hydroxyproline has been researched along with Abnormalities, Autosome in 5 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In patients with Klinefelter's syndrome at the age below 11 and above 17 years normal hydroxyproline values were observed." | 1.26 | Urinary total hydroxyproline excretion in patients with Turner's syndrome and Klinefelter's syndrome. ( Jakubowski, L, 1981) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (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 |
|---|---|
| SCHMIDT, M | 1 |
| BARZILAI, D | 1 |
| BEN-MOSHE, H | 1 |
| Jakubowski, L | 1 |
| Kanwar, YS | 1 |
| Krakower, CA | 1 |
| Manaligod, JR | 1 |
| Justice, P | 1 |
| Wong, PW | 1 |
| Douglas, EP | 1 |
| Rosenberg, LE | 1 |
| Durant, JL | 1 |
| Elsas, LJ | 1 |
5 other studies available for hydroxyproline and Abnormalities, Autosome
| Article | Year |
|---|---|
[MARFAN'S SYNDROME].
Topics: Anthropometry; Arachnodactyly; Blood Chemical Analysis; Chromosome Aberrations; Chromosome Disorders | 1963 |
Urinary total hydroxyproline excretion in patients with Turner's syndrome and Klinefelter's syndrome.
Topics: Adolescent; Age Factors; Child; Chromosome Aberrations; Female; Humans; Hydroxyproline; Karyotyping; | 1981 |
Biochemical, morphological and hybrid studies in hyperprolinemic mice.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Animals; Chromosome Aberrations; C | 1975 |
Hyperprolinaemia and gyrate atrophy of the choroid and retina in members of the same family.
Topics: Adult; Atrophy; Child; Choroid; Chromosome Aberrations; Chromosome Disorders; Female; Fundus Oculi; | 1985 |
Familial iminoglycinuria. An inborn error of renal tubular transport.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Genotype; Glycine; Het | 1968 |