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doi: 10.1093/ajcn/81.5.1218

These studies indicate the potential of utilizing the de novo pathway, a less extensively studied pathway, as a therapeutic strategy for metabolic diseases Barth syndrome is a rare disease caused by mutations in the tafazzin gene encoding for cardiolipin (CL), a phospholipid specific for the mitochondria 303

Membranes were blocked in TBS-T containing 5% skim milk for 1 h at room temperature and then incubated with primary antibodies against -catenin, phosphorylated ERK (p-ERK), and -actin (all from Santa Cruz Biotechnology, USA)

USA 112 , 78337838 (2015)

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