phosphatidylcholines has been researched along with Cerebro-Hepato-Renal Syndrome in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (14.29) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hama, K; Ikeda, K; Imanaka, T; Inoue, K; Morita, M; Nagai, T; Nakanishi, H; Nishizawa, C; Satoh, N; Shimozawa, N; Taguchi, R; Yokoyama, K | 1 |
| Abe, Y; Fujiki, Y; Honsho, M; Nakanishi, H; Taguchi, R | 1 |
| Coppens, I; Jayabalasingham, B; Lige, B; Pypaert, M; Zhang, H | 1 |
| Byers, DM; Cook, HW; Logan, HE; Ridgway, ND | 1 |
| Fang, X; Kaduce, TL; Spector, AA | 1 |
| Johnson, D; Poulos, A; Sharp, P | 1 |
| Martinez, M | 1 |
7 other study(ies) available for phosphatidylcholines and Cerebro-Hepato-Renal Syndrome
| Article | Year |
|---|---|
Molecular species of phospholipids with very long chain fatty acids in skin fibroblasts of Zellweger syndrome.
Topics: Adrenoleukodystrophy; Fatty Acids; Fibroblasts; Humans; Phosphatidylcholines; Phospholipids; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry; Zellweger Syndrome | 2013 |
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 |
Role of an ancestral d-bifunctional protein containing two sterol-carrier protein-2 domains in lipid uptake and trafficking in Toxoplasma.
Topics: 17-Hydroxysteroid Dehydrogenases; Amino Acid Sequence; Animals; Biological Transport; Carrier Proteins; Cell Line; Cholesterol; Humans; Hydro-Lyases; Lipid Metabolism; Membrane Lipids; Molecular Sequence Data; Peroxisomal Multifunctional Protein-2; Peroxisomes; Phosphatidylcholines; Protein Processing, Post-Translational; Protozoan Proteins; Recombinant Fusion Proteins; Sequence Alignment; Sterols; Toxoplasma; Zellweger Syndrome | 2009 |
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 |
13-(S)-hydroxyoctadecadienoic acid (13-HODE) incorporation and conversion to novel products by endothelial cells.
Topics: Animals; Aorta, Thoracic; Cattle; Cells, Cultured; Chromatography, High Pressure Liquid; Endothelium, Vascular; Extracellular Space; Fibroblasts; Gas Chromatography-Mass Spectrometry; Humans; Kinetics; Linoleic Acids; Lipid Metabolism; Phosphatidylcholines; Skin; Tritium; Zellweger Syndrome | 1999 |
Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain.
Topics: Adolescent; Adrenoleukodystrophy; Aged; Aged, 80 and over; Brain; Brain Chemistry; Child; Child, Preschool; Chromatography, High Pressure Liquid; Diglycerides; Fatty Acids; Female; Humans; Infant, Newborn; Magnetic Resonance Spectroscopy; Male; Microbodies; Middle Aged; Phosphatidylcholines; Phospholipases A; Refsum Disease; X Chromosome; Zellweger Syndrome | 1991 |
Polyunsaturated fatty acid changes suggesting a new enzymatic defect in Zellweger syndrome.
Topics: Brain; Erythrocytes; Fatty Acids, Unsaturated; Fibroblasts; Humans; Infant; Kidney; Liver; Phosphatidylcholines; Phosphatidylethanolamines; Plasmalogens; Zellweger Syndrome | 1989 |