Attenuation of Progressive Hearing Loss in DBA/2J Mice by Reagents that Affect Epigenetic Modifications Is Associated with Up-Regulation of the Zinc Importer Zip4

Por Mutai, Hideki, Miya, Fuyuki, Fujii, Masato, Tsunoda, Tatsuhiko, Matsunaga, Tatsuo
Publicado no PLoS One (2015)

Gene expression profiling of DBA/2J mice cochleae treated with l-methionine and valproic acid

Por Miya, Fuyuki, Mutai, Hideki, Fujii, Masato, Boroevich, Keith A., Matsunaga, Tatsuo, Tsunoda, Tatsuhiko
Publicado no Genom Data (2015)

Predicting response of bladder cancers to gemcitabine and carboplatin neoadjuvant chemotherapy through genome-wide gene expression profiling

Por KATO, YOICHIRO, ZEMBUTSU, HITOSHI, TAKATA, RYO, MIYA, FUYUKI, TSUNODA, TATSUHIKO, OBARA, WATARU, FUJIOKA, TOMOAKI, NAKAMURA, YUSUKE
Publicado em 2011

Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathy

Por Tsutsumi, Makiko, Yokoi, Setsuri, Miya, Fuyuki, Miyata, Masafumi, Kato, Mitsuhiro, Okamoto, Nobuhiko, Tsunoda, Tatsuhiko, Yamasaki, Mami, Kanemura, Yonehiro, Kosaki, Kenjiro, Saitoh, Shinji, Kurahashi, Hiroki
Publicado no Eur J Hum Genet (2016)

Truncating mutation in NFIA causes brain malformation and urinary tract defects

Por Negishi, Yutaka, Miya, Fuyuki, Hattori, Ayako, Mizuno, Kentaro, Hori, Ikumi, Ando, Naoki, Okamoto, Nobuhiko, Kato, Mitsuhiro, Tsunoda, Tatsuhiko, Yamasaki, Mami, Kanemura, Yonehiro, Kosaki, Kenjiro, Saitoh, Shinji
Publicado no Hum Genome Var (2015)

A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations

Por Miya, Fuyuki, Kato, Mitsuhiro, Shiohama, Tadashi, Okamoto, Nobuhiko, Saitoh, Shinji, Yamasaki, Mami, Shigemizu, Daichi, Abe, Tetsuo, Morizono, Takashi, Boroevich, Keith A., Kosaki, Kenjiro, Kanemura, Yonehiro, Tsunoda, Tatsuhiko
Publicado no Sci Rep (2015)

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

Por Shigemizu, Daichi, Aiba, Takeshi, Nakagawa, Hidewaki, Ozaki, Kouichi, Miya, Fuyuki, Satake, Wataru, Toda, Tatsushi, Miyamoto, Yoshihiro, Fujimoto, Akihiro, Suzuki, Yutaka, Kubo, Michiaki, Tsunoda, Tatsuhiko, Shimizu, Wataru, Tanaka, Toshihiro
Publicado no PLoS One (2015)

Identification of a set of genes associated with response to interleukin-2 and interferon-α combination therapy for renal cell carcinoma through genome-wide gene expression profili...

Por MIZUMORI, OSAMU, ZEMBUTSU, HITOSHI, KATO, YOICHIRO, TSUNODA, TATSUHIKO, MIYA, FUYUKI, MORIZONO, TAKASHI, TSUKAMOTO, TAIJI, FUJIOKA, TOMOAKI, TOMITA, YOSHIHIKO, KITAMURA, TADAICHI, OZONO, SEIICHIRO, MIKI, TSUNEHARU, NAITO, SEIJI, AKAZA, HIDEYUKI, NAKAMURA, YUSUKE
Publicado em 2010

Hepatitis C Virus Infection Suppresses the Interferon Response in the Liver of the Human Hepatocyte Chimeric Mouse

Por Tsuge, Masataka, Fujimoto, Yoshifumi, Hiraga, Nobuhiko, Zhang, Yizhou, Ohnishi, Mayu, Kohno, Tomohiko, Abe, Hiromi, Miki, Daiki, Imamura, Michio, Takahashi, Shoichi, Ochi, Hidenori, Hayes, C. Nelson, Miya, Fuyuki, Tsunoda, Tatsuhiko, Chayama, Kazuaki
Publicado em 2011

TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis

Por Yokoi, Setsuri, Ishihara, Naoko, Miya, Fuyuki, Tsutsumi, Makiko, Yanagihara, Itaru, Fujita, Naoko, Yamamoto, Hiroyuki, Kato, Mitsuhiro, Okamoto, Nobuhiko, Tsunoda, Tatsuhiko, Yamasaki, Mami, Kanemura, Yonehiro, Kosaki, Kenjiro, Kojima, Seiji, Saitoh, Shinji, Kurahashi, Hiroki, Natsume, Jun
Publicado no Sci Rep (2015)

A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese

Por Hirokawa, Megumi, Morita, Hiroyuki, Tajima, Tomoyuki, Takahashi, Atsushi, Ashikawa, Kyota, Miya, Fuyuki, Shigemizu, Daichi, Ozaki, Kouichi, Sakata, Yasuhiko, Nakatani, Daisaku, Suna, Shinichiro, Imai, Yasushi, Tanaka, Toshihiro, Tsunoda, Tatsuhiko, Matsuda, Koichi, Kadowaki, Takashi, Nakamura, Yusuke, Nagai, Ryozo, Komuro, Issei, Kubo, Michiaki
Publicado no Eur J Hum Genet (2015)

A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly

Por Negishi, Yutaka, Miya, Fuyuki, Hattori, Ayako, Johmura, Yoshikazu, Nakagawa, Motoo, Ando, Naoki, Hori, Ikumi, Togawa, Takao, Aoyama, Kohei, Ohashi, Kei, Fukumura, Shinobu, Mizuno, Seiji, Umemura, Ayako, Kishimoto, Yoko, Okamoto, Nobuhiko, Kato, Mitsuhiro, Tsunoda, Tatsuhiko, Yamasaki, Mami, Kanemura, Yonehiro, Kosaki, Kenjiro, Nakanishi, Makoto, Saitoh, Shinji
Publicado no BMC Med Genet (2017)