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Human MLL/KMT2A gene exhibits a second breakpoint cluster region for recurrent MLL-USP2 fusions
C. Meyer, BA. Lopes, A. Caye-Eude, H. Cavé, C. Arfeuille, W. Cuccuini, R. Sutton, NC. Venn, SH. Oh, G. Tsaur, G. Escherich, T. Feuchtinger, HJ. Kosasih, SL. Khaw, PG. Ekert, MS. Pombo-de-Oliveira, A. Bidet, B. Djahanschiri, I. Ebersberger, M....
Jazyk angličtina Země Velká Británie
Typ dokumentu dopisy, práce podpořená grantem
NLK
ProQuest Central
od 2000-01-01 do Před 1 rokem
Open Access Digital Library
od 1997-01-01
Nursing & Allied Health Database (ProQuest)
od 2000-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 2000-01-01 do Před 1 rokem
Public Health Database (ProQuest)
od 2000-01-01 do Před 1 rokem
- 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
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
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
Citace poskytuje Crossref.org
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