Search Results - "Suda, Kojiro"

Cytoplasmic zoning by protein phase transition after membrane permeabilization by Sugiyama, Shinju, Suda, Kojiro, Kono, Keiko

“…Abstract Biological membranes, including plasma membrane (PM) and organelle membranes, restrict the flux of ions, molecules and organelles. However, the…”
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Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability by Li, Jialin, Suda, Kojiro, Ueoka, Ibuki, Tanaka, Ryo, Yoshida, Hideki, Okada, Yasushi, Okamoto, Yuji, Hiramatsu, Yu, Takashima, Hiroshi, Yamaguchi, Masamitsu

“…Mutations in the HADHB gene induce dysfunctions in the beta-oxidation of fatty acids and result in a MTP deficiency, which is characterized by clinical…”
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Novel roles of Drosophila FUS and Aub responsible for piRNA biogenesis in neuronal disorders by Wakisaka, Keiko Tsuji, Tanaka, Ryo, Hirashima, Tomoki, Muraoka, Yuuka, Azuma, Yumiko, Yoshida, Hideki, Tokuda, Takahiko, Asada, Satoshi, Suda, Kojiro, Ichiyanagi, Kenji, Ohno, Seiko, Itoh, Masanobu, Yamaguchi, Masamitsu

“…•Aub overexpression enhanced mobility defects induced by the knockdown of Caz.•Caz plays a role in pre-piRNA production.•Knockdown of Caz produced abnormal…”
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Reduction of Rpd3 suppresses defects in locomotive ability and neuronal morphology induced by the knockdown of Drosophila SLC25A46 via an epigenetic pathway by Suda, Kojiro, Muraoka, Yuuka, Ortega-Yáñez, Andrea, Yoshida, Hideki, Kizu, Fuma, Hochin, Teruhisa, Kimura, Hiroshi, Yamaguchi, Masamitsu

“…Mitochondrial dysfunction causes various diseases. Mutations in the SLC25A46 gene have been identified in mitochondrial diseases that are sometimes classified…”
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Neuron-specific knockdown of solute carrier protein SLC25A46a induces locomotive defects, an abnormal neuron terminal morphology, learning disability, and shortened lifespan by Ali, Md Saheb, Suda, Kojiro, Kowada, Ryosuke, Ueoka, Ibuki, Yoshida, Hideki, Yamaguchi, Masamitsu

“…•Neuron-specific dSLC25A46a knockdown resulted in reduced mobility in larvae as well as adults.•Neuron-specific dSLC25A46a knockdown induced an aberrant…”
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Novel Drosophila model for mitochondrial diseases by targeting of a solute carrier protein SLC25A46 by Suda, Kojiro, Ueoka, Ibuki, Azuma, Yumiko, Muraoka, Yuuka, Yoshida, Hideki, Yamaguchi, Masamitsu

“…•Novel Drosophila SLC25A46 knockdown model for mitochondrial diseases was developed.•Neuron-specific knockdown of dSLC25A46 results in locomotive…”
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Drosophila models to study causative genes for human rare intractable neurological diseases by Yamaguchi, Masamitsu, Lee, Im-soon, Jantrapirom, Salinee, Suda, Kojiro, Yoshida, Hideki

“…Drosophila is emerging as a convenient model for investigating human diseases. Functional homologues of almost 75% of human disease-related genes are found in…”
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Genetic screening of the genes interacting with Drosophila FIG4 identified a novel link between CMT-causing gene and long noncoding RNAs by Muraoka, Yuuka, Nakamura, Aya, Tanaka, Ryo, Suda, Kojiro, Azuma, Yumiko, Kushimura, Yukie, Lo Piccolo, Luca, Yoshida, Hideki, Mizuta, Ikuko, Tokuda, Takahiko, Mizuno, Toshiki, Nakagawa, Masanori, Yamaguchi, Masamitsu

“…Neuron-specific knockdown of the dFIG4 gene, a Drosophila homologue of human FIG4 and one of the causative genes for Charcot-Marie-Tooth disease (CMT), reduces…”
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Plasma membrane damage limits replicative lifespan in yeast and induces premature senescence in human fibroblasts by Suda, Kojiro, Moriyama, Yohsuke, Razali, Nurhanani, Chiu, Yatzu, Masukagami, Yumiko, Nishimura, Koutarou, Barbee, Hunter, Takase, Hiroshi, Sugiyama, Shinju, Yamazaki, Yuta, Sato, Yoshikatsu, Higashiyama, Tetsuya, Johmura, Yoshikazu, Nakanishi, Makoto, Kono, Keiko

“…Plasma membrane damage (PMD) occurs in all cell types due to environmental perturbation and cell-autonomous activities. However, cellular outcomes of PMD…”
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