120 related articles for article (PubMed ID: 9354393)
1. Caenorhabditis elegans cDNA for a Menkes/Wilson disease gene homologue and its function in a yeast CCC2 gene deletion mutant.
Sambongi Y; Wakabayashi T; Yoshimizu T; Omote H; Oka T; Futai M
J Biochem; 1997 Jun; 121(6):1169-75. PubMed ID: 9354393
[TBL] [Abstract][Full Text] [Related]
2. The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake.
Yuan DS; Stearman R; Dancis A; Dunn T; Beeler T; Klausner RD
Proc Natl Acad Sci U S A; 1995 Mar; 92(7):2632-6. PubMed ID: 7708696
[TBL] [Abstract][Full Text] [Related]
3. Transcriptional remodelling in response to changing copper levels in the Wilson and Menkes disease model of Saccharomyces cerevisiae.
Cankorur-Cetinkaya A; Eraslan S; Kirdar B
Mol Biosyst; 2013 Nov; 9(11):2889-908. PubMed ID: 24056782
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Analysis of functional domains of Wilson disease protein (ATP7B) in Saccharomyces cerevisiae.
Iida M; Terada K; Sambongi Y; Wakabayashi T; Miura N; Koyama K; Futai M; Sugiyama T
FEBS Lett; 1998 May; 428(3):281-5. PubMed ID: 9654149
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Structure-function analysis of purified Enterococcus hirae CopB copper ATPase: effect of Menkes/Wilson disease mutation homologues.
Bissig KD; Wunderli-Ye H; Duda PW; Solioz M
Biochem J; 2001 Jul; 357(Pt 1):217-23. PubMed ID: 11415452
[TBL] [Abstract][Full Text] [Related]
8. P-type ATPase from the cyanobacterium Synechococcus 7942 related to the human Menkes and Wilson disease gene products.
Phung LT; Ajlani G; Haselkorn R
Proc Natl Acad Sci U S A; 1994 Sep; 91(20):9651-4. PubMed ID: 7937823
[TBL] [Abstract][Full Text] [Related]
9. Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease.
Yamaguchi Y; Heiny ME; Gitlin JD
Biochem Biophys Res Commun; 1993 Nov; 197(1):271-7. PubMed ID: 8250934
[TBL] [Abstract][Full Text] [Related]
10. Quantitative relationship between mutated amino-acid sequence of human copper-transporting ATPases and their related diseases.
Yan S; Wu G
Mol Divers; 2008 May; 12(2):119-29. PubMed ID: 18688737
[TBL] [Abstract][Full Text] [Related]
11. Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases.
Payne AS; Gitlin JD
J Biol Chem; 1998 Feb; 273(6):3765-70. PubMed ID: 9452509
[TBL] [Abstract][Full Text] [Related]
12. Expression of the Wilson disease gene is deficient in the Long-Evans Cinnamon rat.
Yamaguchi Y; Heiny ME; Shimizu N; Aoki T; Gitlin JD
Biochem J; 1994 Jul; 301 ( Pt 1)(Pt 1):1-4. PubMed ID: 8037655
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.
Papur OS; Terzioglu O; Koc A
J Trace Elem Med Biol; 2015; 31():33-6. PubMed ID: 26004889
[TBL] [Abstract][Full Text] [Related]
15. Genetic and molecular basis for copper toxicity.
Harris ZL; Gitlin JD
Am J Clin Nutr; 1996 May; 63(5):836S-41S. PubMed ID: 8615371
[TBL] [Abstract][Full Text] [Related]
16. Sequence, mapping and disruption of CCC2, a gene that cross-complements the Ca(2+)-sensitive phenotype of csg1 mutants and encodes a P-type ATPase belonging to the Cu(2+)-ATPase subfamily.
Fu D; Beeler TJ; Dunn TM
Yeast; 1995 Mar; 11(3):283-92. PubMed ID: 7785328
[TBL] [Abstract][Full Text] [Related]
17. Essential Cys-Pro-Cys motif of Caenorhabditis elegans copper transport ATPase.
Yoshimizu T; Omote H; Wakabayashi T; Sambongi Y; Futai M
Biosci Biotechnol Biochem; 1998 Jun; 62(6):1258-60. PubMed ID: 9692213
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Novel bacterial P-type ATPases with histidine-rich heavy-metal-associated sequences.
Trenor C; Lin W; Andrews NC
Biochem Biophys Res Commun; 1994 Dec; 205(3):1644-50. PubMed ID: 7811248
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
