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Yuichi Kawamura

Explore the profile of Yuichi Kawamura including associated specialties, affiliations and a list of published articles. Areas
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Citations 108
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Recent Articles
1.
Iwagawa T, Fukushima M, Takeuchi S, Kawamura Y, Aihara Y, Ozawa M, et al.
Genes Cells . 2023 Apr; 28(7):482-495. PMID: 37073980
Histone methylation plays a vital role in retinal development. However, the role of histone H3K36 methylation in retinal development is not clear. We examined the role of H3K36 methylation by...
2.
Kawamura Y, Yamanaka K, Poh B, Kuribayashi H, Koso H, Watanabe S
Biochem Biophys Res Commun . 2018 Aug; 503(4):3023-3030. PMID: 30146259
We found that the Zhx2 gene (whose product is known to act as a tumor suppressor in hepatocellular carcinoma) is expressed in embryonic retinal progenitors and in developing cone bipolar...
3.
Kawamura Y, Suga A, Fujimaki T, Yoshitake K, Tsunoda K, Murakami A, et al.
J Hum Genet . 2018 May; 63(8):893-900. PMID: 29760528
The macula is a unique structure in higher primates, where cone and rod photoreceptors show highest density in the fovea and the surrounding area, respectively. The hereditary macular dystrophies represent...
4.
Kato Y, Hanazono G, Fujinami K, Hatase T, Kawamura Y, Iwata T, et al.
Invest Ophthalmol Vis Sci . 2017 Dec; 58(14):6020-6029. PMID: 29196766
Purpose: To report the clinical characteristics of asymptomatic cases with RP1L1 gene mutations in four families with occult macular dystrophy (OMD). Methods: Four asymptomatic cases from four families were selected...
5.
Ueno S, Nakanishi A, Kominami T, Ito Y, Hayashi T, Yoshitake K, et al.
Jpn J Ophthalmol . 2016 Oct; 61(1):92-98. PMID: 27718025
Purpose: The 2 most common causative genes for achromatopsia (ACHM) are CNGA3 and CNGB3; other genes including GNAT2 account for only a small portion of ACHM cases. The cone mosaics...
6.
Fujinami K, Kameya S, Kikuchi S, Ueno S, Kondo M, Hayashi T, et al.
Invest Ophthalmol Vis Sci . 2016 Sep; 57(11):4837-46. PMID: 27623337
Purpose: To determine the clinical and genetic characteristics of Japanese patients with occult macular dystrophy (OMD) in a nationwide multicenter study. Methods: Twenty-three patients from 21 families with clinically diagnosed...
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Kawamura Y, Takahashi O, Ishii T
Psychiatry Clin Neurosci . 2008 Apr; 62(2):152-9. PMID: 18412836
Aim: Although recent epidemiological studies on the pervasive development disorders (PDD) appear to be reporting higher rates of incidence than previously believed, great variation in the reported figures suggests a...