Large-Scale Single-Nucleotide Polymorphism (SNP) and Haplotype Analyses, Using Dense SNP Maps, of 199 Drug-Related Genes in 752 Subjects: the Analysis of the Association between Un...

Por Kamatani, Naoyuki, Sekine, Akihiro, Kitamoto, Takuya, Iida, Aritoshi, Saito, Susumu, Kogame, Akifumi, Inoue, Eisuke, Kawamoto, Manabu, Harigai, Masayoshi, Nakamura, Yusuke
Publicado em 2004

A novel FOXC2 mutation in spinal extradural arachnoid cyst

Por Ogura, Yoji, Fujibayashi, Shunsuke, Iida, Aritoshi, Kou, Ikuyo, Nakajima, Masahiro, Okada, Eijiro, Toyama, Yoshiaki, Iwanami, Akio, Ishii, Ken, Nakamura, Masaya, Matsumoto, Morio, Ikegawa, Shiro
Publicado no Hum Genome Var (2015)

FOXC2 Mutations in Familial and Sporadic Spinal Extradural Arachnoid Cyst

Por Ogura, Yoji, Yabuki, Shoji, Iida, Aritoshi, Kou, Ikuyo, Nakajima, Masahiro, Kano, Hiroki, Shiina, Masaaki, Kikuchi, Shinichi, Toyama, Yoshiaki, Ogata, Kazuhiro, Nakamura, Masaya, Matsumoto, Morio, Ikegawa, Shiro
Publicado em 2013

Identification of HOXD4 Mutations in Spinal Extradural Arachnoid Cyst

Por Ogura, Yoji, Miyake, Noriko, Kou, Ikuyo, Iida, Aritoshi, Nakajima, Masahiro, Takeda, Kazuki, Fujibayashi, Shunsuke, Shiina, Masaaki, Okada, Eijiro, Toyama, Yoshiaki, Iwanami, Akio, Ishii, Ken, Ogata, Kazuhiro, Asahara, Hiroshi, Matsumoto, Naomichi, Nakamura, Masaya, Matsumoto, Morio, Ikegawa, Shiro
Publicado no PLoS One (2015)

Ectopic Expression of Ptf1a Induces Spinal Defects, Urogenital Defects, and Anorectal Malformations in Danforth's Short Tail Mice

Por Semba, Kei, Araki, Kimi, Matsumoto, Ken-ichirou, Suda, Hiroko, Ando, Takashi, Sei, Akira, Mizuta, Hiroshi, Takagi, Katsumasa, Nakahara, Mai, Muta, Mayumi, Yamada, Gen, Nakagata, Naomi, Iida, Aritoshi, Ikegawa, Shiro, Nakamura, Yusuke, Araki, Masatake, Abe, Kuniya, Yamamura, Ken-ichi
Publicado em 2013

Association between Single-Nucleotide Polymorphisms in Selectin Genes and Immunoglobulin A Nephropathy

Por Takei, Takashi, Iida, Aritoshi, Nitta, Kosaku, Tanaka, Toshihiro, Ohnishi, Yozo, Yamada, Ryo, Maeda, Shiro, Tsunoda, Tatsuhiko, Takeoka, Sachiyo, Ito, Kyoko, Honda, Kazuho, Uchida, Keiko, Tsuchiya, Ken, Suzuki, Yasushi, Fujioka, Tomoaki, Ujiie, Takashi, Nagane, Yutaka, Miyano, Satoru, Narita, Ichiei, Gejyo, Fumitake, Nihei, Hiroshi, Nakamura, Yusuke
Publicado em 2002

Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations

Por Wang, Zheng, Iida, Aritoshi, Miyake, Noriko, Nishiguchi, Koji M., Fujita, Kosuke, Nakazawa, Toru, Alswaid, Abdulrahman, Albalwi, Mohammed A., Kim, Ok-Hwa, Cho, Tae-Joon, Lim, Gye-Yeon, Isidor, Bertrand, David, Albert, Rustad, Cecilie F., Merckoll, Else, Westvik, Jostein, Stattin, Eva-Lena, Grigelioniene, Giedre, Kou, Ikuyo, Nakajima, Masahiro, Ohashi, Hirohumi, Smithson, Sarah, Matsumoto, Naomichi, Nishimura, Gen, Ikegawa, Shiro
Publicado no PLoS One (2016)

Mutations in B3GALT6, which Encodes a Glycosaminoglycan Linker Region Enzyme, Cause a Spectrum of Skeletal and Connective Tissue Disorders

Por Nakajima, Masahiro, Mizumoto, Shuji, Miyake, Noriko, Kogawa, Ryo, Iida, Aritoshi, Ito, Hironori, Kitoh, Hiroshi, Hirayama, Aya, Mitsubuchi, Hiroshi, Miyazaki, Osamu, Kosaki, Rika, Horikawa, Reiko, Lai, Angeline, Mendoza-Londono, Roberto, Dupuis, Lucie, Chitayat, David, Howard, Andrew, Leal, Gabriela F., Cavalcanti, Denise, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Watanabe, Shigehiko, Lausch, Ekkehart, Unger, Sheila, Bonafé, Luisa, Ohashi, Hirofumi, Superti-Furga, Andrea, Matsumoto, Naomichi, Sugahara, Kazuyuki, Nishimura, Gen, Ikegawa, Shiro
Publicado em 2013

A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis

Por Ogura, Yoji, Kou, Ikuyo, Miura, Shigenori, Takahashi, Atsushi, Xu, Leilei, Takeda, Kazuki, Takahashi, Yohei, Kono, Katsuki, Kawakami, Noriaki, Uno, Koki, Ito, Manabu, Minami, Shohei, Yonezawa, Ikuho, Yanagida, Haruhisa, Taneichi, Hiroshi, Zhu, Zezhang, Tsuji, Taichi, Suzuki, Teppei, Sudo, Hideki, Kotani, Toshiaki, Watanabe, Kota, Hosogane, Naobumi, Okada, Eijiro, Iida, Aritoshi, Nakajima, Masahiro, Sudo, Akihiro, Chiba, Kazuhiro, Hiraki, Yuji, Toyama, Yoshiaki, Qiu, Yong, Shukunami, Chisa, Kamatani, Yoichiro, Kubo, Michiaki, Matsumoto, Morio, Ikegawa, Shiro
Publicado no Am J Hum Genet (2015)