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Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome.
Taniguchi Y, Nagano C, Sekiguchi K, Tashiro A, Sugawara N, Sakaguchi H, Umeda C, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Kondo A, Nagai S, Nagase H, Iijima K, Miner JH, Nozu K. Taniguchi Y, et al. Among authors: sugawara n. Kidney360. 2021 Oct 15;2(12):1968-1978. doi: 10.34067/KID.0004952021. eCollection 2021 Dec 30. Kidney360. 2021. PMID: 35419533 Free PMC article.
New-onset diabetes after renal transplantation in a patient with a novel HNF1B mutation.
Kanda S, Morisada N, Kaneko N, Yabuuchi T, Nawashiro Y, Tada N, Nishiyama K, Miyai T, Sugawara N, Ishizuka K, Chikamoto H, Akioka Y, Iijima K, Hattori M. Kanda S, et al. Among authors: sugawara n. Pediatr Transplant. 2016 May;20(3):467-71. doi: 10.1111/petr.12690. Epub 2016 Feb 21. Pediatr Transplant. 2016. PMID: 26899772
Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports.
Yoshikawa T, Kamei K, Nagata H, Saida K, Sato M, Ogura M, Ito S, Miyazaki O, Urushihara M, Kondo S, Sugawara N, Ishizuka K, Hamasaki Y, Shishido S, Morisada N, Iijima K, Nagata M, Yoshioka T, Ogata K, Ishikura K. Yoshikawa T, et al. Among authors: sugawara n. Nephrology (Carlton). 2017 Jul;22(7):566-571. doi: 10.1111/nep.12996. Nephrology (Carlton). 2017. PMID: 28621010
SIRPα interacts with nephrin at the podocyte slit diaphragm.
Kajiho Y, Harita Y, Kurihara H, Horita S, Matsunaga A, Tsurumi H, Kanda S, Sugawara N, Miura K, Sekine T, Hattori S, Hattori M, Igarashi T. Kajiho Y, et al. Among authors: sugawara n. FEBS J. 2012 Sep;279(17):3010-21. doi: 10.1111/j.1742-4658.2012.08682.x. Epub 2012 Jul 23. FEBS J. 2012. PMID: 22747997 Free article.
Generation and analyses of R8L barttin knockin mouse.
Nomura N, Tajima M, Sugawara N, Morimoto T, Kondo Y, Ohno M, Uchida K, Mutig K, Bachmann S, Soleimani M, Ohta E, Ohta A, Sohara E, Okado T, Rai T, Jentsch TJ, Sasaki S, Uchida S. Nomura N, et al. Among authors: sugawara n. Am J Physiol Renal Physiol. 2011 Aug;301(2):F297-307. doi: 10.1152/ajprenal.00604.2010. Epub 2011 May 18. Am J Physiol Renal Physiol. 2011. PMID: 21593186 Free article.
Deletion in the Cobalamin Synthetase W Domain-Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary Tract.
Kanda S, Ohmuraya M, Akagawa H, Horita S, Yoshida Y, Kaneko N, Sugawara N, Ishizuka K, Miura K, Harita Y, Yamamoto T, Oka A, Araki K, Furukawa T, Hattori M. Kanda S, et al. Among authors: sugawara n. J Am Soc Nephrol. 2020 Jan;31(1):139-147. doi: 10.1681/ASN.2019040398. Epub 2019 Dec 20. J Am Soc Nephrol. 2020. PMID: 31862704 Free PMC article.
Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency.
Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T. Uematsu M, et al. Among authors: sugawara n. J Hum Genet. 2007;52(12):1040-1043. doi: 10.1007/s10038-007-0211-9. Epub 2007 Oct 30. J Hum Genet. 2007. PMID: 17968484
450 results