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Nazumi A. Yamada, Ph.D. - Publications

Affiliations: 
2002 University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Molecular Biology
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13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2008 Elso C, Lu X, Morrison S, Tarver A, Thompson H, Thurkow H, Yamada NA, Stubbs L. Germline translocations in mice: unique tools for analyzing gene function and long-distance regulatory mechanisms. Journal of the National Cancer Institute. Monographs. 91-5. PMID 18648012 DOI: 10.1093/Jncimonographs/Lgn008  0.382
2006 Hinz JM, Nham PB, Yamada NA, Tebbs RS, Salazar EP, Hinz AK, Mohrenweiser HW, Jones IM, Thompson LH. Four human FANCG polymorphic variants show normal biological function in hamster CHO cells. Mutation Research. 602: 34-42. PMID 17010390 DOI: 10.1016/j.mrfmmm.2006.07.008  0.374
2005 Hinz JM, Yamada NA, Salazar EP, Tebbs RS, Thompson LH. Influence of double-strand-break repair pathways on radiosensitivity throughout the cell cycle in CHO cells. Dna Repair. 4: 782-92. PMID 15951249 DOI: 10.1016/j.dnarep.2005.03.005  0.452
2005 Miller KA, Hinz JM, Yamada NA, Thompson LH, Albala JS. Nuclear localization of Rad51B is independent of Rad51C and BRCA2. Mutagenesis. 20: 57-63. PMID 15701685 DOI: 10.1093/mutage/gei011  0.356
2005 Thompson LH, Hinz JM, Yamada NA, Jones NJ. How Fanconi anemia proteins promote the four Rs: Replication, recombination, repair, and recovery Environmental and Molecular Mutagenesis. 45: 128-142. PMID 15668941 DOI: 10.1002/em.20109  0.333
2005 Tebbs RS, Hinz JM, Yamada NA, Wilson JB, Salazar EP, Thomas CB, Jones IM, Jones NJ, Thompson LH. New insights into the Fanconi anemia pathway from an isogenic FancG hamster CHO mutant. Dna Repair. 4: 11-22. PMID 15533833 DOI: 10.1016/j.dnarep.2004.06.013  0.33
2004 Lamerdin JE, Yamada NA, George JW, Souza B, Christian AT, Jones NJ, Thompson LH. Characterization of the hamster FancG/Xrcc9 gene and mutations in CHO UV40 and NM3 Mutagenesis. 19: 237-244. PMID 15123790 DOI: 10.1093/mutage/geh019  0.47
2004 Yamada NA, Hinz JM, Kopf VL, Segalle KD, Thompson LH. XRCC3 ATPase activity is required for normal XRCC3-Rad51C complex dynamics and homologous recombination. The Journal of Biological Chemistry. 279: 23250-4. PMID 15037616 DOI: 10.1074/JBC.M402247200  0.358
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  0.738
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  0.748
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  0.76
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  0.597
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  0.758
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