메뉴 건너뛰기




Volumn 4, Issue 1, 2011, Pages

DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation

Author keywords

Breakpoint; Cruciform structure; Hairpin structure; Palindrome; Polymorphism; Secondary structure; Translocation

Indexed keywords

CRUCIFORM DNA; PALINDROMIC DNA;

EID: 80052588393     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-4-18     Document Type: Article
Times cited : (7)

References (45)
  • 1
    • 34249907843 scopus 로고    scopus 로고
    • Non-B DNA conformations, mutagenesis and disease
    • DOI 10.1016/j.tibs.2007.04.003, PII S0968000407000916
    • Non-B DNA conformations, mutagenesis and disease. Wells RD, Trends Biochem Sci 2007 32 271 278 10.1016/j.tibs.2007.04.003 17493823 (Pubitemid 46874927)
    • (2007) Trends in Biochemical Sciences , vol.32 , Issue.6 , pp. 271-278
    • Wells, R.D.1
  • 2
    • 34250878426 scopus 로고    scopus 로고
    • Expandable DNA repeats and human disease
    • DOI 10.1038/nature05977, PII NATURE05977
    • Expandable DNA repeats and human disease. Mirkin SM, Nature 2007 447 932 940 10.1038/nature05977 17581576 (Pubitemid 46975760)
    • (2007) Nature , vol.447 , Issue.7147 , pp. 932-940
    • Mirkin, S.M.1
  • 3
    • 25844438495 scopus 로고    scopus 로고
    • Repeat instability: Mechanisms of dynamic mutations
    • DOI 10.1038/nrg1689
    • Repeat instability: mechanisms of dynamic mutations. Pearson CE, Nichol Edamura K, Cleary JD, Nat Rev Genet 2005 6 729 742 10.1038/nrg1689 16205713 (Pubitemid 41400831)
    • (2005) Nature Reviews Genetics , vol.6 , Issue.10 , pp. 729-742
    • Pearson, C.E.1    Edamura, K.N.2    Cleary, J.D.3
  • 4
    • 1542287213 scopus 로고    scopus 로고
    • A non-B-DNA structure at the Bcl-2 major breakpoint region is cleaved by the RAG complex
    • DOI 10.1038/nature02355
    • A non-B-DNA structure at the Bcl-2 major breakpoint region is cleaved by the RAG complex. Raghavan SC, Swanson PC, Wu X, Hsieh CL, Lieber MR, Nature 2004 428 88 93 10.1038/nature02355 14999286 (Pubitemid 38332363)
    • (2004) Nature , vol.428 , Issue.6978 , pp. 88-93
    • Raghavan, S.C.1    Swanson, P.C.2    Wu, X.3    Hsieh, C.-L.4    Lieber, M.R.5
  • 7
    • 77956406859 scopus 로고    scopus 로고
    • The constitutional t(11;22): Implications for a novel mechanism responsible for gross chromosomal rearrangements
    • 10.1111/j.1399-0004.2010.01445.x 20507342
    • The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements. Kurahashi H, Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Clin Genet 2010 78 299 309 10.1111/j.1399-0004.2010.01445.x 20507342
    • (2010) Clin Genet , vol.78 , pp. 299-309
    • Kurahashi, H.1    Inagaki, H.2    Ohye, T.3    Kogo, H.4    Tsutsumi, M.5    Kato, T.6    Tong, M.7    Emanuel, B.S.8
  • 8
    • 0034513406 scopus 로고    scopus 로고
    • Molecular mechanisms for constitutional chromosomal rearragements in humans
    • DOI 10.1146/annurev.genet.34.1.297
    • Molecular mechanisms for constitutional chromosomal rearrangements in humans. Shaffer LG, Lupski JR, Annu Rev Genet 2000 34 297 329 10.1146/annurev.genet.34.1.297 11092830 (Pubitemid 32065924)
    • (2000) Annual Review of Genetics , vol.34 , pp. 297-329
    • Shaffer, L.G.1    Lupski, J.R.2
  • 10
    • 67649557486 scopus 로고    scopus 로고
