Πλοήγηση ανά Συγγραφέα "Loules, G."

Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV (vol 40, pg 353, 2008)

Speletas, M.; Kioumi, A.; Loules, G.; Hytiroglou, P.; Tsitouridis, J.; Christakis, J.; Germenis, A. E. (2013)

Analysis of SLC40A1(Ferroportin 1) gene at mrna level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV

Speletas, M.; Kioumi, A.; Loules, G.; Kalala, F.; Katodritou, E.; Tsitouridis, I.; Hytiroglou, P.; Christakis, J.; Korantzis, I.; Germenis, A. (2007)

Clinical immunology quiz - Case 5

Loules, G.; Kalala, F.; Mamara, A.; Tsitsami, E.; Speletas, M. (2008)

FIP1L1-PDGFRA molecular analysis in the differential diagnosis of eosinophilia

Loules, G.; Kalala, F.; Giannakoulas, N.; Papadakis, E.; Matsouka, P.; Speletas, M. (2009)

Background: Primary eosinophlia associated with the FIP1L1-PDGFRA rearrangement represents a subset of chronic eosinophilic leukaemia (CEL) and affected patients are very sensitive to imatinib treatment. This study was ...

Foxp3 expression in human cancer cells

Karanikas, V.; Speletas, M.; Zamanakou, M.; Kalala, F.; Loules, G.; Kerenidi, T.; Barda, A. K.; Gourgoulianis, K. I.; Germenis, A. E. (2008)

Objective: Transcription factor forkhead box protein 3 (Foxp3) specifically characterizes the thymically derived naturally occurring regulatory T cells (Tregs). Limited evidence indicates that it is also expressed, albeit ...