Aritoshi Iida
University of Tokyo
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Publication
Featured researches published by Aritoshi Iida.
Journal of Human Genetics | 2006
Aritoshi Iida; Hideki Kizawa; Yusuke Nakamura; Shiro Ikegawa
AbstractOsteoarthritis (OA) is a very common bone and joint disease characterized by breakdown of cartilage in the joint. We recently found that an aspartic-acid repeat polymorphism of the asporin gene (ASPN) on chromosome 9 is associated with susceptibility to OA in Japanese. We provide here a high-resolution single nucleotide polymorphism (SNP) map within a 33.4-kb genomic region containing ASPN. A total of 19 SNPs were isolated from the region by systematic screening using 48 Japanese patients with OA: 7 SNPs in the 5′ flanking region, 8 in introns, and 4 in the 3′ untranslated region. Nine SNPs were novel. This high-resolution SNP map will be a useful resource for analyzing genes associated with OA and other bone and joint diseases.
Journal of Human Genetics | 2001
Aritoshi Iida; Yozo Ohnishi; Kouichi Ozaki; Yoko Ariji; Yusuke Nakamura; Toshihiro Tanaka
AbstractWe constructed a high-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the DiGeorge syndrome critical region 2 (DGCR2) gene at chromosome 22q11.2, a human counterpart of mouse seizure-related gene SEZ-12. A total of 102 SNPs were isolated from the region by systematic screening among 48 Japanese individuals: 9 SNPs in the 5′ flanking region, 3 in the 5′ untranslated region, 2 in the coding regions, 77 in introns, 7 in the 3′ untranslated region, and 4 in the 3′ flanking region. By a comparison of our data with SNPs deposited in the dbSNP database in the National Center for Biotechnology Information, 80 SNPs (78.4%) were considered to be novel. The ratio of transition to transversion was 3.08:1. In addition, eight other types of genetic variations (one GA dinucleotide polymorphism and seven insertion/deletion polymorphisms) were discovered. The high-resolution map that we constructed will be a useful resource for analyzing gene scans of complex diseases mapped to this local segment on chromosome 22.
Archive | 2006
Yusuke Nakamura; Akihiro Sekine; Aritoshi Iida; Susumu Saito
Archive | 2001
Yusuke Nakamura; Akihiro Sekine; Aritoshi Iida; Susumu Saito
Archive | 2003
Toshihiro Tanaka; Yozo Ohnishi; Koichi Ozaki; Aritoshi Iida; Yusuke Nakamura; Masatsugu Hori
Archive | 2003
Yusuke Nakamura; Akihiro Sekine; Aritoshi Iida; Susumu Saito
Archive | 2004
Toshihiro Tanaka; Yozo Ohnishi; Kouichi Ozaki; Aritoshi Iida; Masatsugu Hori; Yusuke Nakamura
Archive | 2012
Toshihiro Tanaka; Yusuke Nakamura; Aritoshi Iida; Kouichi Ozaki; Masatsugu Hori
Archive | 2006
Toshihiro Tanaka; Yusuke Nakamura; Yozo Ohnishi; Kouichi Ozaki; Aritoshi Iida; Masatsugu Hori
Archive | 2004
Yusuke Nakamura; Akihiro Sekine; Aritoshi Iida; Susumu Saito; Naoyuki Kamatani