Search Results - "Henkel, G. W."
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Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities
Published in The EMBO journal (15-10-1996)“…PU.1 is a member of the ets family of transcription factors and is expressed exclusively in cells of the hematopoietic lineage. Mice homozygous for a…”
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2
Defective trophoblast function in mice with a targeted mutation of Ets2
Published in Genes & development (01-05-1998)“…Members of the Ets family of transcription factors mediate transcriptional responses of multiple signaling pathways in diverse cell types and organisms…”
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3
Differentiation of the Mononuclear Phagocyte System During Mouse Embryogenesis: The Role of Transcription Factor PU.1
Published in Blood (01-07-1999)“…During mouse embryogenesis, macrophage-like cells arise first in the yolk sac and are produced subsequently in the liver. The onset of liver hematopoiesis is…”
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4
Identification of three genes up‐regulated in PU.1 rescued monocytic precursor cells
Published in International immunology (01-07-2002)“…The requirement of the transcription factor PU.1 for macrophage development has been well documented. However, the target genes regulated by PU.1 controlling…”
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5
Commitment to the Monocytic Lineage Occurs in the Absence of the Transcription Factor PU.1
Published in Blood (01-05-1999)“…Mice homozygous for the disruption of the PU.1 (Spi-1) gene do not produce mature macrophages. In determining the role of PU.1 in macrophage differentiation,…”
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PU.1 But Not Ets-2 Is Essential for Macrophage Development From Embryonic Stem Cells
Published in Blood (15-10-1996)“…Transcription factors play an important role choreographing lineage commitment and expansion of blood cells. Nuclear factors that are expressed primarily or…”
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The transcription factor PU.1 does not regulate lineage commitment but has lineage-specific effects
Published in Journal of leukocyte biology (01-11-1999)“…PU.1 is a transcription factor shown to regulate the expression of many important genes in myeloid and B cells. At birth, mice homozygous for the disruption of…”
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