Year |
Citation |
Score |
2017 |
Impey S, Jopson T, Pelz C, Tafessu A, Fareh F, Zuloaga D, Marzulla T, Riparip LK, Stewart B, Rosi S, Turker MS, Raber J. Bi-directional and shared epigenomic signatures following proton and (56)Fe irradiation. Scientific Reports. 7: 10227. PMID 28860502 DOI: 10.1038/S41598-017-09191-4 |
0.357 |
|
2017 |
Turker MS, Grygoryev D, Lasarev M, Ohlrich A, Rwatambuga FA, Johnson S, Dan C, Eckelmann B, Hryciw G, Mao JH, Snijders AM, Gauny S, Kronenberg A. Simulated space radiation-induced mutants in the mouse kidney display widespread genomic change. Plos One. 12: e0180412. PMID 28683078 DOI: 10.1371/Journal.Pone.0180412 |
0.403 |
|
2016 |
Impey S, Jopson T, Pelz C, Tafessu A, Fareh F, Zuloaga D, Marzulla T, Riparip LK, Stewart B, Rosi S, Turker MS, Raber J. Short- and long-term effects of (56)Fe irradiation on cognition and hippocampal DNA methylation and gene expression. Bmc Genomics. 17: 825. PMID 27776477 DOI: 10.1186/S12864-016-3110-7 |
0.305 |
|
2016 |
Grygoryev D, Gauny S, Lasarev M, Ohlrich A, Kronenberg A, Turker MS. Charged particle mutagenesis at low dose and fluence in mouse splenic T cells. Mutation Research. 788: 32-40. PMID 27055360 DOI: 10.1016/J.Mrfmmm.2016.03.004 |
0.436 |
|
2016 |
Impey S, Pelz C, Tafessu A, Marzulla T, Turker MS, Raber J. Proton irradiation induces persistent and tissue-specific DNA methylation changes in the left ventricle and hippocampus. Bmc Genomics. 17: 273. PMID 27036964 DOI: 10.1186/S12864-016-2581-X |
0.367 |
|
2015 |
Hryciw G, Grygoryev D, Lasarev M, Ohlrich A, Dan C, Madhira R, Eckelmann B, Gauny S, Kronenberg A, Turker MS. Accelerated (48)Ti Ions Induce Autosomal Mutations in Mouse Kidney Epithelium at Low Dose and Fluence. Radiation Research. 184: 367-77. PMID 26397174 DOI: 10.1667/Rr14130.1 |
0.448 |
|
2015 |
Lu Y, Chu A, Wajapeyee N, Turker MS, Glazer PM. Abstract 2887: Epigenetic silencing of the DNA repair genes, BRCA1 and MLH1, induced by hypoxic stress in a pathway dependent on the histone demethylase, LSD1 Cancer Research. 75: 2887-2887. DOI: 10.1158/1538-7445.Am2015-2887 |
0.362 |
|
2014 |
Lu Y, Wajapeyee N, Turker MS, Glazer PM. Silencing of the DNA mismatch repair gene MLH1 induced by hypoxic stress in a pathway dependent on the histone demethylase LSD1. Cell Reports. 8: 501-13. PMID 25043185 DOI: 10.1016/J.Celrep.2014.06.035 |
0.351 |
|
2014 |
Grygoryev D, Dan C, Gauny S, Eckelmann B, Ohlrich AP, Connolly M, Lasarev M, Grossi G, Kronenberg A, Turker MS. Autosomal mutants of proton-exposed kidney cells display frequent loss of heterozygosity on nonselected chromosomes. Radiation Research. 181: 452-63. PMID 24758577 DOI: 10.1667/Rr13654.1 |
0.401 |
|
2014 |
Kronenberg A, Gauny S, Grossi G, Dan C, Grygoryev D, Turker M. Genotoxicity of charged particles of importance in space flight using murine kidney epithelial cells Journal of Radiation Research. 55: i77-i78. DOI: 10.1093/Jrr/Rrt191 |
0.432 |
|
2013 |
Kronenberg A, Gauny S, Kwoh E, Grossi G, Dan C, Grygoryev D, Lasarev M, Turker MS. Comparative analysis of cell killing and autosomal mutation in mouse kidney epithelium exposed to 1 GeV protons in vitro or in vivo. Radiation Research. 179: 511-20. PMID 23560634 DOI: 10.1667/Rr3182.1 |
0.448 |
|
2013 |
Turker MS, Grygoryev D, Dan C, Eckelmann B, Lasarev M, Gauny S, Kwoh E, Kronenberg A. Autosomal mutations in mouse kidney epithelial cells exposed to high-energy protons in vivo or in culture. Radiation Research. 179: 521-9. PMID 23560630 DOI: 10.1667/Rr3174.1 |
0.504 |
|
2013 |
