Publications by authors named "Ryosuke Ishimura"

8Publications

A homozygous pathogenic variant causes a fatal congenital neuropathy.

J Med Genet 2020 Dec 16;57(12):835-842. Epub 2020 Mar 16.

Centre of Medical Research, The University of Western Australia and the Harry Perkins Institute for Medical Research, Perth, Western Australia, Australia

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http://dx.doi.org/10.1136/jmedgenet-2019-106496DOI Listing
December 2020

A novel approach to assess the ubiquitin-fold modifier 1-system in cells.

FEBS Lett 2017 Jan 20;591(1):196-204. Epub 2016 Dec 20.

Department of Biochemistry, Niigata University Graduate School of Medical and Dental Sciences, Japan.

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http://dx.doi.org/10.1002/1873-3468.12518DOI Listing
January 2017

Proteasome dysfunction activates autophagy and the Keap1-Nrf2 pathway.

J Biol Chem 2014 Sep 21;289(36):24944-55. Epub 2014 Jul 21.

From the Department of Biochemistry, School of Medicine, Niigata University, Chuo-ku, Niigata 951-8510, Japan, the Protein Metabolism Project and

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http://dx.doi.org/10.1074/jbc.M114.580357DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155663PMC
September 2014

Dissection of the role of p62/Sqstm1 in activation of Nrf2 during xenophagy.

FEBS Lett 2014 Mar 1;588(5):822-8. Epub 2014 Feb 1.

Protein Metabolism Project, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan; Department of Biochemistry, School of Medicine, Niigata University, Niigata 951-8510, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.febslet.2014.01.045DOI Listing
March 2014