Award

21H00225

Funder: Japan Society for the Promotion of Science

Funded outputs count: 4

Funder award ID: 21H00225

OpenAlex ID: G484674920

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

2022 · Kaori Ishikawa, Yo Honma, et al. · Pharmacological Research · 1

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

2022 · Haruna Tani, Kaori Ishikawa, et al. · Nucleic Acids Research · 18

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

2021 · Sayo Horibe, Kaori Ishikawa, et al. · Oncology Reports · 21

A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome

2021 · Yoshihito Kishita, Kaori Ishikawa, et al. · Scientific Reports · 15