Lu Y, Wajapeyee N, Turker MS, Glazer PM. Abstract 1513:MLH1silencing is caused by hypoxia through epigenetic regulation.. Cancer Research. 73: 1513-1513. DOI: 10.1158/1538-7445.Am2013-1513 |
0.359 |
|
2011 |
Lu Y, Chu A, Turker MS, Glazer PM. Hypoxia-induced epigenetic regulation and silencing of the BRCA1 promoter. Molecular and Cellular Biology. 31: 3339-50. PMID 21670155 DOI: 10.1128/Mcb.01121-10 |
0.356 |
|
2011 |
Oyer JA, Yates PA, Godsey S, Turker MS. Aberrantly silenced promoters retain a persistent memory of the silenced state after long-term reactivation. Mutation Research. 706: 21-7. PMID 21035468 DOI: 10.1016/J.Mrfmmm.2010.10.006 |
0.337 |
|
2010 |
Turker M, Connolly L, Dan C, Lasarev M, Gauny S, Kwoh E, Kronenberg A. Erratum: Comparison of autosomal mutations in mouse kidney epithelial cells exposed to iron ions in situ or in culture. (Radiation Research (2009) 172 (558-566)) Radiation Research. 173. DOI: 10.1667/0033-7587-173.1.124 |
0.416 |
|
2009 |
Landais I, Hiddingh S, McCarroll M, Yang C, Sun A, Turker MS, Snyder JP, Hoatlin ME. Monoketone analogs of curcumin, a new class of Fanconi anemia pathway inhibitors. Molecular Cancer. 8: 133. PMID 20043851 DOI: 10.1186/1476-4598-8-133 |
0.411 |
|
2009 |
Turker MS, Connolly L, Dan C, Lasarev M, Gauny S, Kwoh E, Kronenberg A. Comparison of autosomal mutations in mouse kidney epithelial cells exposed to iron ions in situ or in culture. Radiation Research. 172: 558-66. PMID 19883223 DOI: 10.1667/Rr1805.1 |
0.46 |
|
2009 |
Kronenberg A, Gauny S, Kwoh E, Connolly L, Dan C, Lasarev M, Turker MS. Comparative analysis of cell killing and autosomal mutation in mouse kidney epithelium exposed to 1 GeV/nucleon iron ions in vitro or in situ. Radiation Research. 172: 550-7. PMID 19883222 DOI: 10.1667/Rr1804.1 |
0.468 |
|
2009 |
Oyer JA, Chu A, Brar S, Turker MS. Aberrant epigenetic silencing is triggered by a transient reduction in gene expression. Plos One. 4: e4832. PMID 19279688 DOI: 10.1371/Journal.Pone.0004832 |
0.308 |
|
2009 |
Kisby GE, Olivas A, Park T, Churchwell M, Doerge D, Samson LD, Gerson SL, Turker MS. DNA repair modulates the vulnerability of the developing brain to alkylating agents. Dna Repair. 8: 400-12. PMID 19162564 DOI: 10.1016/J.Dnarep.2008.12.002 |
0.318 |
|
2008 |
Skinner AM, Dan C, Turker MS. The frequency of CC to TT tandem mutations in mismatch repair-deficient cells is increased in a cytosine run. Mutagenesis. 23: 87-91. PMID 18178959 DOI: 10.1093/Mutage/Gem047 |
0.76 |
|
2008 |
Skinner AM, Turker MS. High frequency induction of CC to TT tandem mutations in DNA repair-proficient mammalian cells. Photochemistry and Photobiology. 84: 222-7. PMID 18173724 DOI: 10.1111/J.1751-1097.2007.00224.X |
0.773 |
|
2008 |
Kasameyer E, Connolly L, Lasarev M, Turker MS. The spectra of large second-step mutations are similar for two different mouse autosomes. Mutation Research. 637: 66-72. PMID 17714739 DOI: 10.1016/J.Mrfmmm.2007.07.001 |
0.422 |
|
2007 |
Turker MS, Lasarev M, Connolly L, Kasameyer E, Roessler D. Age-related accumulation of autosomal mutations in solid tissues of the mouse is gender and cell type specific. Aging Cell. 6: 73-86. PMID 17266677 DOI: 10.1111/J.1474-9726.2006.00264.X |
0.417 |
|
2006 |
Connolly L, Lasarev M, Jordan R, Schwartz JL, Turker MS. Atm haploinsufficiency does not affect ionizing radiation mutagenesis in solid mouse tissues. Radiation Research. 166: 39-46. PMID 16808618 DOI: 10.1667/Rr3578.1 |
0.406 |
|
2006 |
