| Year |
Citation |
Score |
| 2008 |
Boyer JC, Hawk JD, Stefanovic L, Farber RA. Sequence-dependent effect of interruptions on microsatellite mutation rate in mismatch repair-deficient human cells. Mutation Research. 640: 89-96. PMID 18242644 DOI: 10.1016/J.Mrfmmm.2007.12.005 |
0.623 |
|
| 2007 |
Lehner KR, Stone MM, Farber RA, Petes TD. Ninety-six haploid yeast strains with individual disruptions of open reading frames between YOR097C and YOR192C, constructed for the Saccharomyces genome deletion project, have an additional mutation in the mismatch repair gene MSH3. Genetics. 177: 1951-3. PMID 17947417 DOI: 10.1534/Genetics.107.079368 |
0.447 |
|
| 2006 |
Fan H, Civalier C, Booker JK, Gulley ML, Prior TW, Farber RA. Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction. The Journal of Molecular Diagnostics : Jmd. 8: 277-81. PMID 16645216 DOI: 10.2353/Jmoldx.2006.050066 |
0.48 |
|
| 2005 |
Fan H, Booker JK, McCandless SE, Shashi V, Fleming A, Farber RA. Mosaicism for an FMR1 gene deletion in a fragile X female. American Journal of Medical Genetics. Part A. 136: 214-7. PMID 15940701 DOI: 10.1002/Ajmg.A.30807 |
0.512 |
|
| 2005 |
Hawk JD, Stefanovic L, Boyer JC, Petes TD, Farber RA. Variation in efficiency of DNA mismatch repair at different sites in the yeast genome. Proceedings of the National Academy of Sciences of the United States of America. 102: 8639-43. PMID 15932942 DOI: 10.1073/Pnas.0503415102 |
0.542 |
|
| 2005 |
Hatch SB, Lightfoot HM, Garwacki CP, Moore DT, Calvo BF, Woosley JT, Sciarrotta J, Funkhouser WK, Farber RA. Microsatellite instability testing in colorectal carcinoma: Choice of markers affects sensitivity of detection of mismatch repair-deficient tumors Clinical Cancer Research. 11: 2180-2187. PMID 15788665 DOI: 10.1158/1078-0432.Ccr-04-0234 |
0.699 |
|
| 2004 |
Hatch SB, Farber RA. Mutation rates in the complex microsatellite MYCL1 and related simple repeats in cultured human cells. Mutation Research. 545: 117-26. PMID 14698421 DOI: 10.1016/J.Mrfmmm.2003.09.015 |
0.773 |
|
| 2003 |
Yamada NA, Parker JM, Farber RA. Mutation frequency analysis of mononucleotide and dinucleotide repeats after oxidative stress. Environmental and Molecular Mutagenesis. 42: 75-84. PMID 12929119 DOI: 10.1002/Em.10179 |
0.782 |
|
| 2003 |
Yamada NA, Castro A, Farber RA. Variation in the extent of microsatellite instability in human cell lines with defects in different mismatch repair genes. Mutagenesis. 18: 277-82. PMID 12714694 DOI: 10.1093/Mutage/18.3.277 |
0.786 |
|
| 2002 |
Yamada NA, Farber RA. Induction of a low level of microsatellite instability by overexpression of DNA polymerase Beta. Cancer Research. 62: 6061-4. PMID 12414629 |
0.786 |
|
| 2002 |
Boyer JC, Yamada NA, Roques CN, Hatch SB, Riess K, Farber RA. Sequence dependent instability of mononucleotide microsatellites in cultured mismatch repair proficient and deficient mammalian cells. Human Molecular Genetics. 11: 707-13. PMID 11912186 DOI: 10.1093/Hmg/11.6.707 |
0.727 |
|
| 2002 |
Yamada NA, Smith GA, Castro A, Roques CN, Boyer JC, Farber RA. Relative rates of insertion and deletion mutations in dinucleotide repeats of various lengths in mismatch repair proficient mouse and mismatch repair deficient human cells. Mutation Research. 499: 213-25. PMID 11827714 DOI: 10.1016/S0027-5107(01)00282-2 |
0.788 |
|
| 2001 |
Roques CN, Boyer JC, Farber RA. Microsatellite mutation rates are equivalent in normal and telomerase-immortalized human fibroblasts. Cancer Research. 61: 8405-7. PMID 11731418 |
0.554 |
|
| 1999 |
Lee JS, Hanford MG, Genova JL, Farber RA. Relative stabilities of dinucleotide and tetranucleotide repeats in cultured mammalian cells. Human Molecular Genetics. 8: 2567-72. PMID 10556306 DOI: 10.1093/Hmg/8.13.2567 |
0.666 |
|
| 1999 |
Twerdi CD, Boyer JC, Farber RA. Relative rates of insertion and deletion mutations in a microsatellite sequence in cultured cells. Proceedings of the National Academy of Sciences of the United States of America. 96: 2875-9. PMID 10077604 DOI: 10.1073/Pnas.96.6.2875 |
0.655 |
|
| 1998 |
Boyer JC, Risinger JI, Farber RA. Stability of microsatellites in myeloid neoplasias. Cancer Genetics and Cytogenetics. 106: 54-61. PMID 9772910 DOI: 10.1016/S0165-4608(98)00043-0 |
0.467 |
|
| 1998 |
Boyer JC, Farber RA. Mutation rate of a microsatellite sequence in normal human fibroblasts. Cancer Research. 58: 3946-9. PMID 9731507 |
0.592 |
|
| 1998 |
