메뉴 건너뛰기




Volumn 54, Issue 1, 1995, Pages 91-95

Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma

Author keywords

Chromosome arm 19q; Chromosome arm lp; Lineage; Loss of heterozygosity; Oligoastrocytoma; Oligodendroglioma

Indexed keywords

ALLELISM; ARTICLE; ASTROCYTOMA; CELL LINEAGE; CHROMOSOME 19Q; CHROMOSOME 1P; CHROMOSOME ARM; CHROMOSOME LOSS; HETEROZYGOSITY; HUMAN; HUMAN CELL; OLIGODENDROGLIOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0028799791     PISSN: 00223069     EISSN: 15546578     Source Type: Journal    
DOI: 10.1097/00005072-199501000-00011     Document Type: Article
Times cited : (340)

References (32)
  • 3
    • 0023708370 scopus 로고
    • Clonal genomic alterations in glioma malignancy stages
    • James CD, Carlbom E, Dumanski JP, et al. Clonal genomic alterations in glioma malignancy stages. Cancer Res 1988;48:5546-51
    • (1988) Cancer Res , vol.48 , pp. 5546-5551
    • James, C.D.1    Carlbom, E.2    Dumanski, J.P.3
  • 4
    • 0023914874 scopus 로고
    • Gene amplification in malignant human gliomas: Clinical and histopathologic aspects
    • Bigner SH, Burger PC, Wong AJ, et al. Gene amplification in malignant human gliomas: Clinical and histopathologic aspects. J Neu-ropathol Exp Neurol 1988;47:191-205
    • (1988) J Neu-Ropathol Exp Neurol , vol.47 , pp. 191-205
    • Bigner, S.H.1    Burger, P.C.2    Wong, A.J.3
  • 5
    • 0026710064 scopus 로고
    • Association of epidermal growth factor receptor gene amplification with loss of chromosome 10 in human glioblastoma multiforme
    • von Deimling A, Louis DN, von Ammon K, et al. Association of epidermal growth factor receptor gene amplification with loss of chromosome 10 in human glioblastoma multiforme. J Neurosurg 1992;77:295-301
    • (1992) J Neurosurg , vol.77 , pp. 295-301
    • Von Deimling, A.1    Louis, D.N.2    Von Ammon, K.3
  • 6
    • 0026730907 scopus 로고
    • Evidence for a tumor suppressor gene on chromosome 19q associated with human astrocytomas, oligodendrogliomas and mixed gliomas
    • von Deimling A, Louis DN, von Ammon K, Petersen I, Wiestler OD, Seizinger BR. Evidence for a tumor suppressor gene on chromosome 19q associated with human astrocytomas, oligodendrogliomas and mixed gliomas. Cancer Res 1992;52:4277-9
    • (1992) Cancer Res , vol.52 , pp. 4277-4279
    • Von Deimling, A.1    Louis, D.N.2    Von Ammon, K.3    Petersen, I.4    Wiestler, O.D.5    Seizinger, B.R.6
  • 7
    • 0028335222 scopus 로고
    • Deletion mapping of a putative tumor suppressor gene on chromosome 19q associated with human gliomas
    • von Deimling A, Nagel J, Bender B, et al. Deletion mapping of a putative tumor suppressor gene on chromosome 19q associated with human gliomas. Int J Cancer 1994;57:676-80
    • (1994) Int J Cancer , vol.57 , pp. 676-680
    • Von Deimling, A.1    Nagel, J.2    Bender, B.3
  • 10
    • 0027261003 scopus 로고
    • Molecular genetics of pediatric brain stem gliomas. Application of PCR techniques to small and archival brain tumor specimens
    • Louis DN, Rubio M-P, Correa KM, Gusella JF, von Deimling A. Molecular genetics of pediatric brain stem gliomas. Application of PCR techniques to small and archival brain tumor specimens. J Neuropathol Exp Neurol 1993;52:507-15
    • (1993) J Neuropathol Exp Neurol , vol.52 , pp. 507-515
    • Louis, D.N.1    Rubio, M.-P.2    Correa, K.M.3    Gusella, J.F.4    Von Deimling, A.5
  • 11
