[HTML][HTML] Mitochondria in Retinal Ganglion Cells: Unraveling the Metabolic Nexus and Oxidative Stress
This review explored the role of mitochondria in retinal ganglion cells (RGCs), which are
essential for visual processing. Mitochondrial dysfunction is a key factor in the pathogenesis …
essential for visual processing. Mitochondrial dysfunction is a key factor in the pathogenesis …
Pyrroloquinoline quinone drives ATP synthesis in vitro and in vivo and provides retinal ganglion cell neuroprotection
A Canovai, JR Tribble, M Jöe, DY Westerlund… - Acta Neuropathologica …, 2023 - Springer
Retinal ganglion cells are highly metabolically active requiring strictly regulated metabolism
and functional mitochondria to keep ATP levels in physiological range. Imbalances in …
and functional mitochondria to keep ATP levels in physiological range. Imbalances in …
Mitophagy in Astrocytes Is Required for the Health of Optic Nerve
Mitochondrial dysfunction in astrocytes has been implicated in the development of various
neurological disorders. Mitophagy, mitochondrial autophagy, is required for proper …
neurological disorders. Mitophagy, mitochondrial autophagy, is required for proper …
Optimisation of AAV-NDI1 Significantly Enhances Its Therapeutic Value for Correcting Retinal Mitochondrial Dysfunction
AAV gene therapy for ocular disease has become a reality with the market authorisation of
LuxturnaTM for RPE65-linked inherited retinal degenerations and many AAV gene therapies …
LuxturnaTM for RPE65-linked inherited retinal degenerations and many AAV gene therapies …
Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy
S Sharma, A Mahadevan, G Narayanappa… - Journal of …, 2024 - Taylor & Francis
Tropical ataxic neuropathy (TAN) is characterised by ataxic polyneuropathy, degeneration of
the posterior columns and pyramidal tracts, optic atrophy, and sensorineural hearing loss. It …
the posterior columns and pyramidal tracts, optic atrophy, and sensorineural hearing loss. It …
RTN4IP1-associated non-syndromic optic neuropathy and rod-cone dystrophy
PR Gupta, K O'Connell, JM Sullivan… - Ophthalmic …, 2024 - Taylor & Francis
Background Biallelic variants in RTN4IP1 are a well-established cause of syndromic and
nonsyndromic early-onset autosomal recessive optic neuropathy. They have more recently …
nonsyndromic early-onset autosomal recessive optic neuropathy. They have more recently …
Identifying therapeutic compounds for autosomal dominant optic atrophy (ADOA) through screening in the nematode C. elegans
F Borbolis, K Palikaras - Methods in cell biology, 2024 - pubmed.ncbi.nlm.nih.gov
Autosomal Dominant Optic Atrophy (ADOA) is a rare neurodegenerative condition,
characterized by the bilateral loss of vision due to the degeneration of retinal ganglion cells …
characterized by the bilateral loss of vision due to the degeneration of retinal ganglion cells …
Mitochondrial Complex I Assembly and Implications for Mitochondrial Disease
LE Formosa - The Dynamic Nature of Mitochondria - taylorfrancis.com
Mitochondria play a central role in cellular metabolism in almost all eukaryotes, and at the
core of this function is the oxidative phosphorylation system. Complex I serves as the entry …
core of this function is the oxidative phosphorylation system. Complex I serves as the entry …