메뉴 건너뛰기




Volumn 119, Issue 3-4, 2007, Pages 196-203

DMD and IL1RAPL1: Two large adjacent genes localized within a common fragile site (FRAXC) have reduced expression in cultured brain tumors

Author keywords

[No Author keywords available]

Indexed keywords

FRAGILE HISTIDINE TRIAD PROTEIN; INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN; INTERLEUKIN 1 RECEPTOR ACCESSORY PROTEIN LIKE 1; RAD51 LIKE 1 PROTEIN; RAD51 PROTEIN; UNCLASSIFIED DRUG;

EID: 39049149919     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000112061     Document Type: Article
Times cited : (28)

References (57)
  • 2
    • 0036131979 scopus 로고    scopus 로고
    • Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells
    • Arlt MF, Miller DE, Beer DG, Glover TW: Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells. Genes Chromosomes Cancer 33:82-92 (2002).
    • (2002) Genes Chromosomes Cancer , vol.33 , pp. 82-92
    • Arlt, M.F.1    Miller, D.E.2    Beer, D.G.3    Glover, T.W.4
  • 5
    • 22244468667 scopus 로고    scopus 로고
    • Loss of FHIT expression in breast cancer is correlated with poor prognostic markers
    • Arun B, Kilic G, Yen C, Foster B, Yardley DA, et al: Loss of FHIT expression in breast cancer is correlated with poor prognostic markers. Cancer Epidemiol Biomarkers Prev 14:1681-1685 (2005).
    • (2005) Cancer Epidemiol Biomarkers Prev , vol.14 , pp. 1681-1685
    • Arun, B.1    Kilic, G.2    Yen, C.3    Foster, B.4    Yardley, D.A.5
  • 6
    • 0030584084 scopus 로고    scopus 로고
    • Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro
    • Baumann P, Benson FE, West SC: Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro. Cell 87:757-766 (1996).
    • (1996) Cell , vol.87 , pp. 757-766
    • Baumann, P.1    Benson, F.E.2    West, S.C.3
  • 8
    • 0034655131 scopus 로고    scopus 로고
    • WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.2-24.1, a region frequently affected in breast cancer
    • Bednarek AK, Laflin KJ, Daniel RL, Liao Q, Hawkins KA, Aldaz CM: WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.2-24.1, a region frequently affected in breast cancer. Cancer Res 60:2140-2145 (2000).
    • (2000) Cancer Res , vol.60 , pp. 2140-2145
    • Bednarek, A.K.1    Laflin, K.J.2    Daniel, R.L.3    Liao, Q.4    Hawkins, K.A.5    Aldaz, C.M.6
  • 9
    • 33644794329 scopus 로고    scopus 로고
    • Human retinoic acid receptor-related orphan receptor alpha1 overexpression protects neurons against oxidative stress-induced apoptosis
    • Boukhtouche F, Vodjdani G, Jarvis CL, Bakouche J, Staels B, et al: Human retinoic acid receptor-related orphan receptor alpha1 overexpression protects neurons against oxidative stress-induced apoptosis. J Neurochem 96:1778-1789 (2006).
    • (2006) J Neurochem , vol.96 , pp. 1778-1789
    • Boukhtouche, F.1    Vodjdani, G.2    Jarvis, C.L.3    Bakouche, J.4    Staels, B.5
  • 10
    • 0038732456 scopus 로고    scopus 로고
    • Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27
    • Cesari R, Martin ES, Calin GA, Pentimalli F, Bichi R, et al: Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27. Proc Natl Acad Sci USA 100:5956-5961 (2003).
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 5956-5961
    • Cesari, R.1    Martin, E.S.2    Calin, G.A.3    Pentimalli, F.4    Bichi, R.5
  • 11
    • 0042522482 scopus 로고    scopus 로고
    • Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer
    • Denison SF, Callahan G, Becker NA, Phillips LA, Smith DI: Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer. Genes Chromosomes Cancer 38:40-52 (2003).
    • (2003) Genes Chromosomes Cancer , vol.38 , pp. 40-52
    • Denison, S.F.1    Callahan, G.2    Becker, N.A.3    Phillips, L.A.4    Smith, D.I.5
  • 12
    • 33747195058 scopus 로고    scopus 로고
    • Trends in brain cancer incidence and survival in the United States: Surveillance, epidemiology, and end results program. 1973 to 2001
    • Deorah S, Lynch CF, Bibenaller ZA, Ryken TC: Trends in brain cancer incidence and survival in the United States: Surveillance, epidemiology, and end results program. 1973 to 2001. Neurosurg Focus 20:E1 (2006).