    • Recent advance in our understanding of the molecular nature of chromosomal abnormalities
    • 10.1038/jhg.2009.35 19373258
    • Recent advance in our understanding of the molecular nature of chromosomal abnormalities. Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T, J Hum Genet 2009 54 253 260 10.1038/jhg.2009.35 19373258
    • (2009) J Hum Genet , vol.54 , pp. 253-260
    • Kurahashi, H.1    Bolor, H.2    Kato, T.3    Kogo, H.4    Tsutsumi, M.5    Inagaki, H.6    Ohye, T.7
  • 11
    • 0034234453 scopus 로고    scopus 로고
    • Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)
    • Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22). Kurahashi H, Shaikh TH, Hu P, Roe BA, Emanuel BS, Budarf ML, Hum Mol Genet 2000 9 1665 1670 10.1093/hmg/9.11.1665 10861293 (Pubitemid 30427003)
    • (2000) Human Molecular Genetics , vol.9 , Issue.11 , pp. 1665-1670
    • Kurahashi, H.1    Shaikh, T.H.2    Hu, P.3    Roe, B.A.4    Emanuel, B.S.5    Budarf, M.L.6
  • 13
    • 0034839213 scopus 로고    scopus 로고
    • The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers
    • DOI 10.1007/s004390100560
    • The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers. Tapia-Paez I, Kost-Alimova M, Hu P, Roe BA, Blennow E, Fedorova L, Imreh S, Dumanski JP, Hum Genet 2001 109 167 177 10.1007/s004390100560 11511922 (Pubitemid 32825557)
    • (2001) Human Genetics , vol.109 , Issue.2 , pp. 167-177
    • Tapia-Paez, I.1    Kost-Alimova, M.2    Hu, P.3    Roe, B.A.4    Blennow, E.5    Fedorova, L.6    Imreh, S.7    Dumanski, J.P.8
  • 15
    • 0035509701 scopus 로고    scopus 로고
    • Long AT-rich palindromes and the constitutional t(11;22) breakpoint
    • Long AT-rich palindromes and the constitutional t(11;22) breakpoint. Kurahashi H, Emanuel BS, Hum Mol Genet 2001 10 2605 2617 10.1093/hmg/10.23.2605 11726547 (Pubitemid 33133401)
    • (2001) Human Molecular Genetics , vol.10 , Issue.23 , pp. 2605-2617
    • Kurahashi, H.1    Emanuel, B.S.2
  • 16
    • 0031025934 scopus 로고    scopus 로고
    • The second case of a t[17;22) in a family with neurofibromatosis type 1: Sequence analysis of the breakpoint regions
    • DOI 10.1007/s004390050346
    • The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions. Kehrer-Sawatzki H, Haussler J, Krone W, Bode H, Jenne DE, Mehnert KU, Tummers U, Assum G, Hum Genet 1997 99 237 247 10.1007/s004390050346 9048928 (Pubitemid 27073329)
    • (1997) Human Genetics , vol.99 , Issue.2 , pp. 237-247
    • Kehrer-Sawatzki, H.1    Haussler, J.2    Krone, W.3    Bode, H.4    Jenne, D.E.5    Mehnert, K.U.6    Tummers, U.7    Assum, G.8
  • 17
    • 0037371163 scopus 로고    scopus 로고
    • The constitutional t(17;22): Another translocation mediated by palindromic AT-rich repeats
    • DOI 10.1086/368062
    • The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats. Kurahashi H, Shaikh T, Takata M, Toda T, Emanuel BS, Am J Hum Genet 2003 72 733 738 10.1086/368062 12557125 (Pubitemid 36255973)
    • (2003) American Journal of Human Genetics , vol.72 , Issue.3 , pp. 733-738
    • Kurahashi, H.1    Shaikh, T.2    Takata, M.3    Toda, T.4    Emanuel, B.S.5
  • 18
    • 0242440822 scopus 로고    scopus 로고
    • A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)
