Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder - Debashree, Bandopadhyay; Kumar, Manish; Keshava Prasad, Thottethodi Subrahmanya; Natarajan, Archana; Christopher, Rita; Nalini, Atchayaram; Bindu, Parayil Sankaran; Gayathri, Narayanappa; Srinivas Bharath, Muchukunte Mukunda (Journal of neurochemistry, 2018)
Keywords: Adolescent; Adult; Biochemical analysis; Bioenergetics; Biopsy; Cell morphology; Coronary artery disease; Cristae; Cytology; Disorders; Fatty acids; Female; Heart diseases; Histochemistry; Histology; human; Humans; Inflammation; Insulin; Lipid metabolism; Lipid Metabolism, Inborn Errors - pathology; Lipid Metabolism, Inborn Errors - physiopathology; lipid storage; Lipids; Lipolysis; Lysergide; Male; Medical treatment; Membrane permeability; Metabolic disorders; Metabolism; Mitochondria; Mitochondria, Muscle - metabolism; Mitochondria, Muscle - pathology; Mitochondria, Muscle - ultrastructure; Mitochondrial DNA; Molecular chains; Muscle, Skeletal - pathology; Muscle, Skeletal - physiopathology; Muscle, Skeletal - ultrastructure; Muscles; Musculoskeletal system; Myopathy; Neurological diseases; Protein structure; Proteins; proteomics; Skeletal muscle; Spectrometry; Storage; Young Adult; lipid storage; proteomics; myopathy; human; mitochondria