384 related articles for article (PubMed ID: 21242307)
1. 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]
2. Clusterin and COMMD1 independently regulate degradation of the mammalian copper ATPases ATP7A and ATP7B.
Materia S; Cater MA; Klomp LW; Mercer JF; La Fontaine S
J Biol Chem; 2012 Jan; 287(4):2485-99. PubMed ID: 22130675
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. 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]
6. 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]
7. Trafficking of the copper-ATPases, ATP7A and ATP7B: role in copper homeostasis.
La Fontaine S; Mercer JF
Arch Biochem Biophys; 2007 Jul; 463(2):149-67. PubMed ID: 17531189
[TBL] [Abstract][Full Text] [Related]
8. Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.
de Bie P; Muller P; Wijmenga C; Klomp LW
J Med Genet; 2007 Nov; 44(11):673-88. PubMed ID: 17717039
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Advances in the understanding of mammalian copper transporters.
Wang Y; Hodgkinson V; Zhu S; Weisman GA; Petris MJ
Adv Nutr; 2011 Mar; 2(2):129-37. PubMed ID: 22332042
[TBL] [Abstract][Full Text] [Related]
11. The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression.
Vonk WI; de Bie P; Wichers CG; van den Berghe PV; van der Plaats R; Berger R; Wijmenga C; Klomp LW; van de Sluis B
Cell Mol Life Sci; 2012 Jan; 69(1):149-63. PubMed ID: 21667063
[TBL] [Abstract][Full Text] [Related]
12. A comparison of the mutation spectra of Menkes disease and Wilson disease.
Hsi G; Cox DW
Hum Genet; 2004 Jan; 114(2):165-72. PubMed ID: 14579150
[TBL] [Abstract][Full Text] [Related]
13. Molecular mechanisms of copper homeostasis.
Lalioti V; Muruais G; Tsuchiya Y; Pulido D; Sandoval IV
Front Biosci (Landmark Ed); 2009 Jun; 14(13):4878-903. PubMed ID: 19482593
[TBL] [Abstract][Full Text] [Related]
14. Mutation in the CPC motif-containing 6th transmembrane domain affects intracellular localization, trafficking and copper transport efficiency of ATP7A protein in mosaic mutant mice--an animal model of Menkes disease.
Lenartowicz M; Grzmil P; Shoukier M; Starzyński R; Marciniak M; Lipiński P
Metallomics; 2012 Feb; 4(2):197-204. PubMed ID: 22089129
[TBL] [Abstract][Full Text] [Related]
15. Quantitative relationship between mutated amino-acid sequence of human copper-transporting ATPases and their related diseases.
Yan S; Wu G
Mol Divers; 2008 May; 12(2):119-29. PubMed ID: 18688737
[TBL] [Abstract][Full Text] [Related]
16. Role of glutaredoxin1 and glutathione in regulating the activity of the copper-transporting P-type ATPases, ATP7A and ATP7B.
Singleton WCJ; McInnes KT; Cater MA; Winnall WR; McKirdy R; Yu Y; Taylor PE; Ke BX; Richardson DR; Mercer JFB; La Fontaine S
J Biol Chem; 2010 Aug; 285(35):27111-27121. PubMed ID: 20566629
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Intracellular targeting of copper-transporting ATPase ATP7A in a normal and Atp7b-/- kidney.
Linz R; Barnes NL; Zimnicka AM; Kaplan JH; Eipper B; Lutsenko S
Am J Physiol Renal Physiol; 2008 Jan; 294(1):F53-61. PubMed ID: 17928409
[TBL] [Abstract][Full Text] [Related]
19. Structure-function analysis of purified Enterococcus hirae CopB copper ATPase: effect of Menkes/Wilson disease mutation homologues.
Bissig KD; Wunderli-Ye H; Duda PW; Solioz M
Biochem J; 2001 Jul; 357(Pt 1):217-23. PubMed ID: 11415452
[TBL] [Abstract][Full Text] [Related]
20. Physiologic function of the Wilson disease gene product, ATP7B.
Bingham MJ; Ong TJ; Summer KH; Middleton RB; McArdle HJ
Am J Clin Nutr; 1998 May; 67(5 Suppl):982S-987S. PubMed ID: 9587140
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
