Injury-induced Cxcl11 and neutrophil signaling drive zebrafish kidney regeneration by generating a nephrogenic niche of Fgf and Wnt expression
Olaleye Olajuyin, Heiko Joachim Schenk, William G. B. Sampson…·Iain A. S. Drummond
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The Rogosin InstituteORCID 0000-0002-2825-7663Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
8 papers
Recent·Most cited
Olaleye Olajuyin, Heiko Joachim Schenk, William G. B. Sampson…·Iain A. S. Drummond
Mohsina Khan, Kyle Bond, Elyse D. Grilli…·Leif H. Oxburgh
This study shows that mitochondrial redistribution in developing proximal tubule cells depends on fluid flow and LRRK2 activity, which is regulated by shear stress.
Caramai N. Kamei, William G. B. Sampson, Carolin Albertz…·Iain A. S. Drummond
This study identifies the roles of canonical and non-canonical Wnt signaling pathways in directing epithelial tubule interconnection during zebrafish kidney regeneration.
Isabel A. López-García, Sunhee Oh, Christopher P. Chaney…·Denise K. Marciano
This study identifies HGF as a key inducer of epithelial tubule anastomosis in vitro and in embryonic kidneys, revealing a proliferation-independent mechanism involving MAPK and MMPs.
Qiuyu Guo, Albert Kim, Bin Li…·Andrew P. McMahon
The paper shows that β-catenin modulates TCF/LEF binding at gene targets, switching from inhibitory to activating complexes during nephron progenitor cell differentiation.
Ashwani Gupta, Prasenjit Sarkar, Jason A. Wertheim…·Leif H. Oxburgh
This study shows that asynchronous mixing of kidney progenitor cells in organoids enhances nephrogenesis and functional features, but stromal overgrowth limits long-term study.
Sarah S. McCarthy, Lindsey Gower, Michele J. Karolak…·Leif H. Oxburgh
This study shows that TGFβ/Smad signaling controls interstitial cell proliferation in the neonatal kidney by inhibiting Wnt/β-catenin signaling to prevent over-proliferation.
Channabasavaiah B. Gurumurthy, Aidan R. O’Brien, Rolen M. Quadros…·Atsushi Yoshiki
The paper re-evaluates the efficiency of a CRISPR-Cas9 method for generating conditional knockout alleles in mice, finding very low success rates and high rates of undesired alleles.