    • 0026849869 scopus 로고
    • A polymorphic microsatellite repeat is located close to the promotor region of the c-fgr proto-oncogene (FGR) at chromosome 1 p36.2-p36.1
    • Patel MS, Mankoo BS, Brickell PM. A polymorphic microsatellite repeat is located close to the promotor region of the c-fgr proto-oncogene (FGR) at chromosome 1 p36.2-p36.1. Hum Mol Genet 1992;1:65
    • (1992) Hum Mol Genet , vol.1 , pp. 65
    • Patel, M.S.1    Mankoo, B.S.2    Brickell, P.M.3
  • 12
  • 13
    • 0026337065 scopus 로고
    • Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms, Human Gene Mapping 11 (1991)
    • Williamson R, Bowcock A, Kidd K, et al. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms, Human Gene Mapping 11 (1991). Cytogenet Cell Genet 1991;58:1190-1832
    • (1991) Cytogenet Cell Genet , vol.58 , pp. 1190-1832
    • Williamson, R.1    Bowcock, A.2    Kidd, K.3
  • 14
    • 0027280787 scopus 로고
    • Trinucleotide repeat polymorphism in the human anti-thrombin III (AT3) gene
    • Perry DJ. Trinucleotide repeat polymorphism in the human anti-thrombin III (AT3) gene. Hum Mol Genet 1993;2:618
    • (1993) Hum Mol Genet , vol.2 , pp. 618
    • Perry, D.J.1
  • 15
    • 0026519209 scopus 로고
    • A tetranucleotide repeat for the F13B locus
    • Nishimura DY, Murray JC. A tetranucleotide repeat for the F13B locus. Nucl Acids Res 1992:20:1167
    • (1992) Nucl Acids Res , vol.20 , pp. 1167
    • Nishimura, D.Y.1    Murray, J.C.2
  • 17
    • 0026667374 scopus 로고
    • A (CA)n dinucleotide repeat assay for evaluating loss of allelic heterozygosity in small and archival human brain tumor specimens
    • Louis D, von Deimling A, Seizinger BR. A (CA)n dinucleotide repeat assay for evaluating loss of allelic heterozygosity in small and archival human brain tumor specimens. Am J Pathol 1992; 141: 777-82
    • (1992) Am J Pathol , vol.141 , pp. 777-782
    • Louis, D.1    Von Deimling, A.2    Seizinger, B.R.3
  • 19
    • 0027714732 scopus 로고
    • A rapid and non radioactive PCR based assay for the detection of allelic loss in human gliomas
    • von Deimling A, Bender B, Louis DN, Wiestler OD. A rapid and non radioactive PCR based assay for the detection of allelic loss in human gliomas. Neuropathol Appl Neurobiol 1993;19:524-9
    • (1993) Neuropathol Appl Neurobiol , vol.19 , pp. 524-529
    • Von Deimling, A.1    Bender, B.2    Louis, D.N.3    Wiestler, O.D.4
  • 20
    • 0028204493 scopus 로고
    • Loci associated with malignant progression in astrocytomas: A candidate on chromosome 19q
    • von Deimling A, Bender B, Jahnke R, et al. Loci associated with malignant progression in astrocytomas: A candidate on chromosome 19q. Cancer Res 1994;54:1397-1401
    • (1994) Cancer Res , vol.54 , pp. 1397-1401
    • Von Deimling, A.1    Bender, B.2    Jahnke, R.3
  • 21
    • 0024670859 scopus 로고
    • Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-myc amplification
    • Fong C-T, Dracopoli NC, White PS, et al. Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: Correlation with N-myc amplification. Proc Natl Acad Sci USA 1989;86:3753-7
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 3753-3757
    • Fong, C.-T.1    Dracopoli, N.C.2    White, P.S.3
  • 22
    • 0025801654 scopus 로고
    • Abnormalities of chromosome 1and loss of heterozygosity on 1 p in primary hepatomas
    • Simon D, Knowles B, Weith A. Abnormalities of chromosome 1and loss of heterozygosity on 1 p in primary hepatomas. Oncogene 1991;6:765-70
