BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 37846526)

  • 1. Copper-independent lysosomal localisation of the Wilson disease protein ATP7B.
    Maji S; Pirozzi M; Ruturaj ; Pandey R; Ghosh T; Das S; Gupta A
    Traffic; 2023 Dec; 24(12):587-609. PubMed ID: 37846526
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Wilson disease protein ATP7B utilizes lysosomal exocytosis to maintain copper homeostasis.
    Polishchuk EV; Concilli M; Iacobacci S; Chesi G; Pastore N; Piccolo P; Paladino S; Baldantoni D; van IJzendoorn SC; Chan J; Chang CJ; Amoresano A; Pane F; Pucci P; Tarallo A; Parenti G; Brunetti-Pierri N; Settembre C; Ballabio A; Polishchuk RS
    Dev Cell; 2014 Jun; 29(6):686-700. PubMed ID: 24909901
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Retromer retrieves the Wilson disease protein ATP7B from endolysosomes in a copper-dependent manner.
    Das S; Maji S; Ruturaj ; Bhattacharya I; Saha T; Naskar N; Gupta A
    J Cell Sci; 2020 Dec; 133(24):. PubMed ID: 33268466
    [TBL] [Abstract][Full Text] [Related]  

  • 4. COMMD1 and PtdIns(4,5)P
    Stewart DJ; Short KK; Maniaci BN; Burkhead JL
    J Cell Sci; 2019 Oct; 132(19):. PubMed ID: 31515276
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Basolateral sorting and transcytosis define the Cu+-regulated translocation of ATP7B to the bile canaliculus.
    Lalioti V; Peiró R; Pérez-Berlanga M; Tsuchiya Y; Muñoz A; Villalba T; Sanchez C; Sandoval IV
    J Cell Sci; 2016 Jun; 129(11):2190-201. PubMed ID: 27034138
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Copper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B).
    Cater MA; La Fontaine S; Mercer JF
    Biochem J; 2007 Jan; 401(1):143-53. PubMed ID: 16939419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular events initiating exit of a copper-transporting ATPase ATP7B from the trans-Golgi network.
    Hasan NM; Gupta A; Polishchuk E; Yu CH; Polishchuk R; Dmitriev OY; Lutsenko S
    J Biol Chem; 2012 Oct; 287(43):36041-50. PubMed ID: 22898812
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cellular copper levels determine the phenotype of the Arg875 variant of ATP7B/Wilson disease protein.
    Gupta A; Bhattacharjee A; Dmitriev OY; Nokhrin S; Braiterman L; Hubbard AL; Lutsenko S
    Proc Natl Acad Sci U S A; 2011 Mar; 108(13):5390-5. PubMed ID: 21406592
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polarized trafficking and copper transport activity of ATP7B: A mutational approach to establish genotype-phenotype correlation in Wilson disease.
    Das S; Mohammed A; Mandal T; Maji S; Verma J; Ruturaj ; Gupta A
    Hum Mutat; 2022 Oct; 43(10):1408-1429. PubMed ID: 35762218
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Regulation of the apico-basolateral trafficking polarity of the homologous copper-ATPases ATP7A and ATP7B.
    Ruturaj ; Mishra M; Saha S; Maji S; Rodriguez-Boulan E; Schreiner R; Gupta A
    J Cell Sci; 2024 Mar; 137(5):. PubMed ID: 38032054
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Wilson disease protein ATP7B resides in the late endosomes with Rab7 and the Niemann-Pick C1 protein.
    Harada M; Kawaguchi T; Kumemura H; Terada K; Ninomiya H; Taniguchi E; Hanada S; Baba S; Maeyama M; Koga H; Ueno T; Furuta K; Suganuma T; Sugiyama T; Sata M
    Am J Pathol; 2005 Feb; 166(2):499-510. PubMed ID: 15681833
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copper directs ATP7B to the apical domain of hepatic cells via basolateral endosomes.
    Nyasae LK; Schell MJ; Hubbard AL
    Traffic; 2014 Dec; 15(12):1344-65. PubMed ID: 25243755
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An αB-Crystallin Peptide Rescues Compartmentalization and Trafficking Response to Cu Overload of ATP7B-H1069Q, the Most Frequent Cause of Wilson Disease in the Caucasian Population.
    Allocca S; Ciano M; Ciardulli MC; D'Ambrosio C; Scaloni A; Sarnataro D; Caporaso MG; D'Agostino M; Bonatti S
    Int J Mol Sci; 2018 Jun; 19(7):. PubMed ID: 29954118
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Altered localisation of the copper efflux transporters ATP7A and ATP7B associated with cisplatin resistance in human ovarian carcinoma cells.
    Kalayda GV; Wagner CH; Buss I; Reedijk J; Jaehde U
    BMC Cancer; 2008 Jun; 8():175. PubMed ID: 18565219
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Critical roles for the COOH terminus of the Cu-ATPase ATP7B in protein stability, trans-Golgi network retention, copper sensing, and retrograde trafficking.
    Braiterman L; Nyasae L; Leves F; Hubbard AL
    Am J Physiol Gastrointest Liver Physiol; 2011 Jul; 301(1):G69-81. PubMed ID: 21454443
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intracellular trafficking of the human Wilson protein: the role of the six N-terminal metal-binding sites.
    Cater MA; Forbes J; La Fontaine S; Cox D; Mercer JF
    Biochem J; 2004 Jun; 380(Pt 3):805-13. PubMed ID: 14998371
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B.
    Braiterman LT; Murthy A; Jayakanthan S; Nyasae L; Tzeng E; Gromadzka G; Woolf TB; Lutsenko S; Hubbard AL
    Proc Natl Acad Sci U S A; 2014 Apr; 111(14):E1364-73. PubMed ID: 24706876
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new Caenorhabditis elegans model to study copper toxicity in Wilson disease.
    Catalano F; O'Brien TJ; Mekhova AA; Sepe LV; Elia M; De Cegli R; Gallotta I; Santonicola P; Zampi G; Ilyechova EY; Romanov AA; Samuseva PD; Salzano J; Petruzzelli R; Polishchuk EV; Indrieri A; Kim BE; Brown AEX; Puchkova LV; Di Schiavi E; Polishchuk RS
    Traffic; 2024 Jan; 25(1):e12920. PubMed ID: 37886910
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.