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Mutations in acylglycerol kinase (AGK) leads to Sengers syndrome, a rare disease characterized by skeletal myopathy, hypertrophic cardiomyopathy, and cataracts. AGK, in vitro, produces lysophosphatidic acid and phosphatidic acid via phosphorylation of monoacylglycerol and diacylglycerol, accordingly...
ORGANISM(S): Homo sapiens (Human) 
2020-06-18 | PXD019826 | Pride
The composition of mitochondrial membrane lipids is crucial to cellular respiration, as seen in Barth syndrome (BTHS), a rare disease affecting skeletal muscle, heart, and neutrophils. In BTHS, mutations in the tafazzin (TAZ) gene reduce remodeling of the mitochondrial phospholipid, cardiolipin, res...
ORGANISM(S): Mus musculus (Mouse) 
2026-05-28 | PXD077710 | Pride
Faundez TMT 12 samples - 2 batches with 24 fractions each
ORGANISM(S): Homo sapiens (Human) 
2023-05-31 | PXD017501 | Pride
Comparison of 2 cell lines by TMT fractionation mass spectrometry
ORGANISM(S): Homo sapiens (Human) 
2023-05-31 | PXD038974 | Pride
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