Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects?
about
Mitochondrial Dysfunction in Cancer and Neurodegenerative Diseases: Spotlight on Fatty Acid Oxidation and Lipoperoxidation Products15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5MEN1, MEN4, and Carney Complex: Pathology and Molecular GeneticsConnecting molecular pathways to hereditary cancer risk syndromesSDHA related tumorigenesis: a new case series and literature review for variant interpretation and pathogenicity.Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatmentHeterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and miceCarney triad, SDH-deficient tumors, and Sdhb+/- mice share abnormal mitochondriaThe genetic landscape of gastrointestinal stromal tumor lacking KIT and PDGFRA mutations.Familial isolated pituitary adenomas (FIPA) and the pituitary adenoma predisposition due to mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene.A MEN1 syndrome with a paraganglioma.Succinate dehydrogenase deficiency is rare in pituitary adenomas.Toward an improved definition of the genetic and tumor spectrum associated with SDH germ-line mutations.The role of genetic and epigenetic changes in pituitary tumorigenesis.Genetics of Cushing's disease: an update.Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas.Overview of the 2017 WHO Classification of Pituitary Tumors.And the GIST is: When one has a GIST, think of an association!The 2017 World Health Organization classification of tumors of the pituitary gland: a summary.Succinate dehydrogenase (SDH)-deficient neoplasia.The role of metabolic enzymes in mesenchymal tumors and tumor syndromes: genetics, pathology, and molecular mechanisms.The adrenal medulla and extra-adrenal paraganglia: then and now.What's new in pituitary pathology?Cushing's disease and co-existing phaeochromocytoma.[New aspects of tumor pathology of the adrenal glands].Genetics of Cushing's Syndrome.A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma
P2860
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P2860
Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects?
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Succinate dehydrogenase (SDHx) ...... II and/or Krebs cycle defects?
@en
type
label
Succinate dehydrogenase (SDHx) ...... II and/or Krebs cycle defects?
@en
prefLabel
Succinate dehydrogenase (SDHx) ...... II and/or Krebs cycle defects?
@en
P2860
P356
P1476
Succinate dehydrogenase (SDHx) ...... II and/or Krebs cycle defects?
@en
P2093
Paraskevi Xekouki
P2860
P304
P356
10.1530/ERC-12-0118
P577
2012-10-30T00:00:00Z