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Volumn 63, Issue 14, 2003, Pages 3866-3871

Detection of mitochondrial DNA mutations in the tumor and cerebrospinal fluid of medulloblastoma patients

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0041742269     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (83)

References (20)
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    • Ceramide-induced apoptosis of D283 medulloblastoma cells requires mitochondrial respiratory chain activity but occurs independently of caspases and is not sensitive to Bcl-xL overexpression
    • Poppe, M., Reimertz, C., Munstermann, G., Kogel, D., and Prehn, J. H. Ceramide-induced apoptosis of D283 medulloblastoma cells requires mitochondrial respiratory chain activity but occurs independently of caspases and is not sensitive to Bcl-xL overexpression. J. Neurochem. 82: 482-494, 2002.
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  • 8
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    • Mutations in SDHC cause autosomal dominant paraganglioma, type 3
    • Niemann, S., and Muller, U. Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat. Genet., 26: 268-270, 2000.
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    • Niemann, S.1    Muller, U.2
  • 9
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    • Nuclear genetic defects of oxidative phosphorylation
    • Shoubridge, E. A. Nuclear genetic defects of oxidative phosphorylation. Hum. Mol. Genet., 10: 2277-2284, 2001.
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 2277-2284
    • Shoubridge, E.A.1
  • 10
    • 0034671551 scopus 로고    scopus 로고
    • Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
    • Gimm, O., Armanios, M., Dziema, H., Neumann, H. P., and Eng, C. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res., 60: 6822-6825, 2000.
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    • Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
    • Astuti, D., Latif, F., Dallol, A., Dahia, P. L., Douglas, F., George, E., Skoldberg, F., Husebye, E. S., Eng, C., and Maher, E. R. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am. J. Hum. Genet., 69: 49-54, 2001.
    • (2001) Am. J. Hum. Genet. , vol.69 , pp. 49-54
    • Astuti, D.1    Latif, F.2    Dallol, A.3    Dahia, P.L.4    Douglas, F.5    George, E.6    Skoldberg, F.7    Husebye, E.S.8    Eng, C.9    Maher, E.R.10
  • 13
    • 0036839776 scopus 로고    scopus 로고
    • Comprehensive scanning of the whole mitochondrial genome for mutations
    • Wong, L-J. C., Liang, M-H., Kwon, H., Park, J., Bai, R., and Tan, D. Comprehensive scanning of the whole mitochondrial genome for mutations. Clin. Chem., 48: 1901-1912, 2002.
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    • Wong, L.-J.C.1    Liang, M.-H.2    Kwon, H.3    Park, J.4    Bai, R.5    Tan, D.6
  • 14
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    • Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresis
    • Chen, T. J., Boles, R., and Wong, L-J. C. Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresis. Clin. Chem., 45: 1162-1167, 1999.
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    • Chen, T.J.1    Boles, R.2    Wong, L.-J.C.3
  • 17
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    • Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer
    • Tan, D-J., Bai, R., and Wong, L-J. C. Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer. Cancer Res., 62: 972-976, 2002.
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    • Kirches, E., Krause, G., Warich-Kirches, M., Weis, S., Schneider, T., Meyer-Puttlitz, B., Mawrin, C., and Dietzmann, K. High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples. Int. J. Cancer, 93: 534-538, 2001.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.