1014 related articles for article (PubMed ID: 17717039)
1. 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]
2. [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]
3. 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]
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. 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]
6. 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]
7. 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]
8. 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]
9. [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]
10. 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]
11. 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]
12. 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]
13. Solution structures of the actuator domain of ATP7A and ATP7B, the Menkes and Wilson disease proteins.
Banci L; Bertini I; Cantini F; Migliardi M; Natile G; Nushi F; Rosato A
Biochemistry; 2009 Aug; 48(33):7849-55. PubMed ID: 19645496
[TBL] [Abstract][Full Text] [Related]
14. Copper transport and its alterations in Menkes and Wilson diseases.
DiDonato M; Sarkar B
Biochim Biophys Acta; 1997 Feb; 1360(1):3-16. PubMed ID: 9061035
[No Abstract] [Full Text] [Related]
15. 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]
16. Function and regulation of the mammalian copper-transporting ATPases: insights from biochemical and cell biological approaches.
Lutsenko S; Petris MJ
J Membr Biol; 2003 Jan; 191(1):1-12. PubMed ID: 12532272
[TBL] [Abstract][Full Text] [Related]
17. Wilson disease.
Harada M
Med Electron Microsc; 2002 Jun; 35(2):61-6. PubMed ID: 12181646
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