    • (2006) Neurosurg Focus , vol.20
    • Deorah, S.1    Lynch, C.F.2    Bibenaller, Z.A.3    Ryken, T.C.4
  • 13
    • 0031043860 scopus 로고    scopus 로고
    • Structure and expression of the human FHIT gene in normal and tumor cells
    • Druck T, Hadaczek P, Fu TB, Ohta M, Siprashvili Z, et al: Structure and expression of the human FHIT gene in normal and tumor cells. Cancer Res 57:504-512 (1997).
    • (1997) Cancer Res , vol.57 , pp. 504-512
    • Druck, T.1    Hadaczek, P.2    Fu, T.B.3    Ohta, M.4    Siprashvili, Z.5
  • 15
    • 0031907862 scopus 로고
    • Orphan nuclear receptor ROR alpha-deficient mice display the cerebellar defects of staggerer
    • Dussaulat I, Fawcett D, Matthyssen A, Bader JA, Giguere V: Orphan nuclear receptor ROR alpha-deficient mice display the cerebellar defects of staggerer. Mech Dev 70:147-153 (1990).
    • (1990) Mech Dev , vol.70 , pp. 147-153
    • Dussaulat, I.1    Fawcett, D.2    Matthyssen, A.3    Bader, J.A.4    Giguere, V.5
  • 16
    • 0031758918 scopus 로고    scopus 로고
    • Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers
    • Engelman JA, Zhang XL, Lisanti MP: Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers. FEBS Lett 436:403-410 (1998).
    • (1998) FEBS Lett , vol.436 , pp. 403-410
    • Engelman, J.A.1    Zhang, X.L.2    Lisanti, M.P.3
  • 18
    • 0025056930 scopus 로고
    • Identification of a chromosome 18q gene that is altered in colorectal cancers
    • Fearon ER, Cho KR, Nigro JM, Kern SE, Simons JW, et al: Identification of a chromosome 18q gene that is altered in colorectal cancers. Science 247:49-56 (1990).
    • (1990) Science , vol.247 , pp. 49-56
    • Fearon, E.R.1    Cho, K.R.2    Nigro, J.M.3    Kern, S.E.4    Simons, J.W.5
  • 19
    • 0242720711 scopus 로고    scopus 로고
    • Preferential integration of human papillomavirus type 18 near the c-Myc locus in cervical carcinoma
    • Ferber MJ, Thorland EC, Brink AA, Rapp AK, Phillips LA, et al: Preferential integration of human papillomavirus type 18 near the c-Myc locus in cervical carcinoma. Oncogene 22:7233-7242 (2003).
    • (2003) Oncogene , vol.22 , pp. 7233-7242
    • Ferber, M.J.1    Thorland, E.C.2    Brink, A.A.3    Rapp, A.K.4    Phillips, L.A.5
  • 20
    • 17844399776 scopus 로고    scopus 로고
    • Patient tumor EGFR and PDGFRA gene amplifications retained in an invasive intracranial xenograft model of glioblastoma multiforme
    • Giannini C, Sarkaria JN, Saito A, Uhm JH, Galanis E, et al: Patient tumor EGFR and PDGFRA gene amplifications retained in an invasive intracranial xenograft model of glioblastoma multiforme. Neuro Oncol 7:164-176 (2005).
    • (2005) Neuro Oncol , vol.7 , pp. 164-176
    • Giannini, C.1    Sarkaria, J.N.2    Saito, A.3    Uhm, J.H.4    Galanis, E.5
  • 21
    • 10744220604 scopus 로고    scopus 로고
    • Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer
    • Ginestier C, Bardou VJ, Popvici C, Charafe-Jauffret E, Bertucci F, et al: Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer. Int J Cancer 107:854-862 (2003).
    • (2003) Int J Cancer , vol.107 , pp. 854-862
    • Ginestier, C.1    Bardou, V.J.2    Popvici, C.3    Charafe-Jauffret, E.4    Bertucci, F.5
  • 22
    • 0021278143 scopus 로고
    • DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
    • Glover TW, Berger C, Coyle J, Echo B: DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:136-145 (1984).
