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Description
  • Chromosomal rearrangements of the human MLL (mixed lineage leukemia) gene are associated with high-risk infant, pediatric, adult and therapy-induced acute leukemias. We used long-distance inverse-polymerase chain reaction to characterize the chromosomal rearrangement of individual acute leukemia patients. We present data of the molecular characterization of 1590 MLL-rearranged biopsy samples obtained from acute leukemia patients. The precise localization of genomic breakpoints within the MLL gene and the involved translocation partner genes (TPGs) were determined and novel TPGs identified. All patients were classified according to their gender (852 females and 745 males), age at diagnosis (558 infant, 416 pediatric and 616 adult leukemia patients) and other clinical criteria. Combined data of our study and recently published data revealed a total of 121 different MLL rearrangements, of which 79 TPGs are now characterized at the molecular level. However, only seven rearrangements seem to be predominantly associated with illegitimate recombinations of the MLL gene (similar to 90%): AFF1/AF4, MLLT3/AF9, MLLT1/ENL, MLLT10/AF10, ELL, partial tandem duplications (MLL PTDs) and MLLT4/AF6, respectively. The MLL breakpoint distributions for all clinical relevant subtypes (gender, disease type, age at diagnosis, reciprocal, complex and therapy-induced translocations) are presented. Finally, we present the extending network of reciprocal MLL fusions deriving from complex rearrangements.
  • Chromosomal rearrangements of the human MLL (mixed lineage leukemia) gene are associated with high-risk infant, pediatric, adult and therapy-induced acute leukemias. We used long-distance inverse-polymerase chain reaction to characterize the chromosomal rearrangement of individual acute leukemia patients. We present data of the molecular characterization of 1590 MLL-rearranged biopsy samples obtained from acute leukemia patients. The precise localization of genomic breakpoints within the MLL gene and the involved translocation partner genes (TPGs) were determined and novel TPGs identified. All patients were classified according to their gender (852 females and 745 males), age at diagnosis (558 infant, 416 pediatric and 616 adult leukemia patients) and other clinical criteria. Combined data of our study and recently published data revealed a total of 121 different MLL rearrangements, of which 79 TPGs are now characterized at the molecular level. However, only seven rearrangements seem to be predominantly associated with illegitimate recombinations of the MLL gene (similar to 90%): AFF1/AF4, MLLT3/AF9, MLLT1/ENL, MLLT10/AF10, ELL, partial tandem duplications (MLL PTDs) and MLLT4/AF6, respectively. The MLL breakpoint distributions for all clinical relevant subtypes (gender, disease type, age at diagnosis, reciprocal, complex and therapy-induced translocations) are presented. Finally, we present the extending network of reciprocal MLL fusions deriving from complex rearrangements. (en)
Title
  • The MLL recombinome of acute leukemias in 2013
  • The MLL recombinome of acute leukemias in 2013 (en)
skos:prefLabel
  • The MLL recombinome of acute leukemias in 2013
  • The MLL recombinome of acute leukemias in 2013 (en)
skos:notation
  • RIV/00216208:11130/13:10196703!RIV14-MSM-11130___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I
http://linked.open...iv/cisloPeriodika
  • 11
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
  • 88621
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11130/13:10196703
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • AML; ALL; acute leukemia; translocation partner genes; chromosomal translocations; MLL (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [497C1DA3B27E]
http://linked.open...i/riv/nazevZdroje
  • Leukemia
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 27
http://linked.open...iv/tvurceVysledku
  • Hofmann, J.
  • Trka, Jan
  • Zuna, Jan
  • Meyer, C.
  • Macintyre, E.
  • Renneville, A.
  • Cave, H.
  • van Dongen, J. J. M.
  • van der Velden, V. H. J.
  • Aleinikova, O.
  • Binato, R.
  • Burmeister, T.
  • Clappier, E.
  • De Braekeleer, E.
  • De Braekeleer, M.
  • Delabesse, E.
  • Emerenciano, M.
  • Fechina, L.
  • Groeger, D.
  • Harris, M. H.
  • Juvonen, V.
  • Kustanovich, A.
  • Lund-Aho, T.
  • Mass-Malo, K.
  • Oh, S. H.
  • Park, T. S.
  • Silva, M. L. M.
  • Tsaur, G.
  • Villarese, P.
  • de Oliveira, M. Pombo
http://linked.open...ain/vavai/riv/wos
  • 000326882500007
issn
  • 0887-6924
number of pages
http://bibframe.org/vocab/doi
  • 10.1038/leu.2013.135
http://localhost/t...ganizacniJednotka
  • 11130
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