Results 31 to 40 of about 766 (123)
Xanthine oxidase activity in thiopurine curative Chinese inflammatory bowel disease patients
Xanthine oxidase (XO) competes with thiopurine S‐methyltransferase (TPMT) and hypoxanthine guanine phosphoribosyltransferase (HPRT) to metabolize azathioprine (AZA)/6‐mercaptopurine (6‐MP) in vivo. A retrospective investigation was performed to detect the activity of XO in thiopurine curative Chinese inflammatory bowel disease (IBD) patients.
Liang Ding +11 more
wiley +1 more source
Urolithiasis in dogs: Evaluation of trends in urolith composition and risk factors (2006‐2018)
Abstract Background Urolithiasis is a common and often recurrent problem in dogs. Objective To evaluate trends in urolith composition in dogs and to assess risk factors for urolithiasis, including age, breed, sex, neuter status, urolith location, and bacterial urolith cultures.
Lucy Kopecny +3 more
wiley +1 more source
Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease
Diabetic type 2 patients compared to nondiabetic patients exhibit an increased risk of developing diabetic kidney disease (DKD), the leading cause of end‐stage renal disease. Hyperglycemia, hypertension, oxidative stress (OS), and genetic background are some of the mechanisms and pathways implicated in DKD pathogenesis.
Athanasios Roumeliotis +12 more
wiley +1 more source
A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle [PDF]
Background Renal syndromes are occasionally reported in domestic animals. Two identical twin Tyrolean Grey calves exhibited weight loss, skeletal abnormalities and delayed development associated with kidney abnormalities and formation of uroliths ...
Piffer, Christian +22 more
core +5 more sources
A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency. [PDF]
Xanthinurias are rare inherited disorders of purine metabolism. Xanthinuria type III is caused by molybdenum cofactor deficiency (MoCD) due to pathogenic variants in MOCS1, MOCS2, MOCS3, or GEPH genes.
Cho SK +13 more
europepmc +2 more sources
International audienceBackground : Xanthinuria type II is a rare autosomal purine disorder. This recessive defect of purine metabolism remains an underrecognized disorder.
Pailloux, Julie +31 more
core +1 more source
Inborn errors of metabolism that may lead to calculus formation within the urinary tract include: adenine phosphoribosyltransferase deficiency, xanthine oxidase deficiency, orotic aciduria (acidosis) type I and alkaptonuria.
Piotr Skrzypczyk +1 more
doaj +1 more source
Xanthinuria in a family of Cavalier King Charles spaniels
Xanthine calculi mere found in a 7-month-old male Cavalier King Charles spaniel with urethral obstruction and renal insufficiency, Because the only two other reported cases of naturally occurring xanthine urolithiasis concerned a Cavalier King Charles ...
Nickel, RF +3 more
core +2 more sources
Leishmaniosis caused by Leishmania infantum in ferrets: Update review
Leishmaniosis in domestic ferrets (Mustela putorius furo) is a disease caused by Leishmania infantum, a parasite transmitted through the bite of an infected female phlebotomine sand fly. Among vertebrates, the dog is the primary domestic reservoir of the
Sergio Villanueva-Saz +8 more
doaj +1 more source
Differential regulation of hypoxanthine and xanthine by obesity in a general population
In the present study, we investigated the associations of obesity with hypoxanthine, xanthine and plasma xanthine oxidoreductase activity in 484 participants from the general population. The concentration of hypoxanthine was independently associated with body mass index and smoking habit, whereas the level of xanthine was associated with parameters of ...
Masato Furuhashi +12 more
wiley +1 more source

