These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

54 related articles for article (PubMed ID: 10801779)

  • 1. 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]  

  • 2. Convergent neofunctionalization by positive Darwinian selection after ancient recurrent duplications of the xanthine dehydrogenase gene.
    Rodríguez-Trelles F; Tarrío R; Ayala FJ
    Proc Natl Acad Sci U S A; 2003 Nov; 100(23):13413-7. PubMed ID: 14576276
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Hypouricaemia in a patient with hereditary xanthinuria type I.
    Maes B; Dedeurwaerdere F
    Lancet; 2024 Apr; 403(10435):1493. PubMed ID: 38614487
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Comprehensive analysis of 124 transcriptomes from 31 tissues in developing, juvenile, and adult Japanese Black cattle.
    Arishima T; Wakaguri H; Nakashima R; Sakakihara S; Kawashima K; Sugimoto Y; Suzuki Y; Sasaki S
    DNA Res; 2022 Aug; 29(5):. PubMed ID: 36047829
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The History of the Molybdenum Cofactor-A Personal View.
    Mendel RR
    Molecules; 2022 Aug; 27(15):. PubMed ID: 35956883
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. The propagation mechanisms of extracellular tau in Alzheimer's disease.
    Wei Y; Liu M; Wang D
    J Neurol; 2022 Mar; 269(3):1164-1181. PubMed ID: 33913022
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of deleterious recessive haplotypes and candidate deleterious recessive mutations in Japanese Black cattle.
    Sasaki S; Watanabe T; Ibi T; Hasegawa K; Sakamoto Y; Moriwaki S; Kurogi K; Ogino A; Yasumori T; Wakaguri H; Muraki E; Miki Y; Yoshida Y; Inoue Y; Tabuchi I; Iwao K; Arishima T; Kawashima K; Watanabe M; Sugano S; Sugimoto Y; Suzuki Y
    Sci Rep; 2021 Mar; 11(1):6687. PubMed ID: 33758295
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Physiology, Development, and Disease Modeling in the
    Cohen E; Sawyer JK; Peterson NG; Dow JAT; Fox DT
    Genetics; 2020 Feb; 214(2):235-264. PubMed ID: 32029579
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. The mononuclear molybdenum enzymes.
    Hille R; Hall J; Basu P
    Chem Rev; 2014 Apr; 114(7):3963-4038. PubMed ID: 24467397
    [No Abstract]   [Full Text] [Related]  

  • 16. Mapping and exome sequencing identifies a mutation in the IARS gene as the cause of hereditary perinatal weak calf syndrome.
    Hirano T; Kobayashi N; Matsuhashi T; Watanabe D; Watanabe T; Takasuga A; Sugimoto M; Sugimoto Y
    PLoS One; 2013; 8(5):e64036. PubMed ID: 23700453
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.
    Ichida K; Amaya Y; Okamoto K; Nishino T
    Int J Mol Sci; 2012 Nov; 13(11):15475-95. PubMed ID: 23203137
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Structural studies of the molybdenum center of mitochondrial amidoxime reducing component (mARC) by pulsed EPR spectroscopy and 17O-labeling.
    Rajapakshe A; Astashkin AV; Klein EL; Reichmann D; Mendel RR; Bittner F; Enemark JH
    Biochemistry; 2011 Oct; 50(41):8813-22. PubMed ID: 21916412
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molybdenum enzymes in higher organisms.
    Hille R; Nishino T; Bittner F
    Coord Chem Rev; 2011 May; 255(9-10):1179-1205. PubMed ID: 21516203
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.