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The Journal of Biological Chemistry|September 27, 2002
Calreticulin differentially modulates calcium uptake and release in the endoplasmic reticulum and mitochondriaSerge Arnaudeau, Maud Frieden, Kimitoshi Nakamura, et al.
Pediatric Transplantation|October 29, 2018
Recovery of severe acute liver failure without transplantation in patients with Wilson diseaseJun Kido, Shirou Matsumoto, Rieko Sakamoto, et al.
Human Genome Variation|June 7, 2017
Clinical manifestations in two patients with pyruvate dehydrogenase deficiency and long-term survivalTakanobu Yoshida, Jun Kido, Hiroshi Mitsubuchi, et al.
Life Science Alliance|November 25, 2021
TICAM-1/TRIF associates with Act1 and suppresses IL-17 receptor-mediated inflammatory responsesYusuke Miyashita, Takahisa Kouwaki, Hirotake Tsukamoto, et al.
Clinical and Experimental Nephrology|December 27, 2022
High-risk screening for Fabry disease in hemodialysis patients in Chiba Prefecture, JapanToshiyuki Imasawa, Kei Murayama, Takaaki Sawada, et al.
Environmental Pollution (Barking, Essex : 1987)|August 24, 2024
Association of phenol exposure during pregnancy and asthma development in children: The Japan Environment and Children's studyShohei Kuraoka, Masako Oda, Takashi Ohba, et al.
BMC Developmental Biology|November 23, 2006
Ultrastructural analysis of development of myocardium in calreticulin-deficient miceMira D Lozyk, Sylvia Papp, Xiaochu Zhang, et al.
Journal of Human Genetics|July 3, 2003
Complete absence of bile and pancreatic ducts in a newborn: a new entity of congenital anomaly in hepato-pancreatic developmentKimitoshi Nakamura, Hiroshi Mitsubuchi, Haruhiko Miyayama, et al.
Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation|November 15, 2019
Pediatric Pure Red Cell Aplasia Caused by Tacrolimus After Living-Donor Liver TransplantSuguru Watanabe, Rieko Sakamoto, Hidekazu Yamamoto, et al.
Case Reports in Neurology|October 21, 2020
Effect of Flunarizine on Alternating Hemiplegia of Childhood in a Patient with the p.E815K Mutation in ATP1A3: A Case ReportShouichirou Kusunoki, Jun Kido, Ken Momosaki, et al.
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