165 related articles for article (PubMed ID: 30758870)
1. Hereditary xanthinuria in a goat.
Vail KJ; Tate NM; Likavec T; Minor KM; Gibbons PM; Rech RR; Furrow E
J Vet Intern Med; 2019 Mar; 33(2):1009-1014. PubMed ID: 30758870
[TBL] [Abstract][Full Text] [Related]
2. Candidate causative variant for xanthinuria in a Domestic Shorthair cat.
Pritchard E; Samaha G; Mizzi K; Boland L; ; Haase B
Anim Genet; 2023 Aug; 54(4):576-580. PubMed ID: 36970934
[TBL] [Abstract][Full Text] [Related]
3. Multiple variants in
Tate NM; Minor KM; Lulich JP; Mickelson JR; Berent A; Foster JD; Petersen KH; Furrow E
Mol Genet Metab Rep; 2021 Dec; 29():100792. PubMed ID: 34584846
[TBL] [Abstract][Full Text] [Related]
4. Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II).
Stiburkova B; Pavelcova K; Petru L; Krijt J
Toxicol Appl Pharmacol; 2018 Aug; 353():102-108. PubMed ID: 29935280
[TBL] [Abstract][Full Text] [Related]
5. A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle.
Murgiano L; Jagannathan V; Piffer C; Diez-Prieto I; Bolcato M; Gentile A; Drögemüller C
BMC Vet Res; 2016 Dec; 12(1):276. PubMed ID: 27919260
[TBL] [Abstract][Full Text] [Related]
6. Deletion of
Sedda D; Mackowiak C; Pailloux J; Culerier E; Dudas A; Rontani P; Erard N; Lefevre A; Mavel S; Emond P; Foucher F; Le Bert M; Quesniaux VFJ; Mihatsch MJ; Ryffel B; Erard-Garcia M
Kidney360; 2021 Nov; 2(11):1793-1806. PubMed ID: 35372998
[TBL] [Abstract][Full Text] [Related]
7. Polymorphism of genes involved in purine metabolism (XDH, AOX1, MOCOS) in kidney transplant recipients receiving azathioprine.
Kurzawski M; Dziewanowski K; Safranow K; Drozdzik M
Ther Drug Monit; 2012 Jun; 34(3):266-74. PubMed ID: 22495427
[TBL] [Abstract][Full Text] [Related]
8. Xanthine urolithiasis in a cat: a case report and evaluation of a candidate gene for xanthine dehydrogenase.
Tsuchida S; Kagi A; Koyama H; Tagawa M
J Feline Med Surg; 2007 Dec; 9(6):503-8. PubMed ID: 17576085
[TBL] [Abstract][Full Text] [Related]
9. Hereditary xanthinuria is not so rare disorder of purine metabolism.
Sebesta I; Stiburkova B; Krijt J
Nucleosides Nucleotides Nucleic Acids; 2018; 37(6):324-328. PubMed ID: 29723117
[TBL] [Abstract][Full Text] [Related]
10. Xanthinuria type I: a rare cause of urolithiasis.
Arikyants N; Sarkissian A; Hesse A; Eggermann T; Leumann E; Steinmann B
Pediatr Nephrol; 2007 Feb; 22(2):310-4. PubMed ID: 17115198
[TBL] [Abstract][Full Text] [Related]
11. Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II.
Ichida K; Matsumura T; Sakuma R; Hosoya T; Nishino T
Biochem Biophys Res Commun; 2001 Apr; 282(5):1194-200. PubMed ID: 11302742
[TBL] [Abstract][Full Text] [Related]
12. Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.
Zhou Y; Zhang X; Ding R; Li Z; Hong Q; Wang Y; Zheng W; Geng X; Fan M; Cai G; Chen X; Wu D
Cell Physiol Biochem; 2015; 35(6):2412-21. PubMed ID: 25967871
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation in xanthine dehydrogenase in a case with xanthinuria in Hunan province of China.
Xu T; Xie X; Zhang Z; Zhao N; Deng Y; Li P
Clin Chim Acta; 2020 May; 504():168-171. PubMed ID: 32067994
[TBL] [Abstract][Full Text] [Related]
14. MOCOS-associated renal syndrome in a Brown Swiss cattle.
Jacinto JGP; Küchler LB; Peters LM; Van der Vekens E; Gurtner C; Seefried FR; Meylan M; Drögemüller C
J Vet Intern Med; 2023; 37(6):2603-2609. PubMed ID: 37675885
[TBL] [Abstract][Full Text] [Related]
15. Identification of a new point mutation in the human molybdenum cofactor sulferase gene that is responsible for xanthinuria type II.
Yamamoto T; Moriwaki Y; Takahashi S; Tsutsumi Z; Tuneyoshi K; Matsui K; Cheng J; Hada T
Metabolism; 2003 Nov; 52(11):1501-4. PubMed ID: 14624414
[TBL] [Abstract][Full Text] [Related]
16. Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria.
Gok F; Ichida K; Topaloglu R
Nephrol Dial Transplant; 2003 Nov; 18(11):2278-83. PubMed ID: 14551354
[TBL] [Abstract][Full Text] [Related]
17. Kidney failure secondary to hereditary xanthinuria due to a homozygous deletion of the XDH gene, in the absence of overt kidney stone disease.
Gonçalves PL; Diniz H; Tavares I; Dória S; Dong J; Kyriss M; Fairbanks L; Oliveira JP
Nephron; 2024 Mar; ():. PubMed ID: 38527446
[TBL] [Abstract][Full Text] [Related]
18. [Xanthinuria type I as the cause of nephrolithiasis in 17-years old girl].
Borucka B; Runowski D; Safranow K; Olszewska M; Jakubowska K; Chlubek D
Pol Merkur Lekarski; 2010 Aug; 29(170):111-4. PubMed ID: 20842824
[TBL] [Abstract][Full Text] [Related]
19. Recombinant Rhodobacter capsulatus xanthine dehydrogenase, a useful model system for the characterization of protein variants leading to xanthinuria I in humans.
Leimkuhler S; Hodson R; George GN; Rajagopalan KV
J Biol Chem; 2003 Jun; 278(23):20802-11. PubMed ID: 12670960
[TBL] [Abstract][Full Text] [Related]
20. Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.
Ichida K; Amaya Y; Kamatani N; Nishino T; Hosoya T; Sakai O
J Clin Invest; 1997 May; 99(10):2391-7. PubMed ID: 9153281
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
