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Volumn 67, Issue 1, 1996, Pages 11-15

Loss of heterozygosity at locus F13β on chromosome 1q in human medulloblastoma

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CHROMOSOME 11P; CHROMOSOME 17P; CHROMOSOME 1P; CHROMOSOME 1Q; CHROMOSOME 9Q; CHROMOSOME MAP; CLINICAL ARTICLE; FEMALE; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; MALE; MEDULLOBLASTOMA; NEUROECTODERM TUMOR; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0030037445     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0215(19960703)67:1<11::AID-IJC3>3.0.CO;2-2     Document Type: Article
Times cited : (32)

References (41)
  • 2
    • 0026532918 scopus 로고
    • Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site
    • BARE, J.W., LEBO, R.V. and EPSTEIN, E.H., JR., Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site. Cancer Res., 52, 1494-1498 (1992).
    • (1992) Cancer Res. , vol.52 , pp. 1494-1498
    • Bare, J.W.1    Lebo, R.V.2    Epstein Jr., E.H.3
  • 4
    • 0025478315 scopus 로고
    • Cytogenetics and molecular genetics of malignant gliomas and medulloblastomas
    • BIGNER, S.H. and VOGELSTEIN, B., Cytogenetics and molecular genetics of malignant gliomas and medulloblastomas. Brain Pathol., 1, 12-18 (1990).
    • (1990) Brain Pathol. , vol.1 , pp. 12-18
    • Bigner, S.H.1    Vogelstein, B.2
  • 5
  • 6
    • 0028926888 scopus 로고
    • Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: One probably imprinted, another associated with N-myc amplification
    • CARON, H. and 12 OTHERS, Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification. Hum. mol. Genet., 4, 535-539 (1995).
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 535-539
    • Caron, H.1
  • 7
    • 0024447257 scopus 로고
    • Loss of heterozygosity on chromosome 1q in human breast cancer
    • CHEN, L.C., DOLLBAUM, C. and SMITH, H.S., Loss of heterozygosity on chromosome 1q in human breast cancer. Proc. nat. Acad. Sci. (Wash.), 86, 7204-7207 (1989).
    • (1989) Proc. Nat. Acad. Sci. (Wash.) , vol.86 , pp. 7204-7207
    • Chen, L.C.1    Dollbaum, C.2    Smith, H.S.3
  • 9
    • 0024998205 scopus 로고
    • Deletion mapping of the medulloblastoma locus on chromosome 17p
    • COGEN, P.H., DANESHVAR, L., METZGER, A.K. and EDWARDS, M.S.B., Deletion mapping of the medulloblastoma locus on chromosome 17p. Genomics, 8, 279-285 (1990).
    • (1990) Genomics , vol.8 , pp. 279-285
    • Cogen, P.H.1    Daneshvar, L.2    Metzger, A.K.3    Edwards, M.S.B.4
  • 10
    • 0027942568 scopus 로고
    • A comprehensive human linkage map with centimorgan density
    • COOPERATIVE HUMAN LINKAGE CENTER (CHLC), A comprehensive human linkage map with centimorgan density. Science. 265, 2049-2054 (1994).
    • (1994) Science , vol.265 , pp. 2049-2054
  • 15
    • 0026498785 scopus 로고
    • Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors
    • FULTS, D., PETRONIO, J., NOBLETT, B.D. and PEDONE, C.A., Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors. Genomics, 14, 799-801 (1992).
    • (1992) Genomics , vol.14 , pp. 799-801
    • Fults, D.1    Petronio, J.2    Noblett, B.D.3    Pedone, C.A.4
  • 16
    • 0026627965 scopus 로고
    • Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
    • GAILANI, M.R., BALE, S.J. and LEFFELL, D.J., Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell, 69, 111-117 (1992).
    • (1992) Cell , vol.69 , pp. 111-117
    • Gailani, M.R.1    Bale, S.J.2    Leffell, D.J.3
  • 22
    • 0028046406 scopus 로고
    • Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors
    • MATHEW, S., MURTY, V.V.V.S., BOSL, G.J. and CHAGANTI, R.S.K., Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Res., 54, 6265-6269 (1994).
    • (1994) Cancer Res. , vol.54 , pp. 6265-6269
    • Mathew, S.1    Murty, V.V.V.S.2    Bosl, G.J.3    Chaganti, R.S.K.4
  • 23
    • 0028040905 scopus 로고
    • Physical mapping of chromosome 17p13.3 in the region of a putative tumor suppressor gene important in medulloblastoma
    • MCDONALD, J.D., DANESHVAR, L., WILLERT, J.R., MATSUMURA, K., WALDMAN, F. and COGEN, P.H., Physical mapping of chromosome 17p13.3 in the region of a putative tumor suppressor gene important in medulloblastoma. Genomics, 23, 229-232 (1994).
    • (1994) Genomics , vol.23 , pp. 229-232
    • Mcdonald, J.D.1    Daneshvar, L.2    Willert, J.R.3    Matsumura, K.4    Waldman, F.5    Cogen, P.H.6
  • 24
    • 0026548844 scopus 로고
    • Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes
