Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Hironori Nagasaka"'
Autor:
Yasuhiro Hara, Yoshihiko Ikeda, Hayato Kimura, Shinsaku Shimamoto, Mao Ishikawa, Kunihisa Kobayashi, Hironori Nagasaka, Hisashi Shimoyama, Ken-ichi Hirano
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 34, Iss , Pp 100960- (2023)
Primary triglyceride deposit cardiomyovasculopathy (P-TGCV), caused by a rare genetic mutation in PNPLA2 encoding adipose triglyceride lipase (ATGL), exhibits severe cardiomyocyte steatosis and heart failure. Here, we report the case of a 51-year-old
Externí odkaz:
https://doaj.org/article/7531a1ac2f99491d95ab7e4d8e40aa22
Autor:
Ming Li, Ken-ichi Hirano, Yoshihiko Ikeda, Masahiro Higashi, Chikako Hashimoto, Bo Zhang, Junji Kozawa, Koichiro Sugimura, Hideyuki Miyauchi, Akira Suzuki, Yasuhiro Hara, Atsuko Takagi, Yasuyuki Ikeda, Kazuhiro Kobayashi, Yoshiaki Futsukaichi, Nobuhiro Zaima, Satoshi Yamaguchi, Rojeet Shrestha, Hiroshi Nakamura, Katsuhiro Kawaguchi, Eiryu Sai, Shu-Ping Hui, Yusuke Nakano, Akinori Sawamura, Tohru Inaba, Yasuhiko Sakata, Yoko Yasui, Yasuyuki Nagasawa, Shintaro Kinugawa, Kazunori Shimada, Sohsuke Yamada, Hiroyuki Hao, Daisaku Nakatani, Tomomi Ide, Tetsuya Amano, Hiroaki Naito, Hironori Nagasaka, Kunihisa Kobayashi, on behalf of the Japan TGCV study group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Triglyceride deposit cardiomyovasculopathy (TGCV) is a phenotype primarily reported in patients carrying genetic mutations in PNPLA2 encoding adipose triglyceride lipase (ATGL) which releases long chain fatty acid (LCFA) as a major energy so
Externí odkaz:
https://doaj.org/article/b62f55ce80454dd6a43a16d72cd67b1d
Autor:
Hisamitsu Hayashi, Sotaro Naoi, Takao Togawa, Yu Hirose, Hiroki Kondou, Yasuhiro Hasegawa, Daiki Abukawa, Mika Sasaki, Koji Muroya, Satoshi Watanabe, Satoshi Nakano, Kei Minowa, Ayano Inui, Akinari Fukuda, Mureo Kasahara, Hironori Nagasaka, Kazuhiko Bessho, Mitsuyoshi Suzuki, Hiroyuki Kusuhara
Publikováno v:
EBioMedicine, Vol 27, Iss C, Pp 187-199 (2018)
Progressive familial intrahepatic cholestasis type 1 (PFIC1), a rare inherited recessive disease resulting from a genetic deficiency in ATP8B1, progresses to liver failure. Because of the difficulty of discriminating PFIC1 from other subtypes of PFIC
Externí odkaz:
https://doaj.org/article/ce1e9672a010451aaf8a48d29e6a166a
Autor:
Hironori Nagasaka, Ichiro Morioka, Mayuko Takuwa, Mariko Nakacho, Mayumi Yoshida, Akihito Ishida, Satoshi Hirayama, Takashi Miida, Hirokazu Tsukahara, Tohru Yorifuji, Kazumoto Iijima
Publikováno v:
Journal of International Medical Research, Vol 46 (2018)
Objective To investigate the basal amino acid metabolism and impact of growth hormone (GH) therapy in short-stature children born small for gestational age (short SGA children). Methods In this age-matched case-control study, the basal blood levels o
Externí odkaz:
https://doaj.org/article/b2a2d0d959784007b15309bec3df616e
Autor:
Satoshi Yamaguchi, Bo Zhang, Takeshi Tomonaga, Utako Seino, Akiko Kanagawa, Masaru Segawa, Hironori Nagasaka, Akira Suzuki, Takashi Miida, Sohsuke Yamada, Yasuyuki Sasaguri, Takefumi Doi, Keijiro Saku, Mitsuyo Okazaki, Yoshihiro Tochino, Ken-ichi Hirano
