Πλοήγηση ανά Συγγραφέα "Aleporou-Marinou, V."
-
Altered expression pattern of integrin alphavbeta3 correlates with actin cytoskeleton in primary cultures of human breast cancer
Havaki, S.; Kouloukoussa, M.; Amawi, K.; Drosos, Y.; Arvanitis, L. D.; Goutas, N.; Vlachodimitropoulos, D.; Vassilaros, S. D.; Katsantoni, E. Z.; Voloudakis-Baltatzis, I.; Aleporou-Marinou, V.; Kittas, C.; Marinos, E. (2007)Background: Integrins are transmembrane adhesion receptors that provide the physical link between the actin cytoskeleton and the extracellular matrix. It has been well established that integrins play a major role in various ... -
CER1 gene variations associated with bone mineral density, bone markers, and early menopause in postmenopausal women
Koromila, T.; Georgoulias, P.; Dailiana, Z.; Ntzani, E. E.; Samara, S.; Chassanidis, C.; Aleporou-Marinou, V.; Kollia, P. (2013)Background: Osteoporosis has a multifactorial pathogenesis characterized by a combination of low bone mass and increased fragility. In our study, we focused on the effects of polymorphisms in CER1 and DKK1 genes, recently ... -
Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and delta beta-thalassemia
Kalamaras, A.; Chassanidis, C.; Samara, M.; Papadakis, M. N.; Vagena, A.; Aleporou-Marinou, V.; Patrinos, G. P.; Kollia, P. (2008) -
The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G > T) in the HBG2 gene promoter
Chassanidis, C.; Kalamaras, A.; Phylactides, M.; Pourfarzad, F.; Likousi, S.; Maroulis, V.; Papadakis, M. N.; Vamvakopoulos, N. K.; Aleporou-Marinou, V.; Patrinos, G. P.; Kollia, P. (2009)Nondeletional hereditary persistence of fetal hemoglobin (nd-HPFH), a rare hereditary condition resulting in elevated levels of fetal hemoglobin (Hb F) in adults, is associated with promoter mutations in the human fetal ... -
Impact of ACE and ApoE polymorphisms on myocardial perfusion: correlation with myocardial single photon emission computed tomographic imaging
Georgoulias, P.; Wozniak, G.; Samara, M.; Chiotoglou, I.; Kontos, A.; Tzavara, C.; Valotassiou, V.; Georgitsi, M.; Aleporou-Marinou, V.; Patrinos, G. P.; Kollia, P. (2009)Coronary artery disease is associated with multiple genetic and environmental risk factors. In this study, we evaluated the correlation of angiotensin l-converting enzyme (ACE) (I/D) and ApoE gene polymorphisms (E2, E3, ... -
Novel Sequence Variations in the CER1 Gene Are Strongly Associated with Low Bone Mineral Density and Risk of Osteoporotic Fracture in Postmenopausal Women
Koromila, T.; Dailiana, Z.; Samara, S.; Chassanidis, C.; Tzavara, C.; Patrinos, G. P.; Aleporou-Marinou, V.; Kollia, P. (2012)Osteoporosis is a common skeletal disease characterized by a combination of low bone mass and increased fragility. In this case-control study, we investigated the possible association of two novel candidate genes, CER1 and ... -
Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion
Satra, M.; Samara, M.; Wosniak, G.; Tzavara, C.; Kontos, A.; Valotassiou, V.; Vamvakopoulos, N. K.; Tsougos, I.; Aleporou-Marinou, V.; Patrinos, G. P.; Kollia, P.; Georgoulias, P. (2011)Aims: Coronary artery disease (CAD) is a significant cause of morbidity and mortality in modern societies. The association between genetic markers and CAD is still poorly understood. In this study, we evaluated the effect ...