PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 24098344-6 2013 Following DOX however, CK-M-OE hearts had better preservation of creatine phosphate and higher CK flux and higher EF as compared to control DOX hearts. Phosphocreatine 65-83 creatine kinase, muscle Mus musculus 23-27 9746466-2 1998 Phosphocreatine (PCr) and ATP concentrations in M-CK-deficient hearts were not significantly different from those in wild-type hearts. Phosphocreatine 0-15 creatine kinase, muscle Mus musculus 48-52 32372868-8 2020 The direct binding activated CK-MM activity in vitro and in vivo, which increased the levels of tissue phosphocreatine and strengthened the function of the creatine kinase/phosphocreatine system in skeletal muscle, thus buffering cellular ATP, delaying exercise-induced lactate accumulation, and improving exercise performance in mice. Phosphocreatine 103-118 creatine kinase, muscle Mus musculus 29-34 32372868-8 2020 The direct binding activated CK-MM activity in vitro and in vivo, which increased the levels of tissue phosphocreatine and strengthened the function of the creatine kinase/phosphocreatine system in skeletal muscle, thus buffering cellular ATP, delaying exercise-induced lactate accumulation, and improving exercise performance in mice. Phosphocreatine 172-187 creatine kinase, muscle Mus musculus 29-34 24098344-6 2013 Following DOX however, CK-M-OE hearts had better preservation of creatine phosphate and higher CK flux and higher EF as compared to control DOX hearts. Phosphocreatine 65-83 creatine kinase, muscle Mus musculus 23-25