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Similar effects were observed in models of glutamine-dependent T-cell acute lymphoblastic leukemia, in which CB-839 alone at a concentration of 1 M was strongly viable, reduced the OCR, and produced synergistic effects when cells were treated in combination with inhibitors of mitochondrial complex I (29)
Endocrine-disrupting chemicals: implications for human health
10.3733/ca.v059n02p109 Calif
Copper Peptide Complex: A Novel Skin Care Ingredient
Splice mutation in the ironsulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance
Severe myoclonic epilepsy of infancy (SMEI) or Dravet syndrome from one point of view may be classified as an idiopathic genetic disorder, since children are healthy and normally developed until onset of the epilepsy, and there is a clear genetic cause (usually a SCN1A defect) in the majority of cases