    • DOI 10.1093/hmg/ddg301
    • A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22). Nimmakayalu MA, Gotter AL, Shaikh TH, Emanuel BS, Hum Mol Genet 2003 12 2817 2825 10.1093/hmg/ddg301 12952865 (Pubitemid 37407118)
    • (2003) Human Molecular Genetics , vol.12 , Issue.21 , pp. 2817-2825
    • Nimmakayalu, M.A.1    Gotter, A.L.2    Shaikh, T.H.3    Emanuel, B.S.4
  • 19
    • 0347287037 scopus 로고    scopus 로고
    • A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2
    • DOI 10.1093/hmg/ddh004
    • A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2. Gotter AL, Shaikh TH, Budarf ML, Rhodes CH, Emanuel BS, Hum Mol Genet 2004 13 103 115 10.1093/hmg/ddh072 14613967 (Pubitemid 38072139)
    • (2004) Human Molecular Genetics , vol.13 , Issue.1 , pp. 103-115
    • Gotter, A.L.1    Shaikh, T.H.2    Budarf, M.L.3    Rhodes, C.H.4    Emanuel, B.S.5
  • 20
    • 34147167259 scopus 로고    scopus 로고
    • A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies
    • DOI 10.1101/gr.6130907
    • A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies. Gotter AL, Nimmakayalu MA, Jalali GR, Hacker AM, Vorstman J, Conforto Duffy D, Medne L, Emanuel BS, Genome Res 2007 17 470 481 10.1101/gr.6130907 17351131 (Pubitemid 46556451)
    • (2007) Genome Research , vol.17 , Issue.4 , pp. 470-481
    • Gotter, A.L.1    Nimmakayalu, M.A.2    Jalali, G.R.3    Hacker, A.M.4    Vorstman, J.5    Duffy, D.C.6    Medne, L.7    Emanuel, B.S.8
  • 22
    • 0034790435 scopus 로고    scopus 로고
    • Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males
    • DOI 10.1038/ng1001-139
    • Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males. Kurahashi H, Emanuel BS, Nat Genet 2001 29 139 140 10.1038/ng1001-139 11586296 (Pubitemid 32952648)
    • (2001) Nature Genetics , vol.29 , Issue.2 , pp. 139-140
    • Kurahashi, H.1    Emanuel, B.S.2
  • 23
    • 15044351972 scopus 로고    scopus 로고
    • Widespread and nonrandom distribution of DNA palindromes in cancer cells provides a structural platform for subsequent gene amplification
    • DOI 10.1038/ng1515
    • Widespread and nonrandom distribution of DNA palindromes in cancer cells provides a structural platform for subsequent gene amplification. Tanaka H, Bergstrom DA, Yao MC, Tapscott SJ, Nat Genet 2005 37 320 327 10.1038/ng1515 15711546 (Pubitemid 41716261)
    • (2005) Nature Genetics , vol.37 , Issue.3 , pp. 320-327
    • Tanaka, H.1    Bergstrom, D.A.2    Yao, M.-C.3    Tapscott, S.J.4
  • 24
    • 34147165221 scopus 로고    scopus 로고
    • Molecular cloning of a translocation breakpoint hotspot in 22q11
    • DOI 10.1101/gr.5769507
    • Molecular cloning of a translocation breakpoint hotspot in 22q11. Kurahashi H, Inagaki H, Hosoba E, Kato T, Ohye T, Kogo H, Emanuel BS, Genome Res 2007 17 461 469 10.1101/gr.5769507 17267815 (Pubitemid 46556450)
    • (2007) Genome Research , vol.17 , Issue.4 , pp. 461-469
    • Kurahashi, H.1    Inagaki, H.2    Hosoba, E.3    Kato, T.4    Ohye, T.5    Kogo, H.6    Emanuel, B.S.7
  • 25
    • 4143085977 scopus 로고    scopus 로고
    • Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations
    • DOI 10.1074/jbc.M400354200
    • Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations. Kurahashi H, Inagaki H, Yamada K, Ohye T, Taniguchi M, Emanuel BS, Toda T, J Biol Chem 2004 279 35377 35383 10.1074/jbc.M400354200 15208332 (Pubitemid 39100537)
    • (2004) Journal of Biological Chemistry , vol.279 , Issue.34 , pp. 35377-35383
    • Kurahashi, H.1    Inagaki, H.2    Yamada, K.3    Ohye, T.4    Taniguchi, M.5    Emanuel, B.S.6    Toda, T.7
  • 26
    • 25444455882 scopus 로고    scopus 로고
    • Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates
    • DOI 10.1002/humu.20228
    • Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates. Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H, Hum Mutat 2005 26 332 342 10.1002/humu.20228 16116616 (Pubitemid 41361801)
    • (2005) Human Mutation , vol.26 , Issue.4 , pp. 332-342
    • Inagaki, H.1    Ohye, T.2    Kogo, H.3    Yamada, K.4    Kowa, H.5    Shaikh, T.H.6    Emanuel, B.S.7    Kurahashi, H.8
  • 27
    • 34047101901 scopus 로고    scopus 로고
    • Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats
    • DOI 10.1093/nar/gkm036
    • Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats. Kogo H, Inagaki H, Ohye T, Kato T, Emanuel BS, Kurahashi H, Nucleic Acids Res 2007 35 1198 1208 10.1093/nar/gkm036 17264116 (Pubitemid 46522972)
    • (2007) Nucleic Acids Research , vol.35 , Issue.4 , pp. 1198-1208
    • Kogo, H.1    Inagaki, H.2    Ohye, T.3    Kato, T.4    Emanuel, B.S.5    Kurahashi, H.6
  • 29
    • 77954166543 scopus 로고    scopus 로고
    • Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm
    • 10.1093/hmg/ddq150 20392709
    • Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm. Tong M, Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Tsutsumi M, Wang J, Emanuel BS, Kurahashi H, Hum Mol Genet 2010 19 2630 2637 10.1093/hmg/ddq150 20392709
    • (2010) Hum Mol Genet , vol.19 , pp. 2630-2637
    • Tong, M.1    Kato, T.2    Yamada, K.3    Inagaki, H.4    Kogo, H.5    Ohye, T.6    Tsutsumi, M.7    Wang, J.8    Emanuel, B.S.9    Kurahashi, H.10
  • 30
    • 59949101230 scopus 로고    scopus 로고
    • Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans
    • 18997000
    • Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans. Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H, Genome Res 2009 19 191 198 18997000
    • (2009) Genome Res , vol.19 , pp. 191-198
    • Inagaki, H.1    Ohye, T.2    Kogo, H.3    Kato, T.4    Bolor, H.5    Taniguchi, M.6    Shaikh, T.H.7    Emanuel, B.S.8    Kurahashi, H.9
  • 31
    • 0037169325 scopus 로고    scopus 로고
    • The Mre11 complex is required for repair of hairpin-capped double-strand breaks and prevention of chromosome rearrangements
    • DOI 10.1016/S0092-8674(02)00614-1
    • The Mre11 complex is required for repair of hairpin-capped double-strand breaks and prevention of chromosome rearrangements. Lobachev KS, Gordenin DA, Resnick MA, Cell 2002 108 183 193 10.1016/S0092-8674(02)00614-1 11832209 (Pubitemid 34161139)
    • (2002) Cell , vol.108 , Issue.2 , pp. 183-193
    • Lobachev, K.S.1    Gordenin, D.A.2    Resnick, M.A.3
  • 32
    • 14844286404 scopus 로고    scopus 로고
    • Chromosomal translocations in yeast induced by low levels of DNA polymerase: A model for chromosome fragile sites
    • DOI 10.1016/j.cell.2004.12.039
