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XB-ANAT-144
Papers associated with glomerulus (and wt1)
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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome., Mann N., J Am Soc Nephrol. March 1, 2021; 32 (3): 580-596. |
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Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4): |
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Notch signaling, wt1 and foxc2 are key regulators of the podocyte gene regulatory network in Xenopus., White JT., Development. June 1, 2010; 137 (11): 1863-73. |
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A reverse genetic screen in the zebrafish identifies crb2b as a regulator of the glomerular filtration barrier., Ebarasi L., Dev Biol. October 1, 2009; 334 (1): 1-9. |
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Cadherin-6 is required for zebrafish nephrogenesis during early development., Kubota F., Int J Dev Biol. January 1, 2007; 51 (2): 123-9. |
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FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17. |
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