310 related articles for article (PubMed ID: 27226607)
1. The Activity of Menkes Disease Protein ATP7A Is Essential for Redox Balance in Mitochondria.
Bhattacharjee A; Yang H; Duffy M; Robinson E; Conrad-Antoville A; Lu YW; Capps T; Braiterman L; Wolfgang M; Murphy MP; Yi L; Kaler SG; Lutsenko S; Ralle M
J Biol Chem; 2016 Aug; 291(32):16644-58. PubMed ID: 27226607
[TBL] [Abstract][Full Text] [Related]
2. Menkes disease.
Bertini I; Rosato A
Cell Mol Life Sci; 2008 Jan; 65(1):89-91. PubMed ID: 17989919
[TBL] [Abstract][Full Text] [Related]
3. Autonomous requirements of the Menkes disease protein in the nervous system.
Hodgkinson VL; Zhu S; Wang Y; Ladomersky E; Nickelson K; Weisman GA; Lee J; Gitlin JD; Petris MJ
Am J Physiol Cell Physiol; 2015 Nov; 309(10):C660-8. PubMed ID: 26269458
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. The lumenal loop Met672-Pro707 of copper-transporting ATPase ATP7A binds metals and facilitates copper release from the intramembrane sites.
Barry AN; Otoikhian A; Bhatt S; Shinde U; Tsivkovskii R; Blackburn NJ; Lutsenko S
J Biol Chem; 2011 Jul; 286(30):26585-94. PubMed ID: 21646353
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Menkes copper-translocating P-type ATPase (ATP7A): biochemical and cell biology properties, and role in Menkes disease.
Voskoboinik I; Camakaris J
J Bioenerg Biomembr; 2002 Oct; 34(5):363-71. PubMed ID: 12539963
[TBL] [Abstract][Full Text] [Related]
8. Transcriptional regulation of the Menkes copper ATPase (Atp7a) gene by hypoxia-inducible factor (HIF2{alpha}) in intestinal epithelial cells.
Xie L; Collins JF
Am J Physiol Cell Physiol; 2011 Jun; 300(6):C1298-305. PubMed ID: 21346155
[TBL] [Abstract][Full Text] [Related]
9. Evidence that translation reinitiation leads to a partially functional Menkes protein containing two copper-binding sites.
Paulsen M; Lund C; Akram Z; Winther JR; Horn N; Møller LB
Am J Hum Genet; 2006 Aug; 79(2):214-29. PubMed ID: 16826513
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. ATP7A-related copper transport diseases-emerging concepts and future trends.
Kaler SG
Nat Rev Neurol; 2011 Jan; 7(1):15-29. PubMed ID: 21221114
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. A single PDZ domain protein interacts with the Menkes copper ATPase, ATP7A. A new protein implicated in copper homeostasis.
Stephenson SE; Dubach D; Lim CM; Mercer JF; La Fontaine S
J Biol Chem; 2005 Sep; 280(39):33270-9. PubMed ID: 16051599
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Alterations in the expression of the Atp7a gene in the early postnatal development of the mosaic mutant mice (Atp7a mo-ms) - An animal model for Menkes disease.
Lenartowicz M; Starzyński R; Wieczerzak K; Krzeptowski W; Lipiński P; Styrna J
Gene Expr Patterns; 2011; 11(1-2):41-7. PubMed ID: 20831904
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux.
Leary SC; Cobine PA; Nishimura T; Verdijk RM; de Krijger R; de Coo R; Tarnopolsky MA; Winge DR; Shoubridge EA
Mol Biol Cell; 2013 Mar; 24(6):683-91. PubMed ID: 23345593
[TBL] [Abstract][Full Text] [Related]
19. Clinical outcomes in Menkes disease patients with a copper-responsive ATP7A mutation, G727R.
Tang J; Donsante A; Desai V; Patronas N; Kaler SG
Mol Genet Metab; 2008 Nov; 95(3):174-81. PubMed ID: 18752978
[TBL] [Abstract][Full Text] [Related]
20. Menkes disease.
Tümer Z; Møller LB
Eur J Hum Genet; 2010 May; 18(5):511-8. PubMed ID: 19888294
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]