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Volumn 102, Issue 2, 1998, Pages 93-99

Pediatric brain tumors: Loss of heterozygosity at 17p and TP53 gene mutations

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; BRAIN TUMOR; CHILD; CHILDHOOD CANCER; CHROMOSOME 17P; CLINICAL ARTICLE; CYTOGENETICS; EXON; FEMALE; HETEROZYGOSITY LOSS; HUMAN; INFANT; MALE; NEWBORN; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; TUMOR SUPPRESSOR GENE;

EID: 0032055899     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(97)00343-9     Document Type: Article
Times cited : (29)

References (18)
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  • 6
    • 0026087925 scopus 로고
    • Loss of heterozygosity on 6q, 16q and 17p in human central nervous system primitive neuroectodermal tumors
    • Thomas GA, Raffel C (1991): Loss of heterozygosity on 6q, 16q and 17p in human central nervous system primitive neuroectodermal tumors. Cancer Res 51:639-643.
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    • Thomas, G.A.1    Raffel, C.2
  • 8
    • 0026634161 scopus 로고
    • Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors
    • Biegel JA, Burk CD, Barr FG, Emanuel BS (1992): Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors. Cancer Res 52:3391-3395.
    • (1992) Cancer Res , vol.52 , pp. 3391-3395
    • Biegel, J.A.1    Burk, C.D.2    Barr, F.G.3    Emanuel, B.S.4
  • 12
    • 0028931287 scopus 로고
    • Deletion of chromosome arm 17p DNA sequences in pediatric high-grade and juvenile pilocytic astrocytomas
    • Willwert JR, Daneshvar L, Sheffield VC, Cohen PH (1995): Deletion of chromosome arm 17p DNA sequences in pediatric high-grade and juvenile pilocytic astrocytomas. Genes Chromosom Cancer 12:165-172.
    • (1995) Genes Chromosom Cancer , vol.12 , pp. 165-172
    • Willwert, J.R.1    Daneshvar, L.2    Sheffield, V.C.3    Cohen, P.H.4
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    • Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma
    • Onadim Z, Cowell JK (1991): Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma. J Med Genet 28:312-316.
    • (1991) J Med Genet , vol.28 , pp. 312-316
    • Onadim, Z.1    Cowell, J.K.2
  • 15
    • 0020210930 scopus 로고
    • Ultrasensitive staining of nucleic acids with silver
    • Biedler JL, Hillard PR, Rill RL (1982): Ultrasensitive staining of nucleic acids with silver. Anal Biochem 126:374-380.
    • (1982) Anal Biochem , vol.126 , pp. 374-380
    • Biedler, J.L.1    Hillard, P.R.2    Rill, R.L.3
  • 17
    • 0027983716 scopus 로고
    • Six microsatellite polymorphisms at candidate and confirmed tumour suppressor gene loci
    • Jones MH, Sato T, Saito H, Tanigami A, Nakamura Y (1994): Six microsatellite polymorphisms at candidate and confirmed tumour suppressor gene loci. Hum Mol Genet 10:1911.
    • (1994) Hum Mol Genet , vol.10 , pp. 1911
    • Jones, M.H.1    Sato, T.2    Saito, H.3    Tanigami, A.4    Nakamura, Y.5
  • 18
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    • Polymorphism at codon 213 within the p53 gene
    • Carbone D, Chiba J, Mitsucloni T (1991): Polymorphism at codon 213 within the p53 gene. Oncogene 6:1691-1692.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.