Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lambrini, Psiouri"'
Autor:
Adamantia Papachatzopoulou, Argyro Sgourou, Aglaia Athanassiadou, Michael Antoniou, Lambrini Psiouri, Samantha Routledge
Publikováno v:
British Journal of Haematology. 124:828-835
The mechanisms by which mutations within the 5' untranslated region (UTR) of the human beta-globin gene (HBB) cause thalassaemia are currently not well understood. We present here the first comprehensive comparative functional analysis of four 'silen
Autor:
Lambrini Psiouri, Vassilis G. Gorgoulis, George M. Maniatis, Gerassimos E. Voutsinas, Liliana Puiu, Anastasia Apostolidou, Eftichia Petrakou, Aglaia Athanassiadou, Adamantia Papachatzopoulou, Athanassios Kotsinas, Evangelos Tzoracoeleftherakis
Publikováno v:
Cancer Letters. 194:91-97
Fas (APO-1/CD95) is a transmembrane receptor protein involved in cell death signaling. Fas receptor and ligand are both expressed in breast cancer cells, however these cells are resistant to apoptosis. Fas gene mutations were detected in hematologica
Autor:
Lambrini Psiouri, Michael Antoniou, Aglaia Athanassiadou, Nicholas C. Zoumbos, Adamandia Papachatzopoulou, Argyro Sgourou, Richard A. Gibbs
Publikováno v:
British Journal of Haematology. 118:671-676
Summary. We have studied the expression of the silent β-thalassaemia term+6 (CG) mutation, at nucleotide 6 after the stop codon within the human β-globin 3′ untranslated regions (3′UTR), by stable transfection in murine erythroleukaemia (MEL) c
Autor:
Argyro, Sgourou, Samantha, Routledge, Michael, Antoniou, Adamantia, Papachatzopoulou, Lambrini, Psiouri, Aglaia, Athanassiadou
Publikováno v:
British journal of haematology. 124(6)
The mechanisms by which mutations within the 5' untranslated region (UTR) of the human beta-globin gene (HBB) cause thalassaemia are currently not well understood. We present here the first comprehensive comparative functional analysis of four 'silen
Autor:
Argyro, Sgourou, Adamandia, Papachatzopoulou, Lambrini, Psiouri, Michael, Antoniou, Nicholas, Zoumbos, Richard, Gibbs, Aglaia, Athanassiadou
Publikováno v:
British journal of haematology. 118(2)
We have studied the expression of the silent beta-thalassaemia term+6 (C--G) mutation, at nucleotide 6 after the stop codon within the human beta-globin 3' untranslated regions (3'UTR), by stable transfection in murine erythroleukaemia (MEL) cells. S
Autor:
George M. Maniatis, Elisabeth Leroy, Achilleas Ilias, Gerassimos E. Voutsinas, Lambrini Psiouri, Aglaia Athanassiadou, Mihael H. Polymeropoulos, Thodoros Papapetropoulos
Publikováno v:
The American Journal of Human Genetics. (2):555-558
We wish to thank Drs. C. Bissas, N. Georgopoulos, P. Ghikas, C. Kremmydas, P. Leonardos, S. Papapetropoulos, and, last but not least, A. Protonotariou, for their great help in sample collection. This work was supported by European Framework Program E