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Page 1
Novel mutation in KIF23 causing congenital dyserythropoietic anemia type III in patients who underwent allogeneic hematopoietic stem cell transplantation.
Fujikawa T, Uemura S, Hasegawa D, Morisada N, Nakamura S, Kozaki A, Saito A, Kishimoto K, Ishida T, Mori T, Yakushijin K, Katayama Y, Yamashita D, Wakamatsu M, Hamada M, Muramatsu H, Takahashi Y, Kosaka Y. Fujikawa T, et al. Among authors: morisada n. Pediatr Blood Cancer. 2024 Jun;71(6):e30736. doi: 10.1002/pbc.30736. Epub 2024 Mar 24. Pediatr Blood Cancer. 2024. PMID: 38523246 No abstract available.
Severe dyslipidaemia, atherosclerosis, and sudden cardiac death in mice lacking all NO synthases fed a high-fat diet.
Yatera Y, Shibata K, Furuno Y, Sabanai K, Morisada N, Nakata S, Morishita T, Toyohira Y, Wang KY, Tanimoto A, Sasaguri Y, Tasaki H, Nakashima Y, Shimokawa H, Yanagihara N, Otsuji Y, Tsutsui M. Yatera Y, et al. Among authors: morisada n. Cardiovasc Res. 2010 Sep 1;87(4):675-82. doi: 10.1093/cvr/cvq092. Epub 2010 Mar 18. Cardiovasc Res. 2010. PMID: 20304785
Crucial vasculoprotective role of the whole nitric oxide synthase system in vascular lesion formation in mice: Involvement of bone marrow-derived cells.
Furuno Y, Morishita T, Toyohira Y, Yamada S, Ueno S, Morisada N, Sugita K, Noguchi K, Sakanashi M, Miyata H, Tanimoto A, Sasaguri Y, Shimokawa H, Otsuji Y, Yanagihara N, Tamura M, Tsutsui M. Furuno Y, et al. Among authors: morisada n. Nitric Oxide. 2011 Oct 30;25(3):350-9. doi: 10.1016/j.niox.2011.06.007. Epub 2011 Jul 13. Nitric Oxide. 2011. PMID: 21767657
Spontaneous development of left ventricular hypertrophy and diastolic dysfunction in mice lacking all nitric oxide synthases.
Shibata K, Yatera Y, Furuno Y, Sabanai K, Morisada N, Nakata S, Morishita T, Yamazaki F, Tanimoto A, Sasaguri Y, Tasaki H, Nakashima Y, Shimokawa H, Yanagihara N, Otsuji Y, Tsutsui M. Shibata K, et al. Among authors: morisada n. Circ J. 2010 Nov;74(12):2681-92. doi: 10.1253/circj.cj-10-0277. Epub 2010 Oct 19. Circ J. 2010. PMID: 20966596 Free article.
A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency.
Nakatani N, Tamura A, Hanafusa H, Nino N, Yamamoto N, Awano H, Tanaka Y, Morisada N, Uemura S, Saito A, Hasegawa D, Nozu K, Kosaka Y. Nakatani N, et al. Among authors: morisada n. Hum Genome Var. 2024 Mar 22;11(1):15. doi: 10.1038/s41439-024-00271-2. Hum Genome Var. 2024. PMID: 38514645 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: morisada n. Pediatr Transplant. 2016 May;20(3):467-71. doi: 10.1111/petr.12690. Epub 2016 Feb 21. Pediatr Transplant. 2016. PMID: 26899772
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