Pages that link to "Q44347017"
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The following pages link to Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas (Q44347017):
Displaying 41 items.
- Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma (Q25255910) (← links)
- 15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5 (Q26798384) (← links)
- Mitochondrial tumour suppressors: a genetic and biochemical update (Q28285094) (← links)
- Targeting heat shock protein 90 for the treatment of malignant pheochromocytoma (Q28486170) (← links)
- Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD. (Q30381330) (← links)
- Cochaperone binding to LYR motifs confers specificity of iron sulfur cluster delivery. (Q33292297) (← links)
- SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes (Q35185252) (← links)
- The TCA cycle and tumorigenesis: the examples of fumarate hydratase and succinate dehydrogenase. (Q35622053) (← links)
- Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas (Q35636300) (← links)
- Genetic defects in the oxidative phosphorylation (OXPHOS) system (Q35680303) (← links)
- K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma. (Q35912876) (← links)
- Mutations of the SDHB and SDHD genes (Q36121952) (← links)
- Genetic testing for pheochromocytoma-associated syndromes (Q36179240) (← links)
- Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function (Q36329838) (← links)
- Genetic insights into OXPHOS defect and its role in cancer (Q36377723) (← links)
- Penetrance and clinical consequences of a gross SDHB deletion in a large family (Q36477811) (← links)
- Acquired hypermethylation of the P16INK4A promoter in abdominal paraganglioma: relation to adverse tumor phenotype and predisposing mutation (Q36613916) (← links)
- The occurrence of SDHB gene mutations in pheochromocytoma (Q36652778) (← links)
- Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma. (Q36696226) (← links)
- Management of head and neck paragangliomas: review of 120 patients (Q37313159) (← links)
- Pathological mechanisms and parent-of-origin effects in hereditary paraganglioma/pheochromocytoma (PGL/PCC) (Q37872637) (← links)
- Oxidative Phosphorylation System in Gastric Carcinomas and Gastritis (Q40119667) (← links)
- Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome (Q40365390) (← links)
- Loss of heterozygosity of succinate dehydrogenase B mutation by direct sequencing in synchronous paragangliomas (Q42081534) (← links)
- L157X nonsense mutation of the succinate dehydrogenase subunit B gene in a Japanese patient with right paraaortic paraganglioma (Q42853743) (← links)
- Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome (Q43688658) (← links)
- Complex II Defect via Down-regulation of Iron-Sulfur Subunit Induces Mitochondrial Dysfunction and Cell Cycle Delay in Iron Chelation-induced Senescence-associated Growth Arrest (Q44598323) (← links)
- Malignant paraganglioma caused by a novel germline mutation of the succinate dehydrogenase D-gene--a case report (Q46795898) (← links)
- An apparently sporadic paraganglioma with an SDHB gene germline mutation presenting at age 68 years. (Q46939617) (← links)
- Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma. (Q47785173) (← links)
- Genetic mechanisms of human hypertension and their implications for blood pressure physiology. (Q48100826) (← links)
- Urinary Bladder Paragangliomas: Analysis of Succinate Dehydrogenase and Outcome (Q50891010) (← links)
- Bronchial Paraganglioma with SDHB Deficiency. (Q53796552) (← links)
- Network-based analysis of oligodendrogliomas predicts novel cancer gene candidates within the region of the 1p/19q co-deletion. (Q55338815) (← links)
- Closely spaced multiple mutations as potential signatures of transient hypermutability in human genes (Q57263735) (← links)
- SDH Mutations in Patients Affected by Paraganglioma Syndromes: A Personal Experience (Q57737932) (← links)
- High-frequency actionable pathogenic exome variants in an average-risk cohort (Q60922248) (← links)
- Mutational load in carotid body tumor (Q64096925) (← links)
- Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p (Q81333176) (← links)
- Bilateral Adrenal Medullary Hyperplasia Associated With an SDHB Mutation (Q82966845) (← links)
- Head and neck paragangliomas: Report of 175 patients (1989-2010) (Q84406350) (← links)