Pages that link to "Q44301583"

The following pages link to Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene. (Q44301583):

Displaying 36 items.

• Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (Q29147460) (← links)
• Mitochondrial dysfunction in bipolar disorder: from 31P-magnetic resonance spectroscopic findings to their molecular mechanisms. (Q30985980) (← links)
• Mitochondrial dysfunction as the molecular basis of bipolar disorder: therapeutic implications. (Q31088436) (← links)
• Molecular, functional, and pathological aspects of the mitochondrial ADP/ATP carrier (Q33997917) (← links)
• Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions (Q34692062) (← links)
• Mitochondrial involvement in psychiatric disorders (Q34994220) (← links)
• A meta-analysis of gene expression quantitative trait loci in brain (Q35150211) (← links)
• Two families with autosomal dominant progressive external ophthalmoplegia (Q35482241) (← links)
• Mitochondriopathies (Q35685889) (← links)
• Misfolding of mutant adenine nucleotide translocase in yeast supports a novel mechanism of Ant1-induced muscle diseases. (Q35754848) (← links)
• Frontal lobe bioenergetic metabolism in depressed adolescents with bipolar disorder: a phosphorus-31 magnetic resonance spectroscopy study (Q36295874) (← links)
• RAPID detection of gene-gene interactions in genome-wide association studies (Q36383401) (← links)
• Mitochondrial diseases: a nosological update. (Q36765849) (← links)
• Dominant membrane uncoupling by mutant adenine nucleotide translocase in mitochondrial diseases (Q37089644) (← links)
• Molecular diagnostics and mitochondrial dysfunction: a future perspective. (Q37206274) (← links)
• Purinergic signaling and energy homeostasis in psychiatric disorders (Q37284060) (← links)
• The mitochondrial ADP/ATP carrier: functional and structural studies in the route of elucidating pathophysiological aspects. (Q37315531) (← links)
• The power of yeast to model diseases of the powerhouse of the cell. (Q37418894) (← links)
• Suppression of mitochondrial DNA instability of autosomal dominant forms of progressive external ophthalmoplegia-associated ANT1 mutations in Podospora anserina (Q37425025) (← links)
• The role of mitochondrial dysfunction in psychiatric disease (Q37785512) (← links)
• Impaired mitochondrial function in psychiatric disorders (Q38003304) (← links)
• MtDNA-maintenance defects: syndromes and genes (Q40955181) (← links)
• Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation (Q43230150) (← links)
• Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder (Q45144296) (← links)
• An isoform shift in the cardiac adenine nucleotide translocase expression alters the kinetic properties of the carrier in dilated cardiomyopathy (Q45765525) (← links)
• Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy (Q46697083) (← links)
• Response to 'POLG1 mutations in bipolar disorders'. (Q47797456) (← links)
• Reduced intracellular pH in the basal ganglia and whole brain measured by 31P-MRS in bipolar disorder (Q48114635) (← links)
• Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes (Q48581868) (← links)
• Identification and molecular characterization of two novel chromosomal deletions associated with autism (Q50304662) (← links)
• Emerging Roles in the Biogenesis of Cytochrome Oxidase for Members of the Mitochondrial Carrier Family (Q61805012) (← links)
• Ant1 mutant mice bridge the mitochondrial and serotonergic dysfunctions in bipolar disorder. (Q64936050) (← links)
• Splice-Break: exploiting an RNA-seq splice junction algorithm to discover mitochondrial DNA deletion breakpoints and analyses of psychiatric disorders. (Q64943976) (← links)
• A hybrid model to study pathological mutations of the human ADP/ATP carriers (Q84058212) (← links)
• Mitochondrial carrier protein overloading and misfolding induce aggresomes and proteostatic adaptations in the cytosol (Q92502784) (← links)
• Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice (Q102379201) (← links)