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Molecular Genetics & Genomic Medicine|June 17, 2025
A Japanese Case of Lenz-Majewski Syndrome With a Novel PTDSS1 VariantYasuko Kobari, Non Miyata, Jun Takayama, et al.American Journal of Human Genetics|July 10, 2003
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlationNaomi Matsumoto, Shigehiko Tamura, Satomi Furuki, et al.Biological & Pharmaceutical Bulletin|May 1, 2024
Inhibition Mechanism of SARS-CoV-2 Infection by a Cholesterol Derivative, Nat-20(S)-yneMana Murae, Shota Sakai, Non Miyata, et al.Journal of Cell Science|May 13, 2020
Recent insights into peroxisome biogenesis and associated diseasesYukio Fujiki, Yuichi Abe, Yuuta Imoto, et al.The Journal of Biological Chemistry|February 8, 2017
Adaptation of a Genetic Screen Reveals an Inhibitor for Mitochondrial Protein Import Component Tim44Non Miyata, Zhiye Tang, Michael A Conti, et al.Molecular Cell|February 11, 2019
Porin Associates with Tom22 to Regulate the Mitochondrial Protein Gate AssemblyHaruka Sakaue, Takuya Shiota, Naoya Ishizaka, et al.American Journal of Human Genetics|October 15, 2013
Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4Gordon J Hildick-Smith, Jeffrey D Cooney, Caterina Garone, et al.The Journal of Clinical Investigation|August 27, 2014
TMEM14C is required for erythroid mitochondrial heme metabolismYvette Y Yien, Raymond F Robledo, Iman J Schultz, et al.Pageof 3