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Japanese Journal of Ophthalmology|January 1, 1993
A multicenter study of typical retinitis pigmentosa in JapanM Hayakawa, M Matsumura, N Ohba, et al.Nihon Shokakibyo Gakkai Zasshi = the Japanese Journal of Gastro-Enterology|March 1, 1993
[Biopsy diagnosis for gastric lymphoma--usefulness and limitation of AgNOR staining]K Yokota, S Okuyama, M Yuki, et al.Journal of Psychiatric Research|November 11, 2021
Increase in the left hippocampal dentate gyrus head volume after a 4-week bright light exposure in healthy participants: A randomized controlled studyHirofumi Hirakawa, Takeshi Terao, Koji Hatano, et al.European Journal of Immunology|March 23, 2010
Identification of the rat NKG2D ligands, RAE1L and RRLT, and their role in allograft rejectionMing Zhuo, Masato Fujiki, Mouer Wang, et al.[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|April 21, 2005
[Analysis of gene mutation in Chinese patients with Reis-Bücklers corneal dystrophy]Xin Tian, Zu-guo Liu, Qin Li, et al.Nippon Ganka Gakkai Zasshi|February 1, 1992
[Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa]Y Hotta, T Shiono, M Hayakawa, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|February 12, 2005
Endothelium-derived hydrogen peroxide accounts for the enhancing effect of an angiotensin-converting enzyme inhibitor on endothelium-derived hyperpolarizing factor-mediated responses in miceTakako Fujiki, Hiroaki Shimokawa, Keiko Morikawa, et al.Human Molecular Genetics|November 18, 1998
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disordersA Imamura, S Tamura, N Shimozawa, et al.Molecular Endocrinology (Baltimore, Md.)|November 11, 2006
1Alpha,25(OH)2D3-induced transrepression by vitamin D receptor through E-box-type elements in the human parathyroid hormone gene promoterMi-sun Kim, Ryoji Fujiki, Akiko Murayama, et al.Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|June 1, 1991
A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathyK Fujiki, Y Hotta, M Hayakawa, et al.Pageof 239