Hanford MG, Rushton BC, Gowen LC, Farber RA. Microsatellite mutation rates in cancer cell lines deficient or proficient in mismatch repair. Oncogene. 16: 2389-93. PMID 9620556 DOI: 10.1038/Sj.Onc.1201751 |
0.642 |
|
| 1996 |
Riedinger KL, Hanford MG, Farber RA. Induction of frameshift mutations in cultured mammalian cells within a transfected sequence containing a poly(dC-dA).poly(dT-dG) microsatellite. Environmental and Molecular Mutagenesis. 28: 276-83. PMID 8908187 DOI: 10.1002/(Sici)1098-2280(1996)28:3<276::Aid-Em12>3.0.Co;2-C |
0.548 |
|
| 1995 |
King SA, Wilson SJ, Farber RA, Kaufmann WK, Cordeiro-Stone M. Xeroderma pigmentosum variant: generation and characterization of fibroblastic cell lines transformed with SV40 large T antigen. Experimental Cell Research. 217: 100-8. PMID 7867708 DOI: 10.1006/Excr.1995.1068 |
0.404 |
|
| 1995 |
Heim RA, Kam-Morgan LN, Binnie CG, Corns DD, Cayouette MC, Farber RA, Aylsworth AS, Silverman LM, Luce MC. Distribution of 13 truncating mutations in the neurofibromatosis 1 gene. Human Molecular Genetics. 4: 975-81. PMID 7655472 DOI: 10.1093/Hmg/4.6.975 |
0.522 |
|
| 1994 |
Farber RA, Petes TD, Dominska M, Hudgens SS, Liskay RM. Instability of simple sequence repeats in a mammalian cell line Human Molecular Genetics. 3: 253-256. PMID 8004091 DOI: 10.1093/Hmg/3.2.253 |
0.513 |
|
| 1992 |
Neuman WL, Le Beau MM, Farber RA, Lindgren V, Westbrook CA. Somatic cell hybrid mapping of human chromosome band 5q31: a region important to hematopoiesis. Cytogenetics and Cell Genetics. 61: 103-6. PMID 1395713 DOI: 10.1159/000133381 |
0.351 |
|
| 1992 |
Neuman WL, Rubin CM, Rios RB, Larson RA, Le Beau MM, Rowley JD, Vardiman JW, Schwartz JL, Farber RA. Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders. Blood. 79: 1501-10. PMID 1347709 DOI: 10.1182/Blood.V79.6.1501.Bloodjournal7961501 |
0.337 |
|
| 1988 |
Farber RA, Phalen T, Neuman WL, Le Beau MM, Wasmuth JJ, Dobbs M. An anonymous DNA segment pTP5E (D5S70) maps to the long arm of chromosome 5 and identifies a Taq I polymorphism. Nucleic Acids Research. 16: 2360. PMID 2895914 DOI: 10.1093/Nar/16.5.2360 |
0.333 |
|
| 1986 |
Farber RA, Zielinski D. Assignment of a processed mouse Aprt pseudogene to the same chromosome as the functional gene. Cytogenetics and Cell Genetics. 42: 198-201. PMID 2875850 DOI: 10.1159/000132278 |
0.365 |
|
| 1985 |
Samuelson LC, Farber RA. Cytological localization of adenosine kinase, nucleoside phosphorylase-1, and esterase-10 genes on mouse chromosome 14. Somatic Cell and Molecular Genetics. 11: 157-65. PMID 2984788 DOI: 10.1007/Bf01534704 |
0.551 |
|
| 1983 |
Lindgren V, Farber RA. Chromosome replication in normal and transformed human lymphocytes. Cancer Genetics and Cytogenetics. 9: 71-9. PMID 6601510 DOI: 10.1016/0165-4608(83)90027-4 |
0.316 |
|
| 1983 |
Eves EM, Farber RA. Expression of recessive Aprt- mutations in mouse CAK cells resulting from chromosome loss and duplication. Somatic Cell Genetics. 9: 771-8. PMID 6581543 DOI: 10.1007/Bf01539479 |
0.495 |
|
| 1983 |
Dubnick M, Chou J, Petes TD, Farber RA. Relationships among DNA sequences of the 1.3 kb EcoRI family of mouse DNA Journal of Molecular Evolution. 19: 115-121. PMID 6100837 DOI: 10.1007/Bf02300749 |
0.365 |
|
| 1982 |
Lindgren V, Farber RA. Chromosome replication in aging human diploid fibroblasts. Experimental Cell Research. 142: 301-7. PMID 7173326 DOI: 10.1016/0014-4827(82)90371-8 |
0.35 |
|
| 1981 |
Eves EM, Farber RA. Chromosome segregation is frequently associated with the expression of recessive mutations in mouse cells. Proceedings of the National Academy of Sciences of the United States of America. 78: 1768-72. PMID 6940188 DOI: 10.1073/Pnas.78.3.1768 |
0.501 |
|
| 1980 |
Farber RA. Patterns of replication of human chromosomes in human x mouse hybrids with different chromosomal compositions. Cytogenetics and Cell Genetics. 27: 246-53. PMID 7438785 DOI: 10.1159/000131493 |
0.334 |
|
| 1979 |
Farber RA, Davidson RL. Maintenance of replication patterns in human-mouse hybrids retaining only one human chromosome. Somatic Cell Genetics. 5: 519-28. PMID 227124 DOI: 10.1007/Bf01538885 |
0.337 |
|
| 1978 |
Farber RA, Davidson RL. Altered pattern of replication of human chromosomes in a human fibroblast-mouse cell hybrid. Proceedings of the National Academy of Sciences of the United States of America. 75: 1470-4. PMID 274734 DOI: 10.1073/Pnas.75.3.1470 |
0.347 |
|
| Show low-probability matches. |
