Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor
about
A key commitment step in erythropoiesis is synchronized with the cell cycle clock through mutual inhibition between PU.1 and S-phase progressionSUMO-specific protease 1 is essential for stabilization of HIF1alpha during hypoxiaRHEX, a novel regulator of human erythroid progenitor cell expansion and erythroblast developmentInsulin-like growth factor-I augments erythropoietin-induced proliferation through enhanced tyrosine phosphorylation of STAT5Identification of a cytokine-induced antiapoptotic molecule anamorsin essential for definitive hematopoiesisTargeted disruption of the ubiquitous CNC-bZIP transcription factor, Nrf-1, results in anemia and embryonic lethality in mice.Fli-1, an Ets-related transcription factor, regulates erythropoietin-induced erythroid proliferation and differentiation: evidence for direct transcriptional repression of the Rb gene during differentiation.The distal region and receptor tyrosines of the Epo receptor are non-essential for in vivo erythropoiesisProtein inhibitor of activated STAT Y (PIASy) and a splice variant lacking exon 6 enhance sumoylation but are not essential for embryogenesis and adult lifeA novel role for erythropoietin during fibrin-induced wound-healing responseErythropoietin stimulates phosphorylation and activation of GATA-1 via the PI3-kinase/AKT signaling pathwaySuppression of Fas-FasL coexpression by erythropoietin mediates erythroblast expansion during the erythropoietic stress response in vivoPI3 kinase is important for Ras, MEK and Erk activation of Epo-stimulated human erythroid progenitorsProgress towards mechanism-based treatment for Diamond-Blackfan anemiaPrimitive and definitive erythropoiesis in mammalsFrom stem cell to red cell: regulation of erythropoiesis at multiple levels by multiple proteins, RNAs, and chromatin modificationsIsolation and characterization of renal erythropoietin-producing cells from genetically produced anemia miceErythropoietin and the use of a transgenic model of erythropoietin-deficient miceCIS3/SOCS-3 suppresses erythropoietin (EPO) signaling by binding the EPO receptor and JAK2The SH2 inositol 5-phosphatase Ship1 is recruited in an SH2-dependent manner to the erythropoietin receptorThe prolactin receptor and severely truncated erythropoietin receptors support differentiation of erythroid progenitorsLnk inhibits erythropoiesis and Epo-dependent JAK2 activation and downstream signaling pathwaysA developmental transition in definitive erythropoiesis: erythropoietin expression is sequentially regulated by retinoic acid receptors and HNF4Nuclear envelope protein Lem2 is required for mouse development and regulates MAP and AKT kinasesFunctions of c-Jun in liver and heart developmentZFP36L2 is required for self-renewal of early burst-forming unit erythroid progenitorsSox6 is necessary for efficient erythropoiesis in adult mice under physiological and anemia-induced stress conditionsAn activated protein kinase C alpha gives a differentiation signal for hematopoietic progenitor cells and mimicks macrophage colony-stimulating factor-stimulated signaling eventsErythropoietin contributes to implantation: ectopic hemoglobin synthesis in decidual cells of miceRole of Gas6 in erythropoiesis and anemia in miceIn vivo regulation of erythropoiesis by chemically inducible dimerization of the erythropoietin receptor intracellular domainThe erythropoietin receptor is a downstream effector of Klotho-induced cytoprotectionKIT associated