about
Childhood adrenocortical tumors: from a clinical to a molecular approachAnalysis of the putative promoter region of the GIP receptor gene (GIPR) in GIP-dependent Cushing's syndrome (CS)Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3.CTNNB1 gene mutations, pituitary transcription factors, and MicroRNA expression involvement in the pathogenesis of adamantinomatous craniopharyngiomas.New strategy for testing efficacy of immunotherapeutic compounds for diabetes in vitro.Absence of functional LIN28B mutations in a large cohort of patients with idiopathic central precocious puberty.Inhibition of the Tcf/beta-catenin complex increases apoptosis and impairs adrenocortical tumor cell proliferation and adrenal steroidogenesis.Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case.The growth hormone receptor exon 3 polymorphism is not associated with height or metabolic traits in healthy young adults.The aurora kinase inhibitor AMG 900 increases apoptosis and induces chemosensitivity to anticancer drugs in the NCI-H295 adrenocortical carcinoma cell line.Unraveling the expression of the oncogene YAP1, a Wnt/beta-catenin target, in adrenocortical tumors and its association with poor outcome in pediatric patients.Postnatal ontogeny of the circadian expression of the adrenal clock genes and corticosterone rhythm in male rats.Sonic hedgehog signaling is active in human adrenal cortex development and deregulated in adrenocortical tumors.Adrenocortical neoplasms in adulthood and childhood: distinct presentation. Review of the clinical, pathological and imaging characteristics.Maternal mood and concordant maternal and infant salivary cortisol during heel lance while in kangaroo care.[Human milk for neonatal pain relief during ophthalmoscopy].Evaluating the roles of follicle-stimulating hormone receptor polymorphisms in gonadal hyperstimulation associated with severe juvenile primary hypothyroidism.Sonic Hedgehog pathway is upregulated in adamantinomatous craniopharyngiomas.Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age.Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly.Wnt/beta-catenin pathway deregulation in childhood adrenocortical tumors.Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphism.Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit.NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype association.Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole.Expression of ACTH receptor pathway genes in glucose-dependent insulinotrophic peptide (GIP)-dependent Cushing's syndrome.A novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome.Homocysteine, folate, hs-C-reactive protein, tumor necrosis factor alpha and inflammatory proteins: are these biomarkers related to nutritional status and cardiovascular risk in childhood-onset systemic lupus erythematosus?Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects.Spindle assembly checkpoint gene expression in childhood adrenocortical tumors (ACT): Overexpression of Aurora kinases A and B is associated with a poor prognosis.Glucocorticoid receptor gene polymorphisms in ACTH-secreting pituitary tumours.Analysis of the putative regulatory region of the gastric inhibitory polypeptide receptor gene in food-dependent Cushing's syndrome.Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and −202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiencyPrimary Hyperparathyroidism as the First Clinical Manifestation of Multiple Endocrine Neoplasia Type 2A in a 5-Year-Old ChildAltered expression of noncanonical Wnt pathway genes in paediatric and adult adrenocortical tumoursHesx1 gene in midline cerebral defectsExpression of ACTH receptor pathway genes in GIP-dependent Cushing's syndrome (CS)[Mineralocorticoid resistance: pseudohypoaldosteronism type 1]A commentary on Association of adiponectin polymorphism with cord blood adiponectin concentrations and intrauterine growthPostnatal growth and cardiometabolic profile in young adults born large for gestational age
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Sonir R Antonini
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Sonir R Antonini
@en
Sonir R Antonini
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Sonir R Antonini
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type
label
Sonir R Antonini
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Sonir R Antonini
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Sonir R Antonini
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Sonir R Antonini
@nl
prefLabel
Sonir R Antonini
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Sonir R Antonini
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Sonir R Antonini
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Sonir R Antonini
@nl
P106
P31
P496
0000-0003-4778-8803