메뉴 건너뛰기




Volumn 207, Issue 4, 2014, Pages 133-140

Analysis of the t(3;8) of hereditary renal cell carcinoma: A palindrome-mediated translocation

Author keywords

FRA3B; Palindrome; PATRR; Renal cell carcinoma; Translocation

Indexed keywords

FRAGILE HISTIDINE TRIAD PROTEIN;

EID: 84901604510     PISSN: 22107762     EISSN: 22107770     Source Type: Journal    
DOI: 10.1016/j.cancergen.2014.03.004     Document Type: Article
Times cited : (19)

References (55)
  • 1
    • 33747871340 scopus 로고    scopus 로고
    • The involvement of non-B DNA structures in gross chromosomal rearrangements
    • Bacolla A., Wojciechowska M., Kosmider B., et al. The involvement of non-B DNA structures in gross chromosomal rearrangements. DNA Repair (Amst) 2006, 5:1161-1170.
    • (2006) DNA Repair (Amst) , vol.5 , pp. 1161-1170
    • Bacolla, A.1    Wojciechowska, M.2    Kosmider, B.3
  • 2
    • 33744944261 scopus 로고    scopus 로고
    • Non-B DNA structure-induced genetic instability
    • Wang G., Vasquez K.M. Non-B DNA structure-induced genetic instability. Mutat Res 2006, 598:103-119.
    • (2006) Mutat Res , vol.598 , pp. 103-119
    • Wang, G.1    Vasquez, K.M.2
  • 3
    • 73749085274 scopus 로고    scopus 로고
    • Non-B DNA structure-induced genetic instability and evolution
    • Zhao J., Bacolla A., Wang G., et al. Non-B DNA structure-induced genetic instability and evolution. Cell Mol Life Sci 2010, 67:43-62.
    • (2010) Cell Mol Life Sci , vol.67 , pp. 43-62
    • Zhao, J.1    Bacolla, A.2    Wang, G.3
  • 4
    • 34249907843 scopus 로고    scopus 로고
    • Non-B DNA conformations, mutagenesis and disease
    • Wells R.D. Non-B DNA conformations, mutagenesis and disease. Trends Biochem Sci 2007, 32:271-278.
    • (2007) Trends Biochem Sci , vol.32 , pp. 271-278
    • Wells, R.D.1
  • 5
    • 0028674914 scopus 로고
    • Long DNA palindromes, cruciform structures, genetic instability and secondary structure repair
    • Leach D.R. Long DNA palindromes, cruciform structures, genetic instability and secondary structure repair. Bioessays 1994, 16:893-900.
    • (1994) Bioessays , vol.16 , pp. 893-900
    • Leach, D.R.1
  • 6
    • 33748620023 scopus 로고    scopus 로고
    • Palindromes and genomic stress fractures: bracing and repairing the damage
    • Lewis S.M., Cote A.G. Palindromes and genomic stress fractures: bracing and repairing the damage. DNA Repair (Amst) 2006, 5:1146-1160.
    • (2006) DNA Repair (Amst) , vol.5 , pp. 1146-1160
    • Lewis, S.M.1    Cote, A.G.2
  • 7
    • 0030837535 scopus 로고    scopus 로고
    • Palindrome resolution and recombination in the mammalian germ line
    • Akgun E., Zahn J., Baumes S., et al. Palindrome resolution and recombination in the mammalian germ line. Mol Cell Biol 1997, 17:5559-5570.
    • (1997) Mol Cell Biol , vol.17 , pp. 5559-5570
    • Akgun, E.1    Zahn, J.2    Baumes, S.3
  • 8
    • 0029871490 scopus 로고    scopus 로고
    • Instability of long inverted repeats within mouse transgenes
    • Collick A., Drew J., Penberth J., et al. Instability of long inverted repeats within mouse transgenes. EMBO J 1996, 15:1163-1171.
    • (1996) EMBO J , vol.15 , pp. 1163-1171
    • Collick, A.1    Drew, J.2    Penberth, J.3
  • 9
    • 0027220892 scopus 로고
    • Inverted DNA repeats: a source of eukaryotic genomic instability
    • Gordenin D.A., Lobachev K.S., Degtyareva N.P., et al. Inverted DNA repeats: a source of eukaryotic genomic instability. Mol Cell Biol 1993, 13:5315-5322.
