Kaori Ishikawa

Tsukuba, 3058575, Japan

Last Updated: 09/26/2026

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Found 38 publications

Investigation of a causal relationship between mtDNA mutations and a mitochondrial respiratory dysfunction in premature aging mice

Investigation of a causal relationship between mtDNA mutations and a mitochondrial respiratory dysfunction in premature aging mice

Journal: Nihon yakurigaku zasshi. Folia pharmacologica Japonica

Published: July 01, 2026

Mitochondria-Dependent Metabolic Reprogramming Enhances Myofibroblast Differentiation and Aggravates Bleomycin-Induced Pulmonary Fibrosis.

Mitochondria-Dependent Metabolic Reprogramming Enhances Myofibroblast Differentiation and Aggravates Bleomycin-Induced Pulmonary Fibrosis.

Journal: Cells

Published: March 11, 2026

Comparative analysis of muscle pathologies and metabolic signaling in mouse models of mitochondrial dysfunction.

Comparative analysis of muscle pathologies and metabolic signaling in mouse models of mitochondrial dysfunction.

Journal: Scientific reports

Published: December 23, 2025

Mitochondrial vulnerability underlies myocarditis from COVID-19 mRNA vaccine.

Mitochondrial vulnerability underlies myocarditis from COVID-19 mRNA vaccine.

Journal: Nature communications

Published: August 20, 2025

Effect of Denervation on Skeletal Muscle Mitochondria in Heterozygous mtDNA Mutator Mice.

Effect of Denervation on Skeletal Muscle Mitochondria in Heterozygous mtDNA Mutator Mice.

Journal: FASEB bioAdvances

Published: March 11, 2025

Mitochondrial Respiratory Dysfunction Is Not Correlated With Mitochondrial Genotype in Premature Aging Mice.

Mitochondrial Respiratory Dysfunction Is Not Correlated With Mitochondrial Genotype in Premature Aging Mice.

Journal: Aging cell

Published: December 28, 2024

Endurance swimming exacerbates mitochondrial myopathy in mice with high mtDNA deletions.

Endurance swimming exacerbates mitochondrial myopathy in mice with high mtDNA deletions.

Journal: Mitochondrion

Published: December 09, 2024

Accumulation of mitochondrial DNA with a point mutation in tRNALeu(UUR) gene induces brain dysfunction in mice.

Accumulation of mitochondrial DNA with a point mutation in tRNALeu(UUR) gene induces brain dysfunction in mice.

Journal: Pharmacological research

Published: May 29, 2024

Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment.

Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment.

Journal: eLife

Published: March 26, 2024

Pearson syndrome-like anemia induced by accumulation of mutant mtDNA and anemia with imbalanced white blood cell lineages induced by Drp1 deletion in a murine model.

Pearson syndrome-like anemia induced by accumulation of mutant mtDNA and anemia with imbalanced white blood cell lineages induced by Drp1 deletion in a murine model.

Journal: Pharmacological research

Published: June 28, 2022

Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation.

Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation.

Journal: Nucleic acids research

Published: January 17, 2022

Mitochondrial DNA mutations are involved in the acquisition of cisplatin resistance in human lung cancer A549 cells.

Mitochondrial DNA mutations are involved in the acquisition of cisplatin resistance in human lung cancer A549 cells.

Journal: Oncology reports

Published: July 08, 2021

Showing 1-12 of 38

Last Updated: 09/26/2026