메뉴 건너뛰기




Volumn 28, Issue 2, 2000, Pages 164-172

Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE MYELOBLASTIC LEUKEMIA; ARTICLE; CANCER SUSCEPTIBILITY; CHROMOSOME 5Q; CHROMOSOME 7Q; CLINICAL ARTICLE; FAMILY STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HETEROZYGOSITY LOSS; HUMAN; MALE; PEDIGREE; PRIORITY JOURNAL;

EID: 0034015768     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(200006)28:2<164::AID-GCC5>3.0.CO;2-2     Document Type: Article
Times cited : (18)

References (40)
  • 1
    • 0020623050 scopus 로고
    • Partial deletion of the lung arm of chromosome 16 and bone marrow eosinophilia in acute nonlymphocytic leukemia: A new association
    • Arthur DC, Bloomfield CD. 1983. Partial deletion of the lung arm of chromosome 16 and bone marrow eosinophilia in acute nonlymphocytic leukemia: a new association. Blood 61:9994-9998.
    • (1983) Blood , vol.61 , pp. 9994-9998
    • Arthur, D.C.1    Bloomfield, C.D.2
  • 2
    • 0027089868 scopus 로고
    • Abnormalities of chromosome 16q in myeloid malignancy: 14 new cases and a review of the literature
    • Betts DR, Rohatiner AZ, Evans ML, Rassam SM, Lister TA, Gibbons B. 1992. Abnormalities of chromosome 16q in myeloid malignancy: 14 new cases and a review of the literature. Leukemia 6:1250-1256.
    • (1992) Leukemia , vol.6 , pp. 1250-1256
    • Betts, D.R.1    Rohatiner, A.Z.2    Evans, M.L.3    Rassam, S.M.4    Lister, T.A.5    Gibbons, B.6
  • 3
    • 0026321407 scopus 로고
    • Statistical methods for multipoint radiation hybrid mapping
    • Boehnke M, Lange K, Cox DR. 1991. Statistical methods for multipoint radiation hybrid mapping. Am J Hum Genet 49:1174-1188.
    • (1991) Am J Hum Genet , vol.49 , pp. 1174-1188
    • Boehnke, M.1    Lange, K.2    Cox, D.R.3
  • 4
    • 0027259409 scopus 로고
    • Clonal evolution in acute myeloid leukemia
    • Busque L, Gilliland G. 1993. Clonal evolution in acute myeloid leukemia. Blood 82:337-342.
    • (1993) Blood , vol.82 , pp. 337-342
    • Busque, L.1    Gilliland, G.2
  • 7
    • 0031811725 scopus 로고    scopus 로고
    • Familial acute myeloid leukemia: Four male members of a single family over three consecutive generations exhibiting anticipation
    • De Lord C, Powles R, Mehta J, Wilson K, Treleaven J, Meller S, Catovsky D. 1998. Familial acute myeloid leukemia: four male members of a single family over three consecutive generations exhibiting anticipation. Br J haematol 100:557-560.
    • (1998) Br J Haematol , vol.100 , pp. 557-560
    • De Lord, C.1    Powles, R.2    Mehta, J.3    Wilson, K.4    Treleaven, J.5    Meller, S.6    Catovsky, D.7
  • 8
    • 0025166061 scopus 로고
    • Characterization of chromosomal anomalies in human breast cancer: A comparison of 30 paradiploid cases with few chromosome changes
    • Dutrillaux B, Gerbault-Seureau M, Zafrani B. 1990. Characterization of chromosomal anomalies in human breast cancer: a comparison of 30 paradiploid cases with few chromosome changes. Cancer Genet Cytogenet 49:203-217.
    • (1990) Cancer Genet Cytogenet , vol.49 , pp. 203-217
    • Dutrillaux, B.1    Gerbault-Seureau, M.2    Zafrani, B.3
  • 11
    • 0031977285 scopus 로고    scopus 로고
    • A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers
    • Filippova GN, Lindblom A, Meincke LJ, Klenova EM, Neiman PE, Collins SJ, Doggett NA, Lobanenkov VV. 1998. A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers. Genes Chromosomes Cancer 22:26-36.
