 Hyperoxaluria
"Hyperoxaluria" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Excretion of an excessive amount of OXALATES in the urine.
| Descriptor ID |
D006959
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| MeSH Number(s) |
C12.777.419.313 C13.351.968.419.313
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hyperoxaluria".
Below are MeSH descriptors whose meaning is more specific than "Hyperoxaluria".
This graph shows the total number of publications written about "Hyperoxaluria" by people in this website by year, and whether "Hyperoxaluria" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyperoxaluria" by people in Profiles.
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Khandrika L, Koul S, Meacham RB, Koul HK. Kidney injury molecule-1 is up-regulated in renal epithelial cells in response to oxalate in vitro and in renal tissues in response to hyperoxaluria in vivo. PLoS One. 2012; 7(9):e44174.
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Knight J, Holmes RP, Cramer SD, Takayama T, Salido E. Hydroxyproline metabolism in mouse models of primary hyperoxaluria. Am J Physiol Renal Physiol. 2012 Mar 15; 302(6):F688-93.
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Wesson JA, Johnson RJ, Mazzali M, Beshensky AM, Stietz S, Giachelli C, Liaw L, Alpers CE, Couser WG, Kleinman JG, Hughes J. Osteopontin is a critical inhibitor of calcium oxalate crystal formation and retention in renal tubules. J Am Soc Nephrol. 2003 Jan; 14(1):139-47.
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Cramer SD, Ferree PM, Lin K, Milliner DS, Holmes RP. The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II. Hum Mol Genet. 1999 Oct; 8(11):2063-9.
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