phosphatidylcholines has been researched along with Peroxisomal Disorders in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Blevins, MS; Braverman, NE; Brodbelt, JS; Cui, W; Fallatah, W; Moser, AB; Shields, SWJ | 1 |
| Abe, Y; Fujiki, Y; Honsho, M; Nakanishi, H; Taguchi, R | 1 |
| Byers, DM; Cook, HW; Logan, HE; Ridgway, ND | 1 |
3 other study(ies) available for phosphatidylcholines and Peroxisomal Disorders
| Article | Year |
|---|---|
Structural Characterization and Quantitation of Ether-Linked Glycerophospholipids in Peroxisome Biogenesis Disorder Tissue by Ultraviolet Photodissociation Mass Spectrometry.
Topics: Animals; Ether; Ethers; Ethyl Ethers; Glycerophospholipids; Mice; Peroxisomal Disorders; Phosphatidylcholines; Phosphatidylethanolamines; Tandem Mass Spectrometry | 2022 |
Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.
Topics: Acyl Coenzyme A; Adrenoleukodystrophy; Animals; Cells, Cultured; Cricetinae; Fatty Acids, Unsaturated; Fibroblasts; Humans; Oxidation-Reduction; Peroxisomal Disorders; Peroxisomes; Phosphatidylcholines; Zellweger Syndrome | 2014 |
Phospholipase D activity is altered in X-linked adrenoleukodystrophy heterozygous carriers, but not in hemizygous patients.
Topics: Carrier State; Cells, Cultured; Choline; Enzyme Activation; Female; Fibroblasts; Genetic Linkage; Humans; Intracellular Signaling Peptides and Proteins; Isoenzymes; Male; Membrane Proteins; Monosomy; Myristoylated Alanine-Rich C Kinase Substrate; Oleic Acid; Peroxisomal Disorders; Phosphatidylcholines; Phospholipase D; Protein Kinase C; Proteins; Sex Chromosome Aberrations; Tetradecanoylphorbol Acetate; X Chromosome; Zellweger Syndrome | 1998 |