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Volumn 68, Issue 2, 2007, Pages 68-71

Novel germline mutations in the SDHB and SDHD genes in Japanese pheochromocytomas

Author keywords

Mutation; Pheochromocytoma; SDH genes

Indexed keywords

SUCCINATE DEHYDROGENASE;

EID: 34347374074     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000099655     Document Type: Article
Times cited : (13)

References (13)
  • 4
    • 0037422207 scopus 로고    scopus 로고
    • Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic pheochromocytomas
    • Benn DE, Croxson MS, Tucker K, Bambach CP, Richardson AL, Debridge L, Pullan PT, Hammond J, Marsh DJ, Robinson BG: Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic pheochromocytomas. Oncogene 2003;22:1358-1364.
    • (2003) Oncogene , vol.22 , pp. 1358-1364
    • Benn, D.E.1    Croxson, M.S.2    Tucker, K.3    Bambach, C.P.4    Richardson, A.L.5    Debridge, L.6    Pullan, P.T.7    Hammond, J.8    Marsh, D.J.9    Robinson, B.G.10
  • 5
    • 0034977649 scopus 로고    scopus 로고
    • Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas
    • Aguiar RCT, Cox G, Pomeroy SL, Dahia PLM: Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas. J Clin Endocrinol Metab 2001;86:2890-2894.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 2890-2894
    • Aguiar, R.C.T.1    Cox, G.2    Pomeroy, S.L.3    Dahia, P.L.M.4
  • 6
    • 0034671551 scopus 로고    scopus 로고
    • Somatic and occult germ-line mutations in SDHD, amitochondrial complex II gene, in nonfamilial pheochromocytoma
    • Gimm O, Armanios M, Dziema H, Neumann HPH, Eng C: Somatic and occult germ-line mutations in SDHD, amitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res 2000;60:6822-6825.
    • (2000) Cancer Res , vol.60 , pp. 6822-6825
    • Gimm, O.1    Armanios, M.2    Dziema, H.3    Neumann, H.P.H.4    Eng, C.5
  • 8
    • 0025054257 scopus 로고
    • Histopathology of benign versus malignant sympathoadrenal paragangliomas: Clinicopathologic study of 120 cases including unusual histopathologic features
    • Linnolia RI, Keiser HR, Steinberg SM, Lack EE: Histopathology of benign versus malignant sympathoadrenal paragangliomas: Clinicopathologic study of 120 cases including unusual histopathologic features. Hum Pathol 1990;21:1168-1180.
    • (1990) Hum Pathol , vol.21 , pp. 1168-1180
    • Linnolia, R.I.1    Keiser, H.R.2    Steinberg, S.M.3    Lack, E.E.4
  • 9
    • 33751528825 scopus 로고    scopus 로고
    • High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: Implications for genetic testing
    • Brouwers FM, Eisenhofer G, Tao JJ, Kant JA, Adams KT, Linehan WM, Pacak K: High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing. J Clin End Metab 2006;91:4505-4509.
    • (2006) J Clin End Metab , vol.91 , pp. 4505-4509
    • Brouwers, F.M.1    Eisenhofer, G.2    Tao, J.J.3    Kant, J.A.4    Adams, K.T.5    Linehan, W.M.6    Pacak, K.7
  • 13
    • 29144484161 scopus 로고    scopus 로고
    • The SDH mutation database: An online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency
    • Bayley JP, Devilee P, Taschner PEM: The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency. BMC Med Genet 2005;6:39.
    • (2005) BMC Med Genet , vol.6 , pp. 39
    • Bayley, J.P.1    Devilee, P.2    Taschner, P.E.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.