Πλοήγηση ανά Συγγραφέα "Vagena, A."
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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) -
FSH modulatory effect on human granulosa cells: a gene-protein candidate for gonadotrophin surge-attenuating factor
Karligiotou, E.; Kollia, P.; Papaggeli, P.; Samara, S.; Vagena, A.; Dafopoulos, K.; Messinis, I. E. (2011)Previous evidence indicates a homology of gonadotrophin surge-attenuating factor (GnSAF) to the carboxyl terminal of human serum albumin (HSA) and the ability of human granulosa cells to produce mRNA transcripts corresponding ... -
Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central Greece compared to the rest of the country
Samara, M.; Chiotoglou, I.; Kalamaras, A.; Likousi, S.; Chassanidis, C.; Vagena, A.; Vagenas, C.; Eftichiadis, E.; Vamvakopoulos, N.; Patrinos, G. P.; Kollia, P. (2007)We have undertaken a large population screening study to identify the molecular basis of hemoglobinopathies in the central Greece region. A total of 845 unrelated beta-thalassemia patients and alpha-, beta-, and delta ...