lysophosphatidic acid has been researched along with Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chandramohan, C; Ghosh, AK; Rajasekharan, R; Ramakrishnan, G | 1 |
| Dereure, O | 1 |
| Kienesberger, PC; Kohlwein, SD; Lass, A; Preiss-Landl, K; Wolinski, H; Zechner, R; Zimmermann, R | 1 |
3 other study(ies) available for lysophosphatidic acid and Syndrome
| Article | Year |
|---|---|
CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Acylation; Adipose Tissue, White; Animals; Esterases; Gene Expression; Humans; Ichthyosis; Lipase; Lipid Metabolism, Inborn Errors; Lysophospholipids; Mice; Mutation; Recombinant Proteins; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Syndrome; Triglycerides | 2008 |
[Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndrome].
Topics: Genes, Recessive; Hair Diseases; Hypotrichosis; Lysophospholipids; Mutation; Receptors, Purinergic P2; Syndrome | 2008 |
Identification of an insulin-regulated lysophospholipase with homology to neuropathy target esterase.
Topics: 3T3-L1 Cells; Animals; Axons; Brain; Carboxylic Ester Hydrolases; Dose-Response Relationship, Drug; Endoplasmic Reticulum; Fasting; Gene Expression Regulation, Enzymologic; Hypoglycemic Agents; Insulin; Lipid Metabolism; Lysophosphatidylcholines; Lysophospholipase; Lysophospholipids; Male; Mice; Organ Specificity; Paralysis; RNA, Messenger; Substrate Specificity; Syndrome | 2008 |