PU.1 is not essential for early myeloid gene expression but is required for terminal myeloid differentiation
Authors:
- Edward W. ScottESEdward W. Scott
- Andrew A. HackAHAndrew A. Hack
- Gloria H. SuGSGloria H. Su
- Daniel G. TenenDTDaniel G. Tenen
- Harinder SinghHSHarinder Singh
- M.Celeste SimonMSM.Celeste Simon
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Cloning of B7-2: a CTLA-4 Counter-Receptor That Costimulates Human T Cell ProliferationScience, 1993
- Mouse beta-globin DNA-binding protein B1 is identical to a proto-oncogene, the transcription factor Spi-1/PU.1, and is restricted in expression to hematopoietic cells and the testis.Molecular and Cellular Biology, 1993
- Granulocyte colony-stimulating factor and its receptorBlood, 1991
- Engraftment after infusion of CD34+ marrow cells in patients with breast cancer or neuroblastomaBlood, 1991
- The gene encoding the stem cell antigen, CD34, is conserved in mouse and expressed in haemopoietic progenitor cell lines, brain, and embryonic fibroblastsInternational Immunology, 1991
- Expression cloning of a receptor for murine granulocyte colony-stimulating factorCell, 1990
- Isolation and Expression of Functional High-Affinity Fc Receptor Complementary DNAsScience, 1989
- Antigen CD34+ marrow cells engraft lethally irradiated baboons.Journal of Clinical Investigation, 1988
- Comparison of three actin-coding sequences in the mouse; Evolutionary relationships between the actin genes of warm-blooded vertebratesJournal of Molecular Evolution, 1986
- Expression of myeloid differentiation antigens on normal and malignant myeloid cells.Journal of Clinical Investigation, 1981