Pages that link to "Q30489322"
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The following pages link to Effects of overexpression of huntingtin proteins on mitochondrial integrity (Q30489322):
Displaying 50 items.
- Mitochondrial Dysfunction in Alzheimer's Disease and the Rationale for Bioenergetics Based Therapies (Q26750081) (← links)
- Defining the role of the Bcl-2 family proteins in Huntington's disease (Q26822846) (← links)
- Mitochondrial morphology-emerging role in bioenergetics (Q26852770) (← links)
- The dynamics of the mitochondrial organelle as a potential therapeutic target (Q26853454) (← links)
- Calcium channel blockers and Alzheimer's disease (Q26866552) (← links)
- Mitochondrial quality control: decommissioning power plants in neurodegenerative diseases (Q27009213) (← links)
- Novel mitochondrial targets for neuroprotection (Q27023108) (← links)
- Impaired mitochondrial dynamics and Nrf2 signaling contribute to compromised responses to oxidative stress in striatal cells expressing full-length mutant huntingtin (Q27312215) (← links)
- S-nitrosylation of Drp1 links excessive mitochondrial fission to neuronal injury in neurodegeneration (Q27694603) (← links)
- Mechanisms of aging-related proteinopathies in Caenorhabditis elegans (Q28077338) (← links)
- The role of insulin/IGF-1 signaling in the longevity of model invertebrates, C. elegans and D. melanogaster (Q28083445) (← links)
- Dynamin-related protein 1 and mitochondrial fragmentation in neurodegenerative diseases (Q28300234) (← links)
- Shaping the role of mitochondria in the pathogenesis of Huntington's disease (Q28384036) (← links)
- Role of oxidative DNA damage in mitochondrial dysfunction and Huntington's disease pathogenesis (Q28386202) (← links)
- Impaired balance of mitochondrial fission and fusion in Alzheimer's disease (Q28854335) (← links)
- Mitochondrial dynamics--fusion, fission, movement, and mitophagy--in neurodegenerative diseases (Q29615646) (← links)
- S-glutathionylation: from molecular mechanisms to health outcomes (Q30398587) (← links)
- Coenzyme Q protects Caenorhabditis elegans GABA neurons from calcium-dependent degeneration (Q30496117) (← links)
- Systems biology analysis of Drosophila in vivo screen data elucidates core networks for DNA damage repair in SCA1. (Q30687417) (← links)
- Metabolic profiling for the identification of Huntington biomarkers by on-line solid-phase extraction capillary electrophoresis mass spectrometry combined with advanced data analysis tools (Q31032933) (← links)
- Huntingtin interacts with the cue domain of gp78 and inhibits gp78 binding to ubiquitin and p97/VCP. (Q33529116) (← links)
- Perturbations in mitochondrial dynamics induced by human mutant PINK1 can be rescued by the mitochondrial division inhibitor mdivi-1. (Q33799876) (← links)
- DISC1 and Huntington's disease--overlapping pathways of vulnerability to neurological disorder? (Q33813559) (← links)
- Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease (Q33814719) (← links)
- Potential therapeutic benefits of strategies directed to mitochondria. (Q34117168) (← links)
- Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease (Q34163054) (← links)
- Increased mitochondrial fission and neuronal dysfunction in Huntington's disease: implications for molecular inhibitors of excessive mitochondrial fission (Q34313991) (← links)
- Therapeutic approaches to preventing cell death in Huntington disease (Q34411338) (← links)
- Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli (Q34605764) (← links)
- Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage (Q34627072) (← links)
- Mutant huntingtin binds the mitochondrial fission GTPase dynamin-related protein-1 and increases its enzymatic activity (Q34634421) (← links)
- Mitochondrial approaches to protect against cardiac ischemia and reperfusion injury. (Q34854255) (← links)
- Recent advances in our understanding of neurodegeneration (Q34999535) (← links)
- The Striatum Is Highly Susceptible to Mitochondrial Oxidative Phosphorylation Dysfunctions (Q35219902) (← links)
- Direct reprogramming of Huntington's disease patient fibroblasts into neuron-like cells leads to abnormal neurite outgrowth, increased cell death, and aggregate formation (Q35294913) (← links)
- Implications of mitochondrial dynamics on neurodegeneration and on hypothalamic dysfunction (Q35708874) (← links)
- Mutant huntingtin's interaction with mitochondrial protein Drp1 impairs mitochondrial biogenesis and causes defective axonal transport and synaptic degeneration in Huntington's disease (Q35747131) (← links)
- Effect of erythropoietin on the expression of dynamin-related protein-1 in rat renal interstitial fibrosis (Q35758909) (← links)
- Mitochondrial dynamics in cancer and neurodegenerative and neuroinflammatory diseases (Q36082495) (← links)
- Caenorhabditis elegans as a model system to study intercompartmental proteostasis: Interrelation of mitochondrial function, longevity, and neurodegenerative diseases (Q36109384) (← links)
- A new Caenorhabditis elegans model of human huntingtin 513 aggregation and toxicity in body wall muscles (Q36304420) (← links)
- PINK1-induced mitophagy promotes neuroprotection in Huntington's disease (Q36347184) (← links)
- Mitochondrial translocation of EGFR regulates mitochondria dynamics and promotes metastasis in NSCLC (Q36545739) (← links)
- Mitochondria-targeted molecules MitoQ and SS31 reduce mutant huntingtin-induced mitochondrial toxicity and synaptic damage in Huntington's disease (Q37178581) (← links)
- S-nitrosylation of dynamin-related protein 1 mediates mutant huntingtin-induced mitochondrial fragmentation and neuronal injury in Huntington's disease (Q37204122) (← links)
- Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle (Q37295056) (← links)
- Mitochondrial structural and functional dynamics in Huntington's disease (Q37356257) (← links)
- Mitochondrial dynamics in Parkinson's disease (Q37364337) (← links)
- Inhibition of mitochondrial fragmentation diminishes Huntington's disease-associated neurodegeneration (Q37384081) (← links)
- What have worm models told us about the mechanisms of neuronal dysfunction in human neurodegenerative diseases? (Q37389590) (← links)