    • Chromosomal translocations in yeast induced by low levels of DNA polymerase a model for chromosome fragile sites. Lemoine FJ, Degtyareva NP, Lobachev K, Petes TD, Cell 2005 120 587 598 10.1016/j.cell.2004.12.039 15766523 (Pubitemid 40343072)
    • (2005) Cell , vol.120 , Issue.5 , pp. 587-598
    • Lemoine, F.J.1    Degtyareva, N.P.2    Lobachev, K.3    Petes, T.D.4
  • 33
    • 34547205070 scopus 로고    scopus 로고
    • An AT-Rich Sequence in Human Common Fragile Site FRA16D Causes Fork Stalling and Chromosome Breakage in S. cerevisiae
    • DOI 10.1016/j.molcel.2007.06.012, PII S1097276507004029
    • An AT-rich sequence in human common fragile site FRA16D causes fork stalling and chromosome breakage in S. cerevisiae. Zhang H, Freudenreich CH, Mol Cell 2007 27 367 379 10.1016/j.molcel.2007.06.012 17679088 (Pubitemid 47126937)
    • (2007) Molecular Cell , vol.27 , Issue.3 , pp. 367-379
    • Zhang, H.1    Freudenreich, C.H.2
  • 34
    • 52049119340 scopus 로고    scopus 로고
    • Mus81-dependent double-strand DNA breaks at in vivo-generated cruciform structures in S. cerevisiae
    • 10.1016/j.molcel.2008.08.025 18922464
    • Mus81-dependent double-strand DNA breaks at in vivo-generated cruciform structures in S. cerevisiae. Cote AG, Lewis SM, Mol Cell 2008 31 800 812 10.1016/j.molcel.2008.08.025 18922464
    • (2008) Mol Cell , vol.31 , pp. 800-812
    • Cote, A.G.1    Lewis, S.M.2
  • 36
    • 33745131837 scopus 로고    scopus 로고
    • Chromosomal translocations mediated by palindromic DNA
    • Chromosomal translocations mediated by palindromic DNA. Kurahashi H, Inagaki H, Ohye T, Kogo H, Kato T, Emanuel BS, Cell Cycle 2006 5 1297 1303 10.4161/cc.5.12.2809 16760666 (Pubitemid 43894284)
    • (2006) Cell Cycle , vol.5 , Issue.12 , pp. 1297-1303
    • Kurahashi, H.1    Inagaki, H.2    Ohye, T.3    Kogo, H.4    Kato, T.5    Emanuel, B.S.6
  • 37
    • 33747874030 scopus 로고    scopus 로고
    • Palindrome-mediated chromosomal translocations in humans
    • DOI 10.1016/j.dnarep.2006.05.035, PII S1568786406001753, Mechanisms of Chromosomal Translocations
    • Palindrome-mediated chromosomal translocations in humans. Kurahashi H, Inagaki H, Ohye T, Kogo H, Kato T, Emanuel BS, DNA Repair (Amst) 2006 5 1136 1145 10.1016/j.dnarep.2006.05.035 (Pubitemid 44291625)
    • (2006) DNA Repair , vol.5 , Issue.9-10 , pp. 1136-1145
    • Kurahashi, H.1    Inagaki, H.2    Ohye, T.3    Kogo, H.4    Kato, T.5    Emanuel, B.S.6
  • 38
    • 77349124038 scopus 로고    scopus 로고
    • De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age
    • 10.1136/jmg.2009.069716 19638350
    • De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age. Thomas NS, Morris JK, Baptista J, Ng BL, Crolla JA, Jacobs PA, J Med Genet 2010 47 112 115 10.1136/jmg.2009.069716 19638350
    • (2010) J Med Genet , vol.47 , pp. 112-115
    • Thomas, N.S.1    Morris, J.K.2    Baptista, J.3    Ng, B.L.4    Crolla, J.A.5    Jacobs, P.A.6
  • 39
    • 78651387587 scopus 로고    scopus 로고
    • Advanced age increases chromosome structural abnormalities in human spermatozoa
    • 10.1038/ejhg.2010.166 21045871
    • Advanced age increases chromosome structural abnormalities in human spermatozoa. Templado C, Donate A, Giraldo J, Bosch M, Estop A, Eur J Hum Genet 2011 19 145 151 10.1038/ejhg.2010.166 21045871
