113 related articles for article (PubMed ID: 11231950)
1. A mutation of the Wilson disease protein, ATP7B, is degraded in the proteasomes and forms protein aggregates.
Harada M; Sakisaka S; Terada K; Kimura R; Kawaguchi T; Koga H; Kim M; Taniguchi E; Hanada S; Suganuma T; Furuta K; Sugiyama T; Sata M
Gastroenterology; 2001 Mar; 120(4):967-74. PubMed ID: 11231950
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Mallory bodies, like the mutant of ATP7B seen in Wilson disease, are aggresomes.
French S
Gastroenterology; 2001 Nov; 121(5):1264-6. PubMed ID: 11706834
[No Abstract] [Full Text] [Related]
5. Copper does not alter the intracellular distribution of ATP7B, a copper-transporting ATPase.
Harada M; Sakisaka S; Kawaguchi T; Kimura R; Taniguchi E; Koga H; Hanada S; Baba S; Furuta K; Kumashiro R; Sugiyama T; Sata M
Biochem Biophys Res Commun; 2000 Sep; 275(3):871-6. PubMed ID: 10973814
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Diverse functional properties of Wilson disease ATP7B variants.
Huster D; Kühne A; Bhattacharjee A; Raines L; Jantsch V; Noe J; Schirrmeister W; Sommerer I; Sabri O; Berr F; Mössner J; Stieger B; Caca K; Lutsenko S
Gastroenterology; 2012 Apr; 142(4):947-956.e5. PubMed ID: 22240481
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Defective cellular localization of mutant ATP7B in Wilson's disease patients and hepatoma cell lines.
Huster D; Hoppert M; Lutsenko S; Zinke J; Lehmann C; Mössner J; Berr F; Caca K
Gastroenterology; 2003 Feb; 124(2):335-45. PubMed ID: 12557139
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase.
La Fontaine S; Theophilos MB; Firth SD; Gould R; Parton RG; Mercer JF
Hum Mol Genet; 2001 Feb; 10(4):361-70. PubMed ID: 11157799
[TBL] [Abstract][Full Text] [Related]
13. Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.
Buiakova OI; Xu J; Lutsenko S; Zeitlin S; Das K; Das S; Ross BM; Mekios C; Scheinberg IH; Gilliam TC
Hum Mol Genet; 1999 Sep; 8(9):1665-71. PubMed ID: 10441329
[TBL] [Abstract][Full Text] [Related]
14. The His1069Gln mutation in the ATP7B gene in Russian patients with Wilson disease.
Ivanova-Smolenskaya IA; Ovchinnikov IV; Karabanov AV; Deineko NL; Poleshchuk VV; Markova ED; Illarioshkin SN
J Med Genet; 1999 Feb; 36(2):174. PubMed ID: 10051024
[No Abstract] [Full Text] [Related]
15. Analysis of functional domains of Wilson disease protein (ATP7B) in Saccharomyces cerevisiae.
Iida M; Terada K; Sambongi Y; Wakabayashi T; Miura N; Koyama K; Futai M; Sugiyama T
FEBS Lett; 1998 May; 428(3):281-5. PubMed ID: 9654149
[TBL] [Abstract][Full Text] [Related]
16. Localization of the Wilson disease protein in murine intestine.
Weiss KH; Wurz J; Gotthardt D; Merle U; Stremmel W; Füllekrug J
J Anat; 2008 Sep; 213(3):232-40. PubMed ID: 18673401
[TBL] [Abstract][Full Text] [Related]
17. Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines.
Chandhok G; Horvath J; Aggarwal A; Bhatt M; Zibert A; Schmidt HH
World J Gastroenterol; 2016 Apr; 22(16):4109-19. PubMed ID: 27122662
[TBL] [Abstract][Full Text] [Related]
18. Wilson disease.
Harada M
Med Electron Microsc; 2002 Jun; 35(2):61-6. PubMed ID: 12181646
[TBL] [Abstract][Full Text] [Related]
19. Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation.
Payne AS; Kelly EJ; Gitlin JD
Proc Natl Acad Sci U S A; 1998 Sep; 95(18):10854-9. PubMed ID: 9724794
[TBL] [Abstract][Full Text] [Related]
20. Proteasome inhibitors: valuable new tools for cell biologists.
Lee DH; Goldberg AL
Trends Cell Biol; 1998 Oct; 8(10):397-403. PubMed ID: 9789328
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
