List of works - Gen Matsumoto

A mutation in secY that causes enhanced SecA insertion and impaired late functions in protein translocation

scientific article published on June 2000

Celastrols as inducers of the heat shock response and cytoprotection.

scientific article

Characterization of a Mutant Form of SecA That Alleviates a SecY Defect at Low Temperature and Shows a Synthetic Defect with SecY Alteration at High Temperature

scientific article published on 01 June 2000

Contribution of hippocampal place cell activity to learning and formation of goal-directed navigation in rats.

scientific article published in January 2003

Cross-seeding fibrillation of Q/N-rich proteins offers new pathomechanism of polyglutamine diseases

scientific article published in April 2009

Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington's model mice

scientific article published on 9 October 2014

Dysregulation of the proteasome increases the toxicity of ALS-linked mutant SOD1.

scientific article

Genetic dissection of SecA: suppressor mutations against the secY205 translocase defect

scientific article published on 01 December 2000

N-Acyldopamine induces aggresome formation without proteasome inhibition and enhances protein aggregation via p62/SQSTM1 expression.

scientific article

Nearest neighbor analysis of the SecYEG complex. 1. Identification of a SecY-SecG interface.

scientific article

Phosphorylation of mitochondrial polyubiquitin by PINK1 promotes Parkin mitochondrial tethering

scientific article

ROCK-phosphorylated vimentin modifies mutant huntingtin aggregation via sequestration of IRBIT.

scientific article

SecY and SecA interact to allow SecA insertion and protein translocation across the Escherichia coli plasma membrane ⬇️

scientific article published on November 3, 1997

Serine 403 Phosphorylation of p62/SQSTM1 Regulates Selective Autophagic Clearance of Ubiquitinated Proteins ⬇️

scientific article published on October 21, 2011

Structural properties and neuronal toxicity of amyotrophic lateral sclerosis-associated Cu/Zn superoxide dismutase 1 aggregates.

scientific article

The Parkinson's Disease-Associated Protein Kinase LRRK2 Modulates Notch Signaling through the Endosomal Pathway.

scientific article published on 10 September 2015

List of works by Gen Matsumoto

A mutation in secY that causes enhanced SecA insertion and impaired late functions in protein translocation

Celastrols as inducers of the heat shock response and cytoprotection.

Characterization of a Mutant Form of SecA That Alleviates a SecY Defect at Low Temperature and Shows a Synthetic Defect with SecY Alteration at High Temperature

Contribution of hippocampal place cell activity to learning and formation of goal-directed navigation in rats.

Cross-seeding fibrillation of Q/N-rich proteins offers new pathomechanism of polyglutamine diseases

Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington's model mice

Dysregulation of the proteasome increases the toxicity of ALS-linked mutant SOD1.

Genetic dissection of SecA: suppressor mutations against the secY205 translocase defect

N-Acyldopamine induces aggresome formation without proteasome inhibition and enhances protein aggregation via p62/SQSTM1 expression.

Nearest neighbor analysis of the SecYEG complex. 1. Identification of a SecY-SecG interface.

Phosphorylation of mitochondrial polyubiquitin by PINK1 promotes Parkin mitochondrial tethering

ROCK-phosphorylated vimentin modifies mutant huntingtin aggregation via sequestration of IRBIT.

SecY and SecA interact to allow SecA insertion and protein translocation across the Escherichia coli plasma membrane ⬇️

Serine 403 Phosphorylation of p62/SQSTM1 Regulates Selective Autophagic Clearance of Ubiquitinated Proteins ⬇️

Structural properties and neuronal toxicity of amyotrophic lateral sclerosis-associated Cu/Zn superoxide dismutase 1 aggregates.

The Parkinson's Disease-Associated Protein Kinase LRRK2 Modulates Notch Signaling through the Endosomal Pathway.