127 related articles for article (PubMed ID: 37846526)
21. 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]
22. Hepatic copper-transporting ATPase ATP7B: function and inactivation at the molecular and cellular level.
Bartee MY; Lutsenko S
Biometals; 2007 Jun; 20(3-4):627-37. PubMed ID: 17268820
[TBL] [Abstract][Full Text] [Related]
23. Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties.
Roy S; McCann CJ; Ralle M; Ray K; Ray J; Lutsenko S; Jayakanthan S
Sci Rep; 2020 Aug; 10(1):13487. PubMed ID: 32778786
[TBL] [Abstract][Full Text] [Related]
24. Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage.
Barnes N; Bartee MY; Braiterman L; Gupta A; Ustiyan V; Zuzel V; Kaplan JH; Hubbard AL; Lutsenko S
Traffic; 2009 Jun; 10(6):767-79. PubMed ID: 19416479
[TBL] [Abstract][Full Text] [Related]
25. Wilson disease protein ATP7B is localized in the late endosomes in a polarized human hepatocyte cell line.
Harada M; Kumemura H; Sakisaka S; Shishido S; Taniguchi E; Kawaguchi T; Hanada S; Koga H; Kumashiro R; Ueno T; Suganuma T; Furuta K; Namba M; Sugiyama T; Sata M
Int J Mol Med; 2003 Mar; 11(3):293-8. PubMed ID: 12579329
[TBL] [Abstract][Full Text] [Related]
26. Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.
Parisi S; Polishchuk EV; Allocca S; Ciano M; Musto A; Gallo M; Perone L; Ranucci G; Iorio R; Polishchuk RS; Bonatti S
Sci Rep; 2018 Apr; 8(1):6247. PubMed ID: 29674751
[TBL] [Abstract][Full Text] [Related]
27. Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis.
Polishchuk EV; Merolla A; Lichtmannegger J; Romano A; Indrieri A; Ilyechova EY; Concilli M; De Cegli R; Crispino R; Mariniello M; Petruzzelli R; Ranucci G; Iorio R; Pietrocola F; Einer C; Borchard S; Zibert A; Schmidt HH; Di Schiavi E; Puchkova LV; Franco B; Kroemer G; Zischka H; Polishchuk RS
Gastroenterology; 2019 Mar; 156(4):1173-1189.e5. PubMed ID: 30452922
[TBL] [Abstract][Full Text] [Related]
28. Role of ATP7B in biliary copper excretion in a human hepatoma cell line and normal rat hepatocytes.
Harada M; Sakisaka S; Terada K; Kimura R; Kawaguchi T; Koga H; Taniguchi E; Sasatomi K; Miura N; Suganuma T; Fujita H; Furuta K; Tanikawa K; Sugiyama T; Sata M
Gastroenterology; 2000 May; 118(5):921-8. PubMed ID: 10784591
[TBL] [Abstract][Full Text] [Related]
29. Human copper transporter ATP7B (Wilson disease protein) forms stable dimers
Jayakanthan S; Braiterman LT; Hasan NM; Unger VM; Lutsenko S
J Biol Chem; 2017 Nov; 292(46):18760-18774. PubMed ID: 28842499
[TBL] [Abstract][Full Text] [Related]
30. DKWSLLL, a versatile DXXXLL-type signal with distinct roles in the Cu(+)-regulated trafficking of ATP7B.
Lalioti V; Hernandez-Tiedra S; Sandoval IV
Traffic; 2014 Aug; 15(8):839-60. PubMed ID: 24831241
[TBL] [Abstract][Full Text] [Related]
31. ATP7B-Deficient Hepatocytes Reveal the Importance of Protein Misfolding Induced at Low Copper Concentration.
Charbonnier P; Chovelon B; Ravelet C; Ngo TD; Chevallet M; Deniaud A
Cells; 2022 Oct; 11(21):. PubMed ID: 36359796
[TBL] [Abstract][Full Text] [Related]
32. Copper-induced translocation of the Wilson disease protein ATP7B independent of Murr1/COMMD1 and Rab7.
Weiss KH; Lozoya JC; Tuma S; Gotthardt D; Reichert J; Ehehalt R; Stremmel W; Füllekrug J
Am J Pathol; 2008 Dec; 173(6):1783-94. PubMed ID: 18974300
[TBL] [Abstract][Full Text] [Related]
33. Communication between the N and C termini is required for copper-stimulated Ser/Thr phosphorylation of Cu(I)-ATPase (ATP7B).
Braiterman LT; Gupta A; Chaerkady R; Cole RN; Hubbard AL
J Biol Chem; 2015 Apr; 290(14):8803-19. PubMed ID: 25666620
[TBL] [Abstract][Full Text] [Related]
34. Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin.
van den Berghe PV; Stapelbroek JM; Krieger E; de Bie P; van de Graaf SF; de Groot RE; van Beurden E; Spijker E; Houwen RH; Berger R; Klomp LW
Hepatology; 2009 Dec; 50(6):1783-95. PubMed ID: 19937698
[TBL] [Abstract][Full Text] [Related]
35. Brief exposure to copper activates lysosomal exocytosis.
Peña K; Coblenz J; Kiselyov K
Cell Calcium; 2015 Apr; 57(4):257-62. PubMed ID: 25620123
[TBL] [Abstract][Full Text] [Related]
36. Copper incorporation into ceruloplasmin is regulated by Niemann-Pick C1 protein.
Yanagimoto C; Harada M; Kumemura H; Abe M; Koga H; Sakata M; Kawaguchi T; Terada K; Hanada S; Taniguchi E; Ninomiya H; Ueno T; Sugiyama T; Sata M
Hepatol Res; 2011 May; 41(5):484-91. PubMed ID: 21518405
[TBL] [Abstract][Full Text] [Related]
37. Structures of the human Wilson disease copper transporter ATP7B.
Yang GM; Xu L; Wang RM; Tao X; Zheng ZW; Chang S; Ma D; Zhao C; Dong Y; Wu S; Guo J; Wu ZY
Cell Rep; 2023 May; 42(5):112417. PubMed ID: 37074913
[TBL] [Abstract][Full Text] [Related]
38. Niemann-Pick C1 protein transports copper to the secretory compartment from late endosomes where ATP7B resides.
Yanagimoto C; Harada M; Kumemura H; Koga H; Kawaguchi T; Terada K; Hanada S; Taniguchi E; Koizumi Y; Koyota S; Ninomiya H; Ueno T; Sugiyama T; Sata M
Exp Cell Res; 2009 Jan; 315(2):119-26. PubMed ID: 19007772
[TBL] [Abstract][Full Text] [Related]
39. Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A.
Lim CM; Cater MA; Mercer JF; La Fontaine S
J Biol Chem; 2006 May; 281(20):14006-14. PubMed ID: 16554302
[TBL] [Abstract][Full Text] [Related]
40. From and to the Golgi - defining the Wilson disease protein road map.
Polishchuk RS; Polishchuk EV
FEBS Lett; 2019 Sep; 593(17):2341-2350. PubMed ID: 31408533
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]