Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Eishi Kuroda"'
Autor:
Haruka Amitani, Hajime Suzuki, Hironori Kobayashi, Masaru Murayama, Nanami Sameshima Uto, Eishi Kuroda, Yoshiki Kobayashi, Momoko Kawabe, Marie Amitani, Akio Inui, Yoshinori Marunaka
Publikováno v:
Frontiers in Aging, Vol 5 (2024)
With the global trend towards longer life expectancies, there’s an increasing emphasis on not just living longer, but also maintaining health and wellbeing into older age. This study explores the efficacy of Ninjin’yoeito (NYT) in the early stage
Externí odkaz:
https://doaj.org/article/6d9277625ebb47c89c8702806095e9fc
AGC2 (Citrin) Deficiency—From Recognition of the Disease till Construction of Therapeutic Procedures
Publikováno v:
Biomolecules, Vol 10, Iss 8, p 1100 (2020)
Can you imagine a disease in which intake of an excess amount of sugars or carbohydrates causes hyperammonemia? It is hard to imagine the intake causing hyperammonemia. AGC2 or citrin deficiency shows their symptoms following sugar/carbohydrates inta
Externí odkaz:
https://doaj.org/article/9c01632737ec497694b63535af6fda9a
Autor:
Eishi Kuroda, Takeyori Saheki, Kazuhiro Eto, David S. Sinasac, Ken Ichi Yamamura, Takashi Kadowaki, Tatsuhiko Furukawa, Qinghua Gao, Yen How Tai, Miharu Ushikai, Katsura Takano, Yoshiko Setogawa, Sumie Furuie, Aki Funahashi, Mitsuaki Moriyama, Izumi Yasuda, Masahisa Horiuchi, Yoichi Nakamura
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9 (1), ⟨10.1038/s41598-019-39627-y⟩
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9 (1), ⟨10.1038/s41598-019-39627-y⟩
Previous studies using citrin/mitochondrial glycerol-3-phosphate (G3P) dehydrogenase (mGPD) double-knockout mice have demonstrated that increased dietary protein reduces the extent of carbohydrate-induced hyperammonemia observed in these mice. This s
Autor:
Kanako Inoue, Tatsuhiko Furukawa, Mitsuaki Moriyama, Akio Inui, Eishi Kuroda, Takeyori Saheki, Takashi Kadowaki, David S. Sinasac, Keiko Kobayashi, Yuki Fujimoto, Sumie Furuie, Hiromi Ono, Kazuhiro Eto, Akihiro Asakawa, Takashi Yamamoto, Ken Ichi Yamamura, Miharu Ushikai
Publikováno v:
Molecular Genetics and Metabolism. 120:306-316
Mice carrying simultaneous homozygous mutations in the genes encoding citrin, the mitochondrial aspartate-glutamate carrier 2 (AGC2) protein, and mitochondrial glycerol-3-phosphate dehydrogenase (mGPD), are a phenotypically representative model of hu
Autor:
Andrea Frassetto, Gilles Besin, Jordan Santana, Joshua R. Schultz, Kimberly Ann Coughlan, Timothy Salerno, Edward J. Miracco, Lin T. Guey, Cosmin Mihai, Jenny Zhuo, Marianne Eybye, Jingsong Cao, Paloma H. Giangrande, Shi Liang, Ding An, E. Sathyajith Kumarasinghe, Mikel Galduroz, Aki Funahashi, Takeyori Saheki, Tatsuhiko Furukawa, Eishi Kuroda, Staci Sabnis, Paolo Martini, Patrick Finn, Christine Lukacs, Kerry Benenato, Becca Levy
Publikováno v:
Mol Ther
Citrin deficiency is an autosomal recessive disorder caused by loss-of-function mutations in SLC25A13, encoding the liver-specific mitochondrial aspartate/glutamate transporter. It has a broad spectrum of clinical phenotypes, including life-threateni
AGC2 (Citrin) Deficiency—From Recognition of the Disease till Construction of Therapeutic Procedures
Publikováno v:
Biomolecules, Vol 10, Iss 1100, p 1100 (2020)
Biomolecules
Biomolecules
Can you imagine a disease in which intake of an excess amount of sugars or carbohydrates causes hyperammonemia? It is hard to imagine the intake causing hyperammonemia. AGC2 or citrin deficiency shows their symptoms following sugar/carbohydrates inta
Autor:
Eishi Kuroda, Shigeo Kure, Osamu Sakamoto, Akio Inui, David S. Sinasac, Yoichi Nakamura, Fumio Endo, Masahide Yazaki, Takeyori Saheki, Masahisa Horiuchi, Chun-Hua Zhang, Akihiro Asakawa, Katsura Takano, Shizuka Rikimaru, Takashi Kadowaki, Shu-ichi Ikeda, Yuki Fujimoto, Mitsuaki Moriyama, Hiroshi Mitsubuchi, Yoshiyuki Okano, Kazuhiro Eto, Ken Ichi Yamamura, Yuan Zong Song, Miharu Ushikai, Kenji Kawabe
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852:1787-1795
The mitochondrial aspartate-glutamate carrier isoform 2 (citrin) and mitochondrial glycerol-3-phosphate dehydrogenase (mGPD) double-knockout mouse has been a useful model of human citrin deficiency. One of the most prominent findings has been markedl
Autor:
Atsushi Tasaki, Barry B. Phillips, Wataru Morita, Akira Yamakawa, Eishi Kuroda, Yoshimitsu Hoshikawa, Taiki Nozaki
Publikováno v:
Arthroscopy: The Journal of Arthroscopic & Related Surgery. 31:1693-1701
To evaluate the outcomes of a combination of an arthroscopic Bankart repair and an open Bristow procedure in relation to the subjective quality of performance in movements that are typical in rugby.Forty shoulders in 38 players who underwent surgery
Autor:
David S. Sinasac, Yukari Yoshidumi, Mana Yokogawa, Miharu Ushikai, Takeyori Saheki, Akihiro Asakawa, Eishi Kuroda, Hiromi Ono, Kanako Inoue, Natsumi Katsura, Kazuhiro Eto, Keiko Kobayashi, Akio Inui, Ken Ichi Yamamura, Takashi Kadowaki, Sumie Furuie
Publikováno v:
Molecular Genetics and Metabolism. 107:322-329
The C57BL/6:Slc23a13(-/-);Gpd2(-/-) double-knockout (a.k.a., citrin/mitochondrial glycerol 3-phosphate dehydrogenase double knockout or Ctrn/mGPD-KO) mouse displays phenotypic attributes of both neonatal intrahepatic cholestasis (NICCD) and adult-ons
Publikováno v:
Journal of spinal disorderstechniques. 25(1)
STUDY DESIGN: Case report. OBJECTIVE: To report a rare case of a penetrating injury to the cauda equina, secondary to a stab wound. SUMMARY OF BACKGROUND DATA: Penetrating injuries affecting the cauda equina by stab wounds, not by gunshot wounds, are