High-density Association Mapping and Interaction Analysis of PLA2R1 and HLA Regions with Idiopathic Membranous Nephropathy in Japanese

por Thiri, Myo, Honda, Kenjiro, Kashiwase, Koichi, Mabuchi, Akihiko, Suzuki, Hodaka, Watanabe, Kimio, Nakayama, Masaaki, Watanabe, Tsuyoshi, Doi, Kent, Tokunaga, Katsushi, Noiri, Eisei
Publicado 2016

Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals

por Liu, Xiaoxi, Kawashima, Minae, Miyagawa, Taku, Otowa, Takeshi, Latt, Khun Zaw, Thiri, Myo, Nishida, Hisami, Sugiyama, Toshiro, Tsurusaki, Yoshinori, Matsumoto, Naomichi, Mabuchi, Akihiko, Tokunaga, Katsushi, Sasaki, Tsukasa
Publicado 2015

Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy

por Latt, Khun Zaw, Honda, Kenjiro, Thiri, Myo, Hitomi, Yuki, Omae, Yosuke, Sawai, Hiromi, Kawai, Yosuke, Teraguchi, Shunsuke, Ueno, Kazuko, Nagasaki, Masao, Mabuchi, Akihiko, Kaga, Hajime, Komatsuda, Atsushi, Tokunaga, Katsushi, Noiri, Eisei
Publicado 2018