hydroxyproline has been researched along with Genetic Diseases in 3 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Li, S | 1 |
| Lu, J | 1 |
| Li, J | 1 |
| Chen, X | 1 |
| Yao, X | 1 |
| Xi, L | 1 |
| Askerova, TA | 1 |
| Iusifova, NA | 1 |
| Gasanova, GT | 1 |
| Kerimova, AR | 1 |
| Rokkones, T | 1 |
| Loken, AC | 1 |
3 other studies available for hydroxyproline and Genetic Diseases
| Article | Year |
|---|---|
HydPred: a novel method for the identification of protein hydroxylation sites that reveals new insights into human inherited disease.
Topics: Amino Acid Sequence; Genetic Diseases, Inborn; Humans; Hydroxylation; Hydroxylysine; Hydroxyproline; | 2016 |
[Diagnostic value of the determination of free oxyproline in hereditary and acquired collagenoses].
Topics: Adult; Aged; Connective Tissue Diseases; Female; Genetic Diseases, Inborn; Humans; Hydroxyproline; M | 2009 |
Congenital renal dysplasia, retinal dysplasia and mental retardation associated with hyperprolinuria and hyper-oh-prolinuria.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Female; Genetic Diseases, Inborn; Hu | 1968 |