phosphatidylcholines has been researched along with alpha-LCAT Deficiency in 21 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (61.90) | 18.7374 |
| 1990's | 3 (14.29) | 18.2507 |
| 2000's | 5 (23.81) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akamatsu, A; Desaki, J; Masuda, Y; Nakaya, Y; Suda, T | 1 |
| Ayyobi, AF; Chan, S; Frohlich, JJ; Hill, JS; John Mancini, GB; McGladdery, SH | 1 |
| Fan, P; Kumagai, K; McMahon, M; Miura, S; Rye, KA; Saku, K; Takeuchi, K; Uehara, Y; Zhang, B | 1 |
| Buckley, JT; Frohlich, J; McLeod, R | 1 |
| Small, DM; Tall, AR | 1 |
| Jain, SK; Mohandas, N; Sensabaugh, GF; Shohet, SB; Shojania, AM | 1 |
| Arakawa, K; Itabe, H; Jimi, S; Saku, K; Takebayashi, S; Uesugi, N; Zhang, B | 1 |
| Hosoya, R; Imanaka, T; Itabe, H; Jimi, S; Karasawa, K; Saku, K; Takano, T; Takebayashi, S | 1 |
| Benlian, P; Chisholm, JW; de Gennes, JL; Dolphin, PJ; Pouliquen, Y; Savoldelli, M; Teh, EM | 1 |
| Cheung, GT; Frohlich, J; Lynn, EG; O, K; Siow, YL | 1 |
| Ahmed, Z; Connelly, PW; Eskandarian, M; Kuksis, A; Maguire, GF; Ng, DS; Ravandi, A; Wylie, J; Xuan, W | 1 |
| Godin, DV; Herring, FG; Maraviglia, B; Weeks, G | 1 |
| Glomset, JA; Verdery, RB | 1 |
| Dobson, RD; Frohlich, J; Rockerbie, RA | 1 |
| Iwamoto, A; Kato, H; Naito, C; Teramoto, T; Watanabe, T; Yamanaka, T | 1 |
| Kuiken, LB; Ragland, JB; Sabesin, SM | 1 |
| Gillett, MP; Owen, JS | 1 |
| Bruckdorfer, KR; Day, RC; Harry, DS; Hope, MJ; Hutton, RA; Lucy, JA; McIntyre, N; Owen, JS | 1 |
| Weed, RI | 1 |
| Blanche, PJ; Forte, TM; Gong, EL; Nichols, AV; Shore, VG; Weisgraber, KH | 1 |
| Pritchard, PH; Subbaiah, PV | 1 |
3 review(s) available for phosphatidylcholines and alpha-LCAT Deficiency
| Article | Year |
|---|---|
Body cholesterol removal: role of plasma high-density lipoproteins.
Topics: Animals; Apolipoproteins; Bile Acids and Salts; Cardiovascular Diseases; Cholesterol; Cholesterol Esters; Chylomicrons; Humans; Hyperlipoproteinemias; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Lipid Bilayers; Lipolysis; Lipoproteins, HDL; Lipoproteins, VLDL; Liposomes; Membranes; Micelles; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Phospholipids; Tangier Disease | 1980 |
Role of LCAT in cholesterol metabolism.
Topics: Acyltransferases; Apolipoproteins; Cholesterol; Chylomicrons; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins; Molecular Conformation; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Protein Conformation; Triglycerides | 1977 |
Membrane structure and its relation to haemolysis.
Topics: Abetalipoproteinemia; Anemia, Sickle Cell; Cell Membrane; Cell Membrane Permeability; Elliptocytosis, Hereditary; Erythrocytes; Erythrocytes, Abnormal; Heinz Bodies; Hematologic Diseases; Hemolysis; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Liver Cirrhosis, Biliary; Phosphatidylcholines; Spherocytosis, Hereditary | 1975 |
18 other study(ies) available for phosphatidylcholines and alpha-LCAT Deficiency
| Article | Year |
|---|---|
Alterations in erythrocyte membrane lipid and its fragility in a patient with familial lecithin:cholesterol acyltrasferase (LCAT) deficiency.
