399 related articles for article (PubMed ID: 11157799)
21. Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?
Forbes JR; Cox DW
Am J Hum Genet; 1998 Dec; 63(6):1663-74. PubMed ID: 9837819
[TBL] [Abstract][Full Text] [Related]
22. Defective localization of the Wilson disease protein (ATP7B) in the mammary gland of the toxic milk mouse and the effects of copper supplementation.
Michalczyk AA; Rieger J; Allen KJ; Mercer JF; Ackland ML
Biochem J; 2000 Dec; 352 Pt 2(Pt 2):565-71. PubMed ID: 11085952
[TBL] [Abstract][Full Text] [Related]
23. Defective copper-induced trafficking and localization of the Menkes protein in patients with mild and copper-treated classical Menkes disease.
Ambrosini L; Mercer JF
Hum Mol Genet; 1999 Aug; 8(8):1547-55. PubMed ID: 10401004
[TBL] [Abstract][Full Text] [Related]
24. Hormonal regulation of the Menkes and Wilson copper-transporting ATPases in human placental Jeg-3 cells.
Hardman B; Michalczyk A; Greenough M; Camakaris J; Mercer JF; Ackland ML
Biochem J; 2007 Mar; 402(2):241-50. PubMed ID: 17109627
[TBL] [Abstract][Full Text] [Related]
25. Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system.
Hsi G; Cullen LM; Macintyre G; Chen MM; Glerum DM; Cox DW
Hum Mutat; 2008 Apr; 29(4):491-501. PubMed ID: 18203200
[TBL] [Abstract][Full Text] [Related]
26. A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network.
Petris MJ; Camakaris J; Greenough M; LaFontaine S; Mercer JF
Hum Mol Genet; 1998 Dec; 7(13):2063-71. PubMed ID: 9817923
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. 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]
31. Menkes and Wilson diseases.
Monaco AP; Chelly J
Adv Genet; 1995; 33():233-53. PubMed ID: 7484454
[No Abstract] [Full Text] [Related]
32. 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]
33. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.
Bull PC; Thomas GR; Rommens JM; Forbes JR; Cox DW
Nat Genet; 1993 Dec; 5(4):327-37. PubMed ID: 8298639
[TBL] [Abstract][Full Text] [Related]
34. Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
Goodyer ID; Jones EE; Monaco AP; Francis MJ
Hum Mol Genet; 1999 Aug; 8(8):1473-8. PubMed ID: 10400994
[TBL] [Abstract][Full Text] [Related]
35. Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease.
Grimes A; Hearn CJ; Lockhart P; Newgreen DF; Mercer JF
Hum Mol Genet; 1997 Jul; 6(7):1037-42. PubMed ID: 9215672
[TBL] [Abstract][Full Text] [Related]
36. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene.
Tanzi RE; Petrukhin K; Chernov I; Pellequer JL; Wasco W; Ross B; Romano DM; Parano E; Pavone L; Brzustowicz LM
Nat Genet; 1993 Dec; 5(4):344-50. PubMed ID: 8298641
[TBL] [Abstract][Full Text] [Related]
37. Molecular mechanisms of copper homeostasis.
Camakaris J; Voskoboinik I; Mercer JF
Biochem Biophys Res Commun; 1999 Aug; 261(2):225-32. PubMed ID: 10425169
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Wilson disease.
Harada M
Med Electron Microsc; 2002 Jun; 35(2):61-6. PubMed ID: 12181646
[TBL] [Abstract][Full Text] [Related]
40. Functional analysis of the N-terminal CXXC metal-binding motifs in the human Menkes copper-transporting P-type ATPase expressed in cultured mammalian cells.
Voskoboinik I; Strausak D; Greenough M; Brooks H; Petris M; Smith S; Mercer JF; Camakaris J
J Biol Chem; 1999 Jul; 274(31):22008-12. PubMed ID: 10419525
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
