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Plos One|August 1, 2012
Genes associated with retinitis pigmentosa and allied diseases are frequently mutated in the general populationKoji M Nishiguchi, Carlo Rivolta
Digital Journal of Ophthalmology : DJO|May 16, 2022
Surgical outcome and pathological findings in macular epiretinal membrane caused by neurofibromatosis type 2Hiroshi Kunikata, Koji M Nishiguchi, Mika Watanabe, et al.
Molecular Therapy. Methods & Clinical Development|May 9, 2017
Spatially and Temporally Regulated NRF2 Gene Therapy Using Mcp-1 Promoter in Retinal Ganglion Cell InjuryKosuke Fujita, Koji M Nishiguchi, Yukihiro Shiga, et al.
Ophthalmic Genetics|February 8, 2019
Macular degeneration as a common cause of visual loss in spinocerebellar ataxia type 1 (SCA1) patientsKoji M Nishiguchi, Masashi Aoki, Toru Nakazawa, et al.
Molecular Vision|February 6, 2004
Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseasesKoji M Nishiguchi, Eliot L Berson, Thaddeus P Dryja
Human Mutation|March 6, 2007
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activityAtsuhiro Kanda, James S Friedman, Koji M Nishiguchi, et al.
Investigative Ophthalmology & Visual Science|February 1, 2008
Retardation of photoreceptor degeneration in the detached retina of rd1 mouseHiroki Kaneko, Koji M Nishiguchi, Makoto Nakamura, et al.
Investigative Ophthalmology & Visual Science|January 4, 2008
Identification of photoreceptor precursors in the pars plana during ocular development and after retinal injuryKoji M Nishiguchi, Hiroki Kaneko, Makoto Nakamura, et al.
Japanese Journal of Ophthalmology|July 30, 2024
Specification of variant interpretation guidelines for inherited retinal dystrophy in JapanKaoru Fujinami, Koji M Nishiguchi, Akio Oishi, et al.
Biochemical and Biophysical Research Communications|November 2, 2019
In vivo imaging of the light response in mouse retinal ganglion cells based on a neuronal activity-dependent promoterKosuke Fujita, Koji M Nishiguchi, Kota Sato, et al.
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