Pages that link to "Q38590033"
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The following pages link to Mitochondrial dynamics and quality control in Huntington's disease. (Q38590033):
Displaying 30 items.
- PPARγ as a therapeutic target to rescue mitochondrial function in neurological disease (Q28069549) (← links)
- Neuronal Mitophagy in Neurodegenerative Diseases (Q29248361) (← links)
- Retinal Ganglion Cells and Circadian Rhythms in Alzheimer's Disease, Parkinson's Disease, and Beyond (Q33634088) (← links)
- The Truncated C-terminal Fragment of Mutant ATXN3 Disrupts Mitochondria Dynamics in Spinocerebellar Ataxia Type 3 Models. (Q33813373) (← links)
- Novel regulatory roles of Mff and Drp1 in E3 ubiquitin ligase MARCH5-dependent degradation of MiD49 and Mcl1 and control of mitochondrial dynamics (Q37686829) (← links)
- Pinocembrin Attenuates Mitochondrial Dysfunction in Human Neuroblastoma SH-SY5Y Cells Exposed to Methylglyoxal: Role for the Erk1/2-Nrf2 Signaling Pathway (Q38725099) (← links)
- Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells. (Q38790183) (← links)
- Modulation of Molecular Chaperones in Huntington's Disease and Other Polyglutamine Disorders. (Q38818474) (← links)
- Neuroglobin and friends (Q39434576) (← links)
- Dynamin-related Protein 1 Inhibition Mitigates Bisphenol A-mediated Alterations in Mitochondrial Dynamics and Neural Stem Cell Proliferation and Differentiation (Q41787156) (← links)
- VCP cooperates with UBXD1 to degrade mitochondrial outer membrane protein MCL1 in model of Huntington's disease (Q45299293) (← links)
- Mitophagy and Mitochondrial Quality Control Mechanisms in the Heart (Q46272529) (← links)
- Increase in Mitochondrial Biogenesis in Neuronal Cells by RNS60, a Physically-Modified Saline, via Phosphatidylinositol 3-Kinase-Mediated Upregulation of PGC1α. (Q47348968) (← links)
- Towards an Understanding of Energy Impairment in Huntington's Disease Brain (Q47442924) (← links)
- From autophagy to mitophagy: the roles of P62 in neurodegenerative diseases. (Q47604057) (← links)
- Searching for Correlations Between the Development of Neurodegenerative Hallmarks: Targeting Huntingtin as a Contributing Factor (Q47710910) (← links)
- Optic neuropathies: the tip of the neurodegeneration iceberg (Q49608453) (← links)
- Patterns of Retinal Ganglion Cell Damage in Neurodegenerative Disorders: Parvocellular vs Magnocellular Degeneration in Optical Coherence Tomography Studies (Q49761625) (← links)
- Mitochondria: A Connecting Link In The Major Depressive Disorder Jigsaw. (Q52670223) (← links)
- A Mitochondria-Associated Oxidative Stress Perspective on Huntington's Disease (Q57072860) (← links)
- Introducing an expanded CAG tract into the huntingtin gene causes a wide spectrum of ultrastructural defects in cultured human cells (Q57454820) (← links)
- Mitochondrial superoxide generation induces a parkinsonian phenotype in zebrafish and huntingtin aggregation in human cells (Q58591586) (← links)
- Regenerative Approaches in Huntington's Disease: From Mechanistic Insights to Therapeutic Protocols (Q59132159) (← links)
- Targeting the proteostasis network in Huntington's disease (Q60922394) (← links)
- Mechanisms and roles of mitophagy in neurodegenerative diseases. (Q64993172) (← links)
- Sodium selenite protects from 3-nitropropionic acid-induced oxidative stress in cultured primary cortical neurons (Q90236449) (← links)
- Axonal transport: Driving synaptic function (Q90639155) (← links)
- Selective vulnerability in neurodegenerative diseases (Q91705233) (← links)
- NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress (Q91930166) (← links)
- A Toolbox for Organelle Mechanobiology Research-Current Needs and Challenges (Q92702206) (← links)