Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epithelia.
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Each niche has an actor: multiple stem cell niches in the preterm kidneyBone morphogenetic protein signaling in nephron progenitor cellsMechanisms of gene activation and repression by Pax proteins in the developing kidneyThe kidney and planar cell polarity.Genetic controls and cellular behaviors in branching morphogenesis of the renal collecting systemRenal stem cells: fact or science fiction?Renal progenitors: Roles in kidney disease and regenerationDevelopment of the Mammalian KidneyConcise Review: Understanding the Renal Progenitor Cell Niche In Vivo to Recapitulate Nephrogenesis In VitroTGF-β signaling plays an essential role in the growth and maintenance of intervertebral disc tissueC-myc as a modulator of renal stem/progenitor cell populationGLI3 repressor controls nephron number via regulation of Wnt11 and Ret in ureteric tip cellsCanonical Wnt9b signaling balances progenitor cell expansion and differentiation during kidney developmentSix2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney developmentOsr1 expression demarcates a multi-potent population of intermediate mesoderm that undergoes progressive restriction to an Osr1-dependent nephron progenitor compartment within the mammalian kidneySall1 balances self-renewal and differentiation of renal progenitor cellsBmp2 and Bmp4 exert opposing effects in hypoxic pulmonary hypertensionNephron organoids derived from human pluripotent stem cells model kidney development and injuryThe number of fetal nephron progenitor cells limits ureteric branching and adult nephron endowment.Retinoic Acid Signaling Coordinates Macrophage-Dependent Injury and Repair after AKI.Bmp7 maintains undifferentiated kidney progenitor population and determines nephron numbers at birthAtlas of gene expression in the developing kidney at microanatomic resolution.Expression of stem cell markers in the human fetal kidneyThe contribution of Notch1 to nephron segmentation in the developing kidney is revealed in a sensitized Notch2 background and can be augmented by reducing Mint dosage.Essential roles of epithelial bone morphogenetic protein signaling during prostatic development.Notch signaling is required for the formation of mesangial cells from a stromal mesenchyme precursor during kidney development.Identification of anchor genes during kidney development defines ontological relationships, molecular subcompartments and regulatory pathways.Patterning a complex organ: branching morphogenesis and nephron segmentation in kidney developmentMorphogenesis and molecular mechanisms involved in human kidney development.Tetracycline inducible gene manipulation in serotonergic neurons.Single cell dissection of early kidney development: multilineage primingDirect transcriptional reprogramming of adult cells to embryonic nephron progenitors.A p53-Pax2 pathway in kidney development: implications for nephrogenesis.Sall1 maintains nephron progenitors and nascent nephrons by acting as both an activator and a repressor.Identification of a multipotent self-renewing stromal progenitor population during mammalian kidney organogenesis.Renal stromal miRNAs are required for normal nephrogenesis and glomerular mesangial survival.Inhibition of Pax2 Transcription Activation with a Small Molecule that Targets the DNA Binding Domain.Induction and patterning of the metanephric nephronGDNF/Ret signaling and renal branching morphogenesis: From mesenchymal signals to epithelial cell behaviors.β-catenin causes renal dysplasia via upregulation of Tgfβ2 and Dkk1
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Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epithelia.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 24 October 2007
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Fate mapping using Cited1-CreE ...... sively to nephronic epithelia.
@en
Fate mapping using Cited1-CreE ...... sively to nephronic epithelia.
@nl
type
label
Fate mapping using Cited1-CreE ...... sively to nephronic epithelia.
@en
Fate mapping using Cited1-CreE ...... sively to nephronic epithelia.
@nl
prefLabel
Fate mapping using Cited1-CreE ...... sively to nephronic epithelia.
@en
Fate mapping using Cited1-CreE ...... sively to nephronic epithelia.
@nl
P2093
P2860
P1476
Fate mapping using Cited1-CreE ...... usively to nephronic epithelia
@en
P2093
Andrew Misfeldt
Douglas P Mortlock
H Scott Baldwin
Karen K Deal
Kelly J Chandler
Mark de Caestecker
Scott Boyle
P2860
P304
P356
10.1016/J.YDBIO.2007.10.014
P407
P577
2007-10-24T00:00:00Z