Nephron organoids derived from human pluripotent stem cells model kidney development and injury - Wikidata - awgldk - TriplyDB

Nephron organoids derived from human pluripotent stem cells model kidney development and injury

Nephron organoids derived from human pluripotent stem cells model kidney development and injury

http://www.wikidata.org/entity/Q29037394

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Generating kidney tissue from pluripotent stem cells Autologous Cells for Kidney Bioengineering Stem Cells Applications in Regenerative Medicine and Disease Therapeutics.Autophagy, Innate Immunity and Tissue Repair in Acute Kidney Injury Modeling Kidney Disease with iPS Cells Translational Prospects and Challenges in Human Induced Pluripotent Stem Cell Research in Drug Discovery Human pluripotent stem cell-derived acinar/ductal organoids generate human pancreas upon orthotopic transplantation and allow disease modelling.Bioprinting of 3D Convoluted Renal Proximal Tubules on Perfusable Chips Human pluripotent stem cell differentiation to functional pancreatic cells for diabetes therapies: Innovations, challenges and future directions.The bioengineered kidney: science or science fiction?Repopulating Decellularized Kidney Scaffolds: An Avenue for Ex Vivo Organ Generation.Growing Kidney Tissue from Stem Cells: How Far from "Party Trick" to Medical Application?Generation of kidney organoids from human pluripotent stem cells Notch signaling promotes nephrogenesis by downregulating Six2.Generation of kidney tubular organoids from human pluripotent stem cells.Repair after nephron ablation reveals limitations of neonatal neonephrogenesis Generation of nephron progenitor cells and kidney organoids from human pluripotent stem cells.Novel fixed z-direction (FiZD) kidney primordia and an organoid culture system for time-lapse confocal imaging.Evolving technology: creating kidney organoids from stem cells.Podocytes and the quest for precision medicines for kidney diseases.The exciting "bench to bedside" journey of cell therapies for acute kidney injury and renal transplantation.Kidney Organoids: A Translational Journey.Regenerative medicine in kidney disease: where we stand and where to go.Organoid technologies meet genome engineering.Induction of nephron progenitors and glomeruli from human pluripotent stem cells.Generation of human muscle fibers and satellite-like cells from human pluripotent stem cells in vitro.Regenerative strategies for kidney engineering.Patient-derived induced pluripotent stem cells in cancer research and precision oncology.How to grow a kidney: patient-specific kidney organoids come of age.Understanding kidney morphogenesis to guide renal tissue regeneration.Making new kidneys: On the road from science fiction to science fact.Growth Factor Regulation in the Nephrogenic Zone of the Developing Kidney.Modeling Cancer with Pluripotent Stem Cells.Engineering kidney cells: reprogramming and directed differentiation to renal tissues.PAX2 is dispensable for in vitro nephron formation from human induced pluripotent stem cells.Evidence of In Vitro Preservation of Human Nephrogenesis at the Single-Cell Level.Bioengineered kidney tubules efficiently excrete uremic toxins.Direct Isolation and Characterization of Human Nephron Progenitors.Gene-Edited Human Kidney Organoids Reveal Mechanisms of Disease in Podocyte Development.Effect of adipose-derived mesenchymal stem cell transplantation on vascular calcification in rats with adenine-induced kidney disease.

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Nephron organoids derived from human pluripotent stem cells model kidney development and injury

http://www.wikidata.org/entity/Q29037394

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2015 nî lūn-bûn

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2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2015年の論文

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Albert Q Lam

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Benjamin S Freedman

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Joseph V Bonventre

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Ryuji Morizane

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Seiji Kishi

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P2860

The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4

Requirement for Wnt3 in vertebrate axis formation

Laser capture-microarray analysis of Lim1 mutant kidney development

Use of dual section mRNA in situ hybridisation/immunohistochemistry to clarify gene expression patterns during the early stages of nephron development in the embryo and in the mature nephron of the adult mouse kidney

The forkhead transcription factor Foxf1 is required for differentiation of extra-embryonic and lateral plate mesoderm

Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system

Gamma-secretase activity is dispensable for mesenchyme-to-epithelium transition but required for podocyte and proximal tubule formation in developing mouse kidney

Crucial roles of Brn1 in distal tubule formation and function in mouse kidney

Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney

Pax2 and pax8 regulate branching morphogenesis and nephron differentiation in the developing kidney

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10.1038/NBT.3392

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11

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33

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M. Todd Valerius

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1027516503

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26458176

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4747858

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