    • (1993) Mol Cell Biol , vol.13 , pp. 5315-5322
    • Gordenin, D.A.1    Lobachev, K.S.2    Degtyareva, N.P.3
  • 10
    • 0035159359 scopus 로고    scopus 로고
    • AT-rich palindromes mediate the constitutional t(11;22) translocation
    • Edelmann L., Spiteri E., Koren K., et al. AT-rich palindromes mediate the constitutional t(11;22) translocation. Am J Hum Genet 2001, 68:1-13.
    • (2001) Am J Hum Genet , vol.68 , pp. 1-13
    • Edelmann, L.1    Spiteri, E.2    Koren, K.3
  • 11
    • 0034234453 scopus 로고    scopus 로고
    • Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)
    • Kurahashi H., Shaikh T.H., Hu P., et al. Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22). Hum Mol Genet 2000, 9:1665-1670.
    • (2000) Hum Mol Genet , vol.9 , pp. 1665-1670
    • Kurahashi, H.1    Shaikh, T.H.2    Hu, P.3
  • 12
    • 34147167259 scopus 로고    scopus 로고
    • Apalindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies
    • Gotter A.L., Nimmakayalu M.A., Jalali G.R., et al. Apalindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies. Genome Res 2007, 17:470-481.
    • (2007) Genome Res , vol.17 , pp. 470-481
    • Gotter, A.L.1    Nimmakayalu, M.A.2    Jalali, G.R.3
  • 13
    • 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
    • Kehrer-Sawatzki H., Haussler J., Krone W., et al. The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions. Hum Genet 1997, 99:237-247.
    • (1997) Hum Genet , vol.99 , pp. 237-247
    • Kehrer-Sawatzki, H.1    Haussler, J.2    Krone, W.3
  • 14
    • 0037371163 scopus 로고    scopus 로고
    • The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats
    • Kurahashi H., Shaikh T., Takata M., et al. The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats. Am J Hum Genet 2003, 72:733-738.
    • (2003) Am J Hum Genet , vol.72 , pp. 733-738
    • Kurahashi, H.1    Shaikh, T.2    Takata, M.3
  • 15
    • 77955570109 scopus 로고    scopus 로고
    • Apalindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21)
    • Sheridan M.B., Kato T., Haldeman-Englert C., et al. Apalindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21). Am J Hum Genet 2010, 87:209-218.
    • (2010) Am J Hum Genet , vol.87 , pp. 209-218
    • Sheridan, M.B.1    Kato, T.2    Haldeman-Englert, C.3
  • 16
    • 0347287037 scopus 로고    scopus 로고
    • Apalindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2
    • Gotter A.L., Shaikh T.H., Budarf M.L., et al. Apalindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2. Hum Mol Genet 2004, 13:103-115.
    • (2004) Hum Mol Genet , vol.13 , pp. 103-115
    • Gotter, A.L.1    Shaikh, T.H.2    Budarf, M.L.3
  • 17
    • 0242440822 scopus 로고    scopus 로고
    • Anovel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)
    • Nimmakayalu M.A., Gotter A.L., Shaikh T.H., et al. Anovel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22). Hum Mol Genet 2003, 12:2817-2825.
    • (2003) Hum Mol Genet , vol.12 , pp. 2817-2825
    • Nimmakayalu, M.A.1    Gotter, A.L.2    Shaikh, T.H.3
  • 18
    • 84881611445 scopus 로고    scopus 로고
    • Chimeric Negative Regulation of p14ARF and TBX1 by a t(9;22) Translocation Associated with Melanoma, Deafness, and DNA Repair Deficiency
    • Tan X., Anzick S.L., Khan S.G., et al. Chimeric Negative Regulation of p14ARF and TBX1 by a t(9;22) Translocation Associated with Melanoma, Deafness, and DNA Repair Deficiency. Hum Mutat 2013, 34:1250-1259.
    • (2013) Hum Mutat , vol.34 , pp. 1250-1259
    • Tan, X.1    Anzick, S.L.2    Khan, S.G.3
  • 19
    • 34147165221 scopus 로고    scopus 로고
    • Molecular cloning of a translocation breakpoint hotspot in 22q11
    • Kurahashi H., Inagaki H., Hosoba E., et al. Molecular cloning of a translocation breakpoint hotspot in 22q11. Genome Res 2007, 17:461-469.
    • (2007) Genome Res , vol.17 , pp. 461-469
    • Kurahashi, H.1    Inagaki, H.2    Hosoba, E.3
  • 20
    • 0018736628 scopus 로고
    • Hereditary renal-cell carcinoma associated with a chromosomal translocation
    • Cohen A.J., Li F.P., Berg S., et al. Hereditary renal-cell carcinoma associated with a chromosomal translocation. NEngl J Med 1979, 301:592-595.
