Keiko Imamura

Kyoto, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 55 publications

Generation of mutant human SOD1 knock-in mouse lines at the Rosa26 locus as a platform for developing genome-editing therapies for amyotrophic lateral sclerosis.

Generation of mutant human SOD1 knock-in mouse lines at the Rosa26 locus as a platform for developing genome-editing therapies for amyotrophic lateral sclerosis.

Journal: Experimental animals

Published: August 10, 2026

Nonlinear combinatorial analysis of blood transcriptomes identifies PRKAR1A as a regulator of TDP-43 pathophysiology in amyotrophic lateral sclerosis.

Nonlinear combinatorial analysis of blood transcriptomes identifies PRKAR1A as a regulator of TDP-43 pathophysiology in amyotrophic lateral sclerosis.

Journal: Biology methods & protocols

Published: January 31, 2026

Lentiviral Vector-Mediated Gene Delivery for iPSC-Related Neuroscience Research.

Lentiviral Vector-Mediated Gene Delivery for iPSC-Related Neuroscience Research.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: November 22, 2025

Apolipoprotein E Deficiency Impairs Human Microglial Proliferation Accompanied by Elevated Cellular Oxidative Stress.

Apolipoprotein E Deficiency Impairs Human Microglial Proliferation Accompanied by Elevated Cellular Oxidative Stress.

Journal: Journal of cellular and molecular medicine

Published: November 20, 2025

Nanofiber-based platform for quantitative analysis of human oligodendrocyte ensheathment with pharmacological perturbations.

Nanofiber-based platform for quantitative analysis of human oligodendrocyte ensheathment with pharmacological perturbations.

Journal: Stem cell reports

Published: September 18, 2025

Neurodegenerative disease and autophagy in iPSC-based models.

Neurodegenerative disease and autophagy in iPSC-based models.

Journal: Neuroscience research

Published: August 27, 2025

Phenotypic screening of human iPSC-derived neurons identifies thienopyridones as neuritogenic small molecules.

Phenotypic screening of human iPSC-derived neurons identifies thienopyridones as neuritogenic small molecules.

Journal: iScience

Published: August 25, 2025

Chemical genomics language model toward reliable and explainable compound-protein interaction exploration.

Chemical genomics language model toward reliable and explainable compound-protein interaction exploration.

Journal: Journal of cheminformatics

Published: June 04, 2025

Protocol for a phase 2 study of bosutinib for amyotrophic lateral sclerosis using real-world data: induced pluripotent stem cell-based drug repurposing for amyotrophic lateral sclerosis medicine (iDReAM) study.

Protocol for a phase 2 study of bosutinib for amyotrophic lateral sclerosis using real-world data: induced pluripotent stem cell-based drug repurposing for amyotrophic lateral sclerosis medicine (iDReAM) study.

Journal: BMJ open

Published: October 26, 2024

iPSC screening identifies CACNA2D2 as a potential therapeutic target for FTLD-Tau.

iPSC screening identifies CACNA2D2 as a potential therapeutic target for FTLD-Tau.

Journal: European journal of cell biology

Published: October 06, 2024

Elimination of the extra chromosome of Dup15q syndrome iPSCs for cellular and molecular investigation.

Elimination of the extra chromosome of Dup15q syndrome iPSCs for cellular and molecular investigation.

Journal: European journal of cell biology

Published: April 17, 2024

Striosome Circuitry Stimulation Inhibits Striatal Dopamine Release and Locomotion.

Striosome Circuitry Stimulation Inhibits Striatal Dopamine Release and Locomotion.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: March 08, 2024

Showing 1-12 of 55

Last Updated: 09/26/2026