Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Yuki Naruke"'
Autor:
Tomohiro Ebihara, Taro Nagatomo, Yohei Sugiyama, Tomoko Tsuruoka, Yoshiteru Osone, Masaru Shimura, Makiko Tajika, Keiko Ichimoto, Yuki Naruke, Nana Akiyama, Sze Chern Lim, Yukiko Yatsuka, Kazuhiro R. Nitta, Yoshihito Kishita, Takuya Fushimi, Atsuko Okazaki, Akira Ohtake, Yasushi Okazaki, Kei Murayama
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 33, Iss , Pp 100912- (2022)
Biallelic deletions extending into the ATPase family AAA-domain containing protein 3A (ATAD3A) gene lead to infantile lethality with severe pontocerebellar hypoplasia (PCH). However, only 12 such cases have been reported worldwide to date, and the ge
Externí odkaz:
https://doaj.org/article/188d708aee554ecca9d11c314c2a3186
Autor:
Keiko Ichimoto, Tomoo Fujisawa, Masaru Shimura, Takuya Fushimi, Makiko Tajika, Ayako Matsunaga, Minako Ogawa-Tominaga, Nana Akiyama, Yuki Naruke, Hiroshi Horie, Tokiko Fukuda, Hideo Sugie, Ayano Inui, Kei Murayama
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 24, Iss , Pp 100601- (2020)
Glycogen storage disease type IV (GSD IV) is a rare inborn metabolic disorder characterized by the accumulation of amylopectin-like glycogen in the liver or other organs. The hepatic subtype may appear normal at birth but rapidly develops to liver ci
Externí odkaz:
https://doaj.org/article/9e938f07756140a19a8f3e32e1aead92
Autor:
Tadashi Shiohama, Ryo Ando, Katsunori Fujii, Hiroki Mukai, Yuki Naruke, Katsuo Sugita, Eiji Kato, Naoki Shimojo
Publikováno v:
Case Reports in Pediatrics, Vol 2017 (2017)
Dandy-Walker malformation (DWM) is a posterior fossa anomaly characterized by hypoplasia and upward rotation of the cerebellar vermis and cystic dilation of the fourth ventricle. The cyst of DWM rarely extends posteriorly to almost completely fill th
Externí odkaz:
https://doaj.org/article/80f34d1707ea4f8c8b3ffb3161b941a6
Autor:
Hiroko Yamammoto, Itsuro Kazukawa, Kyoko Mori, Makiko Kihara, Masanori Minagawa, Shunsuke Shimazaki, Yuki Naruke
Publikováno v:
CEN Case Rep
Fibroblast growth factor 23 (FGF-23), a hormone mainly secreted by osteocytes and osteoblasts, regulates phosphate and vitamin D levels. However, the in vivo significance of FGF-23 is not fully elucidated. This case report describes a 12-year-old gir
Autor:
Yuya Sato, Kai Yamasaki, Yasushi Iwasaki, Akiyoshi Kakita, Mari Yoshida, Manabu Natsumeda, Yukihiko Fujii, Yuki Naruke, Souichi Suenobu, Hiroaki Miyahara, Daiichiro Hasegawa, Yonehiro Kanemura, Hiroyoshi Watanabe, Tomoko Shofuda, Wataru Oohashi, Junichi Yoshimura, Ryo Ando, Akio Akagi, Takashi Taga, Ema Yoshioka, Michio Ozeki, Yoshiki Arakawa, Kenji Ihara, Naoki Okada, Junichi Hara, Yuichi Riku, T. Sakaida, Makiko Yoshida
Publikováno v:
Brain tumor pathology. 38(2)
We previously reported observing GLI3 in medulloblastomas expressing neuronal markers (NM) and/or glial fibrillary acidic protein (GFAP). Furthermore, patients with medulloblastomas expressing NM or GFAP tended to show favorable or poor prognosis, re
Autor:
Masaru Shimura, Hiroshi Horie, Makiko Tajika, Tomoo Fujisawa, Minako Ogawa-Tominaga, Hideo Sugie, Ayano Inui, Yuki Naruke, Tokiko Fukuda, Keiko Ichimoto, Kei Murayama, Ayako Matsunaga, Nana Akiyama, Takuya Fushimi
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 24, Iss, Pp 100601-(2020)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Glycogen storage disease type IV (GSD IV) is a rare inborn metabolic disorder characterized by the accumulation of amylopectin-like glycogen in the liver or other organs. The hepatic subtype may appear normal at birth but rapidly develops to liver ci
Publikováno v:
Clinical neuropathology. 38(1)
Filar lipomas are a subtype of spinal lipomas wherein adipose tissue accumulation is restricted to the filum terminale. Embryologically, filar lipomas are considered to occur because of the failure of secondary neurulation, although the precise mecha
Autor:
Kenji So, Virginia A. LiVolsi, Taiichiro Miyashita, Masahiro Ito, Yuki Naruke, Masahiro Nakashima, Yumi Mihara, Tomoki Origuchi
Publikováno v:
Pathology International. 61:589-592
IgG4-related sclerosing disease (IgG4-RSD) is an inflammatory and fibrosing disorder characterized by lymphoplasmacytic inflammation with infiltration of various organs, including the pancreas, bile ducts, lung, kidney, and retroperitoneum. As for ma
Autor:
Yuki Shimizu-Yoshida, Yuki Naruke, Ichiro Sekine, Masahiro Nakashima, Anatoly F. Tsyb, Hiroyuki Namba, Eugeny Lushnikov, Tatiana Rogounovitch, Pavel O. Roumiantsev, Vladimir Saenko, Hisayoshi Kondo, Aleksander Abrosimov, Shunichi Yamashita, Serik Meirmanov, Masahiro Ito, Noboru Takamura
Publikováno v:
The Journal of Pathology. 202:446-455
Cyclin D1 is a target molecule transcriptionally activated by aberrant beta-catenin in Wnt signalling, while prolyl isomerase Pin1 promotes cyclin D1 overexpression directly or through accumulation of beta-catenin in cancer cells. This study aimed to
Autor:
Fukuzo Matsuya, Yuki Naruke, Yasushi Umezaki, Shinji Khono, Masahiro Nakashima, Masahiro Ito, Mikio Hayashi, Yumi Mihara
Publikováno v:
Pathology International. 61:694-696