Tetsuhiro R Yasuma
Overview
Explore the profile of Tetsuhiro R Yasuma including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
214
Followers
0
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Recent Articles
1.
Nishiguchi K, Tearle R, Liu Y, Oh E, Miyake N, Benaglio P, et al.
Proc Natl Acad Sci U S A
. 2013 Sep;
110(40):16139-44.
PMID: 24043777
We performed whole genome sequencing in 16 unrelated patients with autosomal recessive retinitis pigmentosa (ARRP), a disease characterized by progressive retinal degeneration and caused by mutations in over 50 genes,...
2.
Nishiguchi K, Yasuma T, Tomida D, Nakamura M, Ishikawa K, Kikuchi M, et al.
Invest Ophthalmol Vis Sci
. 2011 Dec;
53(1):508-12.
PMID: 22190594
Purpose: A non-sense mutation at codon 95 in the gene encoding complement factor C9 (C9-R95X) is found most frequently among Japanese. The authors investigated the association between C9-R95X and Japanese...
3.
Takahashi A, Ito Y, Iguchi Y, Yasuma T, Ishikawa K, Terasaki H
Retina
. 2011 Sep;
32(1):127-33.
PMID: 21886022
Purpose: To determine whether the axial length (AL) in highly myopic normal adult eyes with myopic complications in the fellow eyes increases significantly during a 1-year interval and to investigate...
4.
Tomida D, Nishiguchi K, Kataoka K, Yasuma T, Iwata E, Uetani R, et al.
Invest Ophthalmol Vis Sci
. 2011 Feb;
52(6):3193-9.
PMID: 21296829
Purpose: To study the effect of heparin on the development of laser-induced choroidal neovascularization (CNV) and to assess the underlying molecular mechanisms. Methods: Bone marrow transplantation (BMT) was conducted by...
5.
Yasuma T, Nakamura M, Nishiguchi K, Kikuchi M, Kaneko H, Niwa T, et al.
Mol Vis
. 2011 Jan;
16:2923-30.
PMID: 21203342
Purpose: To investigate the association between the serum high sensitivity C-reactive protein (hs-CRP) levels and variants in age-related maculopathy susceptibility 2 (ARMS2)/HtrA serine peptidase 1 (HTRA1) genes in normal subjects...
6.
Nakamura M, Sanuki R, Yasuma T, Onishi A, Nishiguchi K, Koike C, et al.
Mol Vis
. 2010 Mar;
16:425-37.
PMID: 20300565
Purpose: To identify human transient receptor potential cation channel, subfamily M, member 1 (TRPM1) gene mutations in patients with congenital stationary night blindness (CSNB). Methods: We analyzed four different Japanese...
7.
Kondo M, Kondo N, Ito Y, Kachi S, Kikuchi M, Yasuma T, et al.
Retina
. 2009 Aug;
29(9):1242-8.
PMID: 19672216
Purpose: To evaluate the 12-month follow-up results of intravitreal bevacizumab therapy for macular edema secondary to branch retinal vein occlusion and to identify the pretreatment factors that were associated with...