Pages that link to "Q43814295"
Jump to navigation
Jump to search
The following pages link to A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III. (Q43814295):
Displaying 31 items.
- A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability (Q24300577) (← links)
- Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression (Q24317119) (← links)
- Respiratory complex III is required to maintain complex I in mammalian mitochondria (Q24322645) (← links)
- Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene (Q28190016) (← links)
- Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry (Q28393214) (← links)
- Defects in mitochondrial respiratory complexes III and IV, and human pathologies. (Q30331712) (← links)
- A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome (Q30575264) (← links)
- Chronic ethanol consumption increases myocardial mitochondrial DNA mutations: a potential contribution by mitochondrial topoisomerases (Q33767807) (← links)
- De novo mtDNA point mutations are common and have a low recurrence risk. (Q33886230) (← links)
- Coenzyme q and the respiratory chain: coenzyme q pool and mitochondrial supercomplexes (Q33956959) (← links)
- Structural analysis of mitochondrial mutations reveals a role for bigenomic protein interactions in human disease (Q34852419) (← links)
- Mitochondrial encephalomyopathies (Q35085834) (← links)
- Mitochondrial complex I plays an essential role in human respirasome assembly (Q35868845) (← links)
- Alcoholic Cardiomyopathy: Multigenic Changes Underlie Cardiovascular Dysfunction (Q36166171) (← links)
- Mitochondrial DNA and disease (Q36194900) (← links)
- Type II diabetes increases mitochondrial DNA mutations in the left ventricle of the Goto-Kakizaki diabetic rat. (Q36764406) (← links)
- Analysis of Mitochondrial Respiratory Chain Supercomplexes Using Blue Native Polyacrylamide Gel Electrophoresis (BN-PAGE). (Q36773004) (← links)
- Amazing structure of respirasome: unveiling the secrets of cell respiration. (Q37548906) (← links)
- Genomics and genetics in the biology of adaptation to exercise (Q37609488) (← links)
- Respiratory chain supercomplexes: Structures, function and biogenesis. (Q38661650) (← links)
- Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene. (Q40885461) (← links)
- Mutations in mitochondrial complex III uniquely affect complex I in Caenorhabditis elegans (Q41197782) (← links)
- Functional asymmetry and electron flow in the bovine respirasome (Q41600120) (← links)
- A pathogenic cytochrome b mutation reveals new interactions between subunits of the mitochondrial bc1 complex (Q44183071) (← links)
- Significance of respirasomes for the assembly/stability of human respiratory chain complex I. (Q47316196) (← links)
- Synonymous codon usage pattern in mitochondrial CYB gene in pisces, aves, and mammals. (Q53393325) (← links)
- Synergistic Effect of Mitochondrial and Lysosomal Dysfunction in Parkinson's Disease. (Q64915273) (← links)
- Mitochondrial disorders (Q73800862) (← links)
- Mitochondrial encephalomyopathies (Q82029875) (← links)
- Structure of the intact 14-subunit human cytochrome c oxidase (Q90376409) (← links)
- Respiratory supercomplexes act as a platform for complex III-mediated maturation of human mitochondrial complexes I and IV (Q92489077) (← links)