About: CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin´s lymphoma     Goto   Sponge   NotDistinct   Permalink

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  • 4 typy polymorfizmu a 25 mutací (3 již známé mutace a 22 nových mutací) bylo detekováno v genu CEBPA v anylyzovaných vzorcích 390 pacientů. Mutace CEBPA byly nalezeny u 14/152 (9,2%) vzorků pacientů s akutní myeloidní leukémiií (AML), 6/143 (4,2%) vzorků pacientů s myelodysplastickým syndromem (MDS), 2/56 (3,6%) vzorků pacientů s neHodgkinským lymfomem (NHL) a 2/39 (5.1%) vzorků s mnohočetným myelomem (MM). Žádné mutace CEBPA nebyly detekovány u zdravých dárců (41 osob). Diskutujeme jak tyto mutace mohou ovlivnit buněčné funkce C/EBPalfa a blokovat myeloidní diferenciaci (cs)
  • Four types of polymorphism and 25 mutations (3 already known mutations and 22 novel mutations) were detected in CEBPA gene in analysed samples from 390 patients. CEBPA mutations were found in 14/152 (9.2%) of acute myeloid leukemia (AML) patients samples, 6/143 (4.2%) of myelodysplastic syndrome (MDS) patients samples, 2/56 (3,6%) of non-Hodgkin’s lymphoma (NHL) patients samples and 2/39 (5.1%) of multiple myeloma (MM) patients samples. None CEBPA mutations were detected in healthy donors (41 individuals). We discuss how these mutations can affect the cellular function of C/EBPalpha and block the myeloid differentiation
  • Four types of polymorphism and 25 mutations (3 already known mutations and 22 novel mutations) were detected in CEBPA gene in analysed samples from 390 patients. CEBPA mutations were found in 14/152 (9.2%) of acute myeloid leukemia (AML) patients samples, 6/143 (4.2%) of myelodysplastic syndrome (MDS) patients samples, 2/56 (3,6%) of non-Hodgkin’s lymphoma (NHL) patients samples and 2/39 (5.1%) of multiple myeloma (MM) patients samples. None CEBPA mutations were detected in healthy donors (41 individuals). We discuss how these mutations can affect the cellular function of C/EBPalpha and block the myeloid differentiation (en)
Title
  • CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin´s lymphoma
  • CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin´s lymphoma (en)
  • Polymorfizmus a mutace CEBPA u pacientů a akutní myeloidní leukémií, myelodysplastickým syndromem, mnohočetným myelomem a neHodgkinským lymfomem (cs)
skos:prefLabel
  • CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin´s lymphoma
  • CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin´s lymphoma (en)
  • Polymorfizmus a mutace CEBPA u pacientů a akutní myeloidní leukémií, myelodysplastickým syndromem, mnohočetným myelomem a neHodgkinským lymfomem (cs)
skos:notation
  • RIV/00023736:_____/08:00007135!RIV08-MZ0-00023736
http://linked.open.../vavai/riv/strany
  • 401;405
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  • P(NR9045)
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  • 3
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  • 359002
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  • RIV/00023736:_____/08:00007135
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  • acute myeloid leukemia; myelodysplastic syndrome; multiple myeloma; CEBPA mutations; non-Hodgkin ´s lymphoma (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [E39C9D7926F4]
http://linked.open...i/riv/nazevZdroje
  • Blood Cells, Molecules and Diseases
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
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http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 40
http://linked.open...iv/tvurceVysledku
  • Březinová, Jana
  • Klamová, Hana
  • Marková, Jana
  • Salaj, Peter
  • Neuwirtová, R.
  • Nováková, L.
  • Schwarz, Jiří
  • Čermák, Jaroslav
  • Benešová, Kateřina
  • Lemež, P.
  • Fuchs, Ota
  • Kobylka, Petr
  • Kostečka, Arnošt
  • Provazníková, Dana
  • Kočová, M.
  • Maaloufová, Jacqueline
  • Cveková, P.
issn
  • 1079-9796
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