On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
about
Pheochromocytomas and secreting paragangliomasStructural and mechanistic studies on the inhibition of the hypoxia-inducible transcription factor hydroxylases by tricarboxylic acid cycle intermediatesMitochondria-controlled signaling mechanisms of brain protection in hypoxiaPhysiological consequences of complex II inhibition for aging, disease, and the mKATP channelThe mitochondrial SDHD gene is required for early embryogenesis, and its partial deficiency results in persistent carotid body glomus cell activation with full responsiveness to hypoxiaPheochromocytoma: a paradigm for catecholamine-mediated hypertension.No evidence for promoter region methylation of the succinate dehydrogenase and fumarate hydratase tumour suppressor genes in breast cancer.Succinate-to-fumarate ratio as a new metabolic marker to detect the presence of SDHB/D-related paraganglioma: initial experimental and ex vivo findings.Current views on cell metabolism in SDHx-related pheochromocytoma and paragangliomaInhibition of hypoxia-inducible factor (HIF) hydroxylases by citric acid cycle intermediates: possible links between cell metabolism and stabilization of HIF.Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience.Succinate dehydrogenase subunit B inhibits the AMPK-HIF-1α pathway in human ovarian cancer in vitroSensitivity to low-dose/low-LET ionizing radiation in mammalian cells harboring mutations in succinate dehydrogenase subunit C is governed by mitochondria-derived reactive oxygen speciesParagangliomas and paraganglioma syndromes.Phaeochromocytoma: a catecholamine and oxidative stress disorder.Loss of succinate dehydrogenase activity results in dependency on pyruvate carboxylation for cellular anabolism.Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function.Succinate dehydrogenase expression in breast cancer.Clinical features of paraganglioma syndromes.Metabolic modulation of cancer: a new frontier with great translational potential.Chicken or the egg: Warburg effect and mitochondrial dysfunction.Carotid body oxygen sensing and adaptation to hypoxia.Prolyl hydroxylase domain enzymes: important regulators of cancer metabolism.Genomic instability induced by mutant succinate dehydrogenase subunit D (SDHD) is mediated by O2(-•) and H2O2.TRANSCRIPTIONAL AND PHOSPHO-PROTEOMIC SCREENS REVEAL STEM CELL ACTIVATION OF INSULIN-RESISTANCE AND TRANSFORMATION PATHWAYS FOLLOWING A SINGLE MINIMALLY TOXIC EPISODE OF ROS.Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer.Mitonuclear Interactions Mediate Transcriptional Responses to Hypoxia in Drosophila.Sporadic or familial head neck paragangliomas enrolled in a single center: clinical presentation and genotype/phenotype correlations.Unusual cardiac paraganglioma mimicking an atypical carcinoid tumor of the lung.
P2860
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P2860
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
@ast
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
@en
type
label
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
@ast
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
@en
prefLabel
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
@ast
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
@en
P1476
On the association of succinate dehydrogenase mutations with hereditary paraganglioma.
@en
P2093
Bora E Baysal
P304
P356
10.1016/J.TEM.2003.08.004
P577
2003-12-01T00:00:00Z