hydroxyproline has been researched along with Cystinosis in 2 studies
Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.
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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Wellner, D | 1 |
| Meister, A | 1 |
| Tănase-Mogoş, I | 1 |
| Ciortoloman, H | 1 |
| Petrescu, L | 1 |
| Pâtea, P | 1 |
| Popescu, M | 1 |
| Ankăr, V | 1 |
| Grigorescu, G | 1 |
1 review available for hydroxyproline and Cystinosis
| Article | Year |
|---|---|
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 |
1 other study available for hydroxyproline and Cystinosis
| Article | Year |
|---|---|
[Metabolic errors of the cystinuria-lysinuria, cystinosis type detected in the newborn infant and child with renal and ocular diseases].
Topics: Adolescent; Child; Child, Preschool; Cystinosis; Cystinuria; Eye Diseases; Female; Humans; Hydroxypr | 1981 |