BMAL1 and CLOCK proteins exhibit differential association with mitochondrial dynamics, protein synthesis pathways and muscle strength in human muscle - Figueroa‐Toledo, A. M.; Gutiérrez‐Pino, J.; Carriel‐Nesvara, A.; Marchese‐Bittencourt, M.; Zbinden‐Foncea, H.; Castro‐Sepúlveda, M. (The Journal of physiology, 2024)
Keywords: Adult; AKT protein; Animal models; ARNTL Transcription Factors - genetics; ARNTL Transcription Factors - metabolism; Biopsy; BMAL1 protein; circadian clock; CLOCK protein; CLOCK Proteins - genetics; CLOCK Proteins - metabolism; Cristae; Diabetes mellitus; Dynamins - genetics; Dynamins - metabolism; Fusion protein; Humans; Male; Males; Metabolic disorders; Mitochondria; mitochondria cristae density; mitochondria fusion and fission; Mitochondria, Muscle - metabolism; Mitochondria, Muscle - ultrastructure; Mitochondrial Dynamics - physiology; mitochondria–sarcoplasmic reticulum interaction; Mitophagy; Muscle function; Muscle Strength; Muscle, Skeletal - metabolism; Muscle, Skeletal - physiology; Musculoskeletal system; Protein Biosynthesis; Protein synthesis; Proteins; Sarcoplasmic reticulum; Sarcoplasmic Reticulum - metabolism; Signal transduction; Skeletal muscle; Therapeutic targets; TOR protein; TOR Serine-Threonine Kinases - metabolism; Transmission electron microscopy; Young Adult; muscle strength; mitochondria–sarcoplasmic reticulum interaction; mitophagy; mitochondria fusion and fission; circadian clock; mitochondria cristae density