Toshiyuki Yamaji

Years Active: 2020-2023
Publications (10 Years): 5

National Institute of Infectious Diseases

Kyoto University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Institute of Infectious Diseases Sep 01 2015

Japan

Chief, Laboratory II :: Department of Biochemistry and Cell Biology

National Institute of Infectious Diseases Apr 01 2009 - Aug 31 2015

Japan

Senior Research Scientist :: Department of Biochemistry and Cell Biology

National Institute of Infectious Diseases Nov 01 2006 - Mar 31 2009

Japan

Research Scientist :: Department of Biochemistry and Cell Biology

RIKEN FRS Jul 01 2006 - Oct 31 2006

Japan

Researcher :: Glyco-chain Functions Laboratory, Supra-biomolecular System Group

University of California San Francisco Sep 01 2003 - Jun 30 2006

United States

Postdoctoral Researcher :: Department of Anatomy

Education History

Kyoto University Apr 01 1995 - Mar 31 2000

Japan

PHD :: Department of Biochemistry

Publications

Aya Mizuike, Shota Sakai, Kaoru Katoh, Toshiyuki Yamaji, Kentaro Hanada
The C10orf76-PI4KB axis orchestrates CERT-mediated ceramide trafficking to the distal Golgi. The Journal of cell biology 222 (7) (2023)
Aya Mizuike, Shota Sakai, Kaoru Katoh, Toshiyuki Yamaji, Kentaro Hanada
The C10orf76-PI4KB axis orchestrates CERT-mediated ceramide trafficking to the distal Golgi. The Journal of cell biology 222 (7) (2023)
Aya Mizuike, Shota Sakai, Kaoru Katoh, Toshiyuki Yamaji, Kentaro Hanada
The C10orf76-PI4KB axis orchestrates CERT-mediated ceramide trafficking to the distal Golgi. The Journal of cell biology 222 (7) (2023)
Aya Mizuike, Shota Sakai, Kaoru Katoh, Toshiyuki Yamaji, Kentaro Hanada
The C10orf76-PI4KB axis orchestrates CERT-mediated ceramide trafficking to the distal Golgi. The Journal of cell biology 222 (7) (2023)
Kanta Morimoto, Noriko Suzuki, Isei Tanida, Soichiro Kakuta, Yoko Furuta, Yasuo Uchiyama, Kentaro Hanada, Yusuke Suzuki, Toshiyuki Yamaji
Blood group P1 antigen-bearing glycoproteins are functional but less efficient receptors of Shiga toxin than conventional glycolipid-based receptors. The Journal of biological chemistry 295 (28) (2020)

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