Impaired Regulation of Brain Mitochondria by Extramitochondrial Ca2+ in Transgenic Huntington Disease Rats
Open Access
- 1 November 2008
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 283 (45) , 30715-30724
- https://doi.org/10.1074/jbc.m709555200
Abstract
No abstract availableThis publication has 53 references indexed in Scilit:
- High Cyclophilin D Content of Synaptic Mitochondria Results in Increased Vulnerability to Permeability TransitionJournal of Neuroscience, 2007
- Mitochondrial Phosphate–Carrier Deficiency: A Novel Disorder of Oxidative PhosphorylationAmerican Journal of Human Genetics, 2007
- Mitochondrial dysfunction in Huntington’s disease: the bioenergetics of isolated and in situ mitochondria from transgenic miceJournal of Neurochemistry, 2007
- Deranged neuronal calcium signaling and Huntington diseasePublished by Elsevier ,2004
- The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complexHuman Molecular Genetics, 2004
- Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutaminesNature Neuroscience, 2002
- Regulation of the Mitochondrial Ca2+ Uniporter by External Adenine Nucleotides: The Uniporter Behaves Like a Gated Channel Which Is Regulated by Nucleotides and Divalent CationsBiochemistry, 1997
- Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic MiceCell, 1996
- Determination of Fura-2 dissociation constants following adjustment of the apparent Ca-EGTA association constant for temperature and ionic strengthCell Calcium, 1991
- Safranine as a probe of the mitochondrial membrane potentialFEBS Letters, 1976