BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

345 related articles for article (PubMed ID: 26269458)

  • 1. Autonomous requirements of the Menkes disease protein in the nervous system.
    Hodgkinson VL; Zhu S; Wang Y; Ladomersky E; Nickelson K; Weisman GA; Lee J; Gitlin JD; Petris MJ
    Am J Physiol Cell Physiol; 2015 Nov; 309(10):C660-8. PubMed ID: 26269458
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation in the CPC motif-containing 6th transmembrane domain affects intracellular localization, trafficking and copper transport efficiency of ATP7A protein in mosaic mutant mice--an animal model of Menkes disease.
    Lenartowicz M; Grzmil P; Shoukier M; Starzyński R; Marciniak M; Lipiński P
    Metallomics; 2012 Feb; 4(2):197-204. PubMed ID: 22089129
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants.
    La Fontaine S; Firth SD; Lockhart PJ; Brooks H; Camakaris J; Mercer JF
    Hum Mol Genet; 1999 Jun; 8(6):1069-75. PubMed ID: 10332039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Alterations in the expression of the Atp7a gene in the early postnatal development of the mosaic mutant mice (Atp7a mo-ms) - An animal model for Menkes disease.
    Lenartowicz M; Starzyński R; Wieczerzak K; Krzeptowski W; Lipiński P; Styrna J
    Gene Expr Patterns; 2011; 11(1-2):41-7. PubMed ID: 20831904
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Small amounts of functional ATP7A protein permit mild phenotype.
    Møller LB
    J Trace Elem Med Biol; 2015; 31():173-7. PubMed ID: 25172213
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity.
    Schlief ML; West T; Craig AM; Holtzman DM; Gitlin JD
    Proc Natl Acad Sci U S A; 2006 Oct; 103(40):14919-24. PubMed ID: 17003121
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [From gene to disease; Menkes disease: copper deficiency due to an ATP7A-gene defect].
    Aldenhoven M; Klomp LW; van Hasselt PM; de Koning TJ; Visser G
    Ned Tijdschr Geneeskd; 2007 Oct; 151(41):2266-70. PubMed ID: 17987894
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correction of a mouse model of Menkes disease by the human Menkes gene.
    Llanos RM; Ke BX; Wright M; Deal Y; Monty F; Kramer DR; Mercer JF
    Biochim Biophys Acta; 2006 Apr; 1762(4):485-93. PubMed ID: 16488577
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Activity of Menkes Disease Protein ATP7A Is Essential for Redox Balance in Mitochondria.
    Bhattacharjee A; Yang H; Duffy M; Robinson E; Conrad-Antoville A; Lu YW; Capps T; Braiterman L; Wolfgang M; Murphy MP; Yi L; Kaler SG; Lutsenko S; Ralle M
    J Biol Chem; 2016 Aug; 291(32):16644-58. PubMed ID: 27226607
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression.
    Vonk WI; de Bie P; Wichers CG; van den Berghe PV; van der Plaats R; Berger R; Wijmenga C; Klomp LW; van de Sluis B
    Cell Mol Life Sci; 2012 Jan; 69(1):149-63. PubMed ID: 21667063
    [TBL] [Abstract][Full Text] [Related]  

  • 11. L-threo-dihydroxyphenylserine corrects neurochemical abnormalities in a Menkes disease mouse model.
    Donsante A; Sullivan P; Goldstein DS; Brinster LR; Kaler SG
    Ann Neurol; 2013 Feb; 73(2):259-65. PubMed ID: 23224983
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence that translation reinitiation leads to a partially functional Menkes protein containing two copper-binding sites.
    Paulsen M; Lund C; Akram Z; Winther JR; Horn N; Møller LB
    Am J Hum Genet; 2006 Aug; 79(2):214-29. PubMed ID: 16826513
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ATP7A-related copper transport diseases-emerging concepts and future trends.
    Kaler SG
    Nat Rev Neurol; 2011 Jan; 7(1):15-29. PubMed ID: 21221114
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A numerical investigation into possible mechanisms by that the A629P mutant of ATP7A causes Menkes Disease.
    Kouza M; Gowtham S; Seel M; Hansmann UH
    Phys Chem Chem Phys; 2010 Oct; 12(37):11390-7. PubMed ID: 20714486
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.
    Kennerson ML; Nicholson GA; Kaler SG; Kowalski B; Mercer JF; Tang J; Llanos RM; Chu S; Takata RI; Speck-Martins CE; Baets J; Almeida-Souza L; Fischer D; Timmerman V; Taylor PE; Scherer SS; Ferguson TA; Bird TD; De Jonghe P; Feely SM; Shy ME; Garbern JY
    Am J Hum Genet; 2010 Mar; 86(3):343-52. PubMed ID: 20170900
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein.
    Kim BE; Petris MJ
    J Med Genet; 2007 Oct; 44(10):641-6. PubMed ID: 17483305
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease.
    Niciu MJ; Ma XM; El Meskini R; Pachter JS; Mains RE; Eipper BA
    Neurobiol Dis; 2007 Sep; 27(3):278-91. PubMed ID: 17588765
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. The copper-transporting ATPases, menkes and wilson disease proteins, have distinct roles in adult and developing cerebellum.
    Barnes N; Tsivkovskii R; Tsivkovskaia N; Lutsenko S
    J Biol Chem; 2005 Mar; 280(10):9640-5. PubMed ID: 15634671
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disturbed copper transport in humans. Part 1: mutations of the ATP7A gene lead to Menkes disease and occipital horn syndrome.
    Seidel J; Møller LB; Mentzel HJ; Kauf E; Vogt S; Patzer S; Wollina U; Zintl F; Horn N
    Cell Mol Biol (Noisy-le-grand); 2001; 47 Online Pub():OL141-8. PubMed ID: 11936860
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.