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Plos One|July 23, 2013
Sox2 transcriptionally regulates PQBP1, an intellectual disability-microcephaly causative gene, in neural stem progenitor cellsChan Li, Hikaru Ito, Kyota Fujita, et al.Cell Reports|August 17, 2023
Mutant α-synuclein propagates via the lymphatic system of the brain in the monomeric stateKyota Fujita, Hidenori Homma, Meihua Jin, et al.Biorxiv : the Preprint Server for Biology|June 12, 2025
PQBP1-dependent alternative RNA splicing underlies high calorie diet-induced cognitive impairmentYong Huang, Hidenori Homma, Xigui Chen, et al.Journal of Human Genetics|July 9, 2010
Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysisShozo Honda, Shin Hayashi, Issei Imoto, et al.Biochemical and Biophysical Research Communications|August 10, 2024
PQBP3/NOL7 is an intrinsically disordered proteinHidenori Homma, Kien Xuan Ngo, Yuki Yoshioka, et al.Biochemical and Biophysical Research Communications|August 17, 2010
Efficiently differentiating vascular endothelial cells from adipose tissue-derived mesenchymal stem cells in serum-free cultureMasamitsu Konno, Tatsuo S Hamazaki, Satsuki Fukuda, et al.Human Molecular Genetics|November 22, 2011
Ataxin-7 associates with microtubules and stabilizes the cytoskeletal networkYoko Nakamura, Kazuhiko Tagawa, Tsutomu Oka, et al.Communications Biology|August 13, 2021
Prediction and verification of the AD-FTLD common pathomechanism based on dynamic molecular network analysisMeihua Jin, Xiaocen Jin, Hidenori Homma, et al.Plos One|January 3, 2009
Nematode homologue of PQBP1, a mental retardation causative gene, is involved in lipid metabolismKeiko Takahashi, Sawako Yoshina, Maekawa Masashi, et al.Journal of Neuroscience Research|October 28, 2008
Progressive decrease in the level of YAPdeltaCs, prosurvival isoforms of YAP, in the spinal cord of transgenic mouse carrying a mutant SOD1 geneNobutoshi Morimoto, Makiko Nagai, Kazunori Miyazaki, et al.Pageof 11