Studies involving disease:Atherosclerosis
| Study ID | Study Title | Species | Institute |
|---|---|---|---|
| ST000305 | Pig Athersclerosis Model | Pig | University of North Carolina |
| ST001434 | Untargeted lipidomics of liver to assess the potential protective role in atherosclerosis progression of A12 antibodies infusion into LDLR-/-mice | Mouse | Centro Nacional de Investigaciones Cardiovasculares Carlos III |
| ST003351 | Incorporation of various fatty acids in long-chain base of sphingolipids in Huh7 cells | Human | Salk Institute for Biological Studies |
| ST003353 | Incorporation of oleate-d9 and elaidate-d17 in long-chain base of sphingolipids in Huh7 cells. | Human | Salk Institute for Biological Studies |
| ST003354 | Incorporation of co-treated oleate-d9 and elaidate-d17 in long-chain base of sphingolipids in Huh7 cells. | Human | Salk Institute for Biological Studies |
| ST003355 | Incorporation of two types of cis and trans fatty acids in long-chain base of sphingolipids in Huh7 cells | Human | Salk Institute for Biological Studies |
| ST003357 | Incorporation of oleate-d9 and elaidate-d17 in sphingolipids in Huh7 cells. | Human | Salk Institute for Biological Studies |
| ST003358 | Secretion of sphingomyelin from Huh7 cells treated with various fatty acids including of oleate-d9 and elaidate-d17. | Human | Salk Institute for Biological Studies |
| ST003359 | Secretion of phosphatidylcholine from Huh7 cells treated with oleate-d9 or elaidate-d17 | Human | Salk Institute for Biological Studies |
| ST003360 | Secretion of sphingomyelin from Huh7 cells treated with oleate-d9 or elaidate-d17 while modulating SPT flux. | Human | Salk Institute for Biological Studies |
| ST003371 | Incorporation of oleate-d9 and elaidate-d17 into membrane lipids of Huh7 cells. | Human | Salk Institute for Biological Studies |
| ST003372 | Incorporation of oleate-d9 and elaidate-d17 into neutral lipids of Huh7 cells. | Human | Salk Institute for Biological Studies |
| ST003373 | Incorporation of oleate-d9 and elaidate-d17 in sphingolipids in Huh7 cells while modulating SPT flux. | Human | Salk Institute for Biological Studies |
| ST003374 | Incorporation of oleate-d9 and elaidate-d17 into complex sphingolipids in Huh7 cells while modulating SPT flux. | Human | Salk Institute for Biological Studies |
| ST003377 | Sphingolipid secretory flux from Huh7 SPTLC3 KO cells | Human | Salk Institute for Biological Studies |
| ST003379 | Impact of high-fat diet enriched in cis or trans fatty acids and myriocin on hepatic lipidome in Ldlr-/- mice | Mouse | Salk Institute for Biological Studies |
| ST003381 | Impact of high-fat diet enriched in cis or trans fatty acids and myriocin on newly synthesized sphingolipids from D2O in circulation in Ldlr-/- mice | Mouse | Salk Institute for Biological Studies |
| ST003382 | Sphingolipid biosynthetic flux in Huh7 SPTLC3 KO cells | Human | Salk Institute for Biological Studies |
| ST003383 | Impact of high-fat diet enriched in cis or trans fatty acids and myriocin on the plasma lipoprotein profile of sphingolipids in Ldlr-/- mice | Mouse | Salk Institute for Biological Studies |
| ST003384 | Impact of high-fat diet enriched in cis or trans fatty acids and myriocin on plasma lipidome in Ldlr-/- mice | Mouse | Salk Institute for Biological Studies |
| ST003391 | Impact of high-fat diet enriched in cis or trans fatty acids and myriocin on plasma sphingolipids in Ldlr-/- mice | Mouse | Salk Institute for Biological Studies |
| ST003392 | Impact of high-fat diet enriched in cis or trans fatty acids and myriocin on hepatic sphingolipids in Ldlr-/- mice | Mouse | Salk Institute for Biological Studies |
| ST003928 | Untargeted metabolomics links imidazole propionate and atherosclerosis | Mouse | Centro Nacional de Investigaciones Cardiovasculares Carlos III |
| ST003929 | Imidazole propionate is a driver and therapeutic target in atherosclerosis (study 1) | Human | Centro Nacional de Investigaciones Cardiovasculares Carlos III |
| ST003932 | Imidazole propionate is a driver and therapeutic target in atherosclerosis (study 2) | Mouse | Centro Nacional de Investigaciones Cardiovasculares Carlos III |
| ST003938 | Host sensing of microbially produced imidazole propionate is a driver and therapeutic target in atherosclerosis | Human | University of Gothenburg |
