Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Christine, Zoi"'
Autor:
Christine Zoi
Τα Μυελοϋπερπλαστικά Νεοπλάσματα είναι κλωνικές διαταραχές των αρχέγονων αιμοποιητικών κυττάρων και χαρακτηρίζονται από πολλαπλασια
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1ba1d3bc28cd56146bf8512225ce629
https://doi.org/10.12681/eadd/35671
https://doi.org/10.12681/eadd/35671
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...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b5c608d1b104b15a87bc8bcee6c3513
https://pubmed.ncbi.nlm.nih.gov/30196743
https://pubmed.ncbi.nlm.nih.gov/30196743
Autor:
Andreas Reiter, Francis H. Grand, Hubert Serve, Claire Hidalgo-Curtis, David Oscier, Amy V. Jones, Thomas Ernst, Katerina Zoi, Carolann McGuire, Andrew J. Hall, Georgia Metzgeroth, Christine Zoi, Nicholas C.P. Cross, Sebastian Kreil, Andrew Chase, Joannah Score, Christian Brandts
Publikováno v:
Blood. 113:6182-6192
Recent evidence has demonstrated that acquired uniparental disomy (aUPD) is a novel mechanism by which pathogenetic mutations in cancer may be reduced to homozygosity. To help identify novel mutations in myeloproliferative neoplasms (MPNs), we perfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5a882438cc25c66090301b01b36d976
https://doi.org/10.1182/blood-2008-12-194548
https://doi.org/10.1182/blood-2008-12-194548
Autor:
Vassiliki Grigoraki, Franck Lellouche, Christine Dosquet, Christine Chomienne, Dimitris Loukopoulos, Bruno Cassinat, Nathalie Parquet, Katerina Zoi, Christophe Marzac, Marie-Hélène Schlageter, William Vainchenker, Christine Zoi, Jean-Jacques Kiladjian, Linda M. Scott, Eirini Kouroupi, Pierre Fenaux
Publikováno v:
British Journal of Haematology. 142:676-679
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca1b7e92b02c74551115c793b192527d
https://doi.org/10.1111/j.1365-2141.2008.07223.x
https://doi.org/10.1111/j.1365-2141.2008.07223.x
Autor:
Rachel Seear, Andreas Reiter, Rüdiger Hehlmann, Beate Schultheis, Dimitris Loukopoulos, Lingyan Zhang, Helen E. White, Evangelos Terpos, Michael Emig, Thomas Ernst, Elisavet-Christine Vervessou, Nicholas C.P. Cross, Andrew Chase, Claire Curtis, David Oscier, Joannah Score, Christine Zoi, Amy V. Jones, Eva Lengfelder, Sebastian Kreil, Katerina Zoi, Katherine Waghorn, Francis H. Grand, Andreas Hochhaus, Richard T. Silver
Publikováno v:
Blood. 106:2162-2168
The analysis of rare chromosomal translocations in myeloproliferative disorders has highlighted the importance of aberrant tyrosine kinase signaling in the pathogenesis of these diseases. Here we have investigated samples from 679 patients and contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c4589177403c1c21f53b5509fa04eae
https://doi.org/10.1182/blood-2005-03-1320
https://doi.org/10.1182/blood-2005-03-1320
Autor:
Eirini, Kouroupi, Katerina, Zoi, Nathalie, Parquet, Christine, Zoi, Jean-Jacques, Kiladjian, Vassiliki, Grigoraki, William, Vainchenker, Franck, Lellouche, Christophe, Marzac, Marie-Hélène, Schlageter, Christine, Dosquet, Linda M, Scott, Pierre, Fenaux, Dimitris, Loukopoulos, Christine, Chomienne, Bruno, Cassinat
Publikováno v:
British journal of haematology. 142(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f41c032f0c2fdb3ce65ff23b3f0e9a65
https://pubmed.ncbi.nlm.nih.gov/18503583
https://pubmed.ncbi.nlm.nih.gov/18503583
Autor:
Issa J, Dahabreh, Katerina, Zoi, Stavroula, Giannouli, Christine, Zoi, Dimitrios, Loukopoulos, Michael, Voulgarelis
Publikováno v:
Leukemia research. 33(1)
A systematic review and meta-analysis was carried out to compare the frequency of clinically significant outcomes between JAK2 V617F positive and wild type patients with essential thrombocythemia (ET). JAK2 V617F positivity in patients with ET was as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::01c65fdbad4e017d5316be811e92ec64
https://pubmed.ncbi.nlm.nih.gov/18632151
https://pubmed.ncbi.nlm.nih.gov/18632151
Publikováno v:
British journal of haematology. 141(1)
CD177 (PRV1) expression is strongly related to polycythaemia vera (PV). Whilst studying CD177 expression in PV patients and controls, individuals with beta-thalassaemia minor were found to display an elevated expression of CD177. The study was expand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::609b31b487ce58d566330bb653649398
https://pubmed.ncbi.nlm.nih.gov/18324972
https://pubmed.ncbi.nlm.nih.gov/18324972
Autor:
Stavroula Giannouli, Michael Voulgarelis, Issa J Dahabreh, Christine Zoi, Haralampos M. Moutsopoulos, Katerina Zoi
Publikováno v:
Medicine. 86(6)
Hypereosinophilic syndrome (HES) is a heterogeneous group of disorders characterized by unexplained persistent primary eosinophilia causing end-organ damage. We conducted a prospective cohort study of patients fulfilling the diagnostic criteria for H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0fee62c729e38a196c648b731380331
https://pubmed.ncbi.nlm.nih.gov/18004179
https://pubmed.ncbi.nlm.nih.gov/18004179
Autor:
Katerina Zoi, Sonja Burgstaller, Andreas Reiter, Christine Zoi, Finella Brito-Babapulle, Helen E. White, G Metzgeroth, C Walz, Daniela Cilloni, Katherine Waghorn, Claude Preudhomme, Sebastian Kreil, Nicholas C.P. Cross
We have investigated the hypothesis that constitutional genetic variation in IL-5 signalling may be associated with the development or severity of FIP1L1-PDGFRA-positive chronic eosinophilic leukaemia (CEL) in humans. We genotyped six single-nucleoti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1490214ce368855a52c45adbb76bfa59
http://hdl.handle.net/2318/21324
http://hdl.handle.net/2318/21324