메뉴 건너뛰기




Volumn 14, Issue 2, 2007, Pages 453-462

Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN RET; PROTEIN SUBUNIT; SUCCINATE DEHYDROGENASE;

EID: 34547819216     PISSN: 13510088     EISSN: None     Source Type: Journal    
DOI: 10.1677/ERC-06-0044     Document Type: Article
Times cited : (30)

References (36)
  • 1
    • 0036805853 scopus 로고    scopus 로고
    • Cytopathies involving mitochondrial complex II
    • Ackrell BA 2002 Cytopathies involving mitochondrial complex II. Molecular Aspects of Medicine 23 369-384.
    • (2002) Molecular Aspects of Medicine , vol.23 , pp. 369-384
    • Ackrell, B.A.1
  • 10
    • 0037431550 scopus 로고    scopus 로고
    • Dannenberg H, De Krijger RR, van der Harst E, Abbou M, Y IJ, Komminoth P & Dinjens WN 2003 Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas. International Journal of Cancer 105 190-195.
    • Dannenberg H, De Krijger RR, van der Harst E, Abbou M, Y IJ, Komminoth P & Dinjens WN 2003 Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas. International Journal of Cancer 105 190-195.
  • 12
    • 0029836333 scopus 로고    scopus 로고
    • Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease
    • Eng C 1996 Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease. New England Journal of Medicine 335 943-951.
    • (1996) New England Journal of Medicine , vol.335 , pp. 943-951
    • Eng, C.1
  • 15
    • 19944425515 scopus 로고    scopus 로고
    • Pheochromocytoma-associated syndromes: Genes, proteins and functions of RET, VHL and SDHx
    • Gimm O 2005 Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx. Familial Cancer 4 17-23.
    • (2005) Familial Cancer , vol.4 , pp. 17-23
    • Gimm, O.1
  • 18
    • 0028000277 scopus 로고
    • Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing
    • Komminoth P, Kunz E, Hiort O, Schroder S, Matias-Guiu X, Christiansen G, Roth J & Heitz PU 1994 Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing. American Journal of Pathology 145 922-929.
    • (1994) American Journal of Pathology , vol.145 , pp. 922-929
    • Komminoth, P.1    Kunz, E.2    Hiort, O.3    Schroder, S.4    Matias-Guiu, X.5    Christiansen, G.6    Roth, J.7    Heitz, P.U.8
  • 30
    • 0037168186 scopus 로고    scopus 로고
    • Absence of somatic SDHD mutations in sporadic neuroendocrine tumors and detection of two germline variants in paraganglioma patients
    • Perren A, Barghorn A, Schmid S, Saremaslani P, Roth J, Heitz PU & Komminoth P 2002 Absence of somatic SDHD mutations in sporadic neuroendocrine tumors and detection of two germline variants in paraganglioma patients. Oncogene 21 7605-7608.
    • (2002) Oncogene , vol.21 , pp. 7605-7608
    • Perren, A.1    Barghorn, A.2    Schmid, S.3    Saremaslani, P.4    Roth, J.5    Heitz, P.U.6    Komminoth, P.7
  • 32
    • 2442446468 scopus 로고    scopus 로고
    • Pheochromocytoma and functional paraganglioma
    • Roman S 2004 Pheochromocytoma and functional paraganglioma. Current Opinion in Oncology 16 8-12.
    • (2004) Current Opinion in Oncology , vol.16 , pp. 8-12
    • Roman, S.1
  • 35
    • 0035688775 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia
    • Thakker RV 2001 Multiple endocrine neoplasia. Hormone Research 56 67-72.
    • (2001) Hormone Research , vol.56 , pp. 67-72
    • Thakker, R.V.1
  • 36
    • 0036731623 scopus 로고    scopus 로고
    • Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene
    • Young AL, Baysal BE, Deb A & Young WF Jr 2002 Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene. Journal of Clinical Endocrinology and Metabolism 87 4101-4105.
    • (2002) Journal of Clinical Endocrinology and Metabolism , vol.87 , pp. 4101-4105
    • Young, A.L.1    Baysal, B.E.2    Deb, A.3    Young Jr, W.F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.