Pages that link to "Q34118893"
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The following pages link to Leber hereditary optic neuropathy (Q34118893):
Displaying 50 items.
- Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin (Q24299240) (← links)
- A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians (Q24531271) (← links)
- The epidemiology of Leber hereditary optic neuropathy in the North East of England (Q24611047) (← links)
- Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease (Q26770152) (← links)
- Successful amelioration of mitochondrial optic neuropathy using the yeast NDI1 gene in a rat animal model (Q27324143) (← links)
- The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity (Q28392028) (← links)
- Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency (Q28512560) (← links)
- The Eye Drop Preservative Benzalkonium Chloride Potently Induces Mitochondrial Dysfunction and Preferentially Affects LHON Mutant Cells (Q30353026) (← links)
- White matter involvement in mitochondrial diseases (Q30981330) (← links)
- Central nervous system manifestations of mitochondrial disorders (Q31058031) (← links)
- Hematological manifestations of primary mitochondrial disorders (Q33375931) (← links)
- Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation (Q33679205) (← links)
- Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C (Q33728325) (← links)
- Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy (Q33821139) (← links)
- Results of Mitochondrial DNA Sequence Analysis in Patients with Clinically Diagnosed Leber's Hereditary Optic Neuropathy (Q33973515) (← links)
- Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation (Q34000675) (← links)
- Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation (Q34007681) (← links)
- Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients (Q34081807) (← links)
- Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand (Q34111207) (← links)
- Survival and axonal regeneration of retinal ganglion cells in adult cats (Q34159148) (← links)
- Adeno-associated virus-mediated gene delivery of the human ND4 complex I subunit in rabbit eyes (Q34275931) (← links)
- Images of photoreceptors in living primate eyes using adaptive optics two-photon ophthalmoscopy (Q34527844) (← links)
- Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene (Q34543018) (← links)
- Mitochondrial disorders with significant ophthalmic manifestations (Q34570365) (← links)
- Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland (Q34615471) (← links)
- A Female Patient with Down Syndrome and Low-Penetrance Leber's Hereditary Optic Neuropathy (Q34792126) (← links)
- Long-term evaluation of Leber's hereditary optic neuropathy-like symptoms in rotenone administered rats (Q34970747) (← links)
- LHON: Mitochondrial Mutations and More (Q35084727) (← links)
- Mitochondrial encephalomyopathies (Q35085834) (← links)
- A review of primary hereditary optic neuropathies (Q35188343) (← links)
- The eye as a window to inborn errors of metabolism (Q35188347) (← links)
- Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genome (Q35445773) (← links)
- Cell response to oxidative stress induced apoptosis in patients with Leber's hereditary optic neuropathy. (Q35478068) (← links)
- Techniques and Pitfalls in the Detection of Pathogenic Mitochondrial DNA Mutations (Q35565985) (← links)
- Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy (Q35629047) (← links)
- Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy? (Q35636297) (← links)
- Mitochondriopathies (Q35685889) (← links)
- Molecular genetic basis of primary inherited optic neuropathies. (Q35944038) (← links)
- Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients (Q36023873) (← links)
- Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family (Q36054550) (← links)
- Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy (Q36119384) (← links)
- Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy. (Q36408711) (← links)
- Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy (Q36511591) (← links)
- Genotype-phenotype correlation of maternally inherited disorders due to mutations in mitochondrial DNA. (Q36686802) (← links)
- Mitochondrial biogenesis: a therapeutic target for neurodevelopmental disorders and neurodegenerative diseases (Q36771650) (← links)
- The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy. (Q36918855) (← links)
- Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy (Q36954801) (← links)
- Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders (Q37023068) (← links)
- A retrospective analysis of characteristics of visual field damage in patients with Leber's hereditary optic neuropathy (Q37034023) (← links)
- Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation (Q37156232) (← links)