105 related articles for article (PubMed ID: 12540288)
1. Drug targets in Menkes disease - prospective developments.
Kodama H; Gu YH; Mizunuma M
Expert Opin Ther Targets; 2001 Oct; 5(5):625-635. PubMed ID: 12540288
[TBL] [Abstract][Full Text] [Related]
2. Clinical manifestations and treatment of Menkes disease and its variants.
Kodama H; Murata Y; Kobayashi M
Pediatr Int; 1999 Aug; 41(4):423-9. PubMed ID: 10453199
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Menkes syndrome and animal models.
Mercer JF
Am J Clin Nutr; 1998 May; 67(5 Suppl):1022S-1028S. PubMed ID: 9587146
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. [From gene to disease; Menkes disease: copper deficiency due to an ATP7A-gene defect].
Aldenhoven M; Klomp LW; van Hasselt PM; de Koning TJ; Visser G
Ned Tijdschr Geneeskd; 2007 Oct; 151(41):2266-70. PubMed ID: 17987894
[TBL] [Abstract][Full Text] [Related]
10. Purification and membrane reconstitution of catalytically active Menkes copper-transporting P-type ATPase (MNK; ATP7A).
Hung YH; Layton MJ; Voskoboinik I; Mercer JF; Camakaris J
Biochem J; 2007 Jan; 401(2):569-79. PubMed ID: 17009961
[TBL] [Abstract][Full Text] [Related]
11. Molecular mechanisms of copper metabolism and the role of the Menkes disease protein.
Harrison MD; Dameron CT
J Biochem Mol Toxicol; 1999; 13(2):93-106. PubMed ID: 9890194
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Menkes' disease: heterozygosity testing by quantitative real-time PCR and the dilemma of therapeutic support].
Rittinger O; Sander G; Schaller A; Gallati S; Mayr H; Sperl W
Klin Padiatr; 2005; 217(5):286-90. PubMed ID: 16167277
[TBL] [Abstract][Full Text] [Related]
14. Pathology, clinical features and treatments of congenital copper metabolic disorders--focus on neurologic aspects.
Kodama H; Fujisawa C; Bhadhprasit W
Brain Dev; 2011 Mar; 33(3):243-51. PubMed ID: 21112168
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease.
Ogawa A; Yamamoto S; Takayanagi M; Kogo T; Kanazawa M; Kohno Y
J Hum Genet; 1999; 44(3):206-9. PubMed ID: 10319589
[TBL] [Abstract][Full Text] [Related]
18. Expression of menkes copper-transporting ATPase, MNK, in the lactating human breast: possible role in copper transport into milk.
Ackland ML; Anikijenko P; Michalczyk A; Mercer JF
J Histochem Cytochem; 1999 Dec; 47(12):1553-62. PubMed ID: 10567439
[TBL] [Abstract][Full Text] [Related]
19. Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux.
Camakaris J; Petris MJ; Bailey L; Shen P; Lockhart P; Glover TW; Barcroft C; Patton J; Mercer JF
Hum Mol Genet; 1995 Nov; 4(11):2117-23. PubMed ID: 8589689
[TBL] [Abstract][Full Text] [Related]
20. Essential role for the Menkes ATPase in activation of extracellular superoxide dismutase: implication for vascular oxidative stress.
Qin Z; Itoh S; Jeney V; Ushio-Fukai M; Fukai T
FASEB J; 2006 Feb; 20(2):334-6. PubMed ID: 16371425
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