    • (2011) Eur J Hum Genet , vol.19 , pp. 145-151
    • Templado, C.1    Donate, A.2    Giraldo, J.3    Bosch, M.4    Estop, A.5
  • 40
    • 35649020743 scopus 로고    scopus 로고
    • Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm
    • DOI 10.1016/j.fertnstert.2007.01.019, PII S001502820700129X
    • Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm. Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Emanuel BS, Kurahashi H, Fertil Steril 2007 88 1446 1448 10.1016/j.fertnstert.2007.01.019 17448469 (Pubitemid 350030085)
    • (2007) Fertility and Sterility , vol.88 , Issue.5 , pp. 1446-1448
    • Kato, T.1    Yamada, K.2    Inagaki, H.3    Kogo, H.4    Ohye, T.5    Emanuel, B.S.6    Kurahashi, H.7
  • 41
    • 77649211158 scopus 로고    scopus 로고
    • Function of sperm chromatin structural elements in fertilization and development
    • 10.1093/molehr/gap080 19748904
    • Function of sperm chromatin structural elements in fertilization and development. Ward WS, Mol Hum Reprod 2010 16 30 36 10.1093/molehr/gap080 19748904
    • (2010) Mol Hum Reprod , vol.16 , pp. 30-36
    • Ward, W.S.1
  • 42
    • 41849149326 scopus 로고    scopus 로고
    • Two different forms of palindrome resolution in the human genome: Deletion or translocation
    • DOI 10.1093/hmg/ddn008
    • Two different forms of palindrome resolution in the human genome: deletion or translocation. Kato T, Inagaki H, Kogo H, Ohye T, Yamada K, Emanuel BS, Kurahashi H, Hum Mol Genet 2008 17 1184 1191 10.1093/hmg/ddn008 18184694 (Pubitemid 351494190)
    • (2008) Human Molecular Genetics , vol.17 , Issue.8 , pp. 1184-1191
    • Kato, T.1    Inagaki, H.2    Kogo, H.3    Ohye, T.4    Yamada, K.5    Emanuel, B.S.6    Kurahashi, H.7
  • 43
    • 69449106659 scopus 로고    scopus 로고
    • Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells
    • 10.1093/hmg/ddp279 19520744
    • Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells. Kurahashi H, Inagaki H, Kato T, Hosoba E, Kogo H, Ohye T, Tsutsumi M, Bolor H, Tong M, Emanuel BS, Hum Mol Genet 2009 18 3397 3406 10.1093/hmg/ddp279 19520744
    • (2009) Hum Mol Genet , vol.18 , pp. 3397-3406
    • Kurahashi, H.1    Inagaki, H.2    Kato, T.3    Hosoba, E.4    Kogo, H.5    Ohye, T.6    Tsutsumi, M.7    Bolor, H.8    Tong, M.9    Emanuel, B.S.10
  • 44
    • 0035065524 scopus 로고    scopus 로고
    • Trinucleotide expansion in haploid germ cells by gap repair
    • DOI 10.1038/86906
    • Trinucleotide expansion in haploid germ cells by gap repair. Kovtun IV, McMurray CT, Nat Genet 2001 27 407 411 10.1038/86906 11279522 (Pubitemid 32268421)
    • (2001) Nature Genetics , vol.27 , Issue.4 , pp. 407-411
    • Kovtun, I.V.1    McMurray, C.T.2
  • 45
    • 14944341949 scopus 로고    scopus 로고
    • Chromatin remodeling in spermatids: A sensitive step for the genetic integrity of the male gamete
    • DOI 10.1080/014850190518134
    • Chromatin remodeling in spermatids: a sensitive step for the genetic integrity of the male gamete. Laberge RM, Boissonneault G, Arch Androl 2005 51 125 133 10.1080/014850190518134 15804867 (Pubitemid 40364871)
    • (2005) Archives of Andrology , vol.51 , Issue.2 , pp. 125-133
    • Laberge, R.-M.1    Boissonneault, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.