Pages that link to "Q37783778"

The following pages link to Mouse models of dominant optic atrophy: what do they tell us about the pathophysiology of visual loss? (Q37783778):

Displaying 10 items.

• The injury resistant ability of melanopsin-expressing intrinsically photosensitive retinal ganglion cells (Q26864570) (← links)
• Opa1 is required for proper mitochondrial metabolism in early development (Q27334237) (← links)
• The optic nerve: a "mito-window" on mitochondrial neurodegeneration (Q34298350) (← links)
• Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function (Q35660977) (← links)
• Retina ganglion cell degeneration in glaucoma: an opportunity missed? A review (Q37992209) (← links)
• Mitochondrial dynamics in neurodegeneration (Q38060435) (← links)
• Autosomal dominant hereditary optic neuropathy (ADOA): a review of the genetics and clinical manifestations of ADOA and ADOA+. (Q38153739) (← links)
• Mitochondrial dysfunction in an Opa1(Q285STOP) mouse model of dominant optic atrophy results from Opa1 haploinsufficiency. (Q42381310) (← links)
• Mitochondrial Fission in Human Diseases (Q46438173) (← links)
• Targeted next-generation sequencing extends the mutational spectrums for OPA1 mutations in Chinese families with optic atrophy (Q89558188) (← links)