The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.
The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.A recurrent stop-codon mutation in succinate dehydrogenase subunit B gene in normal peripheral blood and childhood T-cell acute leukemiaHypoxia-inducible C-to-U coding RNA editing downregulates SDHB in monocytesSequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHAA formalized description of the standard human variant nomenclature in Extended Backus-Naur FormSDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5Instability of succinate dehydrogenase in SDHD polymorphism connects reactive oxygen species production to nuclear and mitochondrial genomic mutations in yeastGlycolysis inhibition for anticancer treatmentSuccinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancerStructural and biochemical analyses reveal insights into covalent flavinylation of the Escherichia coli Complex II homolog quinol:fumarate reductase.The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patientsCurrent views on cell metabolism in SDHx-related pheochromocytoma and paragangliomaThe in-depth evaluation of suspected mitochondrial diseaseIncreased prevalence of malignancy in adult mitochondrial disordersPheochromocytoma in a Twelve-Year-Old Girl with SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome.Selection of reference gene expression in a schizophrenia brain cohort.Mouse models of inherited cancer syndromesDefects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations.Proteomics-Based Identification of Differentially Abundant Proteins from Human Keratinocytes Exposed to Arsenic Trioxide.Hypersensitivity to oxygen and shortened lifespan in a Drosophila mitochondrial complex II mutant.SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromesPituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and micePrevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden.Alterations of metabolic genes and metabolites in cancer.A novel SDHB mutation associated with hereditary head and neck paraganglioma.Structural basis for malfunction in complex II.Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad.SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster DeliveryDynamic changes in the gene expression profile during rat oral carcinogenesis induced by 4-nitroquinoline 1-oxideParagangliomas: clinical overview.The role of mitochondria in pharmacotoxicology: a reevaluation of an old, newly emerging topic.Carney triad can be (rarely) associated with germline succinate dehydrogenase defects.Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1Familiar Papillary Thyroid Carcinoma in a Large Brazilian Family Is Not Associated with Succinate Dehydrogenase Defects.Electron-transfer pathways in the heme and quinone-binding domain of complex II (succinate dehydrogenase).Red Algal Mitochondrial Genomes Are More Complete than Previously Reported.Recent advances in the genetics of SDH-related paraganglioma and pheochromocytomaMitochondrial respiratory chain complexes: apoptosis sensors mutated in cancer?Impaired TCA cycle flux in mitochondria in skeletal muscle from type 2 diabetic subjects: marker or maker of the diabetic phenotype?
P2860
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P2860
The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.
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2005 nî lūn-bûn
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2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
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2005 թվականի նոյեմբերին հրատարակված գիտական հոդված
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2005年の論文
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2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
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2005年论文
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name
The SDH mutation database: an ...... hondrial complex II deficiency
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The SDH mutation database: an ...... ondrial complex II deficiency.
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The SDH mutation database: an ...... ondrial complex II deficiency.
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type
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The SDH mutation database: an ...... hondrial complex II deficiency
@nl
The SDH mutation database: an ...... ondrial complex II deficiency.
@ast
The SDH mutation database: an ...... ondrial complex II deficiency.
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prefLabel
The SDH mutation database: an ...... hondrial complex II deficiency
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The SDH mutation database: an ...... ondrial complex II deficiency.
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The SDH mutation database: an ...... ondrial complex II deficiency.
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P2860
P921
P356
P1433
P1476
The SDH mutation database: an ...... ondrial complex II deficiency.
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P2093
Jean-Pierre Bayley
Peter E M Taschner
P2860
P2888
P356
10.1186/1471-2350-6-39
P407
P577
2005-11-16T00:00:00Z
P5875
P6179
1049903385