    • (1979) NEngl J Med , vol.301 , pp. 592-595
    • Cohen, A.J.1    Li, F.P.2    Berg, S.3
  • 21
    • 34547092923 scopus 로고    scopus 로고
    • Aconstitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma
    • Poland K.S., Azim M., Folsom M., et al. Aconstitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma. Genes Chromosomes Cancer 2007, 46:805-812.
    • (2007) Genes Chromosomes Cancer , vol.46 , pp. 805-812
    • Poland, K.S.1    Azim, M.2    Folsom, M.3
  • 22
    • 0032482964 scopus 로고    scopus 로고
    • The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8
    • Gemmill R.M., West J.D., Boldog F., et al. The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8. Proc Natl Acad Sci USA 1998, 95:9572-9577.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 9572-9577
    • Gemmill, R.M.1    West, J.D.2    Boldog, F.3
  • 23
    • 2042468966 scopus 로고    scopus 로고
    • Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B
    • Boldog F., Gemmill R.M., West J., et al. Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B. Hum Mol Genet 1997, 6:193-203.
    • (1997) Hum Mol Genet , vol.6 , pp. 193-203
    • Boldog, F.1    Gemmill, R.M.2    West, J.3
  • 24
    • 0033595004 scopus 로고    scopus 로고
    • Cancer-specific chromosome alterations in the constitutive fragile region FRA3B
    • Mimori K., Druck T., Inoue H., et al. Cancer-specific chromosome alterations in the constitutive fragile region FRA3B. Proc Natl Acad Sci USA 1999, 96:7456-7461.
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 7456-7461
    • Mimori, K.1    Druck, T.2    Inoue, H.3
  • 25
    • 3543139536 scopus 로고    scopus 로고
    • Two breakpoint clusters at fragile site FRA3B form phased nucleosomes
    • Mulvihill D.J., Wang Y.H. Two breakpoint clusters at fragile site FRA3B form phased nucleosomes. Genome Res 2004, 14:1350-1357.
    • (2004) Genome Res , vol.14 , pp. 1350-1357
    • Mulvihill, D.J.1    Wang, Y.H.2
  • 26
    • 0028169985 scopus 로고
    • Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma
    • Wilke C.M., Guo S.W., Hall B.K., et al. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma. Genomics 1994, 22:319-326.
    • (1994) Genomics , vol.22 , pp. 319-326
    • Wilke, C.M.1    Guo, S.W.2    Hall, B.K.3
  • 27
    • 33748623634 scopus 로고    scopus 로고
    • Common fragile sites as targets for chromosome rearrangements
    • Arlt M.F., Durkin S.G., Ragland R.L., et al. Common fragile sites as targets for chromosome rearrangements. DNA Repair (Amst) 2006, 5:1126-1135.
    • (2006) DNA Repair (Amst) , vol.5 , pp. 1126-1135
    • Arlt, M.F.1    Durkin, S.G.2    Ragland, R.L.3
  • 29
    • 38349186895 scopus 로고    scopus 로고
    • Replication stress induces tumor-like microdeletions in FHIT/FRA3B
    • Durkin S.G., Ragland R.L., Arlt M.F., et al. Replication stress induces tumor-like microdeletions in FHIT/FRA3B. Proc Natl Acad Sci USA 2008, 105:246-251.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 246-251
    • Durkin, S.G.1    Ragland, R.L.2    Arlt, M.F.3
  • 30
    • 0023910775 scopus 로고
    • Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes
    • Glover T.W., Coyle-Morris J.F., Li F.P., et al. Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes. Cancer Genet Cytogenet 1988, 31:69-73.
    • (1988) Cancer Genet Cytogenet , vol.31 , pp. 69-73
    • Glover, T.W.1    Coyle-Morris, J.F.2    Li, F.P.3
  • 31
    • 0034790435 scopus 로고    scopus 로고
    • Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males
    • Kurahashi H., Emanuel B.S. Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males. Nat Genet 2001, 29:139-140.
    • (2001) Nat Genet , vol.29 , pp. 139-140
    • Kurahashi, H.1    Emanuel, B.S.2
  • 32
    • 33144472660 scopus 로고    scopus 로고
    • Genetic variation affects de novo translocation frequency
    • Kato T., Inagaki H., Yamada K., et al. Genetic variation affects de novo translocation frequency. Science 2006, 311:971.
