Pages that link to "Q46774676"
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The following pages link to Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene (Q46774676):
Displaying 50 items.
- Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA (Q21245354) (← links)
- SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma (Q24317137) (← links)
- Diseases of the adrenal medulla (Q24646015) (← links)
- Human Metabolic Enzymes Deficiency: A Genetic Mutation Based Approach (Q26751169) (← links)
- Heritable Cancer Syndromes Related to the Hypoxia Pathway (Q26751590) (← links)
- Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease (Q26770152) (← links)
- Pheochromocytomas and Paragangliomas: Clinical and Genetic Approaches (Q26782841) (← links)
- Succinate Dehydrogenase Loss in Familial Paraganglioma: Biochemistry, Genetics, and Epigenetics (Q26796203) (← links)
- 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5 (Q26798384) (← links)
- Head and neck paragangliomas: clinical and molecular genetic classification (Q27016092) (← links)
- Cancer phenomics: RET and PTEN as illustrative models (Q28278854) (← links)
- The genetics of paragangliomas: a review (Q28288077) (← links)
- Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD. (Q30381330) (← links)
- Current views on cell metabolism in SDHx-related pheochromocytoma and paraganglioma (Q33590969) (← links)
- Molecular markers of paragangliomas/pheochromocytomas (Q33649025) (← links)
- Paragangliomas/Pheochromocytomas: clinically oriented genetic testing (Q33679204) (← links)
- The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3). (Q33998937) (← links)
- Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria (Q34095498) (← links)
- SDH-related pheochromocytoma and paraganglioma (Q34125978) (← links)
- Mutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility (Q34144574) (← links)
- SDH mutations in cancer (Q34201905) (← links)
- 10 rare tumors that warrant a genetics referral. (Q34325954) (← links)
- Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations (Q34471702) (← links)
- Mitochondrial targeting of vitamin E succinate enhances its pro-apoptotic and anti-cancer activity via mitochondrial complex II (Q34536966) (← links)
- Succinate dehydrogenase and fumarate hydratase: linking mitochondrial dysfunction and cancer. (Q34554818) (← links)
- Malignant head and neck paragangliomas in SDHB mutation carriers (Q34643210) (← links)
- Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. (Q34658237) (← links)
- SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes (Q35185252) (← links)
- Succinate dehydrogenase gene mutations in cardiac paragangliomas (Q35668495) (← links)
- Clinicoradiological manifestations of paraganglioma syndromes associated with succinyl dehydrogenase enzyme mutation. (Q35675637) (← links)
- Paragangliomas and paraganglioma syndromes (Q35926265) (← links)
- Genetic-clinical profile of subjects with apparently sporadic extra-adrenal paragangliomas (Q36047090) (← links)
- The genetic basis of pheochromocytoma and paraganglioma: implications for management (Q36067684) (← links)
- Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes (Q36096070) (← links)
- Phaeochromocytoma: a catecholamine and oxidative stress disorder (Q36149357) (← links)
- Genetic testing for pheochromocytoma-associated syndromes (Q36179240) (← links)
- A case of co-existing paraganglioma and thymoma (Q36234153) (← links)
- Rare vertebral metastasis in a case of Hereditary Paraganglioma. (Q36367439) (← links)
- Clinical aspects of SDHx-related pheochromocytoma and paraganglioma (Q36458394) (← links)
- Pheochromocytoma and paraganglioma (Q36467162) (← links)
- Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad (Q36489471) (← links)
- Tricarboxylic acid cycle dysfunction as a cause of human diseases and tumor formation. (Q36499636) (← links)
- Paragangliomas: clinical overview (Q36652765) (← links)
- Clinical use of laboratory tests for the identification of secondary forms of arterial hypertension. (Q36686822) (← links)
- Comparison of clinical and imaging features in succinate dehydrogenase-positive versus sporadic paragangliomas (Q36793727) (← links)
- Pheochromocytoma as a catecholamine producing tumor: implications for clinical practice (Q36827287) (← links)
- Molecular and cellular biology of pheochromocytomas and extra-adrenal paragangliomas (Q36831552) (← links)
- Familial carotid body tumours: is there a role for genetic screening? (Q36886361) (← links)
- Genetic screening for pheochromocytoma: should SDHC gene analysis be included? (Q37004602) (← links)
- Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1 (Q37061297) (← links)