Topics: Adult; Cholesterol; Consanguinity; Erythrocyte Deformability; Erythrocyte Indices; Erythrocyte Membrane; Erythrocytes, Abnormal; Female; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Membrane Fluidity; Membrane Lipids; Osmotic Fragility; Pedigree; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Phosphatidylethanolamines | 2002 |
Lecithin: cholesterol acyltransferase (LCAT) deficiency and risk of vascular disease: 25 year follow-up.
Topics: Adolescent; Adult; Aged; Apolipoproteins B; Female; Follow-Up Studies; Heterozygote; Homozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins, HDL; Male; Middle Aged; Pedigree; Phosphatidylcholines; Ultrasonography; Vascular Diseases | 2004 |
ApoA-I/phosphatidylcholine discs remodels fast-migrating HDL into slow-migrating HDL as characterized by capillary isotachophoresis.
Topics: Apolipoprotein A-I; Electrophoresis, Capillary; High-Density Lipoproteins, Pre-beta; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins, HDL; Monitoring, Physiologic; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines | 2006 |
Action of a microbial glycerophospholipid:cholesterol acyltransferase on plasma from normal and LCAT-deficient subjects.
Topics: Acyltransferases; Aeromonas; Cholesterol; Cholesterol Esters; Humans; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins; Phosphatidylcholines; Time Factors | 1984 |
Hereditary plasma lecithin-cholesterol acyl transferase deficiency: a heterozygous variant with erythrocyte membrane abnormalities.
Topics: Adult; Cholesterol; Erythrocyte Indices; Erythrocyte Membrane; Erythrocytes; Fatty Acids; Female; Heterozygote; Humans; Hydrogen Peroxide; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Lipids; Male; Middle Aged; Pedigree; Phosphatidylcholines | 1982 |
Possible induction of renal dysfunction in patients with lecithin:cholesterol acyltransferase deficiency by oxidized phosphatidylcholine in glomeruli.
Topics: Adult; Child; Cholesterol, LDL; Fluorescent Antibody Technique; Humans; Hypertension, Renal; Kidney Glomerulus; Lecithin Cholesterol Acyltransferase Deficiency; Male; Microscopy, Electron; Mutation; Nephrotic Syndrome; Oxidation-Reduction; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Proteinuria | 1999 |
Metabolism of oxidized phosphatidylcholines formed in oxidized low density lipoprotein by lecithin-cholesterol acyltransferase.
Topics: 1-Alkyl-2-acetylglycerophosphocholine Esterase; Aryldialkylphosphatase; Blood; Cholesterol; Cholesterol Esters; Dithionitrobenzoic Acid; Esterases; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins, HDL; Lipoproteins, LDL; Oxidation-Reduction; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Phospholipases A; Reference Values; Sulfhydryl Reagents | 1999 |
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144.
Topics: Adolescent; Apolipoproteins; Base Sequence; Codon; Cornea; Corneal Opacity; DNA Mutational Analysis; Electrophoresis, Agar Gel; Exons; Female; Frameshift Mutation; Gene Deletion; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Molecular Sequence Data; Phenotype; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Polymerase Chain Reaction | 1999 |
Lipoprotein-X stimulates monocyte chemoattractant protein-1 expression in mesangial cells via nuclear factor-kappa B.
Topics: Amino Acid Sequence; Animals; Calcium Channel Blockers; Cells, Cultured; Chemokine CCL2; Chemotaxis, Leukocyte; Cholesterol; Diglycerides; Diltiazem; Enzyme Inhibitors; Foam Cells; Gene Expression; Genes, Recessive; Glomerular Mesangium; Glomerulosclerosis, Focal Segmental; Humans; Indoles; Lecithin Cholesterol Acyltransferase Deficiency; Lipoprotein-X; Male; Molecular Sequence Data; Monocytes; NF-kappa B; Phosphatidylcholines; Protein Kinase C; Pyrroles; Rats; Rats, Sprague-Dawley; RNA, Messenger; Staurosporine; Type C Phospholipases | 2001 |
Oxidative stress is markedly elevated in lecithin:cholesterol acyltransferase-deficient mice and is paradoxically reversed in the apolipoprotein E knockout background in association with a reduction in atherosclerosis.
