PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 28916646-8 2018 These phosphatidylglycerol changes, however, were milder than in classic infantile-onset SERAC1 cases, which might partially explain the milder SERAC1 phenotype. Phosphatidylglycerols 6-26 serine active site containing 1 Homo sapiens 89-95 28916646-8 2018 These phosphatidylglycerol changes, however, were milder than in classic infantile-onset SERAC1 cases, which might partially explain the milder SERAC1 phenotype. Phosphatidylglycerols 6-26 serine active site containing 1 Homo sapiens 144-150 22683713-5 2012 Complementation of patient fibroblasts with wild-type human SERAC1 by lentiviral infection led to a decrease and partial normalization of the mean ratio of phosphatidylglycerol-34:1 to phosphatidylglycerol-36:1. Phosphatidylglycerols 156-176 serine active site containing 1 Homo sapiens 60-66 22683713-5 2012 Complementation of patient fibroblasts with wild-type human SERAC1 by lentiviral infection led to a decrease and partial normalization of the mean ratio of phosphatidylglycerol-34:1 to phosphatidylglycerol-36:1. Phosphatidylglycerols 185-205 serine active site containing 1 Homo sapiens 60-66 22683713-6 2012 Our data identify SERAC1 as a key player in the phosphatidylglycerol remodeling that is essential for both mitochondrial function and intracellular cholesterol trafficking. Phosphatidylglycerols 48-68 serine active site containing 1 Homo sapiens 18-24 34326751-3 2021 The serine active site-containing 1 (SERAC1) mutation is localized at the mitochondria-associated membranes, which are responsible for encoding a phosphatidylglycerol remodeler essential for both mitochondrial function and intracellular cholesterol trafficking and is thus responsible for the disease. Phosphatidylglycerols 146-166 serine active site containing 1 Homo sapiens 4-35 34326751-3 2021 The serine active site-containing 1 (SERAC1) mutation is localized at the mitochondria-associated membranes, which are responsible for encoding a phosphatidylglycerol remodeler essential for both mitochondrial function and intracellular cholesterol trafficking and is thus responsible for the disease. Phosphatidylglycerols 146-166 serine active site containing 1 Homo sapiens 37-43 25642805-4 2015 Mutations are found in SERAC1, encoding a phosphatidylglycerol remodeling enzyme essential for both mitochondrial function and intracellular cholesterol trafficking. Phosphatidylglycerols 42-62 serine active site containing 1 Homo sapiens 23-29