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Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04126-6
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- Article
Erythroid Krüppel-like factor (EKLF) is active in primitive and definitive erythroid cells and is required for the function of 5'HS3 of the ß-globin locus control region.
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- EMBO Journal, 1998, v. 17, n. 8, p. 2334, doi. 10.1093/emboj/17.8.2334
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- Article
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.
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- Nature Genetics, 2010, v. 42, n. 9, p. 801, doi. 10.1038/ng.630
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- Article
Specificity Protein 2 (Sp2) Is Essential for Mouse Development and Autonomous Proliferation of Mouse Embryonic Fibroblasts.
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- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009587
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- Article
A tissue‐specific knockout reveals that Gata1 is not essential for Sertoli cell function in the mouse.
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- Nucleic Acids Research, 2003, v. 31, n. 18, p. 5405, doi. 10.1093/nar/gkg723
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- Article
Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1B.
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- Human Genomics, 2020, v. 14, n. 1, p. N.PAG, doi. 10.1186/s40246-020-00283-3
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- Article
Comparison of the PU.1 transcriptional regulome and interactome in human and mouse inflammatory dendritic cells.
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- Journal of Leukocyte Biology, 2021, v. 110, n. 4, p. 735, doi. 10.1002/JLB.6A1219-711RRR
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- Article
Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion.
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- American Journal of Hematology, 2017, v. 92, n. 1, p. E2, doi. 10.1002/ajh.24574
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- Article
Robust hematopoietic specification requires the ubiquitous Sp1 and Sp3 transcription factors.
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- Epigenetics & Chromatin, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13072-019-0282-9
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- Article
The mouse KLF1 Nan variant impairs nuclear condensation and erythroid maturation.
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- PLoS ONE, 2019, v. 14, n. 3, p. 1, doi. 10.1371/journal.pone.0208659
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- Article