159 related articles for article (PubMed ID: 12579329)
41. 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]
42. Functional interactions of Cu-ATPase ATP7B with cisplatin and the role of ATP7B in the resistance of cells to the drug.
Leonhardt K; Gebhardt R; Mössner J; Lutsenko S; Huster D
J Biol Chem; 2009 Mar; 284(12):7793-802. PubMed ID: 19141620
[TBL] [Abstract][Full Text] [Related]
43. Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B.
Wan L; Tsai CH; Hsu CM; Huang CC; Yang CC; Liao CC; Wu CC; Hsu YA; Lee CC; Liu SC; Lin WD; Tsai FJ
Hepatology; 2010 Nov; 52(5):1662-70. PubMed ID: 20931554
[TBL] [Abstract][Full Text] [Related]
44. Expression of ATP7B in normal human liver.
Fanni D; Pilloni L; Orrù S; Coni P; Liguori C; Serra S; Lai ML; Uccheddu A; Contu L; Van Eyken P; Faa G
Eur J Histochem; 2005; 49(4):371-8. PubMed ID: 16377579
[TBL] [Abstract][Full Text] [Related]
45. The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders.
Fieten H; Gill Y; Martin AJ; Concilli M; Dirksen K; van Steenbeek FG; Spee B; van den Ingh TS; Martens EC; Festa P; Chesi G; van de Sluis B; Houwen RH; Watson AL; Aulchenko YS; Hodgkinson VL; Zhu S; Petris MJ; Polishchuk RS; Leegwater PA; Rothuizen J
Dis Model Mech; 2016 Jan; 9(1):25-38. PubMed ID: 26747866
[TBL] [Abstract][Full Text] [Related]
46. A new hepatocytic isoform of PLZF lacking the BTB domain interacts with ATP7B, the Wilson disease protein, and positively regulates ERK signal transduction.
Ko JH; Son W; Bae GY; Kang JH; Oh W; Yoo OJ
J Cell Biochem; 2006 Oct; 99(3):719-34. PubMed ID: 16676348
[TBL] [Abstract][Full Text] [Related]
47. Mechanism of tumor resistance to cisplatin mediated by the copper transporter ATP7B.
Dmitriev OY
Biochem Cell Biol; 2011 Apr; 89(2):138-47. PubMed ID: 21455266
[TBL] [Abstract][Full Text] [Related]
48. Defective roles of ATP7B missense mutations in cellular copper tolerance and copper excretion.
Zhu M; Dong Y; Ni W; Wu ZY
Mol Cell Neurosci; 2015 Jul; 67():31-6. PubMed ID: 26032686
[TBL] [Abstract][Full Text] [Related]
49. [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]
50. Correction of the copper transport defect of Menkes patient fibroblasts by expression of two forms of the sheep Wilson ATPase.
Lockhart PJ; La Fontaine S; Firth SD; Greenough M; Camakaris J; Mercer JF
Biochim Biophys Acta; 2002 Nov; 1588(2):189-94. PubMed ID: 12385784
[TBL] [Abstract][Full Text] [Related]
51. Interactions between metal-binding domains modulate intracellular targeting of Cu(I)-ATPase ATP7B, as revealed by nanobody binding.
Huang Y; Nokhrin S; Hassanzadeh-Ghassabeh G; Yu CH; Yang H; Barry AN; Tonelli M; Markley JL; Muyldermans S; Dmitriev OY; Lutsenko S
J Biol Chem; 2014 Nov; 289(47):32682-93. PubMed ID: 25253690
[TBL] [Abstract][Full Text] [Related]
52. Endosomal trafficking of the Menkes copper ATPase ATP7A is mediated by vesicles containing the Rab7 and Rab5 GTPase proteins.
Pascale MC; Franceschelli S; Moltedo O; Belleudi F; Torrisi MR; Bucci C; La Fontaine S; Mercer JF; Leone A
Exp Cell Res; 2003 Dec; 291(2):377-85. PubMed ID: 14644159
[TBL] [Abstract][Full Text] [Related]
53. Development of a high-resolution melting method for the screening of Wilson disease-related ATP7B gene mutations.
Lin CW; Er TK; Tsai FJ; Liu TC; Shin PY; Chang JG
Clin Chim Acta; 2010 Sep; 411(17-18):1223-31. PubMed ID: 20465995
[TBL] [Abstract][Full Text] [Related]
54. Expression in mouse kidney of membrane copper transporters Atp7a and Atp7b.
Moore SD; Cox DW
Nephron; 2002; 92(3):629-34. PubMed ID: 12372948
[TBL] [Abstract][Full Text] [Related]
55. [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]
56. Clinical and genetic analysis of pediatric patients with Wilson disease.
Şimşek Papur Ö; Aşık Akman S; Terzioğlu O
Turk J Gastroenterol; 2015 Sep; 26(5):397-403. PubMed ID: 26215059
[TBL] [Abstract][Full Text] [Related]
57. Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).
Seidel J; Caca K; Schwab SG; Berr F; Wildenauer DB; Mentzel HJ; Horn N; Kauf E
Cell Mol Biol (Noisy-le-grand); 2001; 47 Online Pub():OL149-57. PubMed ID: 11936861
[TBL] [Abstract][Full Text] [Related]
58. Wilson disease: pathogenesis and clinical considerations in diagnosis and treatment.
Rosencrantz R; Schilsky M
Semin Liver Dis; 2011 Aug; 31(3):245-59. PubMed ID: 21901655
[TBL] [Abstract][Full Text] [Related]
59. 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]
60. Distinct functional roles for the Menkes and Wilson copper translocating P-type ATPases in human placental cells.
Hardman B; Michalczyk A; Greenough M; Camakaris J; Mercer J; Ackland L
Cell Physiol Biochem; 2007; 20(6):1073-84. PubMed ID: 17975309
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
