Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Export 26 results:
Author Title Type [ Year] Filters: Keyword is Promoter Regions, Genetic [Clear All Filters]
DNA methylation analysis within the IL2RA gene promoter in youth with autoimmune thyroid disease..
Eur J Clin Invest. 50(3), e13199.
(2020).
(2019).
Capicua controls Toll/IL-1 signaling targets independently of RTK regulation..
Proc Natl Acad Sci U S A. 115(8), 1807-1812.
(2018). Functional analysis of the C. elegans cyld-1 gene reveals extensive similarity with its human homolog..
PLoS One. 13(2), e0191864.
(2018). Major Adipokines and the -420C>G Resistin Gene Polymorphism as Predictors of Acute Ischemic Stroke Severity and In-Hospital Outcome..
J Stroke Cerebrovasc Dis. 27(4), 963-970.
(2018). Gene promoter methylation and protein expression of BRMS1 in uterine cervix in relation to high-risk human papilloma virus infection and cancer..
Tumour Biol. 39(4), 1010428317697557.
(2017). Regulation of expression of the p21 gene by the transcription factor ZNF217 and MDM2..
Biochem Cell Biol. 94(6), 560-568.
(2016).
(2014).
Association of the RANTES gene promoter polymorphisms -28C/G and -403G/A with pneumonia in Greek children..
Int J Immunopathol Pharmacol. 26(3), 681-90.
(2013). Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin..
Ann Hematol. 92(1), 53-8.
(2013). Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy..
Pharmacogenomics. 14(5), 469-83.
(2013). Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutation..
Hum Mol Genet. 22(16), 3187-94.
(2013). Genetics of myasthenia gravis: a case-control association study in the Hellenic population..
Clin Dev Immunol. 2012, 484919.
(2012). Genotype and allele frequencies of heme oxygenase-1 promoter region in a Greek cohort..
Chin Med J (Engl). 124(20), 3408-11.
(2011).
(2011). Association between the heme oxygenase-1 promoter polymorphism and renal transplantation outcome in Greece..
Transplant Proc. 42(7), 2479-85.
(2010). p16 promoter methylation in Pb2+ -exposed individuals..
Clin Toxicol (Phila). 48(2), 124-8.
(2010). Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis..
Brain. 133(Pt 6), 1810-22.
(2010). Inherited GPI deficiency: a disorder of histone hypoacetylation..
Birth Defects Res C Embryo Today. 87(4), 327-34.
(2009). Methylation status of RASSF1A in patients with chronic myeloid leukemia..
Leuk Res. 33(8), 1130-2.
(2009). OCT4B expression in PBMNCs suggests the existence of an alternative OCT4 promoter..
Genes Chromosomes Cancer. 48(12), 1112-4.
(2009).
(2008).
Aberrant p16 promoter methylation among Greek lung cancer patients and smokers: correlation with smoking..
Eur J Cancer Prev. 16(5), 396-402.
(2007). Alien inhibits E2F1 gene expression and cell proliferation..
Biochim Biophys Acta. 1773(9), 1447-54.
(2007). Secretoglobin 2A1 is under selective androgen control mediated by a peculiar binding site for Sp family transcription factors..
Mol Endocrinol. 19(12), 2964-78.
(2005).