Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Katerina, Zoi"'
Autor:
Maria Bousali, Vasiliki Pogka, Giannis Vatsellas, Theodoros Loupis, Emmanouil I. Athanasiadis, Katerina Zoi, Dimitris Thanos, Dimitrios Paraskevis, Andreas Mentis, Timokratis Karamitros
Publikováno v:
Microbiology Spectrum, Vol 10, Iss 6 (2022)
ABSTRACT The first SARS-CoV-2 case in Greece was confirmed on February 26, 2020, and since then, multiple strains have circulated the country, leading to regional and country-wide outbreaks. Our aim is to enlighten the events that took place during t
Externí odkaz:
https://doaj.org/article/964d3a3aa12a4764ade27ae6df80aadb
Autor:
Georgios Dryllis, Elena E. Solomou, Andreas Giannopoulos, Nefeli Giannakopoulou, Panayiotis Panayiotidis, Sevastianos Hatzidavid, Nora-Athina Viniou, Vasiliki Pappa, Theodoros Loupis, Christina-Nefeli Kontandreopoulou, Ioannis Kotsianidis, Katerina Zoi, Athanasios Galanopoulos, Maria Dimou, Argiris Symeonidis, Panagiotis T. Diamantopoulos
Publikováno v:
Leukemia & Lymphoma. 63:729-737
Ribonucleotide Reductase (RNR) is a two-subunit (RRM1, RRM2) enzyme, responsible for the conversion of ribonucleotides to deoxyribonucleotides required for DNA replication. To evaluate RNR as a biomarker of response to 5-azacytidine, we measured RNR
Autor:
Eleftheria Lamprianidou, Chryssoula Kordella, Menelaos Papoutselis, Zoi Bezyrgiannidou, Evangelia Nakou, Spyros Papamichos, Emmanouil Spanoudakis, Andreas Giannopoulos, Katerina Zoi, Ioannis Kotsianidis
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 9, Iss 1, Pp e2017066-e2017066 (2017)
It has been suggested that myeloid neoplasms with isolated isochromosome 17q[MN i(17q)] comprise a distinct entity with poor prognosis. However, literature reports show a considerable clinical and molecular heterogeneity. We describe a 58-year-old ma
Externí odkaz:
https://doaj.org/article/7639c8858b6d4caea051a90f42bc17a6
Autor:
Theodora Koutsouri, Konstantinos E. Stamoulis, Marianna Politou, I. Flesiopoulou, Katerina Zoi, Argyrios Tsantes, Serena Valsami, Andreas Giannopoulos, A. Chaiκali, P. Panos, Argyri Gialeraki, Panagiota Douramani
Publikováno v:
Transfusion Medicine. 29:468-470
Autor:
Thomas Ernst, Andrew Chase, Katerina Zoi, Katherine Waghorn, Claire Hidalgo-Curtis, Joannah Score, Amy Jones, Francis Grand, Andreas Reiter, Andreas Hochhaus, Nicholas C.P. Cross
Publikováno v:
Haematologica, Vol 95, Iss 9 (2010)
Background Aberrant activation of tyrosine kinases, caused by either mutation or gene fusion, is of major importance for the development of many hematologic malignancies, particularly myeloproliferative neoplasms. We hypothesized that hitherto unreco
Externí odkaz:
https://doaj.org/article/2e25c0c073bd4116b81c7fb208c1607b
Autor:
Nicola Trim, William J. Tapper, Nicholas C.P. Cross, F. Lin, Andrew Chase, Jacqueline Boultwood, Lars Forsberg, Jan P. Dumanski, Joannah Score, Catherine Bryant, Andrea Pellagatti, Yvette Hoade, Katerina Zoi, Shalini Singh, Bon Ham Yip, Chiara Rasi
Publikováno v:
Leukemia
Acquired uniparental disomy (aUPD, also known as copy-neutral loss of heterozygosity) is a common feature of cancer cells and characterized by extended tracts of somatically-acquired homozygosity without any concurrent loss or gain of genetic materia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22e29505cee9542c48404d045e207794
https://doi.org/10.1038/s41375-018-0340-5
https://doi.org/10.1038/s41375-018-0340-5
Autor:
Marianna Politou, Michael Voulgarelis, Andreas Giannopoulos, Abraham Pouliakis, Christine Zoi, E. Logothetis, George Dryllis, G. Kreatsas, Amalia Dinou, Konstantinos Konstantopoulos, Evangelia Kouskouni, Katerina Zoi, Catherine Stavropoulos-Giokas
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 33(9)
Background: Recent findings show that a number of single nucleotide polymorphisms (SNPs) within the promoter region of the annexin A5-gene (ANXA5) reduce the expression of the reporter gene...
Η μελέτη μας αρχικά επικεντρώθηκε στον τρόπο με τον οποίο τα φυσιολογικά κύτταρα αποκρίνονται στις βλάβες που προκαλεί η υπεριώδης ακτι
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::88f97a42219d2ce94a2dff95a8fcb897
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2759298
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2759298
Autor:
Emmanouil Spanoudakis, Eleftheria Lamprianidou, Menelaos Papoutselis, Evangelia Nakou, Zoi Bezyrgiannidou, Katerina Zoi, Chryssoula Kordella, Ioannis Kotsianidis, Andreas Giannopoulos, Spyros I. Papamichos
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 9, Iss 1, Pp e2017066-e2017066 (2017)
Mediterranean Journal of Hematology and Infectious Diseases
Mediterranean Journal of Hematology and Infectious Diseases
It has been suggested that myeloid neoplasms with isolated isochromosome 17q [ MN i(17q)] comprise a distinct entity with poor prognosis . However, literature reports show a considerable clinical and molecular heterogeneity. We describe a 58-year-old
Autor:
Katerina Zoi, Nicholas C.P. Cross
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 35(9)
Myeloproliferative neoplasms (MPNs) are a group of related clonal hematologic disorders characterized by excess accumulation of one or more myeloid cell lineages and a tendency to transform to acute myeloid leukemia. Deregulated JAK2 signaling has em