    • (1991) Oncogene , vol.6 , pp. 765-770
    • Simon, D.1    Knowles, B.2    Weith, A.3
  • 24
    • 0028348101 scopus 로고
    • Chromosomal deletions in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression
    • Lindblom A, Ruttledge M, Collins VP, Nordenskjold M, Dumanski JR Chromosomal deletions in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression. Int J Cancer 1994;56:354-7
    • (1994) Int J Cancer , vol.56 , pp. 354-357
    • Lindblom, A.1    Ruttledge, M.2    Collins, V.P.3    Nordenskjold, M.4    Dumanski, J.R.5
  • 25
    • 0028205559 scopus 로고
    • Molecular analysis of chromosome 1 abnormalities in human gliomas reveals frequent loss of lp in oligodendroglial tumors
    • Bello MJ, Vaquero J, de Campos JM, et al. Molecular analysis of chromosome 1 abnormalities in human gliomas reveals frequent loss of lp in oligodendroglial tumors. Int J Cancer 1994;57:172-5
    • (1994) Int J Cancer , vol.57 , pp. 172-175
    • Bello, M.J.1    Vaquero, J.2    De Campos, J.M.3
  • 26
    • 0021211606 scopus 로고
    • Glial fibrillary acidic protein (GFAP) in oligodendroglial tumors: Gliofibrillary oligodendroglioma and transitional oligo-astrocytoma as subtypes of oligodendroglioma
    • Herpers MJHM, Budka H. Glial fibrillary acidic protein (GFAP) in oligodendroglial tumors: Gliofibrillary oligodendroglioma and transitional oligo-astrocytoma as subtypes of oligodendroglioma. Acta Neuropathol 1984;64:265-72
    • (1984) Acta Neuropathol , vol.64 , pp. 265-272
    • Herpers, M.1    Budka, H.2
  • 27
    • 0023881374 scopus 로고
    • Oligodendroglial tumors: An im-munohistochemical and electron microscopic study
    • Sarker C, Roy S, Tandon PN. Oligodendroglial tumors: An im-munohistochemical and electron microscopic study. Cancer 1989;61:1862-6
    • (1989) Cancer , vol.61 , pp. 1862-1866
    • Sarker, C.1    Roy, S.2    Tandon, P.N.3
  • 28
    • 0020538298 scopus 로고
    • A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium
    • Raff MC, Miller RH, Noble M. A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium. Nature 1983;303:390-6
    • (1983) Nature , vol.303 , pp. 390-396
    • Raff, M.C.1    Miller, R.H.2    Noble, M.3
  • 29
    • 0024431243 scopus 로고
    • De la Monte SM. Dual lineage of astrocytomas
    • Bishop MB, de la Monte SM. Dual lineage of astrocytomas. Am J Pathol 1989;135:517-27
    • (1989) Am J Pathol , vol.135 , pp. 517-527
    • Bishop, M.B.1
  • 30
    • 0026629404 scopus 로고
    • P53 Mutations are associated with 17p allelic loss in grade II and grade III astrocytoma
    • von Deimling A, Eibl RH, Ohgaki H, et al. p53 Mutations are associated with 17p allelic loss in grade II and grade III astrocytoma. Cancer Res 1992;52:2987-90
    • (1992) Cancer Res , vol.52 , pp. 2987-2990
    • Von Deimling, A.1    Eibl, R.H.2    Ohgaki, H.3
  • 31
    • 0026547577 scopus 로고
    • P53 Mutation and loss of heterozygosity on chromosomes 17 and 10 during human astrocytoma progression
    • Fults D, Brockmeyer D, Tullous MW, Pedone CA, Cawthon RM. p53 Mutation and loss of heterozygosity on chromosomes 17 and 10 during human astrocytoma progression. Cancer Res 1992;52: 674-9
    • (1992) Cancer Res , vol.52 , pp. 674-679
    • Fults, D.1    Brockmeyer, D.2    Tullous, M.W.3    Pedone, C.A.4    Cawthon, R.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.