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Publications

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

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Author Title [ Type(Desc)] Year
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Journal Article
Georgitsi, M., De Menis E., Cannavò S., Mäkinen M. J., Tuppurainen K., Pauletto P., et al. (2008).  Aryl hydrocarbon receptor interacting protein (AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas.. Clin Endocrinol (Oxf). 69(4), 621-7.
Castrén, E., Ohga Y., Berzaghi M. P., Tzimagiorgis G., Thoenen H., & Lindholm D. (1994).  bcl-2 messenger RNA is localized in neurons of the developing and adult rat brain.. Neuroscience. 61(1), 165-77.
Pyrpasopoulou, A., Kotoula V., Cheva A., Hytiroglou P., Nikolakaki E., Magras I. N., et al. (2004).  Bone morphogenetic protein expression in newborn rat kidneys after prenatal exposure to radiofrequency radiation.. Bioelectromagnetics. 25(3), 216-27.
Tzimagiorgis, G., Adamson M. C., Kozak C. A., & Moschonas N. K. (1991).  Chromosomal mapping of glutamate dehydrogenase gene sequences to mouse chromosomes 7 and 14.. Genomics. 10(1), 83-8.
Kalinderi, K., Bostantjopoulou S., Paisan-Ruiz C., Katsarou Z., Hardy J., & Fidani L. (2009).  Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece.. Neurosci Lett. 452(2), 87-9.
Goulas, A., Apostolidis S., Gigis P., & Mirtsou-Fidani V. (2006).  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.
Protonotariou, E., Meletis G., Chatzopoulou F., Malousi A., Chatzidimitriou D., & Skoura L. (2019).  Emergence of Klebsiella pneumoniae ST11 co-producing NDM-1 and OXA-48 carbapenemases in Greece.. J Glob Antimicrob Resist. 19, 81-82.
Gogas, H., Dafni U., Koon H., Spyropoulou-Vlachou M., Metaxas Y., Buchbinder E., et al. (2010).  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.
van Beek, N., Patsatsi A., Gupta Y., Möller S., Freitag M., Lemcke S., et al. (2015).  A family with atypical Hailey Hailey disease--is there more to the underlying genetics than ATP2C1?. PLoS One. 10(4), e0121253.
Borg, J., Georgitsi M., Aleporou-Marinou V., Kollia P., & Patrinos G. P. (2009).  Genetic recombination as a major cause of mutagenesis in the human globin gene clusters.. Clin Biochem. 42(18), 1839-50.
Alm, E., Broberg E. K., Connor T., Hodcroft E. B., Komissarov A. B., Maurer-Stroh S., et al. (2020).  Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020.. Euro Surveill. 25(32), 
Lederer, C. W., Pavlou E., Makariou C., Hadjilambi G., Andreou N., Hadjigavriel M., et al. (2014).  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.
Speletas, M., Boukas K., Papadopoulou-Alataki E., Tsitsami E., & Germenis A. E. (2009).  Hereditary angioedema in Greek families caused by novel and recurrent mutations.. Hum Immunol. 70(11), 925-9.
Walsh, S., Liu F., Wollstein A., Kovatsi L., Ralf A., Kosiniak-Kamysz A., et al. (2013).  The HIrisPlex system for simultaneous prediction of hair and eye colour from DNA.. Forensic Sci Int Genet. 7(1), 98-115.
Michaelidis, T. M., Tzimagiorgis G., Moschonas N. K., & Papamatheakis J. (1993).  The human glutamate dehydrogenase gene family: gene organization and structural characterization.. Genomics. 16(1), 150-60.
Eleftheriadis, T., Kartsios C., Pissas G., Liakopoulos V., Antoniadi G., Galaktidou G., et al. (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.
Kritis, A. A., Ktistaki E., Barda D., Zannis V. I., & Talianidis I. (1993).  An indirect negative autoregulatory mechanism involved in hepatocyte nuclear factor-1 gene expression.. Nucleic Acids Res. 21(25), 5882-9.
Goulas, A., Triplett E. L., & Taborsky G. (1996).  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.
Mavrothalassitis, G., Tzimagiorgis G., Mitsialis A., Zannis V., Plaitakis A., Papamatheakis J., et al. (1988).  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.
Kalinderi, K., Bostantjopoulou S., Katsarou Z., Clarimón J., & Fidani L. (2012).  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.
Georgitsi, M., Heliövaara E., Paschke R., Kumar A. V. K., Tischkowitz M., Vierimaa O., et al. (2008).  Large genomic deletions in AIP in pituitary adenoma predisposition.. J Clin Endocrinol Metab. 93(10), 4146-51.
Zhao, C., Escalante L. Navarro, Chen H., Benatti T. R., Qu J., Chellapilla S., et al. (2015).  A massive expansion of effector genes underlies gall-formation in the wheat pest Mayetiola destructor.. Curr Biol. 25(5), 613-20.
Caputo, V. S., Costa J. R., Makarona K., Georgiou E., D Layton M., Roberts I., et al. (2013).  Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutation.. Hum Mol Genet. 22(16), 3187-94.
Tzimagiorgis, G., & Moschonas N. K. (1991).  Molecular cloning, structure and expression analysis of a full-length mouse brain glutamate dehydrogenase cDNA.. Biochim Biophys Acta. 1089(2), 250-3.
Nordström, K. J. V., Albani M. C., James G. Velikkakam, Gutjahr C., Hartwig B., Turck F., et al. (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.

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