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Mitsutoshi Setou

Researcher at Hamamatsu University School of Medicine

Publications -  357
Citations -  16724

Mitsutoshi Setou is an academic researcher from Hamamatsu University School of Medicine. The author has contributed to research in topics: Mass spectrometry imaging & Mass spectrometry. The author has an hindex of 62, co-authored 321 publications receiving 15217 citations. Previous affiliations of Mitsutoshi Setou include Graduate University for Advanced Studies & National Presto Industries.

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Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

Yasushi Okazaki, +138 more
- 05 Dec 2002 - 
TL;DR: The present work, completely supported by physical clones, provides the most comprehensive survey of a mammalian transcriptome so far, and is a valuable resource for functional genomics.
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Kinesin superfamily motor protein KIF17 and mLin-10 in NMDA receptor-containing vesicle transport.

TL;DR: Experiments with vesicles containing N-methyl-D-aspartate (NMDA) receptor 2B (NR2B subunit) show that they are transported along microtubules by KIF17, a neuron-specific molecular motor in neuronal dendrites, and this interaction, specific for a neurotransmitter receptor critically important for plasticity in the postsynaptic terminal, may be a regulatory point for synaptic plasticity and neuronal morphogenesis.
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Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ

TL;DR: It is shown that CMT2A patients contain a loss-of-function mutation in the motor domain of the KIF1B gene, clear indication that defects in axonal transport due to a mutated motor protein can underlie human peripheral neuropathy.
Journal ArticleDOI

All kinesin superfamily protein, KIF, genes in mouse and human

TL;DR: The identification and classification of all kinesin superfamily proteins (KIFs) in mouse and human genome transcripts are reported to set the foundation of KIF and intracellular transport research.
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Glutamate-receptor-interacting protein GRIP1 directly steers kinesin to dendrites

TL;DR: It is shown that an AMPA (α-amino-3-hydroxy-5-methylisoxazole-4-propionate) receptor subunit—GluR2-interacting protein (GRIP1)—can directly interact and steer kinesin heavy chains to dendrites as a motor for AMPA receptors.