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 *

297 related articles for article (PubMed ID: 26732058)

  • 1. Mottled Mice and Non-Mammalian Models of Menkes Disease.
    Lenartowicz M; Krzeptowski W; Lipiński P; Grzmil P; Starzyński R; Pierzchała O; Møller LB
    Front Mol Neurosci; 2015; 8():72. PubMed ID: 26732058
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX).
    Perez-Siles G; Grant A; Ellis M; Ly C; Kidambi A; Khalil M; Llanos RM; Fontaine SL; Strickland AV; Züchner S; Bermeo S; Neist E; Brennan-Speranza TC; Takata RI; Speck-Martins CE; Mercer JF; Nicholson GA; Kennerson ML
    Metallomics; 2016 Sep; 8(9):981-92. PubMed ID: 27293072
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [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]  

  • 9. 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]  

  • 10. The mottled mouse as a model for human Menkes disease: identification of mutations in the Atp7a gene.
    Cecchi C; Biasotto M; Tosi M; Avner P
    Hum Mol Genet; 1997 Mar; 6(3):425-33. PubMed ID: 9147646
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copper efflux from murine microvascular cells requires expression of the menkes disease Cu-ATPase.
    Qian Y; Tiffany-Castiglioni E; Welsh J; Harris ED
    J Nutr; 1998 Aug; 128(8):1276-82. PubMed ID: 9687544
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotypic and genetic characterization of the Atp7a(Mo-Tohm) mottled mouse: a new murine model of Menkes disease.
    Mototani Y; Miyoshi I; Okamura T; Moriya T; Meng Y; Yuan Pei X; Kameo S; Kasai N
    Genomics; 2006 Feb; 87(2):191-9. PubMed ID: 16338116
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation analysis provides additional proof that mottled is the mouse homologue of Menkes' disease.
    Reed V; Boyd Y
    Hum Mol Genet; 1997 Mar; 6(3):417-23. PubMed ID: 9147645
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A.
    Ke BX; Llanos RM; Wright M; Deal Y; Mercer JF
    Am J Physiol Regul Integr Comp Physiol; 2006 May; 290(5):R1460-7. PubMed ID: 16397091
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Intragenic deletions at Atp7a in mouse models for Menkes disease.
    Cunliffe P; Reed V; Boyd Y
    Genomics; 2001 Jun; 74(2):155-62. PubMed ID: 11386751
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ATP7A-Regulated Enzyme Metalation and Trafficking in the Menkes Disease Puzzle.
    Horn N; Wittung-Stafshede P
    Biomedicines; 2021 Apr; 9(4):. PubMed ID: 33917579
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. ATP7A (Menkes protein) functions in axonal targeting and synaptogenesis.
    El Meskini R; Crabtree KL; Cline LB; Mains RE; Eipper BA; Ronnett GV
    Mol Cell Neurosci; 2007 Mar; 34(3):409-21. PubMed ID: 17215139
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.