Publikováno v:
Journal of Lipid Research, Vol 55, Iss 5, Pp 905-918 (2014)
The small intestine (SI) is the second-greatest source of HDL in mice. However, the selective evaluation of SI-derived HDL (SI-HDL) has been difficult because even the origin of HDL obtained in vivo from the intestinal lymph duct of anesthetized rode
Externí odkaz:
https://doaj.org/article/99c8014170b140caa8e44cc2ecf1ba6d
Autor:
Ken-ichi Hirano, Hironori Nagasaka, Kazuhiro Kobayashi, Satoshi Yamaguchi, Akira Suzuki, Tatsushi Toda, Manabu Doyu
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 264-268 (2014)
Marked hyperalphalipoproteinemia (HAL) is a heterogeneous syndrome. To clarify the pathophysiological significance of HAL, we compared clinical profiles between marked HAL subjects with and without cholesteryl ester transfer protein (CETP) deficiency
Externí odkaz:
https://doaj.org/article/d4a88b14565a4cc48dbd2cb02a8480d3
Autor:
Akira Suzuki, Hironori Nagasaka, Yasuhiro Ochi, Kazuhiro Kobayashi, Hiroshi Nakamura, Daisaku Nakatani, Satoshi Yamaguchi, Shinobu Yamaki, Atsushi Wada, Yoshihisa Shirata, Shu-Ping Hui, Tatsushi Toda, Hiroshi Kuroda, Hitoshi Chiba, Ken-ichi Hirano
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 249-253 (2014)
Adipose triglyceride lipase (ATGL) deficiency manifesting neutral lipid storage disease with myopathy/triglyceride deposit cardiomyovasculopathy presents distinct fat-containing vacuoles known as Jordans' anomaly in peripheral leucocytes. To develop
Externí odkaz:
https://doaj.org/article/bf277906c092441d8f9c8e0c43788938
Autor:
Haruki Komatsu, Satoshi Hirayama, Ichiro Morioka, Tomonozumi Takatani, Hironori Nagasaka, Takashi Miida, Ken-ichi Hirano, Tohru Yorifuji
Publikováno v:
Nutrition. 50:45-48
Objective CD36 deficiency is characterized by limited cellular long chain fatty acid uptake in the skeletal and cardiac muscles and often causes energy crisis in these muscles. However, suitable treatment for CD36 deficiency remains to be established
Autor:
Ichiro Morioka, Takashi Miida, Kazumoto Iijima, Hironori Nagasaka, Mariko Nakacho, Satoshi Hirayama, Akihito Ishida, Mayuko Takuwa, Tohru Yorifuji, Hirokazu Tsukahara, Mayumi Yoshida
Publikováno v:
Journal of International Medical Research, Vol 46 (2018)
The Journal of International Medical Research
The Journal of International Medical Research
Objective To investigate the basal amino acid metabolism and impact of growth hormone (GH) therapy in short-stature children born small for gestational age (short SGA children). Methods In this age-matched case-control study, the basal blood levels o
Autor:
Satoshi Yamaguchi, Yasuhiro Hara, Akira Suzuki, Yasuyuki Ikeda, Kunihisa Kobayashi, Ken-ichi Hirano, Hironori Nagasaka, Atsuko Takagi, Hideyuki Miyauchi, Yoshihiko Ikeda, Bo Zhang, Masahiro Higashi, Yasuhiro Magata, Toshiaki Aoyama, Ming Li
Publikováno v:
Journal of Oleo Science. 67:983-989
Triglyceride deposit cardiomyovasculopathy (TGCV) is an intractable cardiovascular disease for which a specific treatment is urgently required. In TGCV, adipose triglyceride lipase (ATGL) deficiency results in the abnormal intracellular metabolism of