BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 19095659)

  • 1. Dominant mutants of ceruloplasmin impair the copper loading machinery in aceruloplasminemia.
    di Patti MC; Maio N; Rizzo G; De Francesco G; Persichini T; Colasanti M; Polticelli F; Musci G
    J Biol Chem; 2009 Feb; 284(7):4545-54. PubMed ID: 19095659
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Role of external loops of human ceruloplasmin in copper loading by ATP7B and Ccc2p.
    Maio N; Polticelli F; De Francesco G; Rizzo G; Bonaccorsi di Patti MC; Musci G
    J Biol Chem; 2010 Jul; 285(27):20507-13. PubMed ID: 20430895
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system.
    Hsi G; Cullen LM; Macintyre G; Chen MM; Glerum DM; Cox DW
    Hum Mutat; 2008 Apr; 29(4):491-501. PubMed ID: 18203200
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Functional assessment of the carboxy-terminus of the Wilson disease copper-transporting ATPase, ATP7B.
    Hsi G; Cullen LM; Moira Glerum D; Cox DW
    Genomics; 2004 Mar; 83(3):473-81. PubMed ID: 14962673
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional iron deficiency in toxic milk mutant mice (tx-J) despite high hepatic ferroportin: a critical role of decreased GPI-ceruloplasmin expression in liver macrophages.
    Jończy A; Lipiński P; Ogórek M; Starzyński RR; Krzysztofik D; Bednarz A; Krzeptowski W; Szudzik M; Haberkiewicz O; Miłoń A; Grzmil P; Lenartowicz M
    Metallomics; 2019 Jun; 11(6):1079-1092. PubMed ID: 31011744
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biological effects of mutant ceruloplasmin on hepcidin-mediated internalization of ferroportin.
    Kono S; Yoshida K; Tomosugi N; Terada T; Hamaya Y; Kanaoka S; Miyajima H
    Biochim Biophys Acta; 2010 Nov; 1802(11):968-75. PubMed ID: 20655381
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Biological functions of ceruloplasmin and their deficiency caused by mutation in genes regulating copper and iron metabolism.
    Mzhel'skaya TI
    Bull Exp Biol Med; 2000 Aug; 130(8):719-27. PubMed ID: 11177225
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The copper-iron connection: hereditary aceruloplasminemia.
    Nittis T; Gitlin JD
    Semin Hematol; 2002 Oct; 39(4):282-9. PubMed ID: 12382203
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence for a critical role of ceruloplasmin oxidase activity in iron metabolism of Wilson disease gene knockout mice.
    Merle U; Tuma S; Herrmann T; Muntean V; Volkmann M; Gehrke SG; Stremmel W
    J Gastroenterol Hepatol; 2010 Jun; 25(6):1144-50. PubMed ID: 20594231
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Apical targeting and Golgi retention signals reside within a 9-amino acid sequence in the copper-ATPase, ATP7B.
    Braiterman L; Nyasae L; Guo Y; Bustos R; Lutsenko S; Hubbard A
    Am J Physiol Gastrointest Liver Physiol; 2009 Feb; 296(2):G433-44. PubMed ID: 19033537
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [In vivo expression of copper transporting proteins in rat brain sections].
    Platonova NA; Barabanova SV; Povalikhin RG; Tsymbalenko NV; Danilovskiĭ MA; Voronina OV; Dorokhova II; Puchkovq LV
    Izv Akad Nauk Ser Biol; 2005; (2):141-54. PubMed ID: 16004274
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.
    Papur OS; Terzioglu O; Koc A
    J Trace Elem Med Biol; 2015; 31():33-6. PubMed ID: 26004889
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Copper-dependent trafficking of Wilson disease mutant ATP7B proteins.
    Forbes JR; Cox DW
    Hum Mol Genet; 2000 Aug; 9(13):1927-35. PubMed ID: 10942420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Silencing the Menkes copper-transporting ATPase (Atp7a) gene in rat intestinal epithelial (IEC-6) cells increases iron flux via transcriptional induction of ferroportin 1 (Fpn1).
    Gulec S; Collins JF
    J Nutr; 2014 Jan; 144(1):12-9. PubMed ID: 24174620
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
    de Bie P; van de Sluis B; Burstein E; van de Berghe PV; Muller P; Berger R; Gitlin JD; Wijmenga C; Klomp LW
    Gastroenterology; 2007 Oct; 133(4):1316-26. PubMed ID: 17919502
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Investigation of iron metabolism in mice expressing a mutant Menke's copper transporting ATPase (Atp7a) protein with diminished activity (Brindled; Mo (Br) (/y) ).
    Gulec S; Collins JF
    PLoS One; 2013; 8(6):e66010. PubMed ID: 23776592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.