    • (2006) Science , vol.311 , pp. 971
    • Kato, T.1    Inagaki, H.2    Yamada, K.3
  • 33
    • 18144425478 scopus 로고    scopus 로고
    • Agenome-wide scalable SNP genotyping assay using microarray technology
    • Gunderson K.L., Steemers F.J., Lee G., et al. Agenome-wide scalable SNP genotyping assay using microarray technology. Nat Genet 2005, 37(5):549-554.
    • (2005) Nat Genet , vol.37 , Issue.5 , pp. 549-554
    • Gunderson, K.L.1    Steemers, F.J.2    Lee, G.3
  • 34
    • 0042121256 scopus 로고    scopus 로고
    • Mfold web server for nucleic acid folding and hybridization prediction
    • Zuker M. Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res 2003, 31:3406-3415.
    • (2003) Nucleic Acids Res , vol.31 , pp. 3406-3415
    • Zuker, M.1
  • 35
    • 13344279424 scopus 로고    scopus 로고
    • The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers
    • Ohta M., Inoue H., Cotticelli M.G., et al. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers. Cell 1996, 84:587-597.
    • (1996) Cell , vol.84 , pp. 587-597
    • Ohta, M.1    Inoue, H.2    Cotticelli, M.G.3
  • 36
    • 0033847567 scopus 로고    scopus 로고
    • Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22)
    • Kurahashi H., Shaikh T.H., Zackai E.H., et al. Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22). Am J Hum Genet 2000, 67:763-768.
    • (2000) Am J Hum Genet , vol.67 , pp. 763-768
    • Kurahashi, H.1    Shaikh, T.H.2    Zackai, E.H.3
  • 37
    • 25444455882 scopus 로고    scopus 로고
    • Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates
    • Inagaki H., Ohye T., Kogo H., et al. Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates. Hum Mutat 2005, 26:332-342.
    • (2005) Hum Mutat , vol.26 , pp. 332-342
    • Inagaki, H.1    Ohye, T.2    Kogo, H.3
  • 38
    • 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
    • Tong M., Kato T., Yamada K., et al. Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm. Hum Mol Genet 2010, 19:2630-2637.
    • (2010) Hum Mol Genet , vol.19 , pp. 2630-2637
    • Tong, M.1    Kato, T.2    Yamada, K.3
  • 39
    • 0023789150 scopus 로고
    • Chromosome breakage and recombination at fragile sites
    • Glover T.W., Stein C.K. Chromosome breakage and recombination at fragile sites. Am J Hum Genet 1988, 43:265-273.
    • (1988) Am J Hum Genet , vol.43 , pp. 265-273
    • Glover, T.W.1    Stein, C.K.2
  • 40
    • 69449106659 scopus 로고    scopus 로고
    • Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells
    • Kurahashi H., Inagaki H., Kato T., et al. Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells. Hum Mol Genet 2009, 18:3397-3406.
    • (2009) Hum Mol Genet , vol.18 , pp. 3397-3406
    • Kurahashi, H.1    Inagaki, H.2    Kato, T.3
  • 41
    • 69749121852 scopus 로고    scopus 로고
    • High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications
    • Shaikh T.H., Gai X., Perin J.C., et al. High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. Genome Res 2009, 19:1682-1690.
    • (2009) Genome Res , vol.19 , pp. 1682-1690
    • Shaikh, T.H.1    Gai, X.2    Perin, J.C.3
  • 42
    • 41849149326 scopus 로고    scopus 로고
    • Two different forms of palindrome resolution in the human genome: deletion or translocation
    • Kato T., Inagaki H., Kogo H., et al. Two different forms of palindrome resolution in the human genome: deletion or translocation. Hum Mol Genet 2008, 17:1184-1191.
    • (2008) Hum Mol Genet , vol.17 , pp. 1184-1191
    • Kato, T.1    Inagaki, H.2    Kogo, H.3
  • 43
    • 84862504386 scopus 로고    scopus 로고
    • Chromosomal translocations and palindromic AT-rich repeats
    • Kato T., Kurahashi H., Emanuel B.S. Chromosomal translocations and palindromic AT-rich repeats. Curr Opin Genet Dev 2012, 22:221-228.
    • (2012) Curr Opin Genet Dev , vol.22 , pp. 221-228
    • Kato, T.1    Kurahashi, H.2    Emanuel, B.S.3
  • 44
    • 0026320272 scopus 로고
    • Large-scale stable opening of supercoiled DNA in response to temperature and supercoiling in (A + T)-rich regions that promote low-salt cruciform extrusion
    • Bowater R., Aboul-ela F., Lilley D.M. Large-scale stable opening of supercoiled DNA in response to temperature and supercoiling in (A + T)-rich regions that promote low-salt cruciform extrusion. Biochemistry 1991, 30:11495-11506.