Wang Q, Ponomareva ON, Lasarev M, Turker MS. High frequency induction of mitotic recombination by ionizing radiation in Mlh1 null mouse cells. Mutation Research. 594: 189-98. PMID 16343558 DOI: 10.1016/J.Mrfmmm.2005.09.005 |
0.518 |
|
2005 |
Skinner AM, Turker MS. Oxidative mutagenesis, mismatch repair, and aging. Science of Aging Knowledge Environment : Sage Ke. 2005: re3. PMID 15744047 DOI: 10.1126/Sageke.2005.9.Re3 |
0.714 |
|
2005 |
Shin-Darlak CY, Skinner AM, Turker MS. A role for Pms2 in the prevention of tandem CC --> TT substitutions induced by ultraviolet radiation and oxidative stress. Dna Repair. 4: 51-7. PMID 15533837 DOI: 10.1016/J.Dnarep.2004.08.006 |
0.56 |
|
2004 |
Turker MS, Schwartz JL, Jordan R, Ponomareva ON, Connolly L, Kasameyer E, Lasarev M, Clepper L. Persistence of chromatid aberrations in the cells of solid mouse tissues exposed to 137Cs gamma radiation. Radiation Research. 162: 357-64. PMID 15447047 DOI: 10.1667/Rr3240 |
0.36 |
|
2004 |
Kisby GE, Lesselroth H, Olivas A, Samson L, Gold B, Tanaka K, Turker MS. Role of nucleotide- and base-excision repair in genotoxin-induced neuronal cell death. Dna Repair. 3: 617-27. PMID 15135729 DOI: 10.1016/J.Dnarep.2004.02.005 |
0.324 |
|
2003 |
Yates PA, Burman R, Simpson J, Ponomoreva ON, Thayer MJ, Turker MS. Silencing of mouse Aprt is a gradual process in differentiated cells. Molecular and Cellular Biology. 23: 4461-70. PMID 12808089 DOI: 10.1128/Mcb.23.13.4461-4470.2003 |
0.389 |
|
2003 |
Turker MS. Autosomal mutation in somatic cells of the mouse. Mutagenesis. 18: 1-6. PMID 12473728 DOI: 10.1093/Mutage/18.1.1 |
0.487 |
|
2002 |
Shin CY, Turker MS. A:T --> G:C base pair substitutions occur at a higher rate than other substitution events in Pms2 deficient mouse cells. Dna Repair. 1: 995-1001. PMID 12531009 DOI: 10.1016/S1568-7864(02)00149-0 |
0.461 |
|
2002 |
Turker MS. Gene silencing in mammalian cells and the spread of DNA methylation. Oncogene. 21: 5388-93. PMID 12154401 DOI: 10.1038/Sj.Onc.1205599 |
0.336 |
|
2002 |
Shin CY, Ponomareva ON, Connolly L, Turker MS. A mouse kidney cell line with a G:C --> C:G transversion mutator phenotype. Mutation Research. 503: 69-76. PMID 12052505 DOI: 10.1016/S0027-5107(02)00073-8 |
0.448 |
|
2002 |
Shin CY, Mellon I, Turker MS. Multiple mutations are common at mouse Aprt in genotoxin-exposed mismatch repair deficient cells. Oncogene. 21: 1768-76. PMID 11896608 DOI: 10.1038/Sj.Onc.1205241 |
0.541 |
|
2002 |
Ponomareva ON, Rose JA, Lasarev M, Rasey J, Turker MS. Tissue-specific deletion and discontinuous loss of heterozygosity are signatures for the mutagenic effects of ionizing radiation in solid tissues. Cancer Research. 62: 1518-23. PMID 11888929 |
0.325 |
|
2001 |
Gage BM, Alroy D, Shin CY, Ponomareva ON, Dhar S, Sharma GG, Pandita TK, Thayer MJ, Turker MS. Spontaneously immortalized cell lines obtained from adult Atm null mice retain sensitivity to ionizing radiation and exhibit a mutational pattern suggestive of oxidative stress Oncogene. 20: 4291-4297. PMID 11466609 DOI: 10.1038/Sj.Onc.1204509 |
0.507 |
|
2000 |
Turker MS. Somatic cell mutations: can they provide a link between aging and cancer? Mechanisms of Ageing and Development. 117: 1-19. PMID 10958919 DOI: 10.1016/S0047-6374(00)00133-0 |
0.471 |
|
1999 |
Yates PA, Burman RW, Mummaneni P, Krussel S, Turker MS. Tandem B1 elements located in a mouse methylation center provide a target for de novo DNA methylation. The Journal of Biological Chemistry. 274: 36357-61. PMID 10593928 DOI: 10.1074/Jbc.274.51.36357 |
0.325 |
|
1999 |
