161 related articles for article (PubMed ID: 23024809)
1. A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation.
Piret SE; Esapa CT; Gorvin CM; Head R; Loh NY; Devuyst O; Thomas G; Brown SD; Brown M; Croucher P; Cox R; Thakker RV
PLoS One; 2012; 7(9):e45217. PubMed ID: 23024809
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. XDH gene mutation is the underlying cause of classical xanthinuria: a second report.
Levartovsky D; Lagziel A; Sperling O; Liberman U; Yaron M; Hosoya T; Ichida K; Peretz H
Kidney Int; 2000 Jun; 57(6):2215-20. PubMed ID: 10844591
[TBL] [Abstract][Full Text] [Related]
4. Assignment of human xanthine dehydrogenase gene to chromosome 2p22.
Xu P; Zhu XL; Huecksteadt TP; Brothman AR; Hoidal JR
Genomics; 1994 Sep; 23(1):289-91. PubMed ID: 7829092
[TBL] [Abstract][Full Text] [Related]
5. A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase.
Iguchi A; Sato T; Yamazaki M; Tasaki K; Suzuki Y; Iino N; Hasegawa H; Ichida K; Narita I
CEN Case Rep; 2016 Nov; 5(2):158-162. PubMed ID: 28508967
[TBL] [Abstract][Full Text] [Related]
6. Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function.
Miyazaki S; Hamada T; Sugihara S; Mizuta E; Endo Y; Ohtahara A; Komatsu K; Kuwabara M; Fukuuchi T; Kaneko K; Ichida K; Ogino K; Ninomiya H; Yamamoto K; Nakamura T; Hisatome I
Intern Med; 2022; 61(9):1383-1386. PubMed ID: 35491177
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22.
Rytkönen EM; Halila R; Laan M; Saksela M; Kallioniemi OP; Palotie A; Raivio KO
Cytogenet Cell Genet; 1995; 68(1-2):61-3. PubMed ID: 7956361
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. The presence of xanthine dehydrogenase is crucial for the maturation of the rat kidneys.
Dissanayake LV; Kravtsova O; Lowe M; McCrorey MK; Van Beusecum JP; Palygin O; Staruschenko A
Clin Sci (Lond); 2024 Mar; 138(5):269-288. PubMed ID: 38358003
[TBL] [Abstract][Full Text] [Related]
11. A case of hereditary xanthinuria type 1 accompanied by bilateral renal calculi.
Fujiwara Y; Kawakami Y; Shinohara Y; Ichida K
Intern Med; 2012; 51(14):1879-84. PubMed ID: 22821105
[TBL] [Abstract][Full Text] [Related]
12. Identification of a xanthinuria type I case with mutations of xanthine dehydrogenase in an Afghan child.
Nakamura M; Yuichiro Y; Sass JO; Tomohiro M; Schwab KO; Takeshi N; Tatsuo H; Ichida K
Clin Chim Acta; 2012 Dec; 414():158-60. PubMed ID: 22981351
[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. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria.
Eggermann T; Spengler S; Denecke B; Zerres K; Mache CJ
Clin Nephrol; 2013 Jan; 79(1):78-80. PubMed ID: 23249873
[TBL] [Abstract][Full Text] [Related]
15. Xanthine oxidoreductase depletion induces renal interstitial fibrosis through aberrant lipid and purine accumulation in renal tubules.
Ohtsubo T; Matsumura K; Sakagami K; Fujii K; Tsuruya K; Noguchi H; Rovira II; Finkel T; Iida M
Hypertension; 2009 Oct; 54(4):868-76. PubMed ID: 19667249
[TBL] [Abstract][Full Text] [Related]
16. An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
Gorvin CM; Ahmad BN; Stechman MJ; Loh NY; Hough TA; Leo P; Marshall M; Sethi S; Bentley L; Piret SE; Reed A; Jeyabalan J; Christie PT; Wells S; Simon MM; Mallon AM; Schulz H; Huebner N; Brown MA; Cox RD; Brown SD; Thakker RV
J Bone Miner Res; 2019 Mar; 34(3):497-507. PubMed ID: 30395686
[TBL] [Abstract][Full Text] [Related]
17. Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: biochemical and molecular genetic analysis in two Czech families with xanthinuria type I.
Stiburkova B; Krijt J; Vyletal P; Bartl J; Gerhatova E; Korinek M; Sebesta I
Clin Chim Acta; 2012 Jan; 413(1-2):93-9. PubMed ID: 21963464
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Deletion mutation in Drosophila ma-l homologous, putative molybdopterin cofactor sulfurase gene is associated with bovine xanthinuria type II.
Watanabe T; Ihara N; Itoh T; Fujita T; Sugimoto Y
J Biol Chem; 2000 Jul; 275(29):21789-92. PubMed ID: 10801779
[TBL] [Abstract][Full Text] [Related]
20. [Xanthinuria type 1 in a woman with arthralgias: a combined clinical and molecular genetic investigation].
Därr RW; Lenzner S; Eggermann T; Därr WH
Dtsch Med Wochenschr; 2016 Apr; 141(8):571-4. PubMed ID: 27078247
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]