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Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5.
Yamamura T, Horinouchi T, Adachi T, Terakawa M, Takaoka Y, Omachi K, Takasato M, Takaishi K, Shoji T, Onishi Y, Kanazawa Y, Koizumi M, Tomono Y, Sugano A, Shono A, Minamikawa S, Nagano C, Sakakibara N, Ishiko S, Aoto Y, Kamura M, Harita Y, Miura K, Kanda S, Morisada N, Rossanti R, Ye MJ, Nozu Y, Matsuo M, Kai H, Iijima K, Nozu K. Yamamura T, et al. Among authors: morisada n. Nat Commun. 2020 Jun 2;11(1):2777. doi: 10.1038/s41467-020-16605-x. Nat Commun. 2020. PMID: 32488001 Free PMC article.
Right hypoplastic kidney.
Ogawa A, Kitamura S, Nakayama K, Sugiyama H, Morisada N, Iijima K, Makino H. Ogawa A, et al. Among authors: morisada n. Kidney Int. 2012 Nov;82(9):1037. doi: 10.1038/ki.2012.201. Kidney Int. 2012. PMID: 23064196 Free article. No abstract available.
Natural history of genetically proven autosomal recessive Alport syndrome.
Oka M, Nozu K, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Morisada N, Yan K, Matsuo M, Yoshikawa N, Vorechovsky I, Iijima K. Oka M, et al. Among authors: morisada n. Pediatr Nephrol. 2014 Sep;29(9):1535-44. doi: 10.1007/s00467-014-2797-4. Epub 2014 Mar 15. Pediatr Nephrol. 2014. PMID: 24633401
16q12 microdeletion syndrome in two Japanese boys.
Morisada N, Sekine T, Ishimori S, Tsuda M, Adachi M, Nozu K, Nakanishi K, Tanaka R, Iijima K. Morisada N, et al. Pediatr Int. 2014 Oct;56(5):e75-8. doi: 10.1111/ped.12426. Pediatr Int. 2014. PMID: 25336016
Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing.
Kato T, Morisada N, Nagase H, Nishiyama M, Toyoshima D, Nakagawa T, Maruyama A, Fu XJ, Nozu K, Wada H, Takada S, Iijima K. Kato T, et al. Among authors: morisada n. Brain Dev. 2015 Oct;37(9):911-5. doi: 10.1016/j.braindev.2015.03.002. Epub 2015 Mar 27. Brain Dev. 2015. PMID: 25819767
123 results