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 *

98 related articles for article (PubMed ID: 20849226)

  • 1. Copper metabolism disorders affect testes structure and gamete quality in male mice.
    Kowal M; Lenartowicz M; Pecio A; Gołas A; Błaszkiewicz T; Styrna J
    Syst Biol Reprod Med; 2010 Dec; 56(6):431-44. PubMed ID: 20849226
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Testicular morphology and expression of aromatase in testes of mice with the mosaic mutation (Atp7a mo-ms).
    Kotula-Balak M; Lenartowicz M; Kowal M; Styrna J; Bilińska B
    Theriogenology; 2007 Jan; 67(2):423-34. PubMed ID: 17045330
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Effects of copper supplementation on the structure and content of elements in kidneys of mosaic mutant mice.
    Lenartowicz M; Windak R; Tylko G; Kowal M; Styrna J
    Biol Trace Elem Res; 2010 Aug; 136(2):204-20. PubMed ID: 19830392
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Impaired somatostatin accumulation within the median eminence in mice with mosaic mutation.
    Wojewodzka U; Gajewska A; Gajkowska B; Styrna J; Kochman K
    Neuro Endocrinol Lett; 2004; 25(1-2):78-82. PubMed ID: 15159688
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Copper therapy reduces intravascular hemolysis and derepresses ferroportin in mice with mosaic mutation (Atp7a
    Lenartowicz M; Starzyński RR; Jończy A; Staroń R; Antoniuk J; Krzeptowski W; Grzmil P; Bednarz A; Pierzchała O; Ogórek M; Rajfur Z; Baster Z; Lipiński P
    Biochim Biophys Acta Mol Basis Dis; 2017 Jun; 1863(6):1410-1421. PubMed ID: 28219768
    [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. Pathological structure of the kidney from adult mice with mosaic mutation.
    Lenartowicz M; Kowal M; Buda-Lewandowska D; Styrna J
    J Inherit Metab Dis; 2002 Dec; 25(8):647-59. PubMed ID: 12705495
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Mice with mottled mutation--a model for defective copper metabolism in humans].
    Lenartowicz M
    Postepy Hig Med Dosw; 1998; 52(5):527-41. PubMed ID: 9857676
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Testicular toxicity and sperm quality following copper exposure in Wistar albino rats: ameliorative potentials of L-carnitine.
    Khushboo M; Murthy MK; Devi MS; Sanjeev S; Ibrahim KS; Kumar NS; Roy VK; Gurusubramanian G
    Environ Sci Pollut Res Int; 2018 Jan; 25(2):1837-1862. PubMed ID: 29103113
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical zinc deficiency as early presentation of Wilson disease.
    Van Biervliet S; Küry S; De Bruyne R; Vanakker OM; Schmitt S; Vande Velde S; Blouin E; Bézieau S
    J Pediatr Gastroenterol Nutr; 2015 Apr; 60(4):457-9. PubMed ID: 25825851
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Alterations in kidney morphology in mice with mosaic mutation.
    Lenartowicz M; Sasuła K; Zawadowska B
    Folia Histochem Cytobiol; 2001; 39(3):275-81. PubMed ID: 11534785
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. An overview and update of ATP7A mutations leading to Menkes disease and occipital horn syndrome.
    Tümer Z
    Hum Mutat; 2013 Mar; 34(3):417-29. PubMed ID: 23281160
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.