Masafumi Ohtsubo
Hamamatsu, 4313192, Japan
Last Updated: 09/26/2026
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Found 9 publications
Morphometric analysis of susceptibility to retinal photic injury in rats: A triphasic severity classification based on post-injury phenotypes.
Journal: Experimental eye research
Published: April 24, 2026
Correction to: Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: fine genomic assay of a rare male case with mosaicism.
Journal: Journal of human genetics
Published: January 28, 2021
Development of a time-series shotgun metagenomics database for monitoring microbial communities at the Pacific coast of Japan.
Journal: Scientific reports
Published: August 14, 2020
Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: fine genomic assay of a rare male case with mosaicism.
Journal: Journal of human genetics
Published: May 28, 2020
A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel CDHR1 frameshift and known missense variants.
Journal: Human genome variation
Published: September 22, 2018
The KM-parkin-DB: A Sub-set MutationView Database Specialized for PARK2 (PARKIN) Variants.
Journal: Human mutation
Published: October 02, 2014
The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.
Journal: Journal of human genetics
Published: March 08, 2014
Oligomerization of optineurin and its oxidative stress- or E50K mutation-driven covalent cross-linking: possible relationship with glaucoma pathology.
Journal: PloS one
Published: November 21, 2013
Interaction between optineurin and the bZIP transcription factor NRL.
Journal: Cell biology international
Published: January 30, 2013
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Last Updated: 09/26/2026