    • (1991) Biochemistry , vol.30 , pp. 11495-11506
    • Bowater, R.1    Aboul-ela, F.2    Lilley, D.M.3
  • 45
    • 0025763979 scopus 로고
    • Formation of (dA-dT)n cruciforms in Escherichia coli cells under different environmental conditions
    • Dayn A., Malkhosyan S., Duzhy D., et al. Formation of (dA-dT)n cruciforms in Escherichia coli cells under different environmental conditions. JBacteriol 1991, 173:2658-2664.
    • (1991) JBacteriol , vol.173 , pp. 2658-2664
    • Dayn, A.1    Malkhosyan, S.2    Duzhy, D.3
  • 46
    • 80052588393 scopus 로고    scopus 로고
    • DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation
    • Kato T., Inagaki H., Tong M., et al. DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation. Mol Cytogenet 2011, 4:18.
    • (2011) Mol Cytogenet , vol.4 , pp. 18
    • Kato, T.1    Inagaki, H.2    Tong, M.3
  • 47
    • 33747874030 scopus 로고    scopus 로고
    • Palindrome-mediated chromosomal translocations in humans
    • Kurahashi H., Inagaki H., Ohye T., et al. Palindrome-mediated chromosomal translocations in humans. DNA Repair (Amst) 2006, 5:1136-1145.
    • (2006) DNA Repair (Amst) , vol.5 , pp. 1136-1145
    • Kurahashi, H.1    Inagaki, H.2    Ohye, T.3
  • 48
    • 0034839213 scopus 로고    scopus 로고
    • The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers
    • Tapia-Paez I., Kost-Alimova M., Hu P., et al. The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers. Hum Genet 2001, 109:167-177.
    • (2001) Hum Genet , vol.109 , pp. 167-177
    • Tapia-Paez, I.1    Kost-Alimova, M.2    Hu, P.3
  • 49
    • 68049114586 scopus 로고    scopus 로고
    • Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): clinical features of 63 individuals
    • Carter M.T., St Pierre S.A., Zackai E.H., et al. Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): clinical features of 63 individuals. Am J Med Genet A 2009, 149A:1712-1721.
    • (2009) Am J Med Genet A , vol.149 A , pp. 1712-1721
    • Carter, M.T.1    St Pierre, S.A.2    Zackai, E.H.3
  • 50
    • 33748657156 scopus 로고    scopus 로고
    • Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)
    • Ashley T., Gaeth A.P., Inagaki H., et al. Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22). Am J Hum Genet 2006, 79:524-538.
    • (2006) Am J Hum Genet , vol.79 , pp. 524-538
    • Ashley, T.1    Gaeth, A.P.2    Inagaki, H.3
  • 51
    • 0035154338 scopus 로고    scopus 로고
    • Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma
    • Fang J.M., Arlt M.F., Burgess A.C., et al. Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma. Genes Chromosomes Cancer 2001, 30:292-298.
    • (2001) Genes Chromosomes Cancer , vol.30 , pp. 292-298
    • Fang, J.M.1    Arlt, M.F.2    Burgess, A.C.3
  • 53
    • 13144283613 scopus 로고    scopus 로고
    • Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site
    • Mishmar D., Rahat A., Scherer S.W., et al. Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proc Natl Acad Sci USA 1998, 95:8141-8146.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 8141-8146
    • Mishmar, D.1    Rahat, A.2    Scherer, S.W.3
  • 54
    • 79551661935 scopus 로고    scopus 로고
    • Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site
    • Letessier A., Millot G.A., Koundrioukoff S., et al. Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site. Nature 2011, 470:120-123.
    • (2011) Nature , vol.470 , pp. 120-123
    • Letessier, A.1    Millot, G.A.2    Koundrioukoff, S.3
  • 55
    • 0035826908 scopus 로고    scopus 로고
    • Sequence conservation at human and mouse orthologous common fragile regions, FRA3B/FHIT and Fra14A2/Fhit
    • Shiraishi T., Druck T., Mimori K., et al. Sequence conservation at human and mouse orthologous common fragile regions, FRA3B/FHIT and Fra14A2/Fhit. Proc Natl Acad Sci USA 2001, 98:5722-5727.
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 5722-5727
    • Shiraishi, T.1    Druck, T.2    Mimori, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.