Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Andrea Sipos"'
Autor:
Hajnalka Andrikovics, Tunde Krahling, Katalin Balassa, Gabriella Halm, Andras Bors, Magdalena Koszarska, Arpad Batai, Janos Dolgos, Judit Csomor, Miklos Egyed, Andrea Sipos, Peter Remenyi, Attila Tordai, Tamas Masszi
Publikováno v:
Haematologica, Vol 99, Iss 7 (2014)
Somatic insertions/deletions in the calreticulin gene have recently been discovered to be causative alterations in myeloproliferative neoplasms. A combination of qualitative and quantitative allele-specific polymerase chain reaction, fragment-sizing,
Externí odkaz:
https://doaj.org/article/8bd72f959dff4b9c935b307804b24b15
Autor:
Sarolta Nahajevszky, Hajnalka Andrikovics, Arpad Batai, Emma Adam, Andras Bors, Judit Csomor, Laszlo Gopcsa, Magdalena Koszarska, Andras Kozma, Nora Lovas, Sandor Lueff, Zoltan Matrai, Nora Meggyesi, Janos Sinko, Andrea Sipos, Andrea Varkonyi, Sandor Fekete, Attila Tordai, Tamas Masszi
Publikováno v:
Haematologica, Vol 96, Iss 11 (2011)
Background Prognostic risk stratification according to acquired or inherited genetic alterations has received increasing attention in acute myeloid leukemia in recent years. A germline Janus kinase 2 haplotype designated as the 46/1 haplotype has bee
Externí odkaz:
https://doaj.org/article/ac88012fc4f3488ab632138d40c784fc
Akademický článek
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Autor:
Andrea Sipos
Publikováno v:
Elpis. Filozófiatudományi Folyóirat. 15:73-84
Publikováno v:
Acta Universitatis Sapientiae: Agriculture and Environment, Vol 7, Iss 1, Pp 47-57 (2015)
Our PhD researches include brownfield revitalization,1 the application of the methods of interim utilizations on greeneries,2 and the formation background and potential of community gardens.3 We compared our systems of criteria in hope of extensive r
Autor:
Angela Feczko, András Kozma, Nóra Meggyesi, János Dolgos, András Bors, Judit Reichardt, Emma Ádám, Tamas Masszi, Judit Csomor, Attila Tordai, Magdalena Koszarska, Tamás I. Orbán, Hajnalka Andrikovics, Nóra Lovas, Andrea Sipos, Sandor Fekete, Eniko Lehoczky, Éva Karászi, Árpád Bátai
Publikováno v:
Leukemia & Lymphoma. 54:1028-1035
Mutations of isocitrate dehydrogenase 1 and 2 (IDH1/2) are genetic alterations in acute myeloid leukemia (AML). The aim of our study was to investigate the frequency and prognostic effect of IDH1/2 mutations together followed by an individual analysi
Autor:
Andrea Sipos, Sandor Lueff, Árpád Bátai, Anikó Barta, András Bors, András Kozma, Péter Reményi, Emma Ádám, Attila Tordai, Hajnalka Andrikovics, Gabriella Halm, György Ujj, Sarolta Nahajevszky, Nóra Meggyesi, Sandor Fekete, Tamas Masszi
Publikováno v:
Acta Haematologica. 127:34-42
Background: Additional chromosome abnormalities (ACAs), mutations of the BCR-ABL tyrosine kinase domain (TKD) and BCR-ABL splice variants may cause resistance to first- and second-generation tyrosine kinase inhibitors (TKIs) in chronic myelogenous le
Publikováno v:
Acta Haematologica. 109:124-128
Homogeneous immunoglobulins are frequently detected in the serum of patients undergoing allogeneic bone marrow transplantation (BMT). The aim of the present study was to further characterize the incidence of this phenomenon and its correlations with
Autor:
Judit Csomor, András Bors, Hajnalka Andrikovics, Miklos Egyed, Tamás Masszi, Tunde Krahling, Attila Tordai, Magdalena Koszarska, János Dolgos, Árpád Bátai, Péter Reményi, Katalin Balassa, Andrea Sipos, Gabriella Halm
Publikováno v:
Haematologica. 99(7)
Somatic insertions/deletions in the calreticulin gene have recently been discovered to be causative alterations in myeloproliferative neoplasms. A combination of qualitative and quantitative allele-specific polymerase chain reaction, fragment-sizing,
Autor:
Otto Csacsovszki, Nóra Lovas, Eniko Lehoczky, András Kozma, Péter Reményi, Tunde Krahling, Attila Tordai, Magdalena Koszarska, András Bors, Tamas Masszi, Emma Ádám, Sándor Fekete, Hajnalka Andrikovics, Nóra Meggyesi, Árpád Bátai, János Dolgos, Andrea Sipos
Publikováno v:
Leukemialymphoma. 55(7)
Internal tandem duplications (ITDs) of the fms-like tyrosine kinase 3 (FLT3) gene occur in about 25% of patients with adult acute myeloid leukemia (AML). The aim of our study was to investigate the frequency of FLT3-ITD mutations followed by a detail