hydroxyproline has been researched along with Nephritis, Hereditary 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.
Nephritis, Hereditary: A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
Excerpt | Relevance | Reference |
---|---|---|
", an increased ratio of dextrorotatory (D) to levorotatory (L) amino acid molecules), we studied by high-performance liquid chromatography the renal excretion of the D-form of the basement membrane-specific trans-3-hydroxyproline in patients with Alport syndrome." | 7.68 | Determination of the urinary D/L trans-3-hydroxyproline ratio: a noninvasive screening test for Alport syndrome. ( Arbeiter, K; Lubec, B, 1993) |
", an increased ratio of dextrorotatory (D) to levorotatory (L) amino acid molecules), we studied by high-performance liquid chromatography the renal excretion of the D-form of the basement membrane-specific trans-3-hydroxyproline in patients with Alport syndrome." | 3.68 | Determination of the urinary D/L trans-3-hydroxyproline ratio: a noninvasive screening test for Alport syndrome. ( Arbeiter, K; Lubec, B, 1993) |
"Alport's syndrome is characterised by morphological and structural changes of the renal basement membranes." | 1.28 | Urinary 3-hydroxyproline excretion in Alport's syndrome: a non-invasive screening test? ( Bartosch, B; Lubec, G; Popow, C; Vycudilik, W, 1991) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (40.00) | 18.7374 |
1990's | 2 (40.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
KOPELMAN, H | 1 |
ASATOOR, AM | 1 |
MILNE, MD | 1 |
Morzaria, S | 1 |
Westerberg, BD | 1 |
Kozak, FK | 1 |
Vel'tishchev, IuE | 1 |
Ananenko, AA | 1 |
Daĭkhin, EI | 1 |
Klembovskiĭ, AI | 1 |
Ignatova, MS | 1 |
Lubec, B | 1 |
Arbeiter, K | 1 |
Bartosch, B | 1 |
Vycudilik, W | 1 |
Popow, C | 1 |
Lubec, G | 1 |
1 review available for hydroxyproline and Nephritis, Hereditary
Article | Year |
---|---|
Evidence-based algorithm for the evaluation of a child with bilateral sensorineural hearing loss.
Topics: Algorithms; Child; Connexin 26; Connexins; Ear, Inner; Electrocardiography; Evidence-Based Medicine; | 2005 |
4 other studies available for hydroxyproline and Nephritis, Hereditary
Article | Year |
---|---|
HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Blood; Blood Chemical | 1964 |
[Renal excretion of connective tissue metabolites and the state of the glomerular basement membranes in hereditary nephritis in children].
Topics: Adolescent; Basement Membrane; Child; Child, Preschool; Connective Tissue; Female; Glycosaminoglycan | 1981 |
Determination of the urinary D/L trans-3-hydroxyproline ratio: a noninvasive screening test for Alport syndrome.
Topics: Adolescent; Adult; Biomarkers; Child; Child, Preschool; Chromatography, High Pressure Liquid; Female | 1993 |
Urinary 3-hydroxyproline excretion in Alport's syndrome: a non-invasive screening test?
Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Chromatography, Thin Layer; Female; Humans; | 1991 |