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Tomohiro Yorimitsu

Researcher at University of Tokyo

Publications -  14
Citations -  4582

Tomohiro Yorimitsu is an academic researcher from University of Tokyo. The author has contributed to research in topics: COPII & Endoplasmic reticulum. The author has an hindex of 9, co-authored 13 publications receiving 3652 citations.

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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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Insights into structural and regulatory roles of Sec16 in COPII vesicle formation at ER exit sites

TL;DR: The results indicate that purified Sec16 alone can self-assemble into homo-oligomeric complexes on a planar lipid membrane and plays an important role in regulating Sar1 GTPase activity at the late steps of COPII vesicle formation.
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Molecular mechanisms of Sar/Arf GTPases in vesicular trafficking in yeast and plants.

TL;DR: This review focuses on the current knowledge of Sar/Arf GTPases, highlighting the molecular details of GTPase regulation in vesicle formation in yeast and advances in knowledge of the characteristics of vesicles trafficking in plants.
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REI-1 Is a Guanine Nucleotide Exchange Factor Regulating RAB-11 Localization and Function in C. elegans Embryos

TL;DR: The loss of REI-1 specifically impaired the targeting of RAB-11 to the late-Golgi compartment and the recycling endosomes in embryos and further reduced the RAB -11 distribution to the cleavage furrow, which resulted in cytokinesis delay, suggesting that REi-1 is a GEF specifically regulating the R AB-11 localization and functions in early embryos.
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COPII machinery cooperates with ER-localized Hsp40 to sequester misfolded membrane proteins into ER-associated compartments

TL;DR: Findings point to an as-yet-undefined role of COPII proteins in the formation of ERACs, which are segregated into specialized ER subdomains, termed ER-associated compartments (ERACs) before degradation.