    • (1984) Hum Genet , vol.67 , pp. 136-145
    • Glover, T.W.1    Berger, C.2    Coyle, J.3    Echo, B.4
  • 23
    • 0344002715 scopus 로고    scopus 로고
    • Fhit expression is absent or reduced in a subset of primary head and neck cancer
    • Gotte K, Hadaczek P, Coy JF, Wirtz HW, Riedel F, et al: Fhit expression is absent or reduced in a subset of primary head and neck cancer. Anticancer Res 20:1057-1060 (2000).
    • (2000) Anticancer Res , vol.20 , pp. 1057-1060
    • Gotte, K.1    Hadaczek, P.2    Coy, J.F.3    Wirtz, H.W.4    Riedel, F.5
  • 24
    • 1842581808 scopus 로고    scopus 로고
    • The fragile genes FHIT and WWOX are inactivated coordinately in invasive breast carcinoma
    • Guler G, Uner A, Guler N, Han SY, Iliopoulos D, et al: The fragile genes FHIT and WWOX are inactivated coordinately in invasive breast carcinoma. Cancer 100:1605-1614 (2004).
    • (2004) Cancer , vol.100 , pp. 1605-1614
    • Guler, G.1    Uner, A.2    Guler, N.3    Han, S.Y.4    Iliopoulos, D.5
  • 25
    • 0032527899 scopus 로고    scopus 로고
    • Absence of reduction of Fhit expression in most clear cell renal carcinomas
    • Hadaczek P, Siprashvili Z, Markiewski M, Domagala W, Druck T, et al: Absence of reduction of Fhit expression in most clear cell renal carcinomas. Cancer Res 58:2946-2951 (1998).
    • (1998) Cancer Res , vol.58 , pp. 2946-2951
    • Hadaczek, P.1    Siprashvili, Z.2    Markiewski, M.3    Domagala, W.4    Druck, T.5
  • 26
    • 33845424480 scopus 로고    scopus 로고
    • Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C 1-relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints
    • Helmrich A, Stout-Weider K, Matthaei A, Hermann K, Heiden T, Schrock E: Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C 1-relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints. Int J Cancer 120:48-54 (2007).
    • (2007) Int J Cancer , vol.120 , pp. 48-54
    • Helmrich, A.1    Stout-Weider, K.2    Matthaei, A.3    Hermann, K.4    Heiden, T.5    Schrock, E.6
  • 27
    • 33845625674 scopus 로고    scopus 로고
    • FRA1E common fragile site breaks map within a 370 kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD)
    • Hormozian F, Schmitt JG, Sagulenko E, Schwab M, Savelyeva L: FRA1E common fragile site breaks map within a 370 kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD). Cancer Lett 246:82-91 (2007).
    • (2007) Cancer Lett , vol.246 , pp. 82-91
    • Hormozian, F.1    Schmitt, J.G.2    Sagulenko, E.3    Schwab, M.4    Savelyeva, L.5
  • 29
    • 0034102258 scopus 로고    scopus 로고
    • Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation
    • Jin H, Gardner RJ, Viswesvaraiah R, Muntoni F, Roberts RG: Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation. Eur J Hum Genet 8:87-94 (2000).
    • (2000) Eur J Hum Genet , vol.8 , pp. 87-94
    • Jin, H.1    Gardner, R.J.2    Viswesvaraiah, R.3    Muntoni, F.4    Roberts, R.G.5
  • 30
    • 0032499264 scopus 로고    scopus 로고
    • Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
    • Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, et al: Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392:605-608 (1998).
    • (1998) Nature , vol.392 , pp. 605-608
    • Kitada, T.1    Asakawa, S.2    Hattori, N.3    Matsumine, H.4    Yamamura, Y.5
  • 31
    • 0023614271 scopus 로고
    • Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
    • Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, Feener C, Kunkel LM: Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50:509-517 (1987).
    • (1987) Cell , vol.50 , pp. 509-517
    • Koenig, M.1    Hoffman, E.P.2    Bertelson, C.J.3    Monaco, A.P.4    Feener, C.5    Kunkel, L.M.6
  • 32
    • 0034306548 scopus 로고    scopus 로고
    • The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations
    • Krummel KA, Roberts LR, Kawakami M, Glover TW, Smith DI: The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations. Genomics 69:37-46 (2000).
    • (2000) Genomics , vol.69 , pp. 37-46
    • Krummel, K.A.1    Roberts, L.R.2    Kawakami, M.3    Glover, T.W.4    Smith, D.I.5
  • 33
    • 0032524625 scopus 로고    scopus 로고
    • Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher
    • Lalouette A, Guenet JL, Vriz S: Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher. Genomics 50:9-13 (1998).
