Kollia Panagoula
Kollia Panagoula
National and Kapodistrian University of Athens, Biology, Dept. Genetics and Biotechnology
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα biol.uoa.gr
Παρατίθεται από
Παρατίθεται από
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
K Estrada, U Styrkarsdottir, E Evangelou, YH Hsu, EL Duncan, EE Ntzani, ...
Nature genetics 44 (5), 491-501, 2012
HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update
B Giardine, S van Baal, P Kaimakis, C Riemer, W Miller, M Samara, ...
Human mutation 28 (2), 206-206, 2007
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
B Giardine, J Borg, DR Higgs, KR Peterson, S Philipsen, D Maglott, ...
Nature genetics 43 (4), 295, 2011
Clinical implications for vascular endothelial growth factor in the lung: friend or foe?
AI Papaioannou, K Kostikas, P Kollia, KI Gourgoulianis
Respiratory research 7 (1), 128, 2006
Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies
GP Patrinos, P Kollia, MN Papadakis
Human mutation 26 (5), 399-412, 2005
Hemin-induced acceleration of hemoglobin production in immature cultured erythroid cells: preferential enhancement of fetal hemoglobin
E Fibach, P Kollia, AN Schechter, CT Noguchi, GP Rodgers
Growth hormone, insulin-like growth factor I, and leptin interaction in human cultured lutein granulosa cells steroidogenesis
M Karamouti, P Kollia, A Kallitsaris, N Vamvakopoulos, G Kollios, ...
Fertility and sterility 90 (4), 1444-1450, 2008
The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [Aγ–158C→T] results from two independent gene conversion events
GP Patrinos, P Kollia, A Loutradi-Anagnostou, D Loukopoulos, ...
Human genetics 102 (6), 629-634, 1998
Beta-thalassaemia mutations and the underlying beta gene cluster haplotypes in the Greek population.
P Kollia, PH Karababa, K Sinopoulou, E Voskaridou, M Boussiou, ...
Gene geography: a computerized bulletin on human gene frequencies 6 (1-2), 59-70, 1992
Assessment of gene‐by‐sex interaction effect on bone mineral density
CT Liu, K Estrada, LM Yerges‐Armstrong, N Amin, E Evangelou, G Li, ...
Journal of bone and mineral research 27 (10), 2051-2064, 2012
A critical view of the general public’s awareness and physicians’ opinion of the trends and potential pitfalls of genetic testing in Greece
Y Mai, T Koromila, A Sagia, DN Cooper, G Vlachopoulos, G Lagoumintzis, ...
Personalized Medicine 8 (5), 551-561, 2011
Analysis of the κ light chain variable region in multiple myeloma
C Kosmas, NA Viniou, K Stamato poulos, NS Courtenay‐Luck, ...
British journal of haematology 94 (2), 306-317, 1996
Transferrin receptor-1 and 2 expression in chronic lymphocytic leukemia
T Smilevska, K Stamatopoulos, M Samara, C Belessi, A Tsompanakou, ...
Leukemia research 30 (2), 183-189, 2006
Telomerase reverse transcriptase mRNA expression in peripheral lymphocytes of patients with chronic HBV and HCV infections
M Satra, GN Dalekos, P Kollia, N Vamvakopoulos, A Tsezou
Journal of viral hepatitis 12 (5), 488-493, 2005
Origin and diversification of the clonogenic cell in multiple myeloma: lessons from the immunoglobulin repertoire
C Kosmas, K Stamatopoulos, N Stavroyianni, K Zoi, C Belessi, N Viniou, ...
Leukemia 14 (10), 1718-1726, 2000
Expression profile of osteoprotegerin, RANK and RANKL genes in the femoral head of patients with avascular necrosis
S Samara, Z Dailiana, C Chassanidis, T Koromila, L Papatheodorou, ...
Experimental and Molecular Pathology 96 (1), 9-14, 2014
Predictive role of cytokine gene polymorphisms for the development of femoral head osteonecrosis
S Samara, P Kollia, Z Dailiana, C Chassanidis, L Papatheodorou, ...
Disease markers 33 (4), 215-221, 2012
Expression of human serum albumin (HSA) mRNA in human granulosa cells: potential correlation of the 95 amino acid long carboxyl terminal of HSA to gonadotrophin surge …
E Karligiotou, P Kollia, A Kallitsaris, IE Messinis
Human Reproduction 21 (3), 645-650, 2006
Prenatal Diagnosis of Thalassemia and of the Sickle Cell Syndromes in Greecea
D Loukopoulos, A Hadji, M Papadakis, P Karababa, K Sinopoulou, ...
Annals of the New York Academy of Sciences 612 (1), 226-236, 1990
Molecular evidence for transferrin receptor 2 expression in all FAB subtypes of acute myeloid leukemia
P Kollia, M Samara, K Stamatopoulos, C Belessi, N Stavroyianni, ...
Leukemia research 27 (12), 1101-1103, 2003
Δεν είναι δυνατή η εκτέλεση της ενέργειας από το σύστημα αυτή τη στιγμή. Προσπαθήστε ξανά αργότερα.
Άρθρα 1–20