    • (1998) Genes Chromosomes Cancer , vol.22 , pp. 26-36
    • Filippova, G.N.1    Lindblom, A.2    Meincke, L.J.3    Klenova, E.M.4    Neiman, P.E.5    Collins, S.J.6    Doggett, N.A.7    Lobanenkov, V.V.8
  • 12
    • 0031045309 scopus 로고    scopus 로고
    • NF-E2p18/mafK is required in DMSO-induced differentiation of Friend erythroleukemia cells by enhancing NF-E2 activity
    • Francastel C, Poindessous-Jazat V, Augery-Bourget Y, Robert-Lezenes J. 1997. NF-E2p18/mafK is required in DMSO-induced differentiation of Friend erythroleukemia cells by enhancing NF-E2 activity. Leukemia 11:273-280.
    • (1997) Leukemia , vol.11 , pp. 273-280
    • Francastel, C.1    Poindessous-Jazat, V.2    Augery-Bourget, Y.3    Robert-Lezenes, J.4
  • 14
    • 0030924499 scopus 로고    scopus 로고
    • The genetics of familial leukemia
    • Horwitz M. 1997. The genetics of familial leukemia. Leukemia 11:1347-1359.
    • (1997) Leukemia , vol.11 , pp. 1347-1359
    • Horwitz, M.1
  • 15
    • 0029760542 scopus 로고    scopus 로고
    • A family inheriting different subtypes of acute myelogenous leukemia
    • Horwitz M, Sabath DE, Smithson WA, Radich J. 1996. A family inheriting different subtypes of acute myelogenous leukemia. Am J Hematol 52:295-304.
    • (1996) Am J Hematol , vol.52 , pp. 295-304
    • Horwitz, M.1    Sabath, D.E.2    Smithson, W.A.3    Radich, J.4
  • 17
    • 0031014544 scopus 로고    scopus 로고
    • Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22
    • Iida A, Isobe R, Yoshimoto M, Kasumi F, Nakamura Y, Emi M. 1997. Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22. Br J Cancer 75:264-267.
    • (1997) Br J Cancer , vol.75 , pp. 264-267
    • Iida, A.1    Isobe, R.2    Yoshimoto, M.3    Kasumi, F.4    Nakamura, Y.5    Emi, M.6
  • 18
    • 0029080316 scopus 로고
    • Conditional expression of the ubiquitous transcription factor MafK induces erythroleukemia cell differentiation
    • Igarashi K, Itoh K, Hayashi N, Nishizawa M, Yamamoto M. 1995. Conditional expression of the ubiquitous transcription factor MafK induces erythroleukemia cell differentiation. Proc Natl Acad Sci USA 92:7445-7449.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 7445-7449
    • Igarashi, K.1    Itoh, K.2    Hayashi, N.3    Nishizawa, M.4    Yamamoto, M.5
  • 20
    • 0027378164 scopus 로고
    • Cytogenetic deletion maps of hematologic neoplasms: Circumstantial evidence for tumor suppressor loci
    • Johansson B, Mertens F, Mitelman F. 1993. Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer 8:205-218.
    • (1993) Genes Chromosomes Cancer , vol.8 , pp. 205-218
    • Johansson, B.1    Mertens, F.2    Mitelman, F.3
  • 21
    • 0029886532 scopus 로고    scopus 로고
    • Parametric and nonparamctric linkage analysis: A unified multipoint approach
    • Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. 1996. Parametric and nonparamctric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363.
    • (1996) Am J Hum Genet , vol.58 , pp. 1347-1363
    • Kruglyak, L.1    Daly, M.J.2    Reeve-Daly, M.P.3    Lander, E.S.4
  • 23
    • 0021183587 scopus 로고
    • Heritable fragile site in cancer
    • Le Beau MM, Rowley JD. 1984. Heritable fragile site in cancer Nature 308:607-608.
