About: Constantine A Stratakis

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

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rdf:type	Item
description	ikertzailea (eu) researcher (en) 연구원 (ko) araştırmacı (tr) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky)
rdfs:label	Constantine A Stratakis (en) Constantine A Stratakis (nl) Constantine A Stratakis (ast)
skos:prefLabel	Constantine A Stratakis (en) Constantine A Stratakis (nl) Constantine A Stratakis (ast)
name	Constantine A Stratakis (en) Constantine A Stratakis (nl) Constantine A Stratakis (ast)
instance of	wds:Q69146861-EB5CB8DF-7B4A-4753-BD57-57B79C4846A9
instance of	Homo sapiens
Nationale Thesaurus voor Auteursnamen ID	wds:Q69146861-15c18f56-8db5-4a42-967d-dc0e15bae782
occupation	wds:Q69146861-EA89C64A-F790-4333-8786-2501184DB9AB
sex or gender	wds:Q69146861-B5A09DDE-0525-4301-B392-1BA0F35285FC
VIAF ID	wds:Q69146861-1CCCF2C2-2712-4B45-99D4-61CCFEF62FBC
IdRef ID	wds:Q69146861-3965EB08-A9C2-419E-9CBD-7D116639D372
WorldCat Identities ID (superseded)	wds:Q69146861-40E530AB-DEA2-485F-818B-37799BB37479
National Library of Israel J9U ID	wds:Q69146861-E0EBEB90-A7EA-4E95-BD1B-5B8B98837B02
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p240488997
VIAF ID	http://viaf.org/viaf/273923581
IdRef ID	http://www.idref.fr/066935318/id
Nationale Thesaurus voor Auteursnamen ID	240488997
occupation	researcher
sex or gender	male
VIAF ID	273923581
IdRef ID	066935318
WorldCat Identities ID (superseded)	lccn-n2002011393
National Library of Israel J9U ID	987007378752105171
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69146861
is author of	Metabolome profiling by HRMAS NMR spectroscopy of pheochromocytomas and paragangliomas detects SDH deficiency: clinical and pathophysiological implications Carney triad, SDH-deficient tumors, and Sdhb+/- mice share abnormal mitochondria Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects? Genetics of carney triad: recurrent losses at chromosome 1 but lack of germline mutations in genes associated with paragangliomas and gastrointestinal stromal tumors. Pituitary pathology in Carney complex patients Clinical and molecular genetics of acromegaly: MEN1, Carney complex, McCune-Albright syndrome, familial acromegaly and genetic defects in sporadic tumors A novel, non-functional, COL1A1 polymorphism is not associated with lumbar disk disease in young male Greek subjects unlike that of the Sp1 site Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia ARMC5 mutations in macronodular adrenal hyperplasia with Cushing's syndrome A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia Protein kinase A effects of an expressed PRKAR1A mutation associated with aggressive tumors Serial analysis of gene expression in adrenocortical hyperplasia caused by a germline PRKAR1A mutation Cushing's syndrome and fetal features resurgence in adrenal cortex-specific Prkar1a knockout mice Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation mTOR pathway is activated by PKA in adrenocortical cells and participates in vivo to apoptosis resistance in primary pigmented nodular adrenocortical disease (PPNAD). How does cAMP/protein kinase A signaling lead to tumors in the adrenal cortex and other tissues? Cushing syndrome caused by adrenocortical tumors and hyperplasias (corticotropin- independent Cushing syndrome) Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes Activation of cyclic AMP signaling leads to different pathway alterations in lesions of the adrenal cortex caused by germline PRKAR1A defects versus those due to somatic GNAS mutations Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours Phosphodiesterase 11A (PDE11A) gene defects in patients with acth-independent macronodular adrenal hyperplasia (AIMAH): functional variants may contribute to genetic susceptibility of bilateral adrenal tumors Constitutive activation of PKA catalytic subunit in adrenal Cushing's syndrome The cAMP pathway and the control of adrenocortical development and growth Genetics of adrenal tumors associated with Cushing's syndrome: a new classification for bilateral adrenocortical hyperplasias Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors Carney complex and McCune Albright syndrome: an overview of clinical manifestations and human molecular genetics 17q22-24 chromosomal losses and alterations of protein kinase a subunit expression and activity in adrenocorticotropin-independent macronodular adrenal hyperplasia. Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysio New genetic insights in familial hyperaldosteronism Endocrine abnormalities in patients with Fanconi anemia Endocrine tumours in neurofibromatosis type 1, tuberous sclerosis and related syndromes Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation The Effects of SOM230 on Cell Proliferation and Adrenocorticotropin Secretion in Human Corticotroph Pituitary Adenomas Succinate dehydrogenase mutation underlies global epigenomic divergence in gastrointestinal stromal tumor Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad Gastric stromal tumors in Carney triad are different clinically, pathologically, and behaviorally from sporadic gastric gastrointestinal stromal tumors: findings in 104 cases Detection of adrenocorticotropin-secreting pituitary adenomas by magnetic resonance imaging in children and adolescents with cushing disease. Large-cell calcifying Sertoli cell tumors of the testes in pediatrics Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype Use of aromatase inhibitors in large cell calcifying sertoli cell tumors: effects on gynecomastia, growth velocity, and bone age ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences The Gene of the Ubiquitin-Specific Protease 8 Is Frequently Mutated in Adenomas Causing Cushing's Disease Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease Screening for GPR101 defects in pediatric pituitary corticotropinomas Corticotropinoma as a Component of Carney Complex. Cushing's syndrome Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations E pluribus unum? The main protein kinase A catalytic subunit (PRKACA), a likely oncogene, and cortisol-producing tumors Germline PRKACA amplification leads to Cushing syndrome caused by 3 adrenocortical pathologic phenotypes. Familial gastrointestinal stromal tumors and germ-line mutations. Selective loss of MEG3 expression and intergenic differentially methylated region hypermethylation in the MEG3/DLK1 locus in human clinically nonfunctioning pituitary adenomas Carney complex: an update The complex of myxomas, spotty skin pigmentation and endocrine overactivity (Carney complex): imaging findings with clinical and pathological correlation Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update Clinical and molecular genetics of Carney complex Carney complex: one more entity with skin and bone manifestations. A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex X-linked acrogigantism syndrome: clinical profile and therapeutic responses Integrated genomic analysis of nodular tissue in macronodular adrenocortical hyperplasia: progression of tumorigenesis in a disorder associated with multiple benign lesions

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