Zobrazeno 1 - 10
of 60
pro vyhledávání: '"D M, Turnbull"'
Publikováno v:
Neuropathology and Applied Neurobiology
Mitochondrial respiratory chain defects are an important cause of inherited disorders affecting approximately 1 in 5000 people in the UK population. Collectively these disorders are termed ‘mitochondrial diseases’ and they result from either mito
Publikováno v:
International Journal of Peptide Research and Therapeutics. 10:353-360
Autor:
P F, Chinnery, D M, Turnbull
Publikováno v:
QJM. 90:657-667
Publikováno v:
Methods in molecular medicine. 38
Since the first demonstration that mutations of the mitochondrial genome were associated with human disease, more than 100 pathological mitochondrial DNA (mtDNA) defects have been characterized in patients with a broad spectrum of clinical manifestat
Publikováno v:
Methods in molecular medicine. 38
Although the precise mechanisms of the aging process remain poorly understood, a plausible theory for cellular dysfunction and deterioration during aging involves mitochondria (1, 2). The major function of mitochondria is to generate energy for cellu
Publikováno v:
Biochemical Medicine and Metabolic Biology. 51:35-42
The measurement of individual respiratory chain complexes is an important component of the investigation of diseases due to mitochondrial dysfunction. We have evaluated assays which measure complexes I to IV in human skeletal muscle mitochondria and
Publikováno v:
Handbook of clinical neurology. 86
Publikováno v:
Current topics in developmental biology. 77
Mitochondria are ubiquitous organelles that are intimately involved in many cellular processes, but whose principal task is to provide the energy necessary for normal cell functioning and maintenance. Disruption of this energy supply can have devasta
Autor:
D A, Cottrell, D M, Turnbull
Publikováno v:
Nestle Nutrition workshop series. Clinicalperformance programme. 6