Pages that link to "Q28281393"
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The following pages link to Mitochondrial disorders (Q28281393):
Displaying 50 items.
- Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies (Q21296841) (← links)
- MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome (Q24300779) (← links)
- Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease (Q24302215) (← links)
- Structural insight into processive human mitochondrial DNA synthesis and disease-related polymerase mutations (Q24336678) (← links)
- Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome (Q24672059) (← links)
- Mitochondrial DNA mutations in human disease (Q24676881) (← links)
- Mitochondria in White, Brown, and Beige Adipocytes (Q26748753) (← links)
- When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis? (Q26777744) (← links)
- Primer removal during mammalian mitochondrial DNA replication (Q26797996) (← links)
- Mitochondrial Oxidative Stress, Mitochondrial DNA Damage and Their Role in Age-Related Vascular Dysfunction (Q26799985) (← links)
- Mitochondrial tRNA mutations and disease (Q26828352) (← links)
- Leber hereditary optic neuropathy: current perspectives (Q26863599) (← links)
- Evolutionary defined role of the mitochondrial DNA in fertility, disease and ageing (Q27024089) (← links)
- A splicing mutation in the novel mitochondrial protein DNAJC11 causes motor neuron pathology associated with cristae disorganization, and lymphoid abnormalities in mice (Q27316380) (← links)
- Biochemical diagnosis of mitochondrial disorders (Q27990527) (← links)
- Toward a therapy for mitochondrial disease (Q28080024) (← links)
- Sensory neuron diseases (Q28252053) (← links)
- Mitochondrial rejuvenation after induced pluripotency (Q28476352) (← links)
- Association of mitochondrial antioxidant enzymes with mitochondrial DNA as integral nucleoid constituents (Q28581179) (← links)
- Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study (Q30447289) (← links)
- Correlative 3D superresolution fluorescence and electron microscopy reveal the relationship of mitochondrial nucleoids to membranes (Q30513904) (← links)
- Central nervous system manifestations of mitochondrial disorders (Q31058031) (← links)
- MRI and the diagnosis of multiple sclerosis: expanding the concept of "no better explanation". (Q31061704) (← links)
- EFNS guidelines on the molecular diagnosis of mitochondrial disorders (Q33516950) (← links)
- Secondary dystonia-clinical clues and syndromic associations (Q33636395) (← links)
- Fall in circulating mononuclear cell mitochondrial DNA content in human sepsis (Q33666825) (← links)
- Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy (Q33917481) (← links)
- rAAV/ABAD-DP-6His attenuates oxidative stress-induced injury of PC12 cells (Q34128067) (← links)
- Small Circular DNAs in Human Pathology (Q34178090) (← links)
- Therapeutic prospects for mitochondrial disease (Q34205124) (← links)
- Mitochondrial ATP synthase: architecture, function and pathology. (Q34211463) (← links)
- New MT-ND6 and NDUFA1 mutations in mitochondrial respiratory chain disorders. (Q34286815) (← links)
- The neuro-ophthalmology of mitochondrial disease (Q34338783) (← links)
- Gene therapy for the treatment of mitochondrial DNA disorders (Q34401459) (← links)
- Surveyor Nuclease: a new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects. (Q34416995) (← links)
- Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health. (Q34472544) (← links)
- Neuroimaging of mitochondrial disease. (Q34593678) (← links)
- Comprehensive association testing of common mitochondrial DNA variation in metabolic disease (Q34658510) (← links)
- Increased protein nitration in mitochondrial diseases: evidence for vessel wall involvement. (Q34751597) (← links)
- Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutations (Q34763439) (← links)
- Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. (Q34820993) (← links)
- Mitochondrial encephalopathy, lactic acidosis, and stroke-like episode syndrome presenting with prolonged visual aura (Q34996511) (← links)
- Mitochondrial DNA mutations in disease and aging (Q35018267) (← links)
- In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis (Q35089820) (← links)
- Mice lacking TR4 nuclear receptor develop mitochondrial myopathy with deficiency in complex I. (Q35135711) (← links)
- Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome (Q35266396) (← links)
- Maternally inherited mitochondrial DNA disease in consanguineous families (Q35591692) (← links)
- A Role for the Mitochondrial Protein Mrpl44 in Maintaining OXPHOS Capacity (Q35722253) (← links)
- Epigenetics, epidemiology and mitochondrial DNA diseases. (Q35832776) (← links)
- Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficiencies (Q35893619) (← links)