Depletion of HNRNPA1 induces peroxisomal autophagy by regulating PEX1 expression
Open Access
- 1 March 2021
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 545, 69-74
Abstract
No abstract availableKeywords
Funding Information
- National Research Foundation of Korea
This publication has 30 references indexed in Scilit:
- The Pex1-G844D mouse: A model for mild human Zellweger spectrum disorderMolecular Genetics and Metabolism, 2014
- hnRNP A1: The Swiss Army Knife of Gene ExpressionInternational Journal of Molecular Sciences, 2013
- Heterogeneous nuclear ribonucleoprotein A1 in health and neurodegenerative disease: From structural insights to post-transcriptional regulatory rolesMolecular and Cellular Neuroscience, 2013
- Autophagy sequesters damaged lysosomes to control lysosomal biogenesis and kidney injuryThe EMBO Journal, 2013
- Role of peroxisomes in ROS/RNS-metabolism: Implications for human diseaseBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2012
- Genetics and molecular basis of human peroxisome biogenesis disordersBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2012
- Monitoring autophagic flux by an improved tandem fluorescent-tagged LC3 (mTagRFP-mWasabi-LC3) reveals that high-dose rapamycin impairs autophagic flux in cancer cellsAutophagy, 2012
- Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasisHuman Molecular Genetics, 2010
- Heterogeneous Nuclear Ribonucleoprotein A1 Regulates Cyclin D1 and c-myc Internal Ribosome Entry Site Function through Akt SignalingJournal of Biological Chemistry, 2008
- The AAA peroxins Pex1p and Pex6p function as dislocases for the ubiquitinated peroxisomal import receptor Pex5pBiochemical Society Transactions, 2008