    • (1984) Nature , vol.308 , pp. 607-608
    • Le Beau, M.M.1    Rowley, J.D.2
  • 25
    • 0028952036 scopus 로고
    • Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia
    • Liu PP, Hajra A, Wijmenga C, Collins FS. 1995. Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia. Blood 86:2289-2302.
    • (1995) Blood , vol.86 , pp. 2289-2302
    • Liu, P.P.1    Hajra, A.2    Wijmenga, C.3    Collins, F.S.4
  • 28
    • 0023890361 scopus 로고
    • Central nervous system involvement in acute nonlymphocytic leukemia with inv(16)(p13q22)
    • Ohyashiki K, Ohyashiki JH, Iwabuchi A, Ito H, Toyama K. 1988. Central nervous system involvement in acute nonlymphocytic leukemia with inv(16)(p13q22). Leukemia 2:398-399.
    • (1988) Leukemia , vol.2 , pp. 398-399
    • Ohyashiki, K.1    Ohyashiki, J.H.2    Iwabuchi, A.3    Ito, H.4    Toyama, K.5
  • 30
    • 0039513062 scopus 로고
    • Computer-simulation methods in human linkage analysis
    • Ott J. 1989. Computer-simulation methods in human linkage analysis. Proc Natl Acad Sci USA 86:4175-4178.
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 4175-4178
    • Ott, J.1
  • 31
    • 0027970838 scopus 로고
    • Chromosomal translocations in human cancer
    • Rabbitts TH. 1994. Chromosomal translocations in human cancer. Nature 372:143-149.
    • (1994) Nature , vol.372 , pp. 143-149
    • Rabbitts, T.H.1
  • 32
    • 0017182228 scopus 로고
    • The role of cytogenetics in hematology
    • Rowley JD. 1976. The role of cytogenetics in hematology. Blood 48:1-7.
    • (1976) Blood , vol.48 , pp. 1-7
    • Rowley, J.D.1
  • 34
    • 0026655447 scopus 로고
    • Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monsomy 7
    • Shannon KM, Turhan AG, Rogers PCJ, Kan YW. 1995. Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monsomy 7. Genomics 14:121-125.
    • (1995) Genomics , vol.14 , pp. 121-125
    • Shannon, K.M.1    Turhan, A.G.2    Rogers, P.C.J.3    Kan, Y.W.4
  • 38
    • 0000801438 scopus 로고
    • SLINK: A general simulation program for linkage analysis
    • Weeks DE, Ott J, Lathrop GM. 1990. SLINK: a general simulation program for linkage analysis. Am J Hum Genet 47:A204.
    • (1990) Am J Hum Genet , vol.47
    • Weeks, D.E.1    Ott, J.2    Lathrop, G.M.3
  • 39
    • 0029145745 scopus 로고
    • The molecular biology of myeloproliferative disorders as revealed by chromosomal abnormalities
    • Zeleznik-Le NJ, Nucifora G, Rowley JD. 1995. The molecular biology of myeloproliferative disorders as revealed by chromosomal abnormalities. Semin Hematol 32:201-219.
    • (1995) Semin Hematol , vol.32 , pp. 201-219
    • Zeleznik-Le, N.J.1    Nucifora, G.2    Rowley, J.D.3
  • 40
    • 0030927835 scopus 로고    scopus 로고
    • Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map
    • Zhao N, Stoffel A, Wang PW, Eisenbart JD, Espinosa R 3rd, Larson RA, Le Beau MM. 1997. Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map. Proc Natl Acad Sci USA 94:6948-6953.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 6948-6953
    • Zhao, N.1    Stoffel, A.2    Wang, P.W.3    Eisenbart, J.D.4    Espinosa R. III5    Larson, R.A.6    Le Beau, M.M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.