Seishi Kato
Overview
Explore the profile of Seishi Kato including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
317
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Iwanami M, Oishi A, Ogino K, Seko Y, Nishida-Shimizu T, Yoshimura N, et al.
Mol Vis
. 2019 Dec;
25:766-779.
PMID: 31814702
Purpose: To elucidate the variant spectrum of the gene in a large cohort of Japanese patients with autosomal recessive and simplex retinitis pigmentosa (arRP and sRP). Methods: We performed a...
2.
Seko Y, Iwanami M, Miyamoto-Matsui K, Takita S, Aoi N, Umezawa A, et al.
Stem Cell Res Ther
. 2018 Oct;
9(1):279.
PMID: 30359287
Background: Generation of induced photoreceptors holds promise for in vitro modeling of intractable retinal diseases. Retinitis pigmentosa is an inherited retinal dystrophy that leads to visual impairment. The EYS gene...
3.
Iwanami M, Oshikawa M, Nishida T, Nakadomari S, Kato S
Invest Ophthalmol Vis Sci
. 2012 Feb;
53(2):1033-40.
PMID: 22302105
Purpose: To screen for disease-causing mutations in the Eyes shut homolog (EYS) gene in Japanese patients with retinitis pigmentosa (RP). Methods. Blood samples were obtained from 68 RP patients and...
4.
Oshikawa M, Tsutsui C, Ikegami T, Fuchida Y, Matsubara M, Toyama S, et al.
Invest Ophthalmol Vis Sci
. 2011 Jun;
52(9):6662-70.
PMID: 21697133
PURPOSE. To collect an entire set of full-length cDNA clones derived from human retina-derived cell lines and to identify full-length transcripts for retinal preferentially expressed genes. METHODS. The full-length cDNA...
5.
Kato S, Oshikawa M, Ohtoko K
Methods Mol Biol
. 2011 Mar;
729:53-70.
PMID: 21365483
Full-length complementary DNAs (cDNAs) are an essential resource for functional genomics. Recently, we have developed a simple and efficient method for preparing a full-length cDNA library from a small amount...
6.
Oshikawa M, Usami R, Kato S
Mol Vis
. 2009 Mar;
15:482-94.
PMID: 19262745
Purpose: The aim of this study was to characterize the arylsulfatase I (ARSI) gene that has been shown to be preferentially expressed in the human retinal pigment epithelium cell line...
7.
Oshikawa M, Sugai Y, Usami R, Ohtoko K, Toyama S, Kato S
DNA Res
. 2008 May;
15(3):123-36.
PMID: 18487259
Recently, we have developed a vector-capping method for constructing a full-length cDNA library. In the present study, we performed in-depth analysis of the vector-capped cDNA library prepared from a single...
8.
Ando Y, Ohmori M, Ohtake H, Ohtoko K, Toyama S, Usami R, et al.
Mol Vis
. 2007 Jul;
13:1038-44.
PMID: 17653048
Purpose: To identify nucleotide sequence variations in the rhodopsin (RHO) gene of Japanese patients with retinitis pigmentosa (RP) in order to search for mutations or haplotypes responsible for RP. Methods:...
9.
Aoyama T, Kamata K, Yamanaka N, Takeuchi Y, Higashihara M, Kato S
Nephrol Dial Transplant
. 2006 Jan;
21(4):1073-81.
PMID: 16431884
Background: Nephrin is an essential protein for maintaining the normal structure of the podocyte foot process and the glomerular filtration barrier. To analyse the mechanism of proteinuria and treatment of...
10.
Kato S, Ohtoko K, Ohtake H, Kimura T
DNA Res
. 2005 Aug;
12(1):53-62.
PMID: 16106752
Full-length cDNAs play an essential role in identifying genes and determining their promoter regions. Here we describe a simple method for constructing a full-length cDNA library, which has the following...