Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nikolaos I. Anagnostopoulos"'
Autor:
Georgios Kakiopoulos, Athina Markou, Nikolaos I Anagnostopoulos, Konstantinos Liapis, Theodora Kounadi, George Piaditis, Sophia Vlachou
Publikováno v:
The Lancet. 389:2261-2262
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::496e1cc658a060fca6fd1c36db8f5c23
https://doi.org/10.1016/s0140-6736(17)31374-0
https://doi.org/10.1016/s0140-6736(17)31374-0
Autor:
Emmanuel Kanavakis, Theodore K. Christopoulos, Penelope C. Ioannou, Nikolaos I. Anagnostopoulos, Margarita Petropoulou, Jan Traeger-Synodinos, Alexandra Iliadi
Publikováno v:
Analytical Chemistry. 83:6545-6551
In somatic (acquired) point mutations, the challenge is to quantify minute amounts of the mutant allele in the presence of a large excess of the normal allele that differs only in a single base pair. We report two bioluminometric methods that enable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e3674d39a6a0f242b1bc137cec5842
https://doi.org/10.1021/ac200810h
https://doi.org/10.1021/ac200810h
Autor:
Jan Traeger-Synodinos, Emmanuel Kanavakis, Theodore K. Christopoulos, Vaya Tsiakalou, Ioanna Savvidou, Nikolaos I. Anagnostopoulos, Penelope C. Ioannou, Margarita Petropoulou
Publikováno v:
Analytical Chemistry. 81:8596-8602
Unlike the inherited mutations, which are present in all cells, somatic (acquired) mutations occur only in certain cells of the body and, quite often, are oncogenic. Quantification of mutant allele burden (percentage of the mutant allele) is critical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ac4dced6117023516e0284fe00c1e6e
https://doi.org/10.1021/ac901584a
https://doi.org/10.1021/ac901584a
Autor:
Evangelos Terpos, Athina Mougiou, Alexandra Kouraklis, Aria Chatzivassili, Evridiki Michalis, Nicholas Giannakoulas, Eleni Manioudaki, Anna Lazaridou, Vassiliki Bakaloudi, Maria Protopappa, Dimitra Liapi, Elisavet Grouzi, Agapi Parharidou, Argyris Symeonidis, Garoufalia Kokkini, Nikolaos P. Laoutaris, George Vaipoulos, Nikolaos I. Anagnostopoulos, John I. Christakis, John Meletis, Konstantinos L. Bourantas, Nicholas C. Zoumbos, Xenophon Yataganas, Nora-Athina Viniou for The Greek MDS Study Grou
Publikováno v:
British Journal of Haematology. 118:174-180
Summary. Treatment with recombinant human erythropoietin (rHuEpo) improves anaemia in approximately 20% of patients with myelodysplastic syndromes (MDS). We investigated the potential advantage of a prolonged administration of rHuEpo to achieve highe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee2787cd342e537b2c174d0b1856bfc8
https://doi.org/10.1046/j.1365-2141.2002.03583.x
https://doi.org/10.1046/j.1365-2141.2002.03583.x
Autor:
Jan Traeger-Synodinos, Alexandra Iliadi, Emmanuel Kanavakis, Penelope C. Ioannou, Nikolaos I. Anagnostopoulos, Jessica K. Konstantou, Theodore K. Christopoulos
Publikováno v:
Analytical and bioanalytical chemistry. 397(5)
During the last 5 years, it was discovered that the JAK2V617F somatic mutation is present in virtually all patients with polycythemia vera and a large proportion of patients with essential thrombocythemia, primary myelofibrosis, and refractory anemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7977c38e5da8e47fd72f54e594250f6
https://pubmed.ncbi.nlm.nih.gov/20428846
https://pubmed.ncbi.nlm.nih.gov/20428846
Autor:
Vasilios, Xanthopoulos, Athanasios G, Galanopoulos, Georgios, Paterakis, Dimitra, Apessou, Theodoros, Argyrakos, Eleni, Goumakou, Stephanos I, Papadhimitriou, Ioanna, Savvidou, Maria, Georgiakaki, Nikolaos I, Anagnostopoulos
Publikováno v:
European journal of haematology. 80(2)
Intravascular lymphoma is an extremely rare, disseminated, and aggressive extranodal CD20+ non-Hodgkin's lymphoma characterized by the presence of lymphoma cells only in the lumina of small vessels. We report a 72-year-old woman with a diagnosis of i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2beedb88f4c49626da18aaa80d0b098
https://pubmed.ncbi.nlm.nih.gov/18076638
https://pubmed.ncbi.nlm.nih.gov/18076638
Autor:
Evangelos, Terpos, Athina, Mougiou, Alexandra, Kouraklis, Aria, Chatzivassili, Evridiki, Michalis, Nicholas, Giannakoulas, Eleni, Manioudaki, Anna, Lazaridou, Vassiliki, Bakaloudi, Maria, Protopappa, Dimitra, Liapi, Elisavet, Grouzi, Agapi, Parharidou, Argyris, Symeonidis, Garoufalia, Kokkini, Nikolaos P, Laoutaris, George, Vaipoulos, Nikolaos I, Anagnostopoulos, John I, Christakis, John, Meletis, Konstantinos L, Bourantas, Nicholas C, Zoumbos, Xenophon, Yataganas, Nora-Athina, Viniou
Treatment with recombinant human erythropoietin (rHuEpo) improves anaemia in approximately 20% of patients with myelodysplastic syndromes (MDS). We investigated the potential advantage of a prolonged administration of rHuEpo to achieve higher erythro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c61b8204ae44a7164ffa211e8a957935
http://olympias.lib.uoi.gr/jspui/handle/123456789/18988
http://olympias.lib.uoi.gr/jspui/handle/123456789/18988
Autor:
Demetrios A. Spandidos, Nikolaos I. Anagnostopoulos, M. Ergazaki, Vasiliki Grigoraki, Dora M. Gougopoulou, Hippokratis Kiaris
Publikováno v:
Stem cells (Dayton, Ohio). 14(6)
The levels of expression and the incidence of codon 12 point mutations of the ras family genes were studied in 18 cases of leukemia, seven with acute myeloblastic leukemia (AML), three with acute lymphoblastic leukemia (ALL), four cases with chronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67db8603792e2c978cdd917a541dbf7f
https://pubmed.ncbi.nlm.nih.gov/8948029
https://pubmed.ncbi.nlm.nih.gov/8948029