intracellular tyrosines play an essential role in EpoR co-signalingISG15 modulates development of the erythroid lineageA heme export protein is required for red blood cell differentiation and iron homeostasisTranscription elongation factor S-II is required for definitive hematopoiesis.Hypoxia-inducible factor-2 (HIF-2) regulates hepatic erythropoietin in vivoDefining an EPOR- regulated transcriptome for primary progenitors, including Tnfr-sf13c as a novel mediator of EPO- dependent erythroblast formationBcl-xL prevents apoptosis of late-stage erythroblasts but does not mediate the antiapoptotic effect of erythropoietinFunctional conservation of erythropoietin signaling in zebrafish
P2860
Q21145791-91DDEA3D-D51B-489A-A4FA-CC897A4DB44CQ24299542-B5F9E394-03DC-447F-B23A-2E0046450403Q24301698-A8DFC042-475F-4E78-B5E7-8779B2E08202Q24308850-30696B82-89F2-486D-960F-C67F3CF94227Q24309295-7BAAC718-DED9-4AC6-BA5A-2E75C41E603DQ24317348-A8793C3D-046D-437E-9C06-9C1AFC20EACEQ24517781-A909CD14-273C-4F9F-B776-DC477DE5E92FQ24550897-64CDADEB-182D-470B-B906-98C3AF06B952Q24561977-E0A1924D-CF33-40F8-BDB4-E8F0200513AFQ24685419-C41C6C40-7DAC-41B1-8804-FB8673DABB3DQ24685447-6736F4B0-D330-4262-AE2F-26D196071F50Q24685620-F6D72B30-B3C3-431F-BD7D-4F74E3A9F857Q24804854-ED465D43-CED5-4C9D-A321-E82014B85EBEQ26823710-17E49953-46E6-4CB2-A187-B282EFD4C89BQ26851586-524E2C15-64B2-484D-9F6B-E2B080F7228CQ26860339-3C7EB840-A99A-41E1-8BBB-82194AEC3BCCQ27317145-16E5B4F4-46F2-490D-AC47-D9134FC4C783Q28075785-6BD72062-D3BE-4E81-A7A1-4632A30C3A21Q28140132-6C97D5B9-88C3-4333-92D7-B7E623842EB1Q28144156-1EF13BB4-CB83-4729-81C4-55BF584CB13DQ28238908-DE1324CF-FEA6-4EAD-BB3D-72A227383F31Q28306960-A6913B0F-C560-4ECB-B0B4-1D1961CE6809Q28362273-9CFDC337-DACE-4E91-BC43-841E97452701Q28504504-45613883-76E3-4A3D-A3C3-9CCAD5DCFBD6Q28505770-8A3316DA-AD4A-4F2E-97B3-E9E28A8D432AQ28508201-7B8EDCC1-649F-4134-A2A2-59731EA0E657Q28509188-71F8701F-DA1F-4B29-B244-CF0A430D5A1EQ28511819-70E76672-C13D-4A78-B7CF-438D6211B971Q28513266-20B6691C-808A-4B30-95CA-B3005477D291Q28513935-D533C7B8-9A53-4C1D-9CE7-94E0A7146F9EQ28544690-922019AF-B6BA-4386-9877-6F37CA1776EBQ28565261-14AC5FCD-FD00-441F-9381-A7D58ED86533Q28588986-4DC8B446-418D-4CBC-B570-B3C57D78F1F1Q28591120-C8B36055-D26B-430B-93F0-D17D40731A94Q28592039-C61C59D1-CEA0-47F7-B722-396A80A97C96Q28592668-57A639CF-63A4-4B66-8B0B-C5E44055513FQ28594830-922BE119-EA64-460B-B843-EE933FB17DE5Q28727049-3ABCA718-9A25-466A-9AE8-F55D982D02D4Q28972292-0D6FC5EC-4852-4791-B956-744459E6CD22Q30480096-A3FBAE26-DF65-48F9-91D8-0A8AF462DCDF
P2860
Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor
description
1995 nî lūn-bûn
@nan
1995 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Generation of committed erythr ...... or the erythropoietin receptor
@ast
Generation of committed erythr ...... or the erythropoietin receptor
@en
Generation of committed erythr ...... or the erythropoietin receptor
@nl
type
label
Generation of committed erythr ...... or the erythropoietin receptor
@ast
Generation of committed erythr ...... or the erythropoietin receptor
@en
Generation of committed erythr ...... or the erythropoietin receptor
@nl
prefLabel
Generation of committed erythr ...... or the erythropoietin receptor
@ast
Generation of committed erythr ...... or the erythropoietin receptor
@en
Generation of committed erythr ...... or the erythropoietin receptor
@nl
P3181
P1433
P1476
Generation of committed erythr ...... or the erythropoietin receptor
@en
P3181
P356
10.1016/0092-8674(95)90234-1
P407
P577
1995-10-06T00:00:00Z