Growth Inhibition of Cultured Human Liver Carcinoma Cells by Ki-energy (Life-energy): Scientific Evidence for Ki-effects on Cancer Cells

by Ohnishi, S. Tsuyoshi, Ohnishi, Tomoko, Nishino, Kozo, Tsurusaki, Yoshinori, Yamaguchi, Masayoshi
Published 2005

Performance Comparison of Bench-Top Next Generation Sequencers Using Microdroplet PCR-Based Enrichment for Targeted Sequencing in Patients with Autism Spectrum Disorder

by Koshimizu, Eriko, Miyatake, Satoko, Okamoto, Nobuhiko, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Matsumoto, Naomichi
Published 2013

‘Cortical cerebellar atrophy' dwindles away in the era of next-generation sequencing

by Yoshida, Kunihiro, Miyatake, Satoko, Kinoshita, Tomomi, Doi, Hiroshi, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Matsumoto, Naomichi
Published 2014

Pathogenic mutations in two families with congenital cataract identified with whole-exome sequencing

by Kondo, Yukiko, Saitsu, Hirotomo, Miyamoto, Toshinobu, Lee, Byung Joo, Nishiyama, Kiyomi, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Doi, Hiroshi, Miyake, Noriko, Kim, Jeong Hun, Yu, Young Suk, Matsumoto, Naomichi
Published 2013

Somatic mutations in GLI3 and OFD1 involved in sonic hedgehog signaling cause hypothalamic hamartoma

by Saitsu, Hirotomo, Sonoda, Masaki, Higashijima, Takefumi, Shirozu, Hiroshi, Masuda, Hiroshi, Tohyama, Jun, Kato, Mitsuhiro, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Mizuguchi, Takeshi, Miyatake, Satoko, Miyake, Noriko, Kameyama, Shigeki, Matsumoto, Naomichi
Published 2016

A novel PITX2 mutation causing iris hypoplasia

by Kimura, Masashi, Tokita, Yoshihito, Machida, Junichiro, Shibata, Akio, Tatematsu, Tadashi, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Miyachi, Hitoshi, Shimozato, Kazuo, Matsumoto, Naomichi, Nakashima, Mitsuko
Published 2014

Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome

by Imagawa, Eri, Fukai, Ryoko, Behnam, Mahdiyeh, Goyal, Manisha, Nouri, Narges, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Salehi, Mansour, Kapoor, Seema, Tanaka, Fumiaki, Miyake, Noriko, Matsumoto, Naomichi
Published 2015

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

by 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
Published 2015

DNA methylation and gene expression dynamics during spermatogonial stem cell differentiation in the early postnatal mouse testis

by Kubo, Naoki, Toh, Hidehiro, Shirane, Kenjiro, Shirakawa, Takayuki, Kobayashi, Hisato, Sato, Tetsuya, Sone, Hidetoshi, Sato, Yasuyuki, Tomizawa, Shin-ichi, Tsurusaki, Yoshinori, Shibata, Hiroki, Saitsu, Hirotomo, Suzuki, Yutaka, Matsumoto, Naomichi, Suyama, Mikita, Kono, Tomohiro, Ohbo, Kazuyuki, Sasaki, Hiroyuki
Published 2015

Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder

by Hashimoto, Ryota, Nakazawa, Takanobu, Tsurusaki, Yoshinori, Yasuda, Yuka, Nagayasu, Kazuki, Matsumura, Kensuke, Kawashima, Hitoshi, Yamamori, Hidenaga, Fujimoto, Michiko, Ohi, Kazutaka, Umeda-Yano, Satomi, Fukunaga, Masaki, Fujino, Haruo, Kasai, Atsushi, Hayata-Takano, Atsuko, Shintani, Norihito, Takeda, Masatoshi, Matsumoto, Naomichi, Hashimoto, Hitoshi
Published 2016

De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firing

by Saitsu, Hirotomo, Akita, Tenpei, Tohyama, Jun, Goldberg-Stern, Hadassa, Kobayashi, Yu, Cohen, Roni, Kato, Mitsuhiro, Ohba, Chihiro, Miyatake, Satoko, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Fukuda, Atsuo, Matsumoto, Naomichi
Published 2015

Duplication of the NPHP1 gene in patients with autism spectrum disorder and normal intellectual ability: a case series

by Yasuda, Yuka, Hashimoto, Ryota, Fukai, Ryoko, Okamoto, Nobuhiko, Hiraki, Yoko, Yamamori, Hidenaga, Fujimoto, Michiko, Ohi, Kazutaka, Taniike, Masako, Mohri, Ikuko, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Matsumoto, Naomichi, Miyake, Noriko, Takeda, Masatoshi
Published 2014

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome

by Hempel, Annmarie, Pagnamenta, Alistair T, Blyth, Moira, Mansour, Sahar, McConnell, Vivienne, Kou, Ikuyo, Ikegawa, Shiro, Tsurusaki, Yoshinori, Matsumoto, Naomichi, Lo-Castro, Adriana, Plessis, Ghislaine, Albrecht, Beate, Battaglia, Agatino, Taylor, Jenny C, Howard, Malcolm F, Keays, David, Sohal, Aman Singh, Kühl, Susanne J, Kini, Usha, McNeill, Alisdair
Published 2016

Human genetic variation database, a reference database of genetic variations in the Japanese population

by Higasa, Koichiro, Miyake, Noriko, Yoshimura, Jun, Okamura, Kohji, Niihori, Tetsuya, Saitsu, Hirotomo, Doi, Koichiro, Shimizu, Masakazu, Nakabayashi, Kazuhiko, Aoki, Yoko, Tsurusaki, Yoshinori, Morishita, Shinichi, Kawaguchi, Takahisa, Migita, Osuke, Nakayama, Keiko, Nakashima, Mitsuko, Mitsui, Jun, Narahara, Maiko, Hayashi, Keiko, Funayama, Ryo, Yamaguchi, Daisuke, Ishiura, Hiroyuki, Ko, Wen-Ya, Hata, Kenichiro, Nagashima, Takeshi, Yamada, Ryo, Matsubara, Yoichi, Umezawa, Akihiro, Tsuji, Shoji, Matsumoto, Naomichi, Matsuda, Fumihiko
Published 2016