| P2093 | author name string | Naomi Chadderton | |
| | Arpad Palfi | |
| | G Jane Farrar | |
| | Sophia Millington-Ward | |
| | Daniel M Maloney | |
| P2860 | cites work | The mitochondrial deubiquitinase USP30 opposes parkin-mediated mitophagy | Q24298748 |
| | Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration | Q24624430 |
| | The pathways of mitophagy for quality control and clearance of mitochondria | Q27009206 |
| | Mitochondrial respiratory-chain diseases | Q29614474 |
| | Altered bioenergetics and enhanced resistance to oxidative stress in human retinal pigment epithelial cells from donors with age-related macular degeneration | Q33784315 |
| | Lysosomal-mediated waste clearance in retinal pigment epithelial cells is regulated by CRYBA1/βA3/A1-crystallin via V-ATPase-MTORC1 signaling | Q33831329 |
| | Glycolytic reliance promotes anabolism in photoreceptors | Q33879266 |
| | Vitamin B3 modulates mitochondrial vulnerability and prevents glaucoma in aged mice | Q34551476 |
| | Genetically encoded fluorescent indicator for imaging NAD(+)/NADH ratio changes in different cellular compartments | Q35431784 |
| | Investigating mitochondria as a target for treating age-related macular degeneration | Q35572570 |
| | Quantification of Oxygen Consumption in Retina Ex Vivo Demonstrates Limited Reserve Capacity of Photoreceptor Mitochondria | Q36424989 |
| | Gene Therapy for Leber Hereditary Optic Neuropathy: Initial Results | Q37618929 |
| | Glucose, lactate, and shuttling of metabolites in vertebrate retinas | Q38388203 |
| | Mitochondrial DNA content in breast cancer: Impact on in vitro and in vivo phenotype and patient prognosis | Q41260173 |
| | Biochemical adaptations of the retina and retinal pigment epithelium support a metabolic ecosystem in the vertebrate eye. | Q41671792 |
| | Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathy | Q41821755 |
| | NMNAT1 variants cause cone and cone-rod dystrophy | Q48220798 |
| | Mitochondrial Dysfunction: A Novel Potential Driver of Epithelial-to-Mesenchymal Transition in Cancer. | Q49708541 |
| | Building and decoding ubiquitin chains for mitophagy | Q49864965 |
| | Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T>C mutation altered the assembly and function of complex I, apoptosis and mitophagy. | Q51734734 |
| | Pyruvate kinase M2 regulates photoreceptor structure, function, and viability. | Q51751194 |
| | Aerobic Glycolysis Is Essential for Normal Rod Function and Controls Secondary Cone Death in Retinitis Pigmentosa. | Q55274674 |
| | Pyruvate kinase M2 isoform deletion in cone photoreceptors results in age-related cone degeneration. | Q55424201 |
| | Apoptosis inducing factor deficiency causes retinal photoreceptor degeneration. The protective role of the redox compound methylene blue | Q57299773 |
| | NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype | Q88412753 |
| | Mitochondrial quality control in AMD: does mitophagy play a pivotal role? | Q88733084 |
| | Protective roles of autophagy in retinal pigment epithelium under high glucose condition via regulating PINK1/Parkin pathway and BNIP3L | Q90249496 |
| | Mitochondrial dysfunctions, endothelial progenitor cells and diabetic retinopathy | Q90695858 |
| | Organelle Turnover: A USP30 Safety Catch Restrains the Trigger for Mitophagy and Pexophagy | Q90817587 |
| | A Role for βA3/A1-Crystallin in Type 2 EMT of RPE Cells Occurring in Dry Age-Related Macular Degeneration | Q90884789 |
| P304 | page(s) | 275-279 | |
| P577 | publication date | 2019-01-01 | |
| P1433 | published in | Advances in Experimental Medicine and Biology | Q4686385 |
| P1476 | title | Retinal Bioenergetics: New Insights for Therapeutics | |
| P478 | volume | 1185 | |