Turker MS. The establishment and maintenance of DNA methylation patterns in mouse somatic cells. Seminars in Cancer Biology. 9: 329-37. PMID 10547341 DOI: 10.1006/Scbi.1999.0133 |
0.301 |
|
1999 |
Burman RW, Popovich BW, Jacky PB, Turker MS. Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. Human Molecular Genetics. 8: 2293-302. PMID 10545610 DOI: 10.1093/Hmg/8.12.2293 |
0.463 |
|
1999 |
Burman RW, Yates PA, Green LD, Jacky PB, Turker MS, Popovich BW. Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect. American Journal of Human Genetics. 65: 1375-86. PMID 10521303 DOI: 10.1086/302628 |
0.385 |
|
1999 |
Turker MS. Estimation of mutation frequencies in normal mammalian cells and the development of cancer. Seminars in Cancer Biology. 8: 407-19. PMID 10191175 DOI: 10.1006/Scbi.1998.0112 |
0.445 |
|
1997 |
Walker KA, Jennings CD, Pulliam J, Ogburn C, Martin GM, Urano M, Turker MS. A cell line selected for resistance to ionizing radiation exhibits cross resistance to other genotoxic agents and a mutator phenotype for loss of heterozygosity events Somatic Cell and Molecular Genetics. 23: 111-121. PMID 9330639 DOI: 10.1007/Bf02679970 |
0.478 |
|
1997 |
Khattar NH, Turker MS. A role for certain mouse Aprt sequences in resistance to toxic adenine analogs. Somatic Cell and Molecular Genetics. 23: 51-61. PMID 9218001 DOI: 10.1007/Bf02679955 |
0.391 |
|
1997 |
Turker MS, Bestor TH. Formation of methylation patterns in the mammalian genome. Mutation Research. 386: 119-30. PMID 9113113 DOI: 10.1016/S1383-5742(96)00048-8 |
0.311 |
|
1997 |
Turker MS, Pieretti M, Kumar S. Molecular evidence for the induction of large interstitial deletions on mouse chromosome 8 by ionizing radiation. Mutation Research. 374: 201-8. PMID 9100844 DOI: 10.1016/S0027-5107(96)00230-8 |
0.486 |
|
1997 |
Turker M. Somatic cell mutation: The mouse APRT model Clinical Biochemistry. 30: 288. DOI: 10.1016/S0009-9120(97)87819-8 |
0.321 |
|
1995 |
Mummaneni P, Walker KA, Bishop PL, Turker MS. Epigenetic gene inactivation induced by a cis-acting methylation center. The Journal of Biological Chemistry. 270: 788-92. PMID 7822312 DOI: 10.1074/Jbc.270.2.788 |
0.322 |
|
1995 |
Pieretti M, Powell DE, Gallion HH, Conway PS, Case EA, Turker MS. Hypermethylation at a chromosome 17 "hot spot" is a common event in ovarian cancer. Human Pathology. 26: 398-401. PMID 7705818 DOI: 10.1016/0046-8177(95)90140-X |
0.305 |
|
1995 |
Khattar NH, Jennings CD, Walker KA, Turker MS. Isolation and characterization of mutations in the mouse APRT gene that encode functional enzymes with resistance to toxic adenine analogs Advances in Experimental Medicine and Biology. 370: 665-670. PMID 7660992 DOI: 10.1007/978-1-4615-2584-4_138 |
0.369 |
|
1995 |
Turker M, Walker KA, Jennings CD, Mellon I, Yusufji A, Urano M. Spontaneous and ionizing radiation induced mutations involve large events when selecting for loss of an autosomal locus Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 329: 97-105. PMID 7603506 DOI: 10.1016/0027-5107(95)00046-L |
0.495 |
|
1994 |
Ogburn CE, Turker MS, Kavanagh TJ, Disteche CM, Smith AC, Fukuchi Ki, Martin GM. Oxygen-resistant multipotent embryonic carcinoma cell lines exhibit antimutator phenotypes Somatic Cell and Molecular Genetics. 20: 361-370. PMID 7825058 DOI: 10.1007/Bf02257453 |
0.366 |
|
1994 |
Turker MS, Mummaneni P, Cooper GE. The mouse APRT gene as a model for studying epigenetic gene inactivation. Advances in Experimental Medicine and Biology. 370: 647-52. PMID 7660987 DOI: 10.1007/978-1-4615-2584-4_134 |
0.427 |
|
1993 |
