Motokazu Tsujikawa
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Explore the profile of Motokazu Tsujikawa including associated specialties, affiliations and a list of published articles.
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100
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1747
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Recent Articles
1.
Fukushima Y, Takahashi S, Nakamura M, Inoue T, Fujieda Y, Sato T, et al.
J Clin Med
. 2024 Sep;
13(17).
PMID: 39274287
: The aim of this paper was to investigate the protein concentrations of high-temperature requirement A 1 (HTRA1) and transforming growth factor-β (TGF-β) in the vitreous humor of patients with...
2.
Kubo K, Oie Y, Koto R, Nishida N, Kai C, Maeno S, et al.
Cornea
. 2024 Aug;
44(4):412-417.
PMID: 39167633
Purpose: To analyze the corneal phenotypes of Japanese patients with myotonic dystrophy type 1 (DM1). Methods: We included patients with DM1 who were diagnosed with clinical neuromuscular symptoms by neurologists...
3.
Maeno S, Oie Y, Koto R, Nishida N, Yamashita A, Yoshioka M, et al.
Cornea
. 2024 Feb;
43(7):805-811.
PMID: 38300219
Purpose: The aim of this study was to investigate the association between cytosine-thymine-guanine trinucleotide repeat (TNR) expansion in TCF4 and the clinical phenotypes of corneal densitometry or anterior segment morphology...
4.
Sato S, Morimoto T, Fujikado T, Tanaka S, Sai S, Tsujikawa M, et al.
Case Rep Ophthalmol
. 2024 Jan;
15(1):8-14.
PMID: 38179148
Hexokinase 1 () gene is the cause of autosomal dominant retinitis pigmentosa (RP) 79. To date, only E874K mutation has been reported as the causative mutation in patients with nonsyndromic...
5.
Sato S, Morimoto T, Fujikado T, Tanaka S, Tsujikawa M, Nishida K
Case Rep Ophthalmol
. 2023 Jan;
13(3):847-854.
PMID: 36605038
Extensive macular atrophy with pseudodrusen (EMAP) is a relatively newly proposed clinical entity that was first reported in 2009. Although no definitive diagnostic criteria have been defined, characteristic findings can...
6.
Shiraki N, Maruyama K, Hayashi R, Oguchi A, Murakawa Y, Katayama T, et al.
Stem Cell Reports
. 2022 Jan;
17(2):221-230.
PMID: 35030319
Microglia are the resident immune cells of the central nervous system (CNS). They govern the immunogenicity of the retina, which is considered to be part of the CNS; however, it...
7.
Watanabe S, Hayashi R, Sasamoto Y, Tsujikawa M, Ksander B, Frank M, et al.
iScience
. 2021 Jul;
24(6):102688.
PMID: 34195566
Human induced pluripotent stem cells (hiPSCs) can generate a multiplicity of organoids, yet no compelling evidence currently exists as to whether or not these contain tissue-specific, holoclone-forming stem cells. Here,...
8.
Ganzen L, Ko M, Zhang M, Xie R, Chen Y, Zhang L, et al.
Sci Rep
. 2021 Jun;
11(1):11432.
PMID: 34075074
Retinitis Pigmentosa (RP) is a mostly incurable inherited retinal degeneration affecting approximately 1 in 4000 individuals globally. The goal of this work was to identify drugs that can help patients...
9.
Nishiguchi K, Miya F, Mori Y, Fujita K, Akiyama M, Kamatani T, et al.
Commun Biol
. 2021 Jan;
4(1):140.
PMID: 33514863
The genetic basis of Japanese autosomal recessive retinitis pigmentosa (ARRP) remains largely unknown. Herein, we applied a 2-step genome-wide association study (GWAS) in 640 Japanese patients. Meta-GWAS identified three independent...
10.
Nagahara Y, Tsujikawa M, Koto R, Uesugi K, Sato S, Kawasaki S, et al.
Am J Pathol
. 2020 Oct;
190(12):2330-2342.
PMID: 33011110
Gelatinous drop-like corneal dystrophy (GDLD) is a severe inherited corneal dystrophy characterized by subepithelial corneal amyloid deposition. We had previously succeeded in identifying the responsible gene, TACSTD2, and subsequently found...