Histochemical localisation of mitochondrial enzyme activity in human optic nerve and retina
about
Linezolid-induced optic neuropathy: a mitochondrial disorder?Leber hereditary optic neuropathy: current perspectivesA neurodegenerative perspective on mitochondrial optic neuropathiesDominant optic atrophy.A model of Costeff Syndrome reveals metabolic and protective functions of mitochondrial OPA3.Mitochondrial disorders and the eye.Leber hereditary optic neuropathyMitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.OPA1 expression in the normal rat retina and optic nerveThe neuro-ophthalmology of mitochondrial diseaseA hypothesis to explain ganglion cell death caused by vascular insults at the optic nerve head: possible implication for the treatment of glaucomaRetinal function and structure in Ant1-deficient mice.Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.A biomechanical paradigm for axonal insult within the optic nerve head in aging and glaucoma.LHON: Mitochondrial Mutations and More.The distributions of mitochondria and sodium channels reflect the specific energy requirements and conduction properties of the human optic nerve head.The association between systemic oxidative stress and ocular blood flow in patients with normal-tension glaucoma.Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targets.Mathematically modeling the involvement of axons in Leber's hereditary optic neuropathy.Inherited mitochondrial optic neuropathies.Intraocular pressure elevation induces mitochondrial fission and triggers OPA1 release in glaucomatous optic nerveMini-Review: Impaired Axonal Transport and Glaucoma.Functional Expression of Electron Transport Chain and FoF1-ATP Synthase in Optic Nerve Myelin Sheath.Chemical and material communication between the optic nerves in rats.Characterization of Ca2+ signalling in postnatal mouse retinal ganglion cells: involvement of OPA1 in Ca2+ clearance.Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.Expression of antiapoptotic and proapoptotic molecules in diabetic retinas.Pathophysiology of primary open-angle glaucoma from a neuroinflammatory and neurotoxicity perspective: a review of the literature.Optic neuropathies: the tip of the neurodegeneration iceberg.Normal tension glaucoma: review of current understanding and mechanisms of the pathogenesis.Juxtapapillary choroid is thinner in normal-tension glaucoma than in healthy eyes.Genotype–phenotype correlations in mitochondrial optic neuropathies
P2860
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P2860
Histochemical localisation of mitochondrial enzyme activity in human optic nerve and retina
description
1999 nî lūn-bûn
@nan
1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Histochemical localisation of ...... n human optic nerve and retina
@ast
Histochemical localisation of ...... n human optic nerve and retina
@en
type
label
Histochemical localisation of ...... n human optic nerve and retina
@ast
Histochemical localisation of ...... n human optic nerve and retina
@en
prefLabel
Histochemical localisation of ...... n human optic nerve and retina
@ast
Histochemical localisation of ...... n human optic nerve and retina
@en
P2093
P2860
P356
P1476
Histochemical localisation of ...... n human optic nerve and retina
@en
P2093
Andrews RM
Griffiths PG
Johnson MA
Turnbull DM
P2860
P304
P356
10.1136/BJO.83.2.231
P407
P577
1999-02-01T00:00:00Z