SLC52A3, A Brown–Vialetto–van Laere syndrome candidate gene is essential for mouse development, but dispensable for motor neuron differentiation

Por Intoh, Atsushi, Suzuki, Naoki, Koszka, Kathryn, Eggan, Kevin
Publicado no Hum Mol Genet (2016)

Hemilaminectomy for Removal of Extramedullary or Extradural Spinal Cord Tumors: Medium to Long-Term Clinical Outcomes

Por Naganawa, Toshitaka, Miyamoto, Kei, Hosoe, Hideo, Suzuki, Naoki, Shimizu, Katsuji
Publicado em 2011

Cantilever Transforaminal Lumbar Interbody Fusion for Upper Lumbar Degenerative Diseases (Minimum 2 Years Follow Up)

Por Hioki, Akira, Miyamoto, Kei, Hosoe, Hideo, Sugiyama, Seiichi, Suzuki, Naoki, Shimizu, Katsuji
Publicado em 2011

CT examination of the head of the Baikal seal (Phoca sibirica)

Por ENDO, HIDEKI, SASAKI, HIROYUKI, HAYASHI, YOSHIHIRO, PETROV, EVAGENY A., AMANO, MASAO, SUZUKI, NAOKI, MIYAZAKI, NOBUYUKI
Publicado em 1999

Two Cases of Elderly-Onset Hereditary Neuropathy with Liability to Pressure Palsy Manifesting Bilateral Peroneal Nerve Palsies

Por Kawaguchi, Norihiko, Suzuki, Naoki, Tateyama, Maki, Takai, Yoshiki, Misu, Tatsuro, Nakashima, Ichiro, Itoyama, Yasuto, Aoki, Masashi
Publicado em 2012

Associations between Single-Nucleotide Polymorphisms in Corticotropin-Releasing Hormone-Related Genes and Irritable Bowel Syndrome

Por Sasaki, Ayaka, Sato, Naoko, Suzuki, Naoki, Kano, Michiko, Tanaka, Yukari, Kanazawa, Motoyori, Aoki, Masashi, Fukudo, Shin
Publicado no PLoS One (2016)

Corticotropin-Releasing Hormone Receptor 1 Gene Variants in Irritable Bowel Syndrome

Por Sato, Naoko, Suzuki, Naoki, Sasaki, Ayaka, Aizawa, Emiko, Obayashi, Takeshi, Kanazawa, Motoyori, Mizuno, Tomoko, Kano, Michiko, Aoki, Masashi, Fukudo, Shin
Publicado em 2012

The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTD

Por Suzuki, Naoki, Maroof, Asif, Merkle, Florian T, Koszka, Kathryn, Intoh, Atsushi, Armstrong, Ian, Moccia, Rob, Davis-Dusenbery, Brandi N, Eggan, Kevin
Publicado no Nat Neurosci (2013)

NO production results in suspension-induced muscle atrophy through dislocation of neuronal NOS

Por Suzuki, Naoki, Motohashi, Norio, Uezumi, Akiyoshi, Fukada, So-ichiro, Yoshimura, Tetsuhiko, Itoyama, Yasuto, Aoki, Masashi, Miyagoe-Suzuki, Yuko, Takeda, Shin’ichi
Publicado em 2007

Design and synthesis of the superionic conductor Na(10)SnP(2)S(12)

Por Richards, William D., Tsujimura, Tomoyuki, Miara, Lincoln J., Wang, Yan, Kim, Jae Chul, Ong, Shyue Ping, Uechi, Ichiro, Suzuki, Naoki, Ceder, Gerbrand
Publicado no Nat Commun (2016)

Sporadic Inclusion Body Myositis Manifesting as Isolated Muscle Weakness of the Finger Flexors Three Years after Disease Onset

Por Suwa, Yuichi, Suzuki, Naoki, Soga, Temma, Harada, Ryuhei, Shibui, Aya, Kuroda, Hiroshi, Izumi, Rumiko, Tateyama, Maki, Nakashima, Ichiro, Sonoo, Masahiro, Aoki, Masashi
Publicado no Intern Med (2016)

Corticotropin-Releasing Hormone Receptor 2 Gene Variants in Irritable Bowel Syndrome

Por Komuro, Hazuki, Sato, Naoko, Sasaki, Ayaka, Suzuki, Naoki, Kano, Michiko, Tanaka, Yukari, Yamaguchi-Kabata, Yumi, Kanazawa, Motoyori, Warita, Hitoshi, Aoki, Masashi, Fukudo, Shin
Publicado no PLoS One (2016)

Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencing

Por Izumi, Rumiko, Niihori, Tetsuya, Takahashi, Toshiaki, Suzuki, Naoki, Tateyama, Maki, Watanabe, Chigusa, Sugie, Kazuma, Nakanishi, Hirotaka, Sobue, Gen, Kato, Masaaki, Warita, Hitoshi, Aoki, Yoko, Aoki, Masashi
Publicado no Neurol Genet (2015)

