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Journal Abstract Search

470 related items for PubMed ID: 11062460

  • 1. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
    Niemann S, Müller U.
    Nat Genet; 2000 Nov; 26(3):268-70. PubMed ID: 11062460
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  • 2. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.
    Benn DE, Croxson MS, Tucker K, Bambach CP, Richardson AL, Delbridge L, Pullan PT, Hammond J, Marsh DJ, Robinson BG.
    Oncogene; 2003 Mar 06; 22(9):1358-64. PubMed ID: 12618761
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  • 4. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.
    Taschner PE, Jansen JC, Baysal BE, Bosch A, Rosenberg EH, Bröcker-Vriends AH, van Der Mey AG, van Ommen GJ, Cornelisse CJ, Devilee P.
    Genes Chromosomes Cancer; 2001 Jul 06; 31(3):274-81. PubMed ID: 11391798
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  • 5. A role for mitochondrial enzymes in inherited neoplasia and beyond.
    Eng C, Kiuru M, Fernandez MJ, Aaltonen LA.
    Nat Rev Cancer; 2003 Mar 06; 3(3):193-202. PubMed ID: 12612654
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  • 6. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
    Taschner PE, Bröcker-Vriends AH, van der Mey AG.
    Ned Tijdschr Geneeskd; 2002 Nov 16; 146(46):2188-90. PubMed ID: 12467161
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  • 9. Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.
    Bayley JP, van Minderhout I, Weiss MM, Jansen JC, Oomen PH, Menko FH, Pasini B, Ferrando B, Wong N, Alpert LC, Williams R, Blair E, Devilee P, Taschner PE.
    BMC Med Genet; 2006 Jan 11; 7():1. PubMed ID: 16405730
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  • 11. [Optic atrophy and ataxia (complex II deficiency-mutation in Fp subunit gene of succinate dehydrogenase)].
    Goto Y.
    Nihon Rinsho; 2002 Apr 11; 60 Suppl 4():376-7. PubMed ID: 12013890
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