glycine has been researched along with Lipidoses in 5 studies
Lipidoses: Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Drug-induced phospholipidosis is one of the significant concerns in drug development, especially in safety assessment and noninvasive diagnostic tool is highly desirable." | 1.46 | Biomarker discovery for drug-induced phospholipidosis: phenylacetylglycine to hippuric acid ratio in urine and plasma as potential markers. ( Higaki, K; Horinouchi, A; Kamiguchi, H; Mori, I; Murabayashi, M, 2017) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kamiguchi, H | 1 |
| Murabayashi, M | 1 |
| Mori, I | 1 |
| Horinouchi, A | 1 |
| Higaki, K | 1 |
| GEROK, W | 1 |
| PABST, K | 1 |
| Perkoff, GT | 1 |
| Palo, J | 1 |
| Saifer, A | 1 |
| Kolkmann, W | 1 |
2 reviews available for glycine and Lipidoses
| Article | Year |
|---|---|
[ON THE PATHOPHYSIOLOGY AND CLINICAL MANIFESTATIONS OF DISORDERS OF RENAL TUBULAR PARTIAL FUNCTION].
Topics: Acidosis; Acidosis, Renal Tubular; Amino Acids; Cystinuria; Diabetes Insipidus; Glycine; Glycosuria; | 1965 |
The hereditary renal diseases.
Topics: Acidosis, Renal Tubular; Bone Diseases; Chronic Kidney Disease-Mineral and Bone Disorder; Cystinuria | 1967 |
3 other studies available for glycine and Lipidoses
| Article | Year |
|---|---|
Biomarker discovery for drug-induced phospholipidosis: phenylacetylglycine to hippuric acid ratio in urine and plasma as potential markers.
Topics: Animals; Biomarkers; Drug Monitoring; Glycine; Hippurates; Lipidoses; Metabolomics; Phospholipids; R | 2017 |
The amino acid composition of gray matter ganglioside-peptides of normal human and Tay-Sachs brains.
Topics: Alanine; Amino Acids; Aspartic Acid; Brain Chemistry; Chromatography, Ion Exchange; Cystine; Ganglio | 1970 |
[Findings concerning the glia in diffuse and focally disseminated types of infantile spongy neurodystrophy].
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases; Demyelinating Diseases; Glycine; Humans; Infan | 1968 |