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Current Biology : CB|May 14, 2025
Neofunctionalization of VAMP7 opened up a plant-unique vacuolar transport pathwayMasaru Fujimoto, Yutaro Shimizu, Yoko Ito, et al.
Journal of Inherited Metabolic Disease|February 20, 2013
A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiencyNaeem Shafqat, Kate L Kavanagh, Jörn Oliver Sass, et al.
Genome Biology and Evolution|November 27, 2015
Eukaryotic Components Remodeled Chloroplast Nucleoid Organization during the Green Plant EvolutionYusuke Kobayashi, Mari Takusagawa, Naomi Harada, et al.
The Journal of Physical Chemistry. B|May 20, 2016
Phase Transition and Dynamics in Imidazolium-Based Ionic Liquid Crystals through a Metastable Highly Ordered Smectic PhaseYoko Nozaki, Keito Yamaguchi, Kenji Tomida, et al.
Gynecologic Oncology Reports|January 2, 2023
Thoracic spinal metastasis as recurrence of borderline Brenner tumor without local recurrence: A case reportTomoaki Fujita, Aya Takeya, Haruka Miyata, et al.
Proteomics|February 3, 2015
Quantitative proteomics of Arabidopsis shoot microsomal proteins reveals a cross-talk between excess zinc and iron deficiencySajad Majeed Zargar, Rie Kurata, Shoko Inaba, et al.
Cancer Causes & Control : CCC|October 10, 2009
Reproductive factors, exogenous female hormone use and breast cancer risk in Japanese: the Miyagi Cohort StudyMasaaki Kawai, Yuko Minami, Shinichi Kuriyama, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|November 7, 2015
Complete bone regeneration in hemophilic pseudotumor of the mandibleHiroki Otsuka, Michio Ozeki, Kaori Kanda, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|May 6, 2022
Influences of protein levels on the cerebrospinal fluid distribution of ceftazidime & ceftriaxone in the cerebrospinal fluid of patients with inflamed meningitisNaoki Ichinose, Gakushi Yoshikawa, Eri Fukao, et al.
Molecular Genetics and Metabolism|March 27, 2002
Identification and characterization of temperature-sensitive mild mutations in three Japanese patients with nonsevere forms of very-long-chain acyl-CoA dehydrogenase deficiencyYuichi Takusa, Toshiyuki Fukao, Masahiko Kimura, et al.
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