Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma. - Test2 - elhamkhani - TriplyDB

Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma.

Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma.

http://www.wikidata.org/entity/Q36898854

about

Murine models and cell lines for the investigation of pheochromocytoma: applications for future therapies?Connecting molecular pathways to hereditary cancer risk syndromes Current views on cell metabolism in SDHx-related pheochromocytoma and paraganglioma A new specific succinate-glutamate metabolomic hallmark in SDHx-related paragangliomas.Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes.Staging and functional characterization of pheochromocytoma and paraganglioma by 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography.Neurofibromatosis-related phaeochromocytoma: two cases with large tumours and elevated plasma methoxytyramine.The genetic basis of pheochromocytoma and paraganglioma: implications for management Subclinical phaeochromocytoma.Phaeochromocytoma: a catecholamine and oxidative stress disorder.Pheochromocytoma - update on disease management.Genetic screening for von Hippel-Lindau gene mutations in non-syndromic pheochromocytoma: low prevalence and false-positives or misdiagnosis indicate a need for caution.Molecular and therapeutic advances in the diagnosis and management of malignant pheochromocytomas and paragangliomas Double stable isotope ultra performance liquid chromatographic-tandem mass spectrometric quantification of tissue content and activity of phenylethanolamine N-methyltransferase, the crucial enzyme responsible for synthesis of epinephrine Genotype-specific abnormalities in mitochondrial function associate with distinct profiles of energy metabolism and catecholamine content in pheochromocytoma and paraganglioma.Plasma-free vs deconjugated metanephrines for diagnosis of phaeochromocytoma Role of hypoxia and HIF2α in development of the sympathoadrenal cell lineage and chromaffin cell tumors with distinct catecholamine phenotypic features.Hypoxia-inducible factor signaling in pheochromocytoma: turning the rudder in the right direction.Diagnostic tests and biomarkers for pheochromocytoma and extra-adrenal paraganglioma: from routine laboratory methods to disease stratification.Screening for pheochromocytomas and paragangliomas.Pathophysiology and diagnosis of disorders of the adrenal medulla: focus on pheochromocytoma.Genetic status determines (18) F-FDG uptake in pheochromocytoma/paraganglioma.PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics.Update on Adrenal Tumours in 2017 World Health Organization (WHO) of Endocrine Tumours.Pheochromocytomas and paragangliomas in humans and dogs.Novel insights into the polycythemia-paraganglioma-somatostatinoma syndrome.Integrated whole-body PET/MRI with 18F-FDG, 18F-FDOPA, and 18F-FDA in paragangliomas in comparison with PET/CT: NIH first clinical experience with a single-injection, dual-modality imaging protocol.Pheochromocytoma: The First Metabolic Endocrine Cancer.Novel germline SDHD mutation: diagnosis and implications to the patient.Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families.The impact of changes in drug availability for hemodynamic management in pheochromocytoma: prêt-à-porter or tailor-made?New Perspectives on Pheochromocytoma and Paraganglioma: Toward a Molecular Classification.Metabologenomics of Phaeochromocytoma and Paraganglioma: An Integrated Approach for Personalised Biochemical and Genetic Testing.Quantitative 18F-DOPA PET/CT in pheochromocytoma: the relationship between tumor secretion and its biochemical phenotype.New Insights into the Nuclear Imaging Phenotypes of Cluster 1 Pheochromocytoma and Paraganglioma.[Mutations in succinate dehydrogenase and DNA methylation].Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma

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P2860

Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma.

http://www.wikidata.org/entity/Q36898854

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Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma.

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Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma.

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Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma.

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Endocrine-related cancer

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Catecholamine metabolomic and secretory phenotypes in phaeochromocytoma.

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Gennady Bratslavsky

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Graeme Eisenhofer

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Henri J Timmers

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Jacques W M Lenders

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Massimo Mannelli

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Nan Qin

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Peter Friberg

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Stefan K Grebe

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Thanh-Truc Huynh

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W Marston Linehan

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P2860

Catecholamine Metabolism: A Contemporary View with Implications for Physiology and Medicine

The hypoxia-responsive transcription factor EPAS1 is essential for catecholamine homeostasis and protection against heart failure during embryonic development

A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas

Biochemical diagnosis of pheochromocytoma: which test is best?

Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer

Hypoxia inducible factor (HIF)-2 alpha is required for the development of the catecholaminergic phenotype of sympathoadrenal cells

Abnormal sympathoadrenal development and systemic hypotension in PHD3-/- mice

The Warburg effect is genetically determined in inherited pheochromocytomas

Physiological aspects of exocytosis in chromaffin cells of the adrenal medulla.

Molecular and cellular biology of pheochromocytomas and extra-adrenal paragangliomas.

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1

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18

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Stefan R. Bornstein

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2010-12-21T00:00:00Z

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21051559

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3671349

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