about
Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadismA genetic basis for functional hypothalamic amenorrheaStress-activated cap'n'collar transcription factors in aging and human diseaseProteasome dysfunction in Drosophila signals to an Nrf2-dependent regulatory circuit aiming to restore proteostasis and prevent premature aging.Hepatic Fgf21 Expression Is Repressed after Simvastatin Treatment in Miceβ-Klotho deficiency protects against obesity through a crosstalk between liver, microbiota, and brown adipose tissue.Congenital idiopathic hypogonadotropic hypogonadism: evidence of defects in the hypothalamus, pituitary, and testes.Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.Serine phosphorylation of insulin receptor substrate-1: a novel target for the reversal of insulin resistance.Erythropoietin abuse and erythropoietin gene doping: detection strategies in the genomic era.Nrf2 represses FGF21 during long-term high-fat diet-induced obesity in mice.Genetic activation of Nrf2 signaling is sufficient to ameliorate neurodegenerative phenotypes in a Drosophila model of Parkinson's disease.Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations.Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.Educational Level Is Related to Physical Fitness in Patients with Type 2 Diabetes - A Cross-Sectional StudyAn ancient founder mutation in PROKR2 impairs human reproduction.Keap1/Nrf2 signaling regulates oxidative stress tolerance and lifespan in DrosophilaRedox Status and Proteostasis in Ageing and Disease.Trial of recombinant follicle-stimulating hormone pretreatment for GnRH-induced fertility in patients with congenital hypogonadotropic hypogonadism.Deciphering genetic disease in the genomic era: the model of GnRH deficiency.Columnar cell variant of papillary thyroid carcinoma: Cytomorphological characteristics of 11 cases with histological correlation and literature review.Nrf2 activation diminishes during adipocyte differentiation of ST2 cells.KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.Very low expression of PD-L1 in medullary thyroid carcinomaFunctional significance of the thyrotropin receptor germline polymorphism D727E.Hippocrates and genomic medicine.Pharmacogenetic principles in the Hippocratic writings.FNA diagnosis of poorly differentiated thyroid carcinoma. A review of the recent literature.Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism.A Simple Protocol for High Efficiency Protein Isolation After RNA Isolation from Mouse Thyroid and Other Very Small Tissue Samples.Endocrine and neuroendocrine cytopathology.Rapid Remission of Graves' Hyperthyroidism Without Thionamides Under Immunosuppressive Treatment for Concomitant Autoimmune Hepatitis.Molecular medicine: a lifetime of learning, teaching and caring.The Bethesda System for Reporting Thyroid Cytopathology explained for practitioners: Frequently Asked Questions.[Subclinical hypothyroidism : should we still treat elderly patients? Clinical implications of a new trial in primary care].Apoptosis: the suicide solution in cancer treatment and chemoprevention.Oestrogen receptor beta (ERbeta) is abundantly expressed in normal colonic mucosa, but declines in colon adenocarcinoma paralleling the tumour's dedifferentiation.Uptake of 99mTc-MIBI by Sclerosing Pneumocytoma Raising a False Suspicion of Metastasis From Medullary Thyroid Carcinoma.Raman spectroscopy for the preoperative diagnosis of thyroid cancer and its subtypes: an in vitro proof-of-concept study
P50
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P50
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wetenschapper
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հետազոտող
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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Gerasimos P Sykiotis
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P106
P31
P496
0000-0002-9565-4941