Glutathione-conjugating and membrane-remodeling activity of GDAP1 relies on amphipathic C-terminal domain
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Title
Glutathione-conjugating and membrane-remodeling activity of GDAP1 relies on amphipathic C-terminal domain
Authors
Keywords
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Journal
Scientific Reports
Volume 6, Issue 1, Pages -
Publisher
Springer Nature
Online
2016-11-14
DOI
10.1038/srep36930
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Related references
Note: Only part of the references are listed.- Lack of GDAP1 Induces Neuronal Calcium and Mitochondrial Defects in a Knockout Mouse Model of Charcot-Marie-Tooth Neuropathy
- (2015) Manuela Barneo-Muñoz et al. PLoS Genetics
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- Junctophilin-1 is a modifier gene of GDAP1-related Charcot–Marie–Tooth disease
- (2014) David Pla-Martín et al. HUMAN MOLECULAR GENETICS
- Redox Regulation of Store-Operated Ca2+ Entry
- (2013) Paula Nunes et al. ANTIOXIDANTS & REDOX SIGNALING
- Charcot-Marie-Tooth disease-associated mutants of GDAP1 dissociate its roles in peroxisomal and mitochondrial fission
- (2013) Nina Huber et al. EMBO REPORTS
- Silencing of the Charcot–Marie–Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry
- (2013) David Pla-Martín et al. NEUROBIOLOGY OF DISEASE
- SnapShot: Membrane Curvature Sensors and Generators
- (2012) Hongying Shen et al. CELL
- The intracellular redox state is a core determinant of mitochondrial fusion
- (2012) Timothy Shutt et al. EMBO REPORTS
- Mechanisms of Membrane Curvature Sensing
- (2011) Bruno Antonny Annual Review of Biochemistry
- Glutathione transferases: a structural perspective
- (2011) Aaron Oakley DRUG METABOLISM REVIEWS
- Dual localization of glutathione S-transferase in the cytosol and mitochondria: implications in oxidative stress, toxicity and disease
- (2011) Haider Raza FEBS Journal
- Charcot–Marie–Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential
- (2011) Rebecca Noack et al. HUMAN MOLECULAR GENETICS
- Mitofusin 2 Regulates STIM1 Migration from the Ca2+Store to the Plasma Membrane in Cells with Depolarized Mitochondria
- (2011) Karthika Singaravelu et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
- (2011) M. Zimon et al. NEUROLOGY
- A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K
- (2011) Julien Cassereau et al. Orphanet Journal of Rare Diseases
- Membrane Remodeling Induced by the Dynamin-Related Protein Drp1 Stimulates Bax Oligomerization
- (2010) Sylvie Montessuit et al. CELL
- Membrane curvature during peroxisome fission requires Pex11
- (2010) Łukasz Opaliński et al. EMBO JOURNAL
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- (2009) Shinji Goto et al. FREE RADICAL BIOLOGY AND MEDICINE
- GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance
- (2009) Axel Niemann et al. NEUROBIOLOGY OF DISEASE
- Targeting and Function of the Mitochondrial Fission Factor GDAP1 Are Dependent on Its Tail-Anchor
- (2009) Konstanze M. Wagner et al. PLoS One
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