Πλοήγηση ανά Συγγραφέα "Kitsiou-Tzeli, S."

The c.504T > C (p.Asn168Asn) polymorphism in the ABCB4 gene as a predisposing factor for intrahepatic cholestasis of pregnancy in Greece

Kitsiou-Tzeli, S.; Traeger-Synodinos, J.; Giannatou, E.; Kaminopetros, P.; Roma, E.; Makrythanasis, P.; Tsezou, A. (2010)

Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization

Manolakos, E.; Kefalas, K.; Neroutsou, R.; Lagou, M.; Kosyakova, N.; Ewers, E.; Ziegler, M.; Weise, A.; Tsoplou, P.; Rapti, S. M.; Papoulidis, I.; Anastasakis, E.; Garas, A.; Sotiriou, S.; Eleftheriades, M.; Peitsidis, P.; Malathrakis, D.; Thomaidis, L.; Kitsos, G.; Orru, S.; Liehr, T.; Petersen, M. B.; Kitsiou-Tzeli, S. (2010)

Small supernumerary marker chromosomes (sSMCs) cannot be identified or characterized unambiguously by conventional cytogenetic banding techniques. Until recently, the large variety of marker chromosomes, as well as the ...

Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3

Christopoulou, G.; Tzetis, M.; Konstantinidou, A. E.; Tsezou, A.; Kanavakis, E.; Kitsiou-Tzeli, S.; Velissariou, V. (2012)

Ring chromosomes are rare cytogenetic findings and are mostly associated with an abnormal phenotype. We report on the prenatal diagnosis of a ring chromosome 10 in a fetus in which talipes equinovarus was incidentally found ...

Genetic Polymorphisms in the UGT1A1 gene and breast cancer risk in Greek women

Tsezou, A.; Tzetis, M.; Giannatou, E.; Gennatas, C.; Pampanos, A.; Kanavakis, E.; Kitsiou-Tzeli, S. (2007)

Uridine diphospho-glucuronosyltransferase 1 (UGT1A1) is involved in estradiol glucuronidation, which may play a central role in the etiology of breast cancer. A common insertion/ deletion polymorphism in the TATAA-box of ...

Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population

Tsezou, A.; Tzetis, M.; Giannatou, E.; Spanos, I.; Roma, E.; Fretzayas, A.; Kanavakis, E.; Kitsiou-Tzeli, S. (2009)

We investigated the hypothesis that coinheritance of the common A(TA)(n)TAA promoter mutation at the UGT1A1 locus associated with Gilbert syndrome is a risk factor for gallstone formation in a homogeneous adult population, ...

Gilbert's syndrome as a predisposing factor for idiopathic cholelithiasis in children

Kitsiou-Tzeli, S.; Kanavakis, E.; Tzetis, M.; Kavazarakis, E.; Galla, A.; Tsezou, A. (2003)

hTERT regulation by NF-kappa B and c-myc in irradiated HER2-positive breast cancer cells

Papanikolaou, V.; Athanassiou, E.; Dubos, S.; Dimou, I.; Papathanasiou, I.; Kitsiou-Tzeli, S.; Kappas, C.; Tsezou, A. (2011)

Purpose: Telomerase activity (TA), frequently observed in cancer, compensates for telomere shortening thus preventing cell senescence and conferring resistance to therapy. In the present study, we investigated the expression ...

Influence of Interleukin 1 alpha (IL-1 alpha), IL-4, and IL-6 Polymorphisms on Genetic Susceptibility to Chronic Osteomyelitis

Tsezou, A.; Poultsides, L.; Kostopoulou, F.; Zintzaras, E.; Satra, M.; Kitsiou-Tzeli, S.; Malizos, K. N. (2008)

The association between cytokine gene polymorphisms and chronic osteomyelitis was investigated in order to determine whether genetic variability in cytokine genes predisposes to osteomyelitis susceptibility. Significant ...