Publication for Gfi1b and Klf1
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| mmu | Gfi1b | growth factor independent 1B | 14582 | [link] | ||
| mmu | Klf1 | Kruppel-like factor 1 (erythroid) | 16596 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 21695229 | 0.99 | Gfi-1b, EpoR, and Klf1 (Figure 3C and Figure 4). |
| 0.98 | Gfi-1b, Klf1, and EpoR are significantly downregulated (Figure 3C). | |
| 0.97 | Gfi-1b, the erythropoietin receptor (EpoR), and the erythroid kruppel-like factor Klf1 promote erythroid differentiation. | |
| 0.67 | Gfi1b, and EpoR are transcribed from the negative strand (right to left), whereas Sfpi1 (PU.1) and Klf1 are expressed in the sense direction (left to right). | |
| 25564442 | 0.99 | Gfi1b, Pu.1/Sfpi1 and Klf1 was down-regulated in Gata1&2KO endothelial cells (Fig6D), implying that Gata1 and/or 2 is required for the induction of the hematopoietic transcription factor network that enables the emergence of HS/PCs from hemogenic endothelium. |
| 0.98 | Klf1, Gfi1b). | |
| 22412390 | 0.99 | Gfi1b Klf1 and Klf3, are up-regulated in CD34- cells (Figure 1). |
| 29300724 | 0.98 | Gfi1b and Klf1) were downregulated in wild type CD31high CMPs compared to wild type CD31low CMPs, reflecting the megakaryocytic/erythroid lineage commitment which accompanies CD31 downregulation in the CMP compartment and demonstrating that CD31low and CD31high CMPs represent transcriptionally distinct progenitor subsets. |
| 0.93 | Gfi1b, Klf1 and Gata2, plus the megakaryocytic/erythroid lineage markers Itga2b, Pf4 and Epor (S7R Fig), were all expressed at comparable levels in Runx1-del/del CD31low CMPs to CD31high CMPs (of all genotypes). | |
| 29861167 | 0.98 | KLF1, NFE2, and GFI1B genes and their regulons, was the most stable core of response across all hemogenic subsets. |
| 0.86 | KLF1, and GFI1B regulons were not active, while, SOX17 and SOX18 regulons displayed slight increases in their regulon-level signal in non-HE. | |
| 31996238 | 0.98 | Gfi1b, Klf1, and Tal1 encode transcription factors which are known to be critically involved in erythropoiesis. |
| 0.96 | Gfi1b, Tal1, Klf1, Epor, and Cldn13. | |
| 21057528 | 0.98 | Gfi-1b and eklf. |
| 24752325 | 0.98 | Gfi1b, Klf1, and Tal1, the latter three confirmed by RT-PCR analysis (Figure 8). |
| 24800817 | 0.98 | KLF1, remained similarly regulated during development in Gfi1b knockout fetal liver cells and wt controls (Figure 8A). |
| 27888632 | 0.98 | KLF1 (5.0-fold, p<0.0001), GFI1B (2.5-fold, p<0.0001), LMO2 (1.7-fold, p<0.001) and TAL1 (2.3-fold, p<0.0001) were downregulated in CD34+ CB cells constitutively expressing VENTX. |
| 29968757 | 0.98 | Gfi1b Klf1, and Ikzf1, known to maintain embryonic blood cells were found in the synergistic transcriptional core of the embryonic primitive erythrocyte subpopulation (Supplementary Data 1). |
| 30206223 | 0.98 | Klf1, Gata1 and Gfi1b. |
| 24711581 | 0.97 | Gfi-1b-/- progenitors had initiated the erythroid program as they expressed many lineage-restricted genes, including Klf1/Eklf and Erythropoietin receptor. |
| 27713415 | 0.97 | Klf1 (Fig. 3e), which are known to regulate primitive erythropoiesis during embryogenesis, as well as Gfi1b (Fig. 3e). |
| 29472540 | 0.97 | KLF1, and GFI1b. |
| 24035353 | 0.96 | Gfi1b, Nfia and Klf1), and negatively correlates with a lymphomyeloid module (characterized by Flt3, Sell, Cebpa and Notch1). |
| 30814124 | 0.96 | Klf1, Gfi1b, or Runx1 were unaffected (Fig 5G). |
| 23159334 | 0.95 | eklf and gfi-1b) or increased transcript level (scl, hba) at the 5' end, whereas the levels of 3' transcripts were significantly reduced for all tested erythroid genes (Fig. 6A). |
| 27207878 | 0.95 | Klf1, Gfi1b and Gata1 expression, characteristic of erythroid lineage progenitors, similar to Clusters 1-6 in the original study (Figure 1c in). |
| 23675896 | 0.94 | Klf1, Gfi1b) are known to play different roles in the primitive versus definitive erythroid lineages; thus the scores of individual genes are expected to vary across the lineages and likely reflect the underlying biology. |
The preparation time of this page was 0.0 [sec].
