glycine has been researched along with Cystinosis in 8 studies
Cystinosis: A metabolic disease characterized by the defective transport of CYSTINE across the lysosomal membrane due to mutation of a membrane protein cystinosin. This results in cystine accumulation and crystallization in the cells causing widespread tissue damage. In the KIDNEY, nephropathic cystinosis is a common cause of RENAL FANCONI SYNDROME.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In order to clarify the hyperglycinemic effect of cysteamine treatment in children with nephropathic cystinosis, we measured [15N]-glycine turnover in three affected patients." | 7.66 | Cysteamine inhibition of [15N]-glycine turnover in cystinosis and of glycine cleavage system in vitro. ( Nissim, I; Schneider, A; Segal, S; Yudkoff, M, 1981) |
| "In order to clarify the hyperglycinemic effect of cysteamine treatment in children with nephropathic cystinosis, we measured [15N]-glycine turnover in three affected patients." | 3.66 | Cysteamine inhibition of [15N]-glycine turnover in cystinosis and of glycine cleavage system in vitro. ( Nissim, I; Schneider, A; Segal, S; Yudkoff, M, 1981) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (87.50) | 18.7374 |
| 1990's | 1 (12.50) | 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 |
|---|---|
| MILNE, MD | 1 |
| Wellner, D | 1 |
| Meister, A | 1 |
| Yudkoff, M | 1 |
| Nissim, I | 1 |
| Schneider, A | 1 |
| Segal, S | 1 |
| Greco, GM | 1 |
| Magli, A | 1 |
| Sakarcan, A | 1 |
| Aricheta, R | 1 |
| Baum, M | 1 |
| Kroll, WA | 1 |
| Becker, FL | 1 |
| Schneider, JA | 1 |
| Kroll, S | 2 |
| Zebisch, P | 2 |
| Toussaint, W | 2 |
3 reviews available for glycine and Cystinosis
| Article | Year |
|---|---|
[RENAL TUBULAR DISEASES, WITH SPECIAL REFERENCE TO AMINOACIDURIA].
Topics: Cystinosis; Cystinuria; Galactosemias; Genetics, Medical; Glycine; Hepatolenticular Degeneration; Hu | 1964 |
A survey of inborn errors of amino acid metabolism and transport in man.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Branched-Chain; Biological Transport | 1981 |
[Eye manifestations of amino acid disorders].
Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria | 1978 |
5 other studies available for glycine and Cystinosis
| Article | Year |
|---|---|
Cysteamine inhibition of [15N]-glycine turnover in cystinosis and of glycine cleavage system in vitro.
Topics: Coenzyme A; Cysteamine; Cystinosis; Decarboxylation; Glycine; Humans; In Vitro Techniques; Kinetics; | 1981 |
Intracellular cystine loading causes proximal tubule respiratory dysfunction: effect of glycine.
Topics: Animals; Cystine; Cystinosis; Glycine; In Vitro Techniques; Kidney Tubules, Proximal; Models, Biolog | 1992 |
Measurement of intracellular amino acids in cultured skin fibroblasts. The effect of storage on cystine recovery and evaluation of three methods of cell preparation.
Topics: Alanine; Amino Acids; Cells, Cultured; Cysteine; Cystinosis; Edetic Acid; Female; Fibroblasts; Freez | 1974 |
[Hereditary amino acid metabolism disorders. Indications for early diagnosis].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; | 1972 |
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Labora | 1972 |