Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL-USP2 fusions
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu dopisy, práce podpořená grantem
PubMed
30899083
PubMed Central
PMC6756029
DOI
10.1038/s41375-019-0451-7
PII: 10.1038/s41375-019-0451-7
Knihovny.cz E-zdroje
- MeSH
- histonlysin-N-methyltransferasa genetika MeSH
- kohortové studie MeSH
- leukemie genetika MeSH
- lidé MeSH
- protoonkogenní protein MLL genetika MeSH
- rekombinantní fúzní proteiny genetika MeSH
- thiolesterasa ubikvitinu genetika MeSH
- translokace genetická genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- dopisy MeSH
- práce podpořená grantem MeSH
- Názvy látek
- histonlysin-N-methyltransferasa MeSH
- KMT2A protein, human MeSH Prohlížeč
- protoonkogenní protein MLL MeSH
- rekombinantní fúzní proteiny MeSH
- thiolesterasa ubikvitinu MeSH
- USP2 protein, human MeSH Prohlížeč
Centro Ricerca Tettamanti Clinica Pediatrica University of Milano Bicocca Monza Italy
Children's Cancer Institute Australia University of NSW Sydney Sydney Australia
Children's Cancer Research Institute Medical University of Vienna Vienna Austria
DCAL Institute of Pharmaceutical Biology Goethe University Frankfurt Frankfurt am Main Germany
Department of Clinical Chemistry and Laboratory Division Turku University Hospital Turku Finland
Department of Cytogenetics Saint Louis Hospital Paris France
Department of Genetics AP HP Robert Debré Paris Diderot University Paris France
Department of Laboratory Medicine Inje University College of Medicine Busan Korea
Division of Clinical Research Research Center Instituto Nacional de Cancer Rio de Janeiro Brazil
Laboratoire d'Hématologie University Hospital Brest CHU de Bordeaux Bordeaux France
Senckenberg Climate and Research Centre Frankfurt am Main 60325 Germany
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The KMT2A recombinome of acute leukemias in 2023