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 *

420 related articles for article (PubMed ID: 9587140)

  • 1. Physiologic function of the Wilson disease gene product, ATP7B.
    Bingham MJ; Ong TJ; Summer KH; Middleton RB; McArdle HJ
    Am J Clin Nutr; 1998 May; 67(5 Suppl):982S-987S. PubMed ID: 9587140
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copper transport and its alterations in Menkes and Wilson diseases.
    DiDonato M; Sarkar B
    Biochim Biophys Acta; 1997 Feb; 1360(1):3-16. PubMed ID: 9061035
    [No Abstract]   [Full Text] [Related]  

  • 3. Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.
    de Bie P; Muller P; Wijmenga C; Klomp LW
    J Med Genet; 2007 Nov; 44(11):673-88. PubMed ID: 17717039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase.
    La Fontaine S; Theophilos MB; Firth SD; Gould R; Parton RG; Mercer JF
    Hum Mol Genet; 2001 Feb; 10(4):361-70. PubMed ID: 11157799
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of the Wilson disease gene is deficient in the Long-Evans Cinnamon rat.
    Yamaguchi Y; Heiny ME; Shimizu N; Aoki T; Gitlin JD
    Biochem J; 1994 Jul; 301 ( Pt 1)(Pt 1):1-4. PubMed ID: 8037655
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Copper transporting P-type ATPases and human disease.
    Cox DW; Moore SD
    J Bioenerg Biomembr; 2002 Oct; 34(5):333-8. PubMed ID: 12539960
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders.
    Fieten H; Gill Y; Martin AJ; Concilli M; Dirksen K; van Steenbeek FG; Spee B; van den Ingh TS; Martens EC; Festa P; Chesi G; van de Sluis B; Houwen RH; Watson AL; Aulchenko YS; Hodgkinson VL; Zhu S; Petris MJ; Polishchuk RS; Leegwater PA; Rothuizen J
    Dis Model Mech; 2016 Jan; 9(1):25-38. PubMed ID: 26747866
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cellular copper transport and metabolism.
    Harris ED
    Annu Rev Nutr; 2000; 20():291-310. PubMed ID: 10940336
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [From gene to disease: copper-transporting P ATPases alteration].
    Garcia Hejl C; Vrignaud C; Garcia C; Ceppa F
    Pathol Biol (Paris); 2009 May; 57(3):272-9. PubMed ID: 19046832
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional analysis of copper homeostasis in cell culture models: a new perspective on internal copper transport.
    Harris ED; Qian Y; Tiffany-Castiglioni E; Lacy AR; Reddy MC
    Am J Clin Nutr; 1998 May; 67(5 Suppl):988S-995S. PubMed ID: 9587141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structure-function analysis of purified Enterococcus hirae CopB copper ATPase: effect of Menkes/Wilson disease mutation homologues.
    Bissig KD; Wunderli-Ye H; Duda PW; Solioz M
    Biochem J; 2001 Jul; 357(Pt 1):217-23. PubMed ID: 11415452
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clusterin (apolipoprotein J), a molecular chaperone that facilitates degradation of the copper-ATPases ATP7A and ATP7B.
    Materia S; Cater MA; Klomp LW; Mercer JF; La Fontaine S
    J Biol Chem; 2011 Mar; 286(12):10073-83. PubMed ID: 21242307
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters.
    Kuo YM; Gitschier J; Packman S
    Hum Mol Genet; 1997 Jul; 6(7):1043-9. PubMed ID: 9215673
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression in mouse kidney of membrane copper transporters Atp7a and Atp7b.
    Moore SD; Cox DW
    Nephron; 2002; 92(3):629-34. PubMed ID: 12372948
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Menkes and Wilson diseases.
    Monaco AP; Chelly J
    Adv Genet; 1995; 33():233-53. PubMed ID: 7484454
    [No Abstract]   [Full Text] [Related]  

  • 16. Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?
    Forbes JR; Cox DW
    Am J Hum Genet; 1998 Dec; 63(6):1663-74. PubMed ID: 9837819
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular mechanisms of copper homeostasis.
    Camakaris J; Voskoboinik I; Mercer JF
    Biochem Biophys Res Commun; 1999 Aug; 261(2):225-32. PubMed ID: 10425169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Structure and function of ATP7A and ATP7B proteins--Cu-transporting ATPases].
    Lenartowicz M; Krzeptowski W
    Postepy Biochem; 2010; 56(3):317-27. PubMed ID: 21117320
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Advances in the understanding of mammalian copper transporters.
    Wang Y; Hodgkinson V; Zhu S; Weisman GA; Petris MJ
    Adv Nutr; 2011 Mar; 2(2):129-37. PubMed ID: 22332042
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A comparison of the mutation spectra of Menkes disease and Wilson disease.
    Hsi G; Cox DW
    Hum Genet; 2004 Jan; 114(2):165-72. PubMed ID: 14579150
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.