    • (1998) Genomics , vol.50 , pp. 9-13
    • Lalouette, A.1    Guenet, J.L.2    Vriz, S.3
  • 35
    • 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 SW, Nyakatura G, Hinzmann B, 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 95:2311-2319 (1998).
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 2311-2319
    • Mishmar, D.1    Rahat, A.2    Scherer, S.W.3    Nyakatura, G.4    Hinzmann, B.5
  • 38
    • 32944460958 scopus 로고    scopus 로고
    • WWOX - the FRA16D cancer gene: Expression correlation with breast cancer progression and prognosis
    • Pluciennik E, Kusinska R, Potemski P, Kubiak R, Kordek R, Bednarek AK: WWOX - the FRA16D cancer gene: expression correlation with breast cancer progression and prognosis. Eur J Surg Oncol 32:153-157 (2006).
    • (2006) Eur J Surg Oncol , vol.32 , pp. 153-157
    • Pluciennik, E.1    Kusinska, R.2    Potemski, P.3    Kubiak, R.4    Kordek, R.5    Bednarek, A.K.6
  • 39
    • 39049128328 scopus 로고    scopus 로고
    • WWOX, a chromosomal fragile site gene and its role in cancer
    • Ramos D, Aldaz CM: WWOX, a chromosomal fragile site gene and its role in cancer. Adv Exp Med Biol 587:149-159 (2006).
    • (2006) Adv Exp Med Biol , vol.587 , pp. 149-159
    • Ramos, D.1    Aldaz, C.M.2
  • 40
    • 4644319208 scopus 로고    scopus 로고
    • Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: Possible association with an inherited disease and cancer
    • Rozier L, El-Achkar E, Apiou F, Debatisse M: Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer. Oncogene 23:6872-6880 (2004).
    • (2004) Oncogene , vol.23 , pp. 6872-6880
    • Rozier, L.1    El-Achkar, E.2    Apiou, F.3    Debatisse, M.4
  • 41
    • 29244489245 scopus 로고    scopus 로고
    • The neurobeachin gene spans the common fragile site FRA13A
    • Savelyeva L, Sagulenko E, Schmitt JG, Schwab M: The neurobeachin gene spans the common fragile site FRA13A. Hum Genet 118:551-558 (2006).
    • (2006) Hum Genet , vol.118 , pp. 551-558
    • Savelyeva, L.1    Sagulenko, E.2    Schmitt, J.G.3    Schwab, M.4
  • 42
    • 33344454749 scopus 로고    scopus 로고
    • The role of dystrophin in the central nervous system: A mini review
    • Sekiguchi M: The role of dystrophin in the central nervous system: a mini review. Acta Myol 24:93-97 (2005).
    • (2005) Acta Myol , vol.24 , pp. 93-97
    • Sekiguchi, M.1
  • 43
    • 0027325816 scopus 로고
    • Cloning of human, mouse and fission yeast recombination genes homolgous to RAD51 and recA
    • Shinohara A, Ogawa H, Matsuda Y, Ushio N, Ikeo K, Ogawa T: Cloning of human, mouse and fission yeast recombination genes homolgous to RAD51 and recA. Nat Genet 4:239-243 (1993).
    • (1993) Nat Genet , vol.4 , pp. 239-243
    • Shinohara, A.1    Ogawa, H.2    Matsuda, Y.3    Ushio, N.4    Ikeo, K.5    Ogawa, T.6
  • 45
    • 0031963434 scopus 로고    scopus 로고
    • Common fragile sites and cancer (review)
    • Smith DI, Huang H, Wang L: Common fragile sites and cancer (review). Int J Oncol 12:187-196 (1998).
    • (1998) Int J Oncol , vol.12 , pp. 187-196
    • Smith, D.I.1    Huang, H.2    Wang, L.3
  • 46
    • 30144442771 scopus 로고    scopus 로고
    • Common fragile sites, extremely large genes, neural development and cancer
    • Smith DI, Zhu Y, McAvoy S, Kuhn R: Common fragile sites, extremely large genes, neural development and cancer. Cancer Lett 232:48-57 (2006).
    • (2006) Cancer Lett , vol.232 , pp. 48-57
    • Smith, D.I.1    Zhu, Y.2    McAvoy, S.3    Kuhn, R.4
  • 49
    • 0033810575 scopus 로고    scopus 로고
    • The clinical significance of fragile sites on human chromosomes
    • Sutherland GR, Baker E: The clinical significance of fragile sites on human chromosomes. Clin Genet 58:157-161 (2000).
