About: A novel MGB probe-based assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPMI (nucleophosmin) exon 12 mutations     Goto   Sponge   NotDistinct   Permalink

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Description
  • Insertions into exon 12 of NPM1 gene represent the most frequent molecular aberration in the subgroup of patients with AML otherwise showing normal karyotype. Therefore, NPM1 mutations may be used as a marker for quantification of minimal residual disease (MRD). Here we propose highly sensitive and reproducible MGB probe-based method for MRD.
  • Insertions into exon 12 of NPM1 gene represent the most frequent molecular aberration in the subgroup of patients with AML otherwise showing normal karyotype. Therefore, NPM1 mutations may be used as a marker for quantification of minimal residual disease (MRD). Here we propose highly sensitive and reproducible MGB probe-based method for MRD. (en)
  • Inzerce v exonu 12 genu pro NPM1 představují nejčastější molekulární aberaci detekovanou u AML pacientů s normálním karyotypem. Tyto mutace mohou být navíc využity pro sledování minimální reziduální choroby. Představujeme novou vysoce senzitivní a reprodukovatelnou metodu sledování MRD založenou na využití specifických MGB sond. (cs)
Title
  • A novel MGB probe-based assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPMI (nucleophosmin) exon 12 mutations
  • A novel MGB probe-based assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPMI (nucleophosmin) exon 12 mutations (en)
  • Nová metoda sledování minimální reziduální choroby u AML pacientů založená na sledování mutací NPM1 genu pomocí MGB sond (cs)
skos:prefLabel
  • A novel MGB probe-based assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPMI (nucleophosmin) exon 12 mutations
  • A novel MGB probe-based assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPMI (nucleophosmin) exon 12 mutations (en)
  • Nová metoda sledování minimální reziduální choroby u AML pacientů založená na sledování mutací NPM1 genu pomocí MGB sond (cs)
skos:notation
  • RIV/00216224:14110/08:00027835!RIV09-MSM-14110___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM0021622430)
http://linked.open...iv/cisloPeriodika
  • 1
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 354369
http://linked.open...ai/riv/idVysledku
  • RIV/00216224:14110/08:00027835
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • minimal residual disease; AML; NPM1; MGB (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [1B85823552CC]
http://linked.open...i/riv/nazevZdroje
  • Hematologica the hematology journal
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 93
http://linked.open...iv/tvurceVysledku
  • Dvořáková, Dana
  • Lengerová, Martina
  • Mayer, Jiří
  • Pospíšilová, J.
  • Ohlídalová, D.
http://linked.open...n/vavai/riv/zamer
issn
  • 0390-6078
number of pages
http://localhost/t...ganizacniJednotka
  • 14110
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