Six2 Defines and Regulates a Multipotent Self-Renewing Nephron Progenitor Population throughout Mammalian Kidney Development
Top Cited Papers
- 7 August 2008
- journal article
- research article
- Published by Elsevier BV in Cell Stem Cell
- Vol. 3 (2), 169-181
- https://doi.org/10.1016/j.stem.2008.05.020
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epitheliaDevelopmental Biology, 2008
- The cdx Genes and Retinoic Acid Control the Positioning and Segmentation of the Zebrafish PronephrosPLoS Genetics, 2007
- Cessation of renal morphogenesis in miceDevelopmental Biology, 2007
- The prepattern transcription factor Irx3 directs nephron segment identityGenes & Development, 2007
- Notch2, but not Notch1, is required for proximal fate acquisition in the mammalian nephronDevelopment, 2007
- Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidneyThe EMBO Journal, 2006
- Cells compete for Decapentaplegic survival factor to prevent apoptosis in Drosophila wing developmentNature, 2002
- Regulation of Cre Recombinase Activity by Mutated Estrogen Receptor Ligand-Binding DomainsBiochemical and Biophysical Research Communications, 1997
- BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning.Genes & Development, 1995
- A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye.Genes & Development, 1995