Topics: Alleles; Animals; Aorta; Apolipoproteins E; Area Under Curve; Arteriosclerosis; Aryldialkylphosphatase; Chromatography, Liquid; Esterases; Genotype; Isoprostanes; Lecithin Cholesterol Acyltransferase Deficiency; Lipids; Mice; Mice, Knockout; Oxidative Stress; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Superoxides; Time Factors | 2002 |
Detection of erythrocyte membrane structural abnormalities in lecithin: cholesterol acyltransferase deficiency using a spin label approach.
Topics: Electron Spin Resonance Spectroscopy; Erythrocyte Membrane; Erythrocytes; Female; Heterozygote; Homozygote; Humans; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Male; Membrane Fluidity; Phosphatidylcholines; Temperature | 1979 |
Gas-chromatographic analysis of patterns of fatty acids of cholesteryl esters and phosphatidylcholine.
Topics: Adult; Arteriosclerosis; Cholesterol Esters; Chromatography, Gas; Fatty Acids; Humans; Infant, Newborn; Lecithin Cholesterol Acyltransferase Deficiency; Linoleic Acids; Oleic Acids; Phosphatidylcholines | 1979 |
Lipid compositions of plasma major lipoproteins and lipoprotein lipase activity in hypolipidemic and hyperlipidemic siblings with familial LCAT deficiency.
Topics: Adult; Cholesterol; Female; Heparin; Humans; Hyperlipidemias; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Lipids; Lipoprotein Lipase; Lipoproteins; Lysophosphatidylcholines; Male; Phosphatidylcholines; Phospholipids; Triglycerides | 1978 |
Lipoprotein abnormalities in galactosamine hepatitis: a model of experimental lecithin:cholesterol acyltransferase deficiency.
Topics: Acute Disease; Animals; Chemical and Drug Induced Liver Injury; Cholesterol; Cholesterol Esters; Disease Models, Animal; Female; Galactosamine; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Lipids; Lipoproteins; Lysophosphatidylcholines; Phosphatidylcholines; Phospholipids; Rats | 1978 |
Lecithin:cholesterol acyltransferase deficiency associated with hepatic schistosomiasis mansoni.
Topics: Adult; Animals; Cholesterol; Cholesterol Esters; Erythrocytes; Female; Humans; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Lipids; Male; Mice; Middle Aged; Phosphatidylcholines; Phospholipids; Schistosoma mansoni; Schistosomiasis | 1978 |
Lecithin:cholesterol acyltransferase deficiency and cell membrane lipids and function in human liver disease.
Topics: Blood Platelets; Cell Membrane Permeability; Cholesterol; Erythrocyte Membrane; Erythrocytes; Humans; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Liver Diseases; Membrane Lipids; Phosphatidylcholines; Phospholipids; Sodium | 1978 |
Discoidal complexes containing apolipoprotein E and their transformation by lecithin-cholesterol acyltransferase.
Topics: Apolipoproteins E; Chemical Phenomena; Chemistry, Physical; Cholesterol; Cholic Acid; Cholic Acids; Dialysis; Electrophoresis, Polyacrylamide Gel; Humans; Immunoblotting; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins, HDL; Microscopy, Electron; Particle Size; Phosphatidylcholine-Sterol O-Acyltransferase; Phosphatidylcholines; Ultracentrifugation | 1989 |
Molecular species of phosphatidylcholine in familial lecithin-cholesterol acyltransferase deficiency: effect of enzyme supplementation.
Topics: Adult; Chromatography, High Pressure Liquid; Female; Humans; Hypolipoproteinemias; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins; Male; Molecular Structure; Phosphatidylcholines | 1989 |