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Page 1
Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2.
Yoshimoto S, Harahap NI, Hamamura Y, Ar Rochmah M, Shima A, Morisada N, Shinohara M, Saito T, Saito K, Lai PS, Matsuo M, Awano H, Morioka I, Iijima K, Nishio H. Yoshimoto S, et al. Among authors: morisada n. Hum Genome Var. 2016 Dec 1;3:16040. doi: 10.1038/hgv.2016.40. eCollection 2016. Hum Genome Var. 2016. PMID: 27917293 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.
Metabolomics analysis of umbilical cord blood clarifies changes in saccharides associated with delivery method.
Hashimoto F, Nishiumi S, Miyake O, Takeichi H, Chitose M, Ohtsubo H, Ishimori S, Ninchoji T, Hashimura Y, Kaito H, Morisada N, Morioka I, Fukuoka H, Yoshida M, Iijima K. Hashimoto F, et al. Among authors: morisada n. Early Hum Dev. 2013 May;89(5):315-20. doi: 10.1016/j.earlhumdev.2012.10.010. Epub 2012 Nov 22. Early Hum Dev. 2013. PMID: 23178109
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
123 results