glycine has been researched along with Lecithin Cholesterol Acyltransferase Deficiency in 2 studies
Lecithin Cholesterol Acyltransferase Deficiency: An autosomal recessive disorder of lipoprotein metabolism caused by mutation of LECITHIN CHOLESTEROL ACYLTRANSFERASE gene. It is characterized by low HDL-cholesterol levels, and the triad of CORNEAL OPACITIES; HEMOLYTIC ANEMIA; and PROTEINURIA with renal failure.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wiebusch, H | 1 |
| Cullen, P | 1 |
| Owen, JS | 1 |
| Collins, D | 1 |
| Sharp, PS | 1 |
| Funke, H | 1 |
| Assmann, G | 1 |
| Moriyama, K | 1 |
| Sasaki, J | 1 |
| Arakawa, F | 1 |
| Takami, N | 1 |
| Maeda, E | 1 |
| Matsunaga, A | 1 |
| Takada, Y | 1 |
| Midorikawa, K | 1 |
| Yanase, T | 1 |
| Yoshino, G | 1 |
2 other studies available for glycine and Lecithin Cholesterol Acyltransferase Deficiency
| Article | Year |
|---|---|
Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene.
Topics: Adolescent; Aged; Amino Acid Sequence; Arginine; Base Sequence; Female; Glycine; Heterozygote; Human | 1995 |
Two novel point mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in LCAT deficiency: LCAT (G873 deletion) and LCAT (Gly344-->Ser).
Topics: Adult; Amino Acid Sequence; Animals; Base Sequence; Blotting, Northern; Cell Line; Cricetinae; Gene | 1995 |