    • (2000) Clin Genet , vol.58 , pp. 157-161
    • Sutherland, G.R.1    Baker, E.2
  • 50
    • 0029061046 scopus 로고
    • The molecular basis of fragile sites in human chromosomes
    • Sutherland GR, Richards RI: The molecular basis of fragile sites in human chromosomes. Curr Opin Genet Dev 5:323-327 (1995a).
    • (1995) Curr Opin Genet Dev , vol.5 , pp. 323-327
    • Sutherland, G.R.1    Richards, R.I.2
  • 51
    • 0028997643 scopus 로고
    • Simple tandem DNA repeats and human genetic disease
    • Sutherland GR, Richards RI: Simple tandem DNA repeats and human genetic disease. Proc Natl Acad Sci USA 92:3636-3641 (1995b).
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 3636-3641
    • Sutherland, G.R.1    Richards, R.I.2
  • 52
    • 33644863950 scopus 로고    scopus 로고
    • A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family
    • Tabolacci E, Pomponi MG, Pietrobono R, Terracciano A, Chiurazzi P, Neri G: A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family. Am J Med Genet A 140:482-487 (2006).
    • (2006) Am J Med Genet A , vol.140 , pp. 482-487
    • Tabolacci, E.1    Pomponi, M.G.2    Pietrobono, R.3    Terracciano, A.4    Chiurazzi, P.5    Neri, G.6
  • 53
    • 0038278610 scopus 로고    scopus 로고
    • Tourette Syndrome Association International Consortium for Genetics: CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder
    • Verkerk AJ, Mathews CA, Hoose M, Eussen BH, Heutink P, Oostra BA: Tourette Syndrome Association International Consortium for Genetics: CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics 82:1-9 (2003).
    • (2003) Genomics , vol.82 , pp. 1-9
    • Verkerk, A.J.1    Mathews, C.A.2    Hoose, M.3    Eussen, B.H.4    Heutink, P.5    Oostra, B.A.6
  • 54
    • 0037327040 scopus 로고    scopus 로고
    • A complex deletion-inversion event results in a chimeric IL1RAPL1-dystrophin transcript and a contiguous gene deletion syndrome
    • Wheway JM, Yau SC, Nihalani V, Ellis D, Irving M, et al: A complex deletion-inversion event results in a chimeric IL1RAPL1-dystrophin transcript and a contiguous gene deletion syndrome. J Med Genet 40:127-131 (2003).
    • (2003) J Med Genet , vol.40 , pp. 127-131
    • Wheway, J.M.1    Yau, S.C.2    Nihalani, V.3    Ellis, D.4    Irving, M.5
  • 55
    • 16644384244 scopus 로고    scopus 로고
    • IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric of DAX1
    • Zhang YH, Huang BL, Niakan KK, McCabe LL, McCabe ER, Dipple KM: IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric of DAX1. Hum Mutat 24:273 (2004).
    • (2004) Hum Mutat , vol.24 , pp. 273
    • Zhang, Y.H.1    Huang, B.L.2    Niakan, K.K.3    McCabe, L.L.4    McCabe, E.R.5    Dipple, K.M.6
  • 56
    • 33749188577 scopus 로고    scopus 로고
    • Aberrant FHIT protein expression in classical Hodgkin's lymphoma: A potential marker
    • Zhao P, Lam AK, Lu YL, Zhong M, Chen LH, Pu XL: Aberrant FHIT protein expression in classical Hodgkin's lymphoma: a potential marker. Pathology 38:399-402 (2006).
    • (2006) Pathology , vol.38 , pp. 399-402
    • Zhao, P.1    Lam, A.K.2    Lu, Y.L.3    Zhong, M.4    Chen, L.H.5    Pu, X.L.6
  • 57
    • 33646706084 scopus 로고    scopus 로고
    • RORA, a large common fragile site gene, is involved in cellular stress response
    • Zhu Y, McAvoy S, Kuhn R, Smith DI: RORA, a large common fragile site gene, is involved in cellular stress response. Oncogene 25:2901-2908 (2006).
    • (2006) Oncogene , vol.25 , pp. 2901-2908
    • Zhu, Y.1    McAvoy, S.2    Kuhn, R.3    Smith, D.I.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.