180 related articles for article (PubMed ID: 16317117)
21. Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2-, AP-1-, and Rab22-dependent steps.
Holloway ZG; Velayos-Baeza A; Howell GJ; Levecque C; Ponnambalam S; Sztul E; Monaco AP
Mol Biol Cell; 2013 Jun; 24(11):1735-48, S1-8. PubMed ID: 23596324
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein.
Kim BE; Petris MJ
J Med Genet; 2007 Oct; 44(10):641-6. PubMed ID: 17483305
[TBL] [Abstract][Full Text] [Related]
24. Multiple Menkes copper ATPase (Atp7a) transcript and protein variants are induced by iron deficiency in rat duodenal enterocytes.
Lu Y; Kim C; Collins JF
J Trace Elem Med Biol; 2012 Jun; 26(2-3):109-14. PubMed ID: 22579041
[TBL] [Abstract][Full Text] [Related]
25. Mutational analysis of the Menkes copper P-type ATPase (ATP7A).
Voskoboinik I; Mar J; Camakaris J
Biochem Biophys Res Commun; 2003 Feb; 301(2):488-94. PubMed ID: 12565888
[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. 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]
28. Human macrophage ATP7A is localized in the trans-Golgi apparatus, controls intracellular copper levels, and mediates macrophage responses to dermal wounds.
Kim HW; Chan Q; Afton SE; Caruso JA; Lai B; Weintraub NL; Qin Z
Inflammation; 2012 Feb; 35(1):167-75. PubMed ID: 21336677
[TBL] [Abstract][Full Text] [Related]
29. Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPases.
La Fontaine SL; Firth SD; Camakaris J; Englezou A; Theophilos MB; Petris MJ; Howie M; Lockhart PJ; Greenough M; Brooks H; Reddel RR; Mercer JF
J Biol Chem; 1998 Nov; 273(47):31375-80. PubMed ID: 9813047
[TBL] [Abstract][Full Text] [Related]
30. Direct interactions of adaptor protein complexes 1 and 2 with the copper transporter ATP7A mediate its anterograde and retrograde trafficking.
Yi L; Kaler SG
Hum Mol Genet; 2015 May; 24(9):2411-25. PubMed ID: 25574028
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Copper-transporting P-type ATPase, ATP7A, confers multidrug resistance and its expression is related to resistance to SN-38 in clinical colon cancer.
Owatari S; Akune S; Komatsu M; Ikeda R; Firth SD; Che XF; Yamamoto M; Tsujikawa K; Kitazono M; Ishizawa T; Takeuchi T; Aikou T; Mercer JF; Akiyama S; Furukawa T
Cancer Res; 2007 May; 67(10):4860-8. PubMed ID: 17510416
[TBL] [Abstract][Full Text] [Related]
33. Conservation of copper-transporting P(IB)-type ATPase function.
Southon A; Palstra N; Veldhuis N; Gaeth A; Robin C; Burke R; Camakaris J
Biometals; 2010 Aug; 23(4):681-94. PubMed ID: 20372979
[TBL] [Abstract][Full Text] [Related]
34. Functional and molecular responses of suckling rat pups and human intestinal Caco-2 cells to copper treatment.
Bauerly KA; Kelleher SL; Lönnerdal B
J Nutr Biochem; 2004 Mar; 15(3):155-62. PubMed ID: 15023397
[TBL] [Abstract][Full Text] [Related]
35. Dynamics of endogenous ATP7A (Menkes protein) in intestinal epithelial cells: copper-dependent redistribution between two intracellular sites.
Nyasae L; Bustos R; Braiterman L; Eipper B; Hubbard A
Am J Physiol Gastrointest Liver Physiol; 2007 Apr; 292(4):G1181-94. PubMed ID: 17158254
[TBL] [Abstract][Full Text] [Related]
36. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.
Kennerson ML; Nicholson GA; Kaler SG; Kowalski B; Mercer JF; Tang J; Llanos RM; Chu S; Takata RI; Speck-Martins CE; Baets J; Almeida-Souza L; Fischer D; Timmerman V; Taylor PE; Scherer SS; Ferguson TA; Bird TD; De Jonghe P; Feely SM; Shy ME; Garbern JY
Am J Hum Genet; 2010 Mar; 86(3):343-52. PubMed ID: 20170900
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Small amounts of functional ATP7A protein permit mild phenotype.
Møller LB
J Trace Elem Med Biol; 2015; 31():173-7. PubMed ID: 25172213
[TBL] [Abstract][Full Text] [Related]
39. Modulation of the cellular pharmacology of cisplatin and its analogs by the copper exporters ATP7A and ATP7B.
Samimi G; Katano K; Holzer AK; Safaei R; Howell SB
Mol Pharmacol; 2004 Jul; 66(1):25-32. PubMed ID: 15213293
[TBL] [Abstract][Full Text] [Related]
40. Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions in ATP7A.
Tümer Z; Birk Møller L; Horn N
Hum Mutat; 2003 Dec; 22(6):457-64. PubMed ID: 14635105
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]