Shinji Hadano
Isehara, Japan
Last Updated: 09/26/2026
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Found 38 publications
The SQSTM1 L341V Variant Associated With Sporadic ALS Promotes the Accumulation of Enlarged Ubiquitin-Positive SQSTM1 Bodies.
Journal: Genes to cells : devoted to molecular & cellular mechanisms
Published: October 24, 2025
Investigation of early axonal phenotypes in an iPSC-derived ALS cellular model using a microfluidic device.
Journal: Frontiers in cellular neuroscience
Published: March 10, 2025
Soymilk yogurt prepared using Pediococcus pentosaceus TOKAI 759m ameliorates cognitive function through gut microbiota modulation in high-fat diet mice.
Journal: Current research in food science
Published: September 15, 2024
Preclinical alternative drug discovery programs for monogenic rare diseases. Should small molecules or gene therapy be used? The case of hereditary spastic paraplegias.
Journal: Drug discovery today
Published: April 09, 2024
Rare CRHR2 and GRM8 variants identified as candidate factors associated with eating disorders in Japanese patients by whole exome sequencing.
Journal: Heliyon
Published: July 11, 2023
Central nervous system specific high molecular weight ALS2/alsin homophilic complex is enriched in mouse brain synaptosomes.
Journal: Biochemical and biophysical research communications
Published: November 07, 2022
Personalized Treatment for Infantile Ascending Hereditary Spastic Paralysis Based on In Silico Strategies.
Journal: Molecules (Basel, Switzerland)
Published: October 03, 2022
Genetic and clinical characteristics of ALS patients with NEK1 gene variants.
Journal: Neurobiology of aging
Published: July 07, 2022
De-erosion of X chromosome dosage compensation by the editing of XIST regulatory regions restores the differentiation potential in hPSCs.
Journal: Cell reports methods
Published: March 18, 2022
SQSTM1, a protective factor of SOD1-linked motor neuron disease, regulates the accumulation and distribution of ubiquitinated protein aggregates in neuron.
Journal: Neurochemistry international
Published: October 08, 2021
AI-based protein structure databases have the potential to accelerate rare diseases research: AlphaFoldDB and the case of IAHSP/Alsin.
Journal: Drug discovery today
Published: September 23, 2021
Last Updated: 09/26/2026