메뉴 건너뛰기




Volumn 114, Issue 1, 1999, Pages 42-50

Karyotypic analyses of hepatoblastoma: Report of two cases and review of the literature suggesting chromosomal loci responsible for the pathogenesis of this disease

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARCINOGENESIS; CASE REPORT; CHILD; CHROMOSOME TRANSLOCATION; FEMALE; GENE LOCUS; HEPATOBLASTOMA; HUMAN; KARYOTYPE; MALE; PARTIAL MONOSOMY; PARTIAL TRISOMY; PRIORITY JOURNAL; TETRASOMY;

EID: 0032837476     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00033-3     Document Type: Article
Times cited : (23)

References (39)
  • 2
    • 0031027719 scopus 로고    scopus 로고
    • Hepatic tumors in children
    • Newman K.D. Hepatic tumors in children. Semin Pediatr Surg. 6:1997;38-41.
    • (1997) Semin Pediatr Surg , vol.6 , pp. 38-41
    • Newman, K.D.1
  • 3
    • 0028270327 scopus 로고
    • Genetic changes in hepatoblastoma
    • Ding S., Michail N.E., Habib N.A. Genetic changes in hepatoblastoma. J Hepatol. 20:1994;672-675.
    • (1994) J Hepatol , vol.20 , pp. 672-675
    • Ding, S.1    Michail, N.E.2    Habib, N.A.3
  • 4
    • 0021932813 scopus 로고
    • Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism
    • Koufos A., Hansen M.F., Copeland N.G., Jenkins N.A., Lampkin B.C., Cavenee W.K. Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism. Nature. 316:1985;330-334.
    • (1985) Nature , vol.316 , pp. 330-334
    • Koufos, A.1    Hansen, M.F.2    Copeland, N.G.3    Jenkins, N.A.4    Lampkin, B.C.5    Cavenee, W.K.6
  • 5
    • 0023789660 scopus 로고
    • Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome
    • Little M.H., Thomson D.B., Hayward N.K., Smith P.J. Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome. Hum Genet. 79:1988;186-189.
    • (1988) Hum Genet , vol.79 , pp. 186-189
    • Little, M.H.1    Thomson, D.B.2    Hayward, N.K.3    Smith, P.J.4
  • 6
    • 0022918905 scopus 로고
    • Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma
    • Hass O.A., Zoubek A., Grümayer E.R., Gadner H. Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma. Cancer Genet Cytogenet. 23:1986;95-104.
    • (1986) Cancer Genet Cytogenet , vol.23 , pp. 95-104
    • Hass, O.A.1    Zoubek, A.2    Grümayer, E.R.3    Gadner, H.4
  • 10
  • 12
    • 0017260918 scopus 로고
    • Establishment of a cell line and its clonal sublines from a patient with hepatoblastoma
    • Doi I. Establishment of a cell line and its clonal sublines from a patient with hepatoblastoma. Gann. 67:1976;1-10.
    • (1976) Gann , vol.67 , pp. 1-10
    • Doi, I.1
  • 13
    • 0019303821 scopus 로고
    • Chromosome analysis in a human hepatoblastoma cell line producing α-fetoprotein
    • Miyamoto K., Taketa K., Yabe T., Miyano K., Sato J. Chromosome analysis in a human hepatoblastoma cell line producing α-fetoprotein. Acta Med Okayama. 34:1980;127-130.
    • (1980) Acta Med Okayama , vol.34 , pp. 127-130
    • Miyamoto, K.1    Taketa, K.2    Yabe, T.3    Miyano, K.4    Sato, J.5
  • 17
  • 18
    • 0025844921 scopus 로고
    • Consistent cytogenetic aberrations in hepatoblastoma: A common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies?
    • Fletcher J.A., Kozakewich H.P., Pavelka K., Grier H.E., Shamberger R.C., Korf B., Morton C.C. Consistent cytogenetic aberrations in hepatoblastoma. a common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies? Genes Chromosom Cancer. 3:1991;37-43.
    • (1991) Genes Chromosom Cancer , vol.3 , pp. 37-43