    • MOLEY, J.F., BROTHER, M.B., FONG, C.-T., WHITE, P.S., BAYLIN, S.B., NELKIN, B., WELLS, S.A. and BRODEUR, G.M., Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes. Cancer Res., 52, 770-774 (1992).
    • (1992) Cancer Res. , vol.52 , pp. 770-774
    • Moley, J.F.1    Brother, M.B.2    Fong, C.-T.3    White, P.S.4    Baylin, S.B.5    Nelkin, B.6    Wells, S.A.7    Brodeur, G.M.8
  • 25
    • 0028918250 scopus 로고
    • Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer
    • NAGAI, H., NEGRINI, M., CARTER, S.L., GILLUM, D.R., ROSENBERG, A.L., SCHWARTZ, G.F. and CROCE, C.M., Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer. Cancer Res., 55, 1752-1757 (1995).
    • (1995) Cancer Res. , vol.55 , pp. 1752-1757
    • Nagai, H.1    Negrini, M.2    Carter, S.L.3    Gillum, D.R.4    Rosenberg, A.L.5    Schwartz, G.F.6    Croce, C.M.7
  • 27
    • 0026519209 scopus 로고
    • A tetranucleotide repeat for the F13B locus
    • NISHIMURA, D.Y. and MURRAY, J.C., A tetranucleotide repeat for the F13B locus. Nucl. Acids Res., 20, 1167 (1992).
    • (1992) Nucl. Acids Res. , vol.20 , pp. 1167
    • Nishimura, D.Y.1    Murray, J.C.2
  • 29
    • 0025649742 scopus 로고
    • Chemotherapy for medulloblastoma/primitive neuroectodermal tumors of the posterior fossa
    • PACKER, R.J., Chemotherapy for medulloblastoma/primitive neuroectodermal tumors of the posterior fossa. Ann. Neurol., 28, 823-828 (1990).
    • (1990) Ann. Neurol. , vol.28 , pp. 823-828
    • Packer, R.J.1
  • 30
    • 0026849869 scopus 로고
    • A polymorphic microsatellite repeat is located close to the promoter region of the c-fgr proto-oncogene (FGR) at chromosome 1p36.2-p36.1
    • PATEL, M.S., MANKOO, B.S. and BRIOCELL, P.M., A polymorphic microsatellite repeat is located close to the promoter region of the c-fgr proto-oncogene (FGR) at chromosome 1p36.2-p36.1. Hum. mol. Genet, 1, 65 (1992).
    • (1992) Hum. Mol. Genet , vol.1 , pp. 65
    • Patel, M.S.1    Mankoo, B.S.2    Briocell, P.M.3
  • 31
    • 0027280787 scopus 로고
    • Trinucleotide repeat polymorphism in the human antithrombin III (AT3) gene
    • PERRY, D.J., Trinucleotide repeat polymorphism in the human antithrombin III (AT3) gene. Hum. mol. Genet., 2, 618 (1993).
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 618
    • Perry, D.J.1
  • 33
    • 0025124584 scopus 로고
    • Reduction to hompzygosity and gene amplification in central nervous system primitive neuroectodermal tumors of childhood
    • RAFFEL, C., GILLES, F.E. and WEINBERG, K.I., Reduction to hompzygosity and gene amplification in central nervous system primitive neuroectodermal tumors of childhood. Cancer Res., 50, 587-591 (1990).
    • (1990) Cancer Res. , vol.50 , pp. 587-591
    • Raffel, C.1    Gilles, F.E.2    Weinberg, K.I.3
  • 35
    • 0028798253 scopus 로고
    • Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas
    • SCHOFIELD, D., WEST, D.C., ANTHONY, D.C., MARSHAL, R. and SKLAR, J., Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas. Amer. J. Pathol., 146, 472-480 (1995).
    • (1995) Amer. J. Pathol. , vol.146 , pp. 472-480
    • Schofield, D.1    West, D.C.2    Anthony, D.C.3    Marshal, R.4    Sklar, J.5
  • 36
    • 0026251312 scopus 로고
    • Descriptive epidemiology of primary central nervous system tumours in children: A population-based study
    • STEVENS, M.C.G., CAMERON, A.H., MUIR, K.R., PARKES, S.E., REID, H. and WHITWELL, H., Descriptive epidemiology of primary central nervous system tumours in children: a population-based study. Clin. Oncol., 3, 323-329 (1991).
    • (1991) Clin. Oncol. , vol.3 , pp. 323-329
    • Stevens, M.C.G.1    Cameron, A.H.2    Muir, K.R.3    Parkes, S.E.4    Reid, H.5    Whitwell, H.6
  • 37
    • 0026087925 scopus 로고
    • Loss of heterozygosity on 6q, 16q, and 17p in human central nervous system primitive neuroectodermal tumors
    • THOMAS, G.A. and RAFFEL, C., Loss of heterozygosity on 6q, 16q, and 17p in human central nervous system primitive neuroectodermal tumors. Cancer Res., 51, 639-643 (1991).
    • (1991) Cancer Res. , vol.51 , pp. 639-643
    • Thomas, G.A.1    Raffel, C.2
  • 41
    • 0028111570 scopus 로고
    • Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas
    • YEH, S.-H., CHEN, P.J., CHEN, H.-L., LAI, M.-Y., WANG, C.-C. and CHEN, D.-S., Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res., 54, 4188-4192 (1994).
    • (1994) Cancer Res. , vol.54 , pp. 4188-4192
    • Yeh, S.-H.1    Chen, P.J.2    Chen, H.-L.3    Lai, M.-Y.4    Wang, C.-C.5    Chen, D.-S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.