Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Misako Okuno"'
Autor:
Ayako Y. Murayama, Ken-ichiro Kuwako, Junko Okahara, Byoung-Il Bae, Misako Okuno, Hiromi Mashiko, Tomomi Shimogori, Christopher A. Walsh, Erika Sasaki, Hideyuki Okano
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Abstract GPR56, a member of the adhesion G protein-coupled receptor family, is abundantly expressed in cells of the developing cerebral cortex, including neural progenitor cells and developing neurons. The human GPR56 gene has multiple presumptive pr
Externí odkaz:
https://doaj.org/article/8805ff715f5d4543bdedcd95bd83ed87
Autor:
Karl J. Windak, Aya C. Yoshida, Ayumi Abe, Masae Sato, Tsuna Serizawa, Kanako Saga, Takuro Yoshimoto, Tomomi Shimogori, Mami Tanaka, Satomi S. Kikuchi, Miyano Sakurai, Mami U, Hirozumi Nishibe, Sachie Suzuki, Mitsuhiro Toki, Kimie Niimi, Tomoko Yoda, Yoshiaki Kita, Eiki Takahashi, Shoji Tatsumoto, Yan Wang, Hideyuki Okano, Tsutomu Hashikawa, Yasuhiro Go, Chihiro Yoshida, Noriyuki Kishi, Misako Okuno, Haruhiko Yamagishi, Keiko Yamashita
Publikováno v:
Neuroscience Research. 128:1-13
Interest in the common marmoset (Callithrix jacchus) as a primate model animal has grown recently, in part due to the successful demonstration of transgenic marmosets. However, there is some debate as to the suitability of marmosets, compared to more
Autor:
Toru Kikuchi, Kikumi Ushijima, Toshikazu Takahashi, Ichiro Yokota, Tsutomu Ogata, Misako Okuno, Kazuhiro Ohkubo, Emiko Tachikawa, Satoshi Narumi, Maki Fukami, Tatsuhiko Urakami, Shoji F. Nakayama, Yoichi Matsubara, Kenichiro Hata, Junichi Arai, Shin Amemiya, Adolescent Diabetes, Kazuhiko Nakabayashi, Shigetaka Sugihara, Tomoyuki Kawamura, Tadayuki Ayabe, Nobuyuki Kikuchi, Akie Nakamura, Kenji Ihara
Publikováno v:
Pediatric Diabetes. 19:243-250
Background Mutations in causative genes for neonatal diabetes or maturity-onset diabetes of the young have been identified in multiple patients with autoantibody-negative type 1 diabetes (T1D). Objectives We aimed to clarify the prevalence and phenot
Autor:
Tatsuhiko Urakami, Shigetaka Sugihara, Masafumi Onodera, Ichiro Yokota, Tomoyuki Kawamura, Shigeru Suga, Tsutomu Ogata, Tadayuki Ayabe, Noriyuki Takubo, Kenichiro Hata, Michiko Okajima, Nobuyuki Kikuchi, Kazuhiko Nakabayashi, Shin Amemiya, Misako Okuno, Junichi Suzuki, Keiko Hayashi, Nobuyuki Watanabe, Yoichi Matsubara, Yoshihito Kasahara, Toru Kikuchi, Maki Fukami
Publikováno v:
Journal of Diabetes Investigation
Aims/Introduction Although genome-wide association studies have identified more than 50 susceptibility genes for type 1 diabetes, low-frequency risk variants could remain unrecognized. The present study aimed to identify novel type 1 diabetes suscept
Autor:
Misako Okuno1,2, Tohru Yorifuji3, Masayo Kagami1, Tadayuki Ayabe1, Tatsuhiko Urakami2, Tomoyuki Kawamura4, Nobuyuki Kikuchi5, Ichiro Yokota6, Toru Kikuchi7, Shin Amemiya7, Junichi Suzuki2, Tsutomu Ogata1,8, Shigetaka Sugihara9, Maki Fukami1 fukami-m@ncchd.go.jp
Publikováno v:
Clinical Pediatric Endocrinology. Jul2016, Vol. 25 Issue 3, p99-102. 4p. 1 Diagram.
Publikováno v:
Endocrine Journal. 63:159-167
We evaluated the efficacy and safety of switching to insulin degludec (IDeg) from insulin glargine (IGlar) as basal-bolus therapy in young people with type 1 diabetes. The subjects were 36 patients, 21.3±1.0 years of age, with type 1 diabetes. IGlar
Autor:
Ichiro Yokota, Misako Okuno, Toru Kikuchi, Shin Amemiya, Nobuyuki Kikuchi, Adolescent Diabetes, Junichi Suzuki, Tomoyuki Kawamura, Masayo Kagami, Tadayuki Ayabe, Shigetaka Sugihara, Tohru Yorifuji, Tsutomu Ogata, Tatsuhiko Urakami, Maki Fukami
Publikováno v:
Clinical Pediatric Endocrinology
Methylation defects in the imprinting locus at chromosome 6q24 result in transient neonatal diabetes and small-for-gestational age (SGA) births (1). These phenotypes are primarily ascribed to the overexpression of PLAGL1, a paternally expressed gene
Autor:
T. Kikuchi, Shin Amemiya, Adolescent Diabetes, Tsutomu Ogata, Kohji Okamura, Ikuma Musha, Kazuhiko Nakabayashi, Misako Okuno, Tomoyuki Kawamura, Yukihide Momozawa, Tatsuhiko Urakami, Nobuyuki Kikuchi, Tadayuki Ayabe, K. Shiga, Michiaki Kubo, Maki Fukami, Akira Ohtake, Akie Nakamura, Ichiro Yokota, Junichi Suzuki, Shigetaka Sugihara
Publikováno v:
Diabetic medicine : a journal of the British Diabetic Association. 35(3)
AIM To examine the contribution of PTPN2 coding variants to the risk of childhood-onset Type 1A diabetes. METHODS PTPN2 mutation analysis was carried out for 169 unrelated Japanese people with childhood-onset Type 1A diabetes. We searched for coding
Publikováno v:
Clinical Pediatric Endocrinology
The first-line pharmacological treatment for patients with maturity-onset diabetes of the young type 1 (MODY1) and maturity-onset diabetes of the young type 3 (MODY3) are sulfonylureas (SUs) or insulin. However, several reports have suggested the pos
Publikováno v:
Journal of Diabetes Investigation
We investigated the efficacy and safety of switching to insulin glulisine (GLU) from other rapid-acting insulin analogs (Ra) in children with type 1 diabetes treated with multiple daily injections of insulin or continuous subcutaneous insulin infusio