hydroxyproline has been researched along with Genetic Predisposition in 7 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 |
|---|---|---|
| " Hyperoxaluria was induced by adding hydroxyproline (HP) to the drinking water." | 3.75 | Dissecting the genetic basis of kidney tubule response to hyperoxaluria using chromosome substitution strains. ( Garrett, MR; Mandel, NS; Roman, RJ; Wiessner, JH, 2009) |
| "Paget's disease of bone affects one or more bones and is characterized by increased bone turnover (remodelling) with hypertrophy and abnormal bone structure with diminished strength leading to deformity and fracture." | 2.40 | [Paget's disease of the bones: diagnosis and treatment]. ( Bijlsma, JW; Huisman, AM; Jacobs, JW; van Paassen, HC, 1999) |
| "Early-onset familial Paget disease of bone (EoPDB) is a rare condition caused by a 27-bp insertion mutation affecting the signal peptide of TNFRSF11A, which encodes RANK." | 1.35 | Clinical and biochemical response of TNFRSF11A-mediated early-onset familial Paget disease to bisphosphonate therapy. ( Imanishi, Y; Nakatsuka, K; Ralston, SH; Riches, PL, 2008) |
| "This inflammation is accompanied by lower levels of CTGF and tissue inhibitor of metalloproteinase-1 gene expression compared with fibrosis-prone C57BL/6 mice." | 1.32 | Connective tissue growth factor is crucial to inducing a profibrotic environment in "fibrosis-resistant" BALB/c mouse lungs. ( Ask, K; Bonniaud, P; Gauldie, J; Kolb, M; Margetts, PJ; Martin, G; Robertson, J, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Belostotsky, R | 1 |
| Frishberg, Y | 1 |
| Li, X | 1 |
| Ding, Y | 1 |
| Liu, Y | 1 |
| Ma, Y | 1 |
| Song, J | 1 |
| Wang, Q | 1 |
| Yang, Y | 1 |
| Riches, PL | 1 |
| Imanishi, Y | 1 |
| Nakatsuka, K | 1 |
| Ralston, SH | 1 |
| Wiessner, JH | 1 |
| Garrett, MR | 1 |
| Roman, RJ | 1 |
| Mandel, NS | 1 |
| Bonniaud, P | 1 |
| Martin, G | 1 |
| Margetts, PJ | 1 |
| Ask, K | 1 |
| Robertson, J | 1 |
| Gauldie, J | 1 |
| Kolb, M | 1 |
| Jacobs, JW | 1 |
| Huisman, AM | 1 |
| van Paassen, HC | 1 |
| Bijlsma, JW | 1 |
| Langdahl, BL | 1 |
| Løkke, E | 1 |
| Carstens, M | 1 |
| Stenkjaer, LL | 1 |
| Eriksen, EF | 1 |
2 reviews available for hydroxyproline and Genetic Predisposition
| Article | Year |
|---|---|
Catabolism of Hydroxyproline in Vertebrates: Physiology, Evolution, Genetic Diseases and New siRNA Approach for Treatment.
Topics: Animals; Evolution, Molecular; Genetic Predisposition to Disease; Glyoxylates; Humans; Hydrogen Pero | 2022 |
[Paget's disease of the bones: diagnosis and treatment].
Topics: Adult; Aged; Alkaline Phosphatase; Arthralgia; Arthroplasty, Replacement; Calcium; Diphosphonates; F | 1999 |
5 other studies available for hydroxyproline and Genetic Predisposition
| Article | Year |
|---|---|
Five Chinese patients with 5-oxoprolinuria due to glutathione synthetase and 5-oxoprolinase deficiencies.
Topics: Amino Acid Metabolism, Inborn Errors; Asian People; Case-Control Studies; Child, Preschool; China; F | 2015 |
Clinical and biochemical response of TNFRSF11A-mediated early-onset familial Paget disease to bisphosphonate therapy.
Topics: Adult; Alkaline Phosphatase; Bone Density Conservation Agents; Creatinine; Diphosphonates; Female; G | 2008 |
Dissecting the genetic basis of kidney tubule response to hyperoxaluria using chromosome substitution strains.
Topics: Animals; Animals, Congenic; Calcium Oxalate; Chromosomes, Mammalian; Disease Models, Animal; Genetic | 2009 |
Connective tissue growth factor is crucial to inducing a profibrotic environment in "fibrosis-resistant" BALB/c mouse lungs.
Topics: Adenoviridae; Animals; Bleomycin; Bronchoalveolar Lavage; Connective Tissue Growth Factor; DNA Prime | 2004 |
Osteoporotic fractures are associated with an 86-base pair repeat polymorphism in the interleukin-1--receptor antagonist gene but not with polymorphisms in the interleukin-1beta gene.
Topics: Adult; Aged; Animals; Biomarkers; Bone Density; Bone Remodeling; Bone Resorption; Case-Control Studi | 2000 |