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The American Journal of Pathology|November 13, 2017
Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral SclerosisMikiko Tada, Hiroshi Doi, Shigeru Koyano, et al.Neuroscience Research|November 1, 2019
Proteomic analysis of exosome-enriched fractions derived from cerebrospinal fluid of amyotrophic lateral sclerosis patientsNoriko Hayashi, Hiroshi Doi, Yoichi Kurata, et al.The Journal of Medical Investigation : JMI|April 25, 2022
Biotin levels in blood and follicular fluid and their associations with pregnancy outcomes in IVF/ICSI patientsRie Yanagihara, Yuri Yamamoto, Takako Kawakita, et al.Brain : a Journal of Neurology|April 1, 2021
Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichmentTakeshi Mizuguchi, Tomoko Toyota, Satoko Miyatake, et al.Clinical and Translational Gastroenterology|November 22, 2023
Non-Pure Intestinal Phenotype as an Indicator of Progression in Sporadic Nonampullary Duodenal Adenomas: A Multicenter Retrospective Cohort StudyRyotaro Uema, Yoshito Hayashi, Masato Komori, et al.Journal of Human Genetics|February 7, 2018
Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutationsHiroshi Doi, Shigeru Koyano, Satoko Miyatake, et al.Neurobiology of Disease|June 24, 2019
Ataxic phenotype with altered Ca<sub>V</sub>3.1 channel property in a mouse model for spinocerebellar ataxia 42Shunta Hashiguchi, Hiroshi Doi, Misako Kunii, et al.Pageof 7