BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 34356852)

  • 1. Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects.
    Peretz H; Lagziel A; Bittner F; Kabha M; Shtauber-Naamati M; Zhuravel V; Usher S; Rump S; Wollers S; Bork B; Mandel H; Falik-Zaccai T; Kalfon L; Graessler J; Zeharia A; Heib N; Shalev H; Landau D; Levartovsky D
    Biomedicines; 2021 Jul; 9(7):. PubMed ID: 34356852
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt.
    Peretz H; Korostishevsky M; Steinberg DM; Kabha M; Usher S; Krause I; Shalev H; Landau D; Levartovsky D
    JIMD Rep; 2020 Jan; 51(1):45-52. PubMed ID: 32071838
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria.
    Peretz H; Naamati MS; Levartovsky D; Lagziel A; Shani E; Horn I; Shalev H; Landau D
    Mol Genet Metab; 2007 May; 91(1):23-9. PubMed ID: 17368066
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Identification of a new mutation in the human xanthine dehydrogenase responsible for xanthinuria type I.
    Collazo Abal C; Romero Santos S; González Mao C; Pazos Lago EC; Barros Angueira F; Castiñeiras Ramos D
    Adv Lab Med; 2021 Nov; 2(4):567-574. PubMed ID: 37360896
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.