Isolated inclusion body myopathy caused by a multisystem proteinopathy–linked hnRNPA1 mutation

Por Izumi, Rumiko, Warita, Hitoshi, Niihori, Tetsuya, Takahashi, Toshiaki, Tateyama, Maki, Suzuki, Naoki, Nishiyama, Ayumi, Shirota, Matsuyuki, Funayama, Ryo, Nakayama, Keiko, Mitsuhashi, Satomi, Nishino, Ichizo, Aoki, Yoko, Aoki, Masashi
Publicado no Neurol Genet (2015)

Proteasome dysfunction induces muscle growth defects and protein aggregation

Por Kitajima, Yasuo, Tashiro, Yoshitaka, Suzuki, Naoki, Warita, Hitoshi, Kato, Masaaki, Tateyama, Maki, Ando, Risa, Izumi, Rumiko, Yamazaki, Maya, Abe, Manabu, Sakimura, Kenji, Ito, Hidefumi, Urushitani, Makoto, Nagatomi, Ryoichi, Takahashi, Ryosuke, Aoki, Masashi
Publicado no J Cell Sci (2014)

Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells

Por Ichiyanagi, Naoki, Fujimori, Koki, Yano, Masato, Ishihara-Fujisaki, Chikako, Sone, Takefumi, Akiyama, Tetsuya, Okada, Yohei, Akamatsu, Wado, Matsumoto, Takuya, Ishikawa, Mitsuru, Nishimoto, Yoshinori, Ishihara, Yasuharu, Sakuma, Tetsushi, Yamamoto, Takashi, Tsuiji, Hitomi, Suzuki, Naoki, Warita, Hitoshi, Aoki, Masashi, Okano, Hideyuki
Publicado no Stem Cell Reports (2016)

Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease()

Por Burberry, Aaron, Suzuki, Naoki, Wang, Jin-Yuan, Moccia, Rob, Mordes, Daniel A., Stewart, Morag, Suzuki-Uematsu, Satomi, Ghosh, Sulagna, Singh, Ajay, Merkle, Florian T., Koszka, Kathryn, Li, Quan-Zhen, Zon, Leonard, Rossi, Derrick J., Trowbridge, Jennifer J., Notarangelo, Luigi D., Eggan, Kevin
Publicado no Sci Transl Med (2016)

Multicenter questionnaire survey for sporadic inclusion body myositis in Japan

Por Suzuki, Naoki, Mori-Yoshimura, Madoka, Yamashita, Satoshi, Nakano, Satoshi, Murata, Ken-ya, Inamori, Yukie, Matsui, Naoko, Kimura, En, Kusaka, Hirofumi, Kondo, Tomoyoshi, Higuchi, Itsuro, Kaji, Ryuji, Tateyama, Maki, Izumi, Rumiko, Ono, Hiroya, Kato, Masaaki, Warita, Hitoshi, Takahashi, Toshiaki, Nishino, Ichizo, Aoki, Masashi
Publicado no Orphanet J Rare Dis (2016)

Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging

Por Tian, Feng, Yang, Wenlong, Mordes, Daniel A., Wang, Jin-Yuan, Salameh, Johnny S., Mok, Joanie, Chew, Jeannie, Sharma, Aarti, Leno-Duran, Ester, Suzuki-Uematsu, Satomi, Suzuki, Naoki, Han, Steve S., Lu, Fa-Ke, Ji, Minbiao, Zhang, Rosanna, Liu, Yue, Strominger, Jack, Shneider, Neil A., Petrucelli, Leonard, Xie, X. Sunney, Eggan, Kevin
Publicado no Nat Commun (2016)

Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B

Por Takahashi, Toshiaki, Aoki, Masashi, Suzuki, Naoki, Tateyama, Maki, Yaginuma, Chikako, Sato, Hitomi, Hayasaka, Miho, Sugawara, Hitomi, Ito, Mariko, Abe-Kondo, Emi, Shimakura, Naoko, Ibi, Tohru, Kuru, Satoshi, Wakayama, Tadashi, Sobue, Gen, Fujii, Naoki, Saito, Toshio, Matsumura, Tsuyoshi, Funakawa, Itaru, Mukai, Eiichiro, Kawanami, Toru, Morita, Mitsuya, Yamazaki, Mineo, Hasegawa, Takashi, Shimizu, Jun, Tsuji, Shoji, Kuzuhara, Shigeki, Tanaka, Hiroyasu, Yoshioka, Masaru, Konno, Hidehiko, Onodera, Hiroshi, Itoyama, Yasuto
Publicado em 2013