+ |
EGR1 | up-regulates
|
Monocyte_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256088 |
|
|
Homo sapiens |
U-937 Cell |
pmid |
sentence |
1864967 |
Finally, we demonstrate that dexamethasone, an inhibitor of monocytic differentiation, blocks the associated increases in EGR-1 and EGR-2 expression. Taken together, the results indicate that the EGR-1 and EGR-2 early response genes are involved in the induction of myeloid leukemia cell differentiation along the monocytic lineage and in the activation of human monocytes. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
JUN | up-regulates
|
Monocyte_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256066 |
|
|
Mus musculus |
Hematopoietic Stem Cell |
pmid |
sentence |
17041602 |
These results show that restoration of c-Jun expression rescues the myelomonocytic differentiation block in preleukemic PU.1-knockdown bone marrow cells, suggesting that c-Jun is a critical downstream target in PU.1-knockdown HSCs. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | HaematopoiesisTranscriptionalControl |
+ |
SPI1 | up-regulates activity
|
Monocyte_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259954 |
|
|
Mus musculus |
Hematopoietic Stem Cell |
pmid |
sentence |
8079170 |
Mice carrying a mutation in the PU.1 locus were generated by gene targeting. Homozygous mutant embryos died at a late gestational stage. [...]An invariant consequence of the mutation was a multilineage defect in the generation of progenitors for B and T lymphocytes, monocytes, and granulocytes. Thus, the developmental programs of lymphoid and myeloid lineages require a common genetic function likely acting at the level of a multipotential progenitor. |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | HaematopoiesisTranscriptionalControl |
+ |
FLI1 | up-regulates activity
|
Monocyte_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259972 |
|
|
Mus musculus |
Hematopoietic Stem Cell |
pmid |
sentence |
23320737 |
The transcription factor Fli-1 regulates monocyte, macrophage and dendritic cell development in mice |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | HaematopoiesisTranscriptionalControl |
+ |
SPI1 | up-regulates
|
Monocyte_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256085 |
|
|
Homo sapiens |
|
pmid |
sentence |
20861919 |
In the myeloid compartment, Gfi1 is part of a regulatory network that determines lineage fate decision between granulocyte and monocyte/macrophage development. In this compartment, Gfi1 antagonizes the function of the transcription factor Pu.1. Pu.1 promotes monocytic differentiation, whereas Gfi1 enhances granulocytic differentiation. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | HaematopoiesisTranscriptionalControl |
+ |
CEBPA | up-regulates activity
|
Monocyte_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-259965 |
|
|
Mus musculus |
Hematopoietic Stem Cell |
pmid |
sentence |
19706798 |
Conditional cebpa deficiency in adult mice blocks the transition from common myeloid progenitors (CMP) to granulocyte monocyte progenitors (GMP) resulting in the accumulation of myeloid blasts |
|
Publications: |
1 |
Organism: |
Mus Musculus |
Pathways: | HaematopoiesisTranscriptionalControl |
+ |
EGR2 | up-regulates
|
Monocyte_differentiation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-256089 |
|
|
Homo sapiens |
U-937 Cell |
pmid |
sentence |
1864967 |
Finally, we demonstrate that dexamethasone, an inhibitor of monocytic differentiation, blocks the associated increases in EGR-1 and EGR-2 expression. Taken together, the results indicate that the EGR-1 and EGR-2 early response genes are involved in the induction of myeloid leukemia cell differentiation along the monocytic lineage and in the activation of human monocytes. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
Pathways: | HaematopoiesisTranscriptionalControl |