Page last updated: 2024-11-06

hydroxyproline and Oxaluria, Primary

hydroxyproline has been researched along with Oxaluria, Primary in 10 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.

Research Excerpts

ExcerptRelevanceReference
"The major clinical manifestation of the Primary Hyperoxalurias (PH) is increased production of oxalate, as a consequence of genetic mutations that lead to aberrant glyoxylate and hydroxyproline metabolism."1.56The effects of the inactivation of Hydroxyproline dehydrogenase on urinary oxalate and glycolate excretion in mouse models of primary hyperoxaluria. ( Buchalski, B; Challa, A; Fargue, S; Holmes, RP; Knight, J; Lowther, WT; Wood, KD, 2020)
"The primary hyperoxalurias are diseases of overproduction of oxalate."1.334-Hydroxyproline metabolism and glyoxylate production: A target for substrate depletion in primary hyperoxaluria? ( Coulter-Mackie, MB, 2006)

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (10.00)29.6817
2010's6 (60.00)24.3611
2020's3 (30.00)2.80

Authors

AuthorsStudies
Belostotsky, R2
Frishberg, Y2
Buchalski, B2
Wood, KD1
Challa, A1
Fargue, S2
Holmes, RP5
Lowther, WT4
Knight, J4
Assimos, DG1
Siener, R1
Hoppe, B1
Löhr, P1
Müller, SC1
Latz, S1
Summitt, CB1
Johnson, LC2
Jönsson, TJ1
Parsonage, D1
Li, X1
Guan, Z1
Inscho, EW1
Liebow, A1
Fitzgerald, K1
Querbes, W1
Todd Lowther, W1
Seboun, E1
Idelson, GH1
Milliner, DS2
Becker-Cohen, R1
Rinat, C1
Monico, CG1
Feinstein, S1
Ben-Shalom, E1
Magen, D1
Weissman, I1
Charon, C1
Riedel, TJ2
Hantgan, RR1
Murray, MS1
Coulter-Mackie, MB1

Reviews

1 review available for hydroxyproline and Oxaluria, Primary

ArticleYear
Catabolism of Hydroxyproline in Vertebrates: Physiology, Evolution, Genetic Diseases and New siRNA Approach for Treatment.
    International journal of molecular sciences, 2022, Jan-17, Volume: 23, Issue:2

    Topics: Animals; Evolution, Molecular; Genetic Predisposition to Disease; Glyoxylates; Humans; Hydrogen Pero

2022

Other Studies

9 other studies available for hydroxyproline and Oxaluria, Primary

ArticleYear
The effects of the inactivation of Hydroxyproline dehydrogenase on urinary oxalate and glycolate excretion in mouse models of primary hyperoxaluria.
    Biochimica et biophysica acta. Molecular basis of disease, 2020, 03-01, Volume: 1866, Issue:3

    Topics: Amino Acid Sequence; Animals; Base Sequence; Calcium; Disease Models, Animal; Female; Glycolates; Hu

2020
Re: The Effects of the Inactivation of Hydroxyproline Dehydrogenase on Urinary Oxalate and Glycolate Excretion in Mouse Models of Primary Hyperoxaluria.
    The Journal of urology, 2020, Volume: 203, Issue:5

    Topics: Animals; Glycolates; Hydroxyproline; Hyperoxaluria; Hyperoxaluria, Primary; Mice; Oxalates; Oxidored

2020
Metabolic profile and impact of diet in patients with primary hyperoxaluria.
    International urology and nephrology, 2018, Volume: 50, Issue:9

    Topics: Acidosis, Renal Tubular; Adolescent; Adult; Calcium; Child; Creatinine; Diet; Diet Records; Humans;

2018
Proline dehydrogenase 2 (PRODH2) is a hydroxyproline dehydrogenase (HYPDH) and molecular target for treating primary hyperoxaluria.
    The Biochemical journal, 2015, Mar-01, Volume: 466, Issue:2

    Topics: Biocatalysis; Catalytic Domain; Enzyme Inhibitors; Flavin-Adenine Dinucleotide; Flavoproteins; Furan

2015
Metabolism of (13)C5-hydroxyproline in mouse models of Primary Hyperoxaluria and its inhibition by RNAi therapeutics targeting liver glycolate oxidase and hydroxyproline dehydrogenase.
    Biochimica et biophysica acta, 2016, Volume: 1862, Issue:2

    Topics: Alcohol Oxidoreductases; Animals; Disease Models, Animal; Hydroxyproline; Hyperoxaluria, Primary; Li

2016
Mutations in DHDPSL are responsible for primary hyperoxaluria type III.
    American journal of human genetics, 2010, Sep-10, Volume: 87, Issue:3

    Topics: Alleles; Amino Acid Sequence; Base Sequence; Child; Child, Preschool; DNA Mutational Analysis; Famil

2010
Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria.
    PloS one, 2011, Volume: 6, Issue:10

    Topics: Amino Acid Sequence; Animals; Apoenzymes; Bacteria; Catalytic Domain; Cattle; Crystallography, X-Ray

2011
4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition.
    Biochimica et biophysica acta, 2012, Volume: 1822, Issue:10

    Topics: Alcohol Oxidoreductases; Animals; Cells, Cultured; CHO Cells; Cricetinae; Glutarates; Humans; Hydrox

2012
4-Hydroxyproline metabolism and glyoxylate production: A target for substrate depletion in primary hyperoxaluria?
    Kidney international, 2006, Volume: 70, Issue:11

    Topics: Adult; Female; Glyoxylates; Humans; Hydroxyproline; Hyperoxaluria, Primary; Male; Oxalates

2006