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Volumn 159, Issue 1, 2005, Pages 27-31

Microarray-based comparative genomic hybridization of pheochromocytoma cell lines from neurofibromatosis knockout mice reveals genetic alterations similar to those in human pheochromocytomas

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CANCER CELL CULTURE; CANCER GENETICS; CARCINOGENESIS; CHROMOSOME 11Q; CHROMOSOME 12; CHROMOSOME 1P; CHROMOSOME 3P; CHROMOSOME 3Q; CHROMOSOME 4; CHROMOSOME 9; CHROMOSOME ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DNA MICROARRAY; GENE DELETION; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC DISORDER; GENOME ANALYSIS; KNOCKOUT GENE; MOUSE; NONHUMAN; PHEOCHROMOCYTOMA CELL; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SPECIES COMPARISON;

EID: 18144397194     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2004.09.018     Document Type: Article
Times cited : (7)

References (15)
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    • A.S. Tischler, T.S. Shih, B.O. Williams, and T. Jacks Characterization of pheochromocytomas in a mouse strain with a targeted disruptive mutation of the neurofibromatosis gene Nf1 Endocr Pathol 6 1995 323 325
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    • Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector
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    • Shizuya, H.1    Birren, B.2    Kim, U.J.3    Mancino, V.4    Slepak, T.5    Tachiiri, Y.6    Simon, M.7
  • 12
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    • Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes
    • J.F. Moley, M.B. Brother, C.T. Fong, P.S. White, S.B. Baylin, B. Nelkin, S.A. Wells, and G.M. Brodeur Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes Cancer Res 52 1992 770 774
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    • 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
  • 13
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    • Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology
    • E. Edstrom, E. Mahlamaki, B. Nord, M. Kjellman, R. Karhu, A. Hoog, N. Goncharov, B.T. Teh, M. Backdahl, and C. Larsson Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology Am J Pathol 156 2000 651 659
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    • High-level expression of receptor tyrosine kinase Ret and responsiveness to Ret-activating ligands in pheochromocytoma cell lines from neurofibromatosis knockout mice
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.