Turker MS, Cooper GE, Bishop PL. Region-specific rates of molecular evolution: a fourfold reduction in the rate of accumulation of "silent" mutations in transcribed versus nontranscribed regions of homologous DNA fragments derived from two closely related mouse species. Journal of Molecular Evolution. 36: 31-40. PMID 8433377 DOI: 10.1007/Bf02407304 |
0.36 |
|
1993 |
Cooper GE, Bishop PL, Turker MS. Hemidemethylation is sufficient for chromatin relaxation and transcriptional activation of methylated aprt gene in mouse P19 embryonal carcinoma cell line. Somatic Cell and Molecular Genetics. 19: 221-9. PMID 7687384 DOI: 10.1007/Bf01233070 |
0.374 |
|
1992 |
Cooper GE, Khattar NH, Bishop PL, Turker MS. At least two distinct epigenetic mechanisms are correlated with high-frequency "switching" for APRT phenotypic expression in mouse embryonal carcinoma stem cells. Somatic Cell and Molecular Genetics. 18: 215-25. PMID 1496418 DOI: 10.1007/Bf01233858 |
0.35 |
|
1992 |
Khattar NH, Cooper GE, DiMartino DL, Bishop PL, Turker MS. Molecular and biochemical elucidation of a cellular phenotype characterized by adenine analogue resistance in the presence of high levels of adenine phosphoribosyltransferase activity. Biochemical Genetics. 30: 635-48. PMID 1296576 DOI: 10.1007/Bf02399812 |
0.438 |
|
1991 |
Turker MS, Mummaneni P, Bishop PL. Region- and cell type-specific de novo DNA methylation in cultured mammalian cells. Somatic Cell and Molecular Genetics. 17: 151-7. PMID 2011793 DOI: 10.1007/Bf01232972 |
0.362 |
|
1991 |
Cooper GE, DiMartino DL, Turker MS. Molecular analysis of APRT deficiency in mouse P19 teratocarcinoma stem cell line. Somatic Cell and Molecular Genetics. 17: 105-16. PMID 2011791 DOI: 10.1007/Bf01232969 |
0.373 |
|
1990 |
Turker MS. Methylation of mouse adenine phosphoribosyltransferase gene is altered upon cellular differentiation and loss of phenotypic expression. Somatic Cell and Molecular Genetics. 16: 331-40. PMID 1699289 DOI: 10.1007/Bf01232461 |
0.356 |
|
1989 |
Turker MS, Stambrook PJ, Tischfield JA, Smith AC, Martin GM. Allelic variation linked to adenine phosphoribosyltransferase locus in mouse teratocarcinoma cell line and feral-derived mouse strains Somatic Cell and Molecular Genetics. 15: 159-166. PMID 2928841 DOI: 10.1007/Bf01535077 |
0.327 |
|
1988 |
Turker MS, Monnat RJ, Fukuchi K, Johnston PA, Ogburn CE, Weller RE, Park JF, Martin GM. A novel class of unstable 6-thioguanine-resistant cells from dog and human kidneys. Cell Biology and Toxicology. 4: 211-23. PMID 3233532 DOI: 10.1007/Bf00119247 |
0.303 |
|
1987 |
Turker MS, Nelson JG, Cummings DJ. A Podospora anserina longevity mutant with a temperature-sensitive phenotype for senescence. Molecular and Cellular Biology. 7: 3199-204. PMID 3670311 DOI: 10.1128/Mcb.7.9.3199 |
0.329 |
|
1985 |
Turker MS, Martin GM. Induction of adenine salvage in mouse cell lines deficient in adenine phosphoribosyltransferase Molecular and Cellular Biology. 5: 2662-2668. PMID 3837181 DOI: 10.1128/Mcb.5.10.2662 |
0.338 |
|
1984 |
Turker MS, Smith AC, Martin GM. High frequency "switching" at the adenine phosphoribosyltransferase locus in multipotent mouse teratocarcinoma stem cells. Somatic Cell and Molecular Genetics. 10: 55-69. PMID 6583853 DOI: 10.1007/Bf01534473 |
0.422 |
|
1984 |
Horn PL, Turker MS, Ogburn CE, Disteche CM, Martin GM. A cloning assay for 6-thioguanine resistance provides evidence against certain somatic mutational theories of aging. Journal of Cellular Physiology. 121: 309-15. PMID 6490730 DOI: 10.1002/Jcp.1041210207 |
0.36 |
|
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