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Glcci1 deficiency leads to proteinuria.
Nishibori Y, Katayama K, Parikka M, Oddsson A, Nukui M, Hultenby K, Wernerson A, He B, Ebarasi L, Raschperger E, Norlin J, Uhlén M, Patrakka J, Betsholtz C, Tryggvason K. Nishibori Y, et al. Among authors: katayama k. J Am Soc Nephrol. 2011 Nov;22(11):2037-46. doi: 10.1681/ASN.2010111147. Epub 2011 Sep 23. J Am Soc Nephrol. 2011. PMID: 21949092 Free PMC article.
Wolf-Hirschhorn syndrome candidate 1-like 1 epigenetically regulates nephrin gene expression.
Ito Y, Katayama K, Nishibori Y, Akimoto Y, Kudo A, Kurayama R, Hada I, Takahashi S, Kimura T, Fukutomi T, Katada T, Suehiro J, Beltcheva O, Tryggvason K, Yan K. Ito Y, et al. Among authors: katayama k. Am J Physiol Renal Physiol. 2017 Jun 1;312(6):F1184-F1199. doi: 10.1152/ajprenal.00305.2016. Epub 2017 Feb 22. Am J Physiol Renal Physiol. 2017. PMID: 28228401 Free article.
USP40 gene knockdown disrupts glomerular permeability in zebrafish.
Takagi H, Nishibori Y, Katayama K, Katada T, Takahashi S, Kiuchi Z, Takahashi SI, Kamei H, Kawakami H, Akimoto Y, Kudo A, Asanuma K, Takematsu H, Yan K. Takagi H, et al. Among authors: katayama k. Am J Physiol Renal Physiol. 2017 Apr 1;312(4):F702-F715. doi: 10.1152/ajprenal.00197.2016. Epub 2017 Feb 1. Am J Physiol Renal Physiol. 2017. PMID: 28148530 Free article.
Podocyte-specific Crb2 knockout mice develop focal segmental glomerulosclerosis.
Tanoue A, Katayama K, Ito Y, Joh K, Toda M, Yasuma T, D'Alessandro-Gabazza CN, Kawachi H, Yan K, Ito M, Gabazza EC, Tryggvason K, Dohi K. Tanoue A, et al. Among authors: katayama k. Sci Rep. 2021 Oct 15;11(1):20556. doi: 10.1038/s41598-021-00159-z. Sci Rep. 2021. PMID: 34654837 Free PMC article.
Gpr116 Receptor Regulates Distinctive Functions in Pneumocytes and Vascular Endothelium.
Niaudet C, Hofmann JJ, Mäe MA, Jung B, Gaengel K, Vanlandewijck M, Ekvärn E, Salvado MD, Mehlem A, Al Sayegh S, He L, Lebouvier T, Castro-Freire M, Katayama K, Hultenby K, Moessinger C, Tannenberg P, Cunha S, Pietras K, Laviña B, Hong J, Berg T, Betsholtz C. Niaudet C, et al. Among authors: katayama k. PLoS One. 2015 Sep 22;10(9):e0137949. doi: 10.1371/journal.pone.0137949. eCollection 2015. PLoS One. 2015. PMID: 26394398 Free PMC article.
COL4A6 is dispensable for autosomal recessive Alport syndrome.
Murata T, Katayama K, Oohashi T, Jahnukainen T, Yonezawa T, Sado Y, Ishikawa E, Nomura S, Tryggvason K, Ito M. Murata T, et al. Among authors: katayama k. Sci Rep. 2016 Jul 5;6:29450. doi: 10.1038/srep29450. Sci Rep. 2016. PMID: 27377778 Free PMC article.
Irradiation prolongs survival of Alport mice.
Katayama K, Kawano M, Naito I, Ishikawa H, Sado Y, Asakawa N, Murata T, Oosugi K, Kiyohara M, Ishikawa E, Ito M, Nomura S. Katayama K, et al. J Am Soc Nephrol. 2008 Sep;19(9):1692-700. doi: 10.1681/ASN.2007070829. Epub 2008 May 14. J Am Soc Nephrol. 2008. PMID: 18480315 Free PMC article.
1,976 results