Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Aryl hydrocarbon receptor interacting protein (AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas..
Clin Endocrinol (Oxf). 69(4), 621-7.
(2008). bcl-2 messenger RNA is localized in neurons of the developing and adult rat brain..
Neuroscience. 61(1), 165-77.
(1994). Bone morphogenetic protein expression in newborn rat kidneys after prenatal exposure to radiofrequency radiation..
Bioelectromagnetics. 25(3), 216-27.
(2004). Chromosomal mapping of glutamate dehydrogenase gene sequences to mouse chromosomes 7 and 14..
Genomics. 10(1), 83-8.
(1991). Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece..
Neurosci Lett. 452(2), 87-9.
(2009). Effect of blood transfusion on gene expression of transforming growth factor beta-1 and the alpha subunit of interleukin-2 receptor in a model of colonic wound healing..
Methods Find Exp Clin Pharmacol. 28(9), 605-8.
(2006). Emergence of Klebsiella pneumoniae ST11 co-producing NDM-1 and OXA-48 carbapenemases in Greece..
J Glob Antimicrob Resist. 19, 81-82.
(2019). Evaluation of six CTLA-4 polymorphisms in high-risk melanoma patients receiving adjuvant interferon therapy in the He13A/98 multicenter trial..
J Transl Med. 8, 108.
(2010). A family with atypical Hailey Hailey disease--is there more to the underlying genetics than ATP2C1?.
PLoS One. 10(4), e0121253.
(2015). Genetic recombination as a major cause of mutagenesis in the human globin gene clusters..
Clin Biochem. 42(18), 1839-50.
(2009). Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020..
Euro Surveill. 25(32),
(2020). Hb Famagusta--analysis of a novel δ-globin chain variant [HBD:c.60C>A] in four families with diverse globin genotypes..
Ann Hematol. 93(9), 1625-7.
(2014). Hereditary angioedema in Greek families caused by novel and recurrent mutations..
Hum Immunol. 70(11), 925-9.
(2009). The HIrisPlex system for simultaneous prediction of hair and eye colour from DNA..
Forensic Sci Int Genet. 7(1), 98-115.
(2013). The human glutamate dehydrogenase gene family: gene organization and structural characterization..
Genomics. 16(1), 150-60.
(1993). Increased plasma angiogenin level is associated and may contribute to decreased T-cell zeta-chain expression in hemodialysis patients..
Ther Apher Dial. 17(1), 48-54.
(2013). An indirect negative autoregulatory mechanism involved in hepatocyte nuclear factor-1 gene expression..
Nucleic Acids Res. 21(25), 5882-9.
(1993). Isolation and characterization of a vitellogenin cDNA from rainbow trout (Oncorhynchus mykiss) and the complete sequence of a phosvitin coding segment..
DNA Cell Biol. 15(7), 605-16.
(1996). Isolation and characterization of cDNA clones encoding human liver glutamate dehydrogenase: evidence for a small gene family..
Proc Natl Acad Sci U S A. 85(10), 3494-8.
(1988). Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population..
Genet Test Mol Biomarkers. 16(8), 974-7.
(2012). Large genomic deletions in AIP in pituitary adenoma predisposition..
J Clin Endocrinol Metab. 93(10), 4146-51.
(2008). A massive expansion of effector genes underlies gall-formation in the wheat pest Mayetiola destructor..
Curr Biol. 25(5), 613-20.
(2015). Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutation..
Hum Mol Genet. 22(16), 3187-94.
(2013). Molecular cloning, structure and expression analysis of a full-length mouse brain glutamate dehydrogenase cDNA..
Biochim Biophys Acta. 1089(2), 250-3.
(1991). Mutation identification by direct comparison of whole-genome sequencing data from mutant and wild-type individuals using k-mers..
Nat Biotechnol. 31(4), 325-30.
(2013).