Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
(2020).
Emergence of Klebsiella pneumoniae ST11 co-producing NDM-1 and OXA-48 carbapenemases in Greece..
J Glob Antimicrob Resist. 19, 81-82.
(2019). mutations in rats and a human polymorphism impair the rate of steroid synthesis..
Biochem J. 474(23), 3985-3999.
(2017). Using CRISPR-Cas9 to Study ERK Signaling in Drosophila..
Methods Mol Biol. 1487, 353-365.
(2017). Regulation of expression of the p21 gene by the transcription factor ZNF217 and MDM2..
Biochem Cell Biol. 94(6), 560-568.
(2016). A family with atypical Hailey Hailey disease--is there more to the underlying genetics than ATP2C1?.
PLoS One. 10(4), e0121253.
(2015). A massive expansion of effector genes underlies gall-formation in the wheat pest Mayetiola destructor..
Curr Biol. 25(5), 613-20.
(2015). 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). Mutational profiling of the RAS, PI3K, MET and b-catenin pathways in cancer of unknown primary: a retrospective study of the Hellenic Cooperative Oncology Group..
Clin Exp Metastasis. 31(7), 761-9.
(2014). Vascular endothelial growth factor polymorphisms and clinical outcome in patients with metastatic breast cancer treated with weekly docetaxel..
Pharmacogenomics J. 14(3), 248-55.
(2014). The HIrisPlex system for simultaneous prediction of hair and eye colour from DNA..
Forensic Sci Int Genet. 7(1), 98-115.
(2013). 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). Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutation..
Hum Mol Genet. 22(16), 3187-94.
(2013). 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). 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).
(2011).
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). The ratio of SRPK1/SRPK1a regulates erythroid differentiation in K562 leukaemic cells..
Biochim Biophys Acta. 1803(12), 1319-31.
(2010). Synonymous polymorphisms at splicing regulatory sites are associated with CpGs in neurodegenerative disease-related genes..
Neuromolecular Med. 12(3), 260-9.
(2010).
(2010). Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece..
Neurosci Lett. 452(2), 87-9.
(2009). Genetic recombination as a major cause of mutagenesis in the human globin gene clusters..
Clin Biochem. 42(18), 1839-50.
(2009). Hereditary angioedema in Greek families caused by novel and recurrent mutations..
Hum Immunol. 70(11), 925-9.
(2009). The natural compound atraric acid is an antagonist of the human androgen receptor inhibiting cellular invasiveness and prostate cancer cell growth..
J Cell Mol Med. 13(8B), 2210-23.
(2009). Novel human pathological mutations. Gene symbol: SLC3A1. Disease: Cystinuria..
Hum Genet. 126(2), 335.
(2009).