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Volumn 17, Issue 2, 2006, Pages 201-202

Genetic analysis of high altitude paragangliomas

Author keywords

[No Author keywords available]

Indexed keywords

ADRENERGIC SYSTEM; ALTITUDE; CAROTID BODY; DIAGNOSTIC PROCEDURE; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENETIC TRAIT; HUMAN; LETTER; PARAGANGLIOMA; PRIORITY JOURNAL;

EID: 33845704224     PISSN: 10463976     EISSN: None     Source Type: Journal    
DOI: 10.1385/EP:17:2:201     Document Type: Letter
Times cited : (13)

References (12)
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    • Nathanson SD, Gaylis H. Multicentric chemodectomata at high altitude. A case report and review of the literature. S Afr Med J 48:1715-1717, 1974.
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  • 3
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    • Chronic hypoxia and chemodectomas in bovines at high altitudes
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    • Arias-Stella, J.1    Bustos, F.2
  • 5
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    • Carotid body tumors in inhabitants of altitudes higher than 2000 meters above sea level
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    • Rodriguez-Cuevas, S.1    Lopez-Garza, J.2    Labastida-Almendaro, S.3
  • 6
    • 3342943223 scopus 로고    scopus 로고
    • Genomic imprinting and environment in hereditary paraganglioma
    • Baysal BE. Genomic imprinting and environment in hereditary paraganglioma. Am J Med Genet C Semin Med Genet 129:85-90, 2004.
    • (2004) Am J Med Genet C Semin Med Genet , vol.129 , pp. 85-90
    • Baysal, B.E.1
  • 7
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    • Malignant pheochromocytoma: Current status and initiatives for future progress
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    • (2004) Endocr Relat Cancer , vol.11 , pp. 423-436
    • Eisenhofer, G.1    Bornstein, S.R.2    Brouwers, F.M.3
  • 8
    • 27244446452 scopus 로고    scopus 로고
    • Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene
    • Schiavi F, Boedeker CC, Bausch B, et al. Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. JAMA 294:2057-2063, 2005.
    • (2005) JAMA , vol.294 , pp. 2057-2063
    • Schiavi, F.1    Boedeker, C.C.2    Bausch, B.3
  • 9
    • 0034977649 scopus 로고    scopus 로고
    • Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas
    • Aguiar RC, Cox G, Pomeroy SL, Dahia PL. Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas. J Clin Endocrinol Metab 86:2890-2894, 2001.
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 2890-2894
    • Aguiar, R.C.1    Cox, G.2    Pomeroy, S.L.3    Dahia, P.L.4
  • 10
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    • A HIF1-alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
    • Dahia PL, Ross KN, Wright ME, et al. A HIF1-alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas. PLoS Genet 1:e8, 2005.
    • (2005) PLoS Genet , vol.1
    • Dahia, P.L.1    Ross, K.N.2    Wright, M.E.3
  • 11
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    • Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma
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  • 12
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    • SDHC mutations in hereditary paraganglioma/pheochromocytoma
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.