 |
Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC, Yao X, Christie DM, Monell C, Arnheim N, Bradley A, Ashley T, Liskay RM. Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nature Genetics. 13: 336-42. PMID 8673133 DOI: 10.1038/ng0796-336 |
0.57 |
|
1995 |
Baker SM, Bronner CE, Zhang L, Plug AW, Robatzek M, Warren G, Elliott EA, Yu J, Ashley T, Arnheim N, Flavell RA, Liskay RM. Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell. 82: 309-19. PMID 7628019 DOI: 10.1016/0092-8674(95)90318-6 |
0.661 |
|
1994 |
Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindblom A. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature. 368: 258-61. PMID 8145827 DOI: 10.1038/368258A0 |
0.473 |
|
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