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Akihide Takeuchi

Researcher at Kyoto University

Publications -  27
Citations -  1305

Akihide Takeuchi is an academic researcher from Kyoto University. The author has contributed to research in topics: Gene & Alternative splicing. The author has an hindex of 17, co-authored 25 publications receiving 1179 citations. Previous affiliations of Akihide Takeuchi include Salk Institute for Biological Studies & Tokyo Medical and Dental University.

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The function of GADD34 is a recovery from a shutoff of protein synthesis induced by ER stress: elucidation by GADD34-deficient mice

TL;DR: Results indicate that GADD34 works as a sensor of ER stress stimuli and recovers cells from shutoff of protein synthesis and up‐regulates Bip and CHOP in MEF of wild‐type mice.
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Na, K-ATPase α3 is a death target of Alzheimer patient amyloid-β assembly

TL;DR: A new neurotoxic mechanism that involves the interaction between patient-derived Aβ assemblies, termed amylospheroids, and the neuron-specific Na+/K+-ATPase α3 subunit (NAKα3) is revealed, which causes neurodegeneration through pre-synaptic calcium overload, which explains earlier observations that such neuronal hyperactivation is an early indicator of AD-related neurodegenersation.
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Heterozygosity with respect to Zfp148 causes complete loss of fetal germ cells during mouse embryogenesis.

TL;DR: Results indicate that two functional alleles of Zfp148 are required for the normal development of fetal germ cells, and that p53 may be required for regulating p53 in the development of germ cells.
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Rectifier of aberrant mRNA splicing recovers tRNA modification in familial dysautonomia

TL;DR: It is found that the levels of modified uridine at the wobble position in cytoplasmic tRNAs are reduced in cells from patients with FD and that treatment with RECTAS increases the expression of IKAP and recovers the tRNA modifications.
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Cloning and Characterization of a Transcription Factor That Binds to the Proximal Promoters of the Two Mouse Type I Collagen Genes

TL;DR: DNA transfection experiments using fusion polypeptides with the yeast GAL4 DNA-binding segment indicated that the C-terminal part of BFCOL1 contained a potential transcriptional activation domain, and it is speculated that BFCol1 participates in the transcriptional control of the two type I collagen genes.