Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Shinobu Ikeda"'
Publikováno v:
Health Science Journal. 12
Single nucleotide polymorphisms (SNPs) related with metabolic syndrome may influence cancer. Our study aimed to replicate association studies of 30 selected polymorphisms pertaining to 21 genes and cancer phenotypes in Japanese elderly population. Al
Autor:
Noriko Sato, Motoji Sawabe, Tetsushi Furukawa, Shinobu Ikeda, Tomio Arai, Seijiro Mori, Khin Thet Thet Zaw, Masaaki Muramatsu, Makiko Mieno, Kaung Si Thu, Tetsuo Sasano, Masashi Tanaka
Publikováno v:
Journal of cardiology. 70(2)
Aim We aimed to study a single nucleotide polymorphism (SNP), rs2106261, in the transcription factor gene, ZFHX3 , in atrial fibrillation (AF) and other related phenotypes by phenome scanning in a Japanese population. Method We retrieved consecutive
Autor:
Makiko Mieno-Naka, Shinobu Ikeda, Tomio Arai, Masaaki Muramatsu, Motoji Sawabe, Kyi Chan Ko, James Tumaini Kengia, Atsuko Hiraishi, Noriko Sato
Publikováno v:
Atherosclerosis. 231:158-162
Background ATP10D belongs to a subfamily of P-type ATPases implicated in phospholipids translocation from the exoplasmic to the cytoplasmic leaflet of cellular biological membrane. Previous genome-wide association study (GWAS) identified that a varia
Publikováno v:
Endocrine Journal. 59:677-684
GLUT4 is a major mediator of glucose removal from the circulation and a key regulator of whole-body glucose homeostasis. Recent studies in south Indian populations revealed that haplotypes of the GLUT4 gene associated with type 2 diabetes. A total of
Autor:
Masaaki Muramatsu, Maung Kyi Chan Ko, Makiko Mieno-Naka, Motoji Sawabe, Shinobu Ikeda, Tomio Arai, Syed Ali Hyder Zaidi, Noriko Sato
Publikováno v:
Journal of Atherosclerosis and Thrombosis. 19:552-558
Aim: Atherosclerotic disease is a major health problem among the elderly, which arises from a complex interaction between genetic and environmental factors. The catechol-O-methyltransferase (COMT) gene encodes an enzyme that degrades catecholamines a
Autor:
Motoji Sawabe, Tomio Arai, Noriko Sato, Shinobu Ikeda, Makiko Naka-Mieno, Masashi Tanaka, Kaung Si Thu, Seijiro Mori, Masaaki Muramatsu
Publikováno v:
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica. 124(8)
The transporter associated with antigen processing 2 (TAP2) gene is involved in the immunological response to tuberculosis (TB) infection. Variations in the TAP2 gene have been associated with TB infection in small population studies in India, Columb
Publikováno v:
Biochemical and Biophysical Research Communications. 405:356-361
Formylpeptide receptor (FPR1) is involved in inflammation, which is important in the pathogenesis of diverse conditions, including common diseases and cancers. To date, little is known about the relationships between FPR1 and such diseases, aside fro
Autor:
Seiichiro Yamamoto, Shinobu Ikeda, Manami Inoue, Shizuka Sasazuki, Tetsuya Otani, Motoki Iwasaki, Shoichiro Tsugane, Tomoyuki Hanaoka
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 15:1341-1347
Background: Although accumulating evidence suggests that Helicobacter pylori plays a role in gastric carcinogenesis, the magnitude of the risk remains uncertain. Aim: We aimed to estimate the magnitude of the risk of gastric cancer associated with H.
Autor:
Yoshiaki Gu, Chiyuki Ishizawa, Koichi Tokuda, Hisakazu Yano, Shinobu Ikeda, Yukari Hirai, Hajime Kanamori, Mitsuo Kaku, Shiro Endo, Masami Takahashi, Tetsuji Aoyagi, David J. Weber, Masumitsu Hatta
Publikováno v:
The Tohoku journal of experimental medicine. 234(2)
Susceptible healthcare personnel (HCP) are at high risk for acquiring and transmitting measles, mumps, rubella, and varicella (MMRV). Presumptive evidence of immunity to MMRV is recommended for HCP. The aim of this investigation was to examine the se
Autor:
Takashi X. Fujisawa, Daiki Toyohisa, Chiho Yatsuga, Naomi Matsuura, Akinobu Hamada, Shota Nishitani, Akemi Tomoda, Shinobu Ikeda, Kazuyuki Shinohara, Masaaki Muramatsu
Publikováno v:
Braindevelopment. 36(7)
This study ascertained the association between attention deficit/hyperactivity disorder (ADHD) in Japanese children and a polymorphism of catechol-O-methyltransferase (COMT), a dopamine-control gene. The secondary aim of the study was the evaluation