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Erythropoiesis defect observed in STAT3 GOF patients with severe anemia
AA. Mauracher, JJM. Eekels, J. Woytschak, A. van Drogen, A. Bosch, S. Prader, M. Felber, M. Heeg, L. Opitz, J. Trück, S. Schroeder, E. Adank, A. Klocperk, E. Haralambieva, D. Zimmermann, S. Tantou, K. Kotsonis, A. Stergiou, MG. Kanariou, S. Ehl,...
Jazyk angličtina Země Spojené státy americké
Typ dokumentu dopisy, práce podpořená grantem
- MeSH
- autoimunitní hemolytická anemie farmakoterapie genetika MeSH
- beta-globiny genetika izolace a purifikace MeSH
- bronchiální astma genetika MeSH
- buněčná diferenciace MeSH
- chelátory železa terapeutické užití MeSH
- dítě MeSH
- erythropoetin metabolismus MeSH
- erytrocyty fyziologie MeSH
- erytropoéza genetika MeSH
- kultivované buňky MeSH
- lidé MeSH
- proliferace buněk MeSH
- receptory erythropoetinu metabolismus MeSH
- regulace genové exprese MeSH
- sekvenování exomu MeSH
- signální transdukce MeSH
- stupeň závažnosti nemoci MeSH
- transkripční faktor STAT3 genetika MeSH
- transkripční faktor STAT5 metabolismus MeSH
- zárodečné mutace genetika MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- Publikační typ
- dopisy MeSH
- práce podpořená grantem MeSH
1st Department of Paediatrics Aghia Sophia Children's Hospital Athens Greece
Department of Immunology University Hospital Zurich University of Zurich Zurich Switzerland
Department of Pathology University and University Hospital Zurich Zurich Switzerland
Division of Haematology University Children's Hospital Zurich Zurich Switzerland
Division of Rheumatology University Children's Hospital Zurich Zurich Switzerland
Functional Genomics Center Zürich University of Zurich ETH Zurich Zurich Switzerland
Institute of Molecular Systems Biology ETH Zurich Zurich Switzerland
Citace poskytuje Crossref.org
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