    • Fletcher, J.A.1    Kozakewich, H.P.2    Pavelka, K.3    Grier, H.E.4    Shamberger, R.C.5    Korf, B.6    Morton, C.C.7
  • 21
    • 0026656557 scopus 로고
    • Undifferentiated "small cell" hepatoblastoma with a unique chromosomal translocation: A case report
    • Hansen K., Bagtas J., Mark H.F., Homans A., Singer D.B. Undifferentiated "small cell" hepatoblastoma with a unique chromosomal translocation. a case report Pediatr Pathol. 12:1992;457-462.
    • (1992) Pediatr Pathol , vol.12 , pp. 457-462
    • Hansen, K.1    Bagtas, J.2    Mark, H.F.3    Homans, A.4    Singer, D.B.5
  • 24
    • 0026596435 scopus 로고
    • Chromosome aberrations in an alpha-fetoprotein-producing hepatoblastoma
    • Annerén G., Nordlinder H., Hedborg F. Chromosome aberrations in an alpha-fetoprotein-producing hepatoblastoma. Genes Chromosom Cancer. 4:1992;99-100.
    • (1992) Genes Chromosom Cancer , vol.4 , pp. 99-100
    • Annerén, G.1    Nordlinder, H.2    Hedborg, F.3
  • 25
    • 0027270811 scopus 로고
    • DNA content measurement can be obtained using archival material for DNA flow cytometry
    • Dressler L.G., Duncan M.H., Varsa E.E., McConnell T.S. DNA content measurement can be obtained using archival material for DNA flow cytometry. Cancer. 72:1993;2033-2041.
    • (1993) Cancer , vol.72 , pp. 2033-2041
    • Dressler, L.G.1    Duncan, M.H.2    Varsa, E.E.3    McConnell, T.S.4
  • 26
    • 0028132075 scopus 로고
    • Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma
    • Tonk V.S., Wilson K.S., Timmons C.F., Schneider N.R. Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma. Genes Chromosom Cancer. 11:1994;199-202.
    • (1994) Genes Chromosom Cancer , vol.11 , pp. 199-202
    • Tonk, V.S.1    Wilson, K.S.2    Timmons, C.F.3    Schneider, N.R.4
  • 27
    • 0030273498 scopus 로고    scopus 로고
    • Significance of extra copies of chromosome 20 and the long arm of chromosome 2 in hepatoblastoma
    • Swarts S., Wisecarver J., Bridge J.A. Significance of extra copies of chromosome 20 and the long arm of chromosome 2 in hepatoblastoma. Cancer Genet Cytogenet. 91:1996;65-67.
    • (1996) Cancer Genet Cytogenet , vol.91 , pp. 65-67
    • Swarts, S.1    Wisecarver, J.2    Bridge, J.A.3
  • 31
    • 0027970838 scopus 로고
    • Chromosomal translocations in human cancer
    • Rabbitts T.H. Chromosomal translocations in human cancer. Nature. 372:1994;143-149.
    • (1994) Nature , vol.372 , pp. 143-149
    • Rabbitts, T.H.1
  • 32
    • 0030999555 scopus 로고    scopus 로고
    • A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
    • Mitelman F., Mertens F., Johansson B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet. 15:1997;417-474.
    • (1997) Nat Genet , vol.15 , pp. 417-474
    • Mitelman, F.1    Mertens, F.2    Johansson, B.3
  • 36
    • 0026341035 scopus 로고
    • Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors
    • Kaneko Y., Homma C., Maseki N., Sakurai M., Hata J. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. Cancer Res. 51:1991;5937-5942.
    • (1991) Cancer Res , vol.51 , pp. 5937-5942
    • Kaneko, Y.1    Homma, C.2    Maseki, N.3    Sakurai, M.4    Hata, J.5
  • 39
    • 0019819011 scopus 로고
    • Break points in chromosome #1 abnormalities of 218 human neoplasms
    • Brito-Babapulle V., Atkin N.B. Break points in chromosome #1 abnormalities of 218 human neoplasms. Cancer Genet Cytogenet. 4:1981;215-225.
    • (1981) Cancer Genet Cytogenet , vol.4 , pp. 215-225
    • Brito-Babapulle, V.1    Atkin, N.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.