These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
305 related articles for article (PubMed ID: 9813047)
1. 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]
2. 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]
3. The Menkes copper transporter is required for the activation of tyrosinase. Petris MJ; Strausak D; Mercer JF Hum Mol Genet; 2000 Nov; 9(19):2845-51. PubMed ID: 11092760 [TBL] [Abstract][Full Text] [Related]
4. Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants. La Fontaine S; Firth SD; Lockhart PJ; Brooks H; Camakaris J; Mercer JF Hum Mol Genet; 1999 Jun; 8(6):1069-75. PubMed ID: 10332039 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Functional analysis and intracellular localization of the human menkes protein (MNK) stably expressed from a cDNA construct in Chinese hamster ovary cells (CHO-K1). La Fontaine S; Firth SD; Lockhart PJ; Brooks H; Parton RG; Camakaris J; Mercer JF Hum Mol Genet; 1998 Aug; 7(8):1293-300. PubMed ID: 9668172 [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. Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: a novel mechanism of regulated trafficking. Petris MJ; Mercer JF; Culvenor JG; Lockhart P; Gleeson PA; Camakaris J EMBO J; 1996 Nov; 15(22):6084-95. PubMed ID: 8947031 [TBL] [Abstract][Full Text] [Related]
9. Intracellular localization of the Menkes and Wilson's disease proteins and their role in intracellular copper transport. Suzuki M; Gitlin JD Pediatr Int; 1999 Aug; 41(4):436-42. PubMed ID: 10453201 [TBL] [Abstract][Full Text] [Related]
10. 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]
12. 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]
13. A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease. Dagenais SL; Adam AN; Innis JW; Glover TW Am J Hum Genet; 2001 Aug; 69(2):420-7. PubMed ID: 11431706 [TBL] [Abstract][Full Text] [Related]
14. The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal. Petris MJ; Mercer JF Hum Mol Genet; 1999 Oct; 8(11):2107-15. PubMed ID: 10484781 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]