Search Results - "Akulevich, Natallia"
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The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl
Published in Human molecular genetics (15-06-2010)“…Papillary thyroid cancer (PTC) among individuals exposed to radioactive iodine in their childhood or adolescence is a major internationally recognized health…”
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Polymorphisms of DNA damage response genes in radiation-related and sporadic papillary thyroid carcinoma
Published in Endocrine-related cancer (01-06-2009)“…Papillary thyroid carcinoma (PTC) etiologically occurs as a radiation-induced or sporadic malignancy. Genetic factors contributing to the susceptibility to…”
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A novel role for thyroid hormone receptor beta in cellular radiosensitivity
Published in Journal of radiation research (01-01-2008)“…Thyroid hormone receptors (THRs) widely govern cell growth, differentiation and metabolism acting in a ligand- and cofactor-dependent manner to modulate…”
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A Novel Role for Thyroid Hormone Receptor Beta in Cellular Radiosensitivity
Published in JOURNAL OF RADIATION RESEARCH (2008)“…Thyroid hormone receptors (THRs) widely govern cell growth, differentiation and metabolism acting in a ligand- and cofactor-dependent manner to modulate…”
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International consensus: ovarian tissue cryopreservation in young Turner syndrome patients: outcomes of an ethical Delphi study including 55 experts from 16 different countries
Published in Human reproduction (Oxford) (01-05-2020)“…Abstract STUDY QUESTION What is the standpoint of an international expert panel on ovarian tissue cryopreservation (OTC) in young females with Turner syndrome…”
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Optimal Pubertal Induction in Girls with Turner Syndrome Using Either Oral or Transdermal Estradiol: A Proposed Modern Strategy
Published in Hormone research in paediatrics (01-01-2019)“…Most girls with Turner syndrome (TS) require pubertal induction with estrogen, followed by long term replacement. However, no adequately powered prospective…”
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Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations
Published in European journal of human genetics : EJHG (01-03-2016)“…Two variants (c.[301_302delAG];[301_302delAG] and c.[150delA];[150delA]) in the PROP1 gene are the most common genetic causes of recessively inherited combined…”
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