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Items: 1 to 20 of 402

1.
2.
3.

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. doi: 10.1007/s11030-008-9084-x. Epub 2008 Aug 8.

PMID:
18688737
4.

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 15;10(4):361-70.

PMID:
11157799
5.

Purification and functional analysis of the copper ATPase CopA of Enterococcus hirae.

Wunderli-Ye H, Solioz M.

Biochem Biophys Res Commun. 2001 Jan 26;280(3):713-9.

PMID:
11162579
6.

Primary structure of two P-type ATPases involved in copper homeostasis in Enterococcus hirae.

Odermatt A, Suter H, Krapf R, Solioz M.

J Biol Chem. 1993 Jun 15;268(17):12775-9.

7.

Copper pumping ATPases: common concepts in bacteria and man.

Solioz M, Odermatt A, Krapf R.

FEBS Lett. 1994 Jun 6;346(1):44-7. Review.

8.

A comparison of the mutation spectra of Menkes disease and Wilson disease.

Hsi G, Cox DW.

Hum Genet. 2004 Jan;114(2):165-72. Epub 2003 Oct 25.

PMID:
14579150
9.

[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. doi: 10.1016/j.patbio.2008.09.004. Epub 2008 Nov 28. French.

PMID:
19046832
10.

Menkes and Wilson diseases.

Monaco AP, Chelly J.

Adv Genet. 1995;33:233-53. Review. No abstract available.

PMID:
7484454
11.

Physiologic function of the Wilson disease gene product, ATP7B.

Bingham MJ, Ong TJ, Summer KH, Middleton RB, McArdle HJ.

Am J Clin Nutr. 1998 May;67(5 Suppl):982S-987S. Review.

PMID:
9587140
12.

The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B.

Tsivkovskii R, Efremov RG, Lutsenko S.

J Biol Chem. 2003 Apr 11;278(15):13302-8. Epub 2003 Jan 27.

14.

[Structure and function of ATP7A and ATP7B proteins--Cu-transporting ATPases].

Lenartowicz M, Krzeptowski W.

Postepy Biochem. 2010;56(3):317-27. Review. Polish.

PMID:
21117320
15.

Induction of the putative copper ATPases, CopA and CopB, of Enterococcus hirae by Ag+ and Cu2+, and Ag+ extrusion by CopB.

Odermatt A, Krapf R, Solioz M.

Biochem Biophys Res Commun. 1994 Jul 15;202(1):44-8.

PMID:
8037745
16.

Mutational analysis of the Menkes copper P-type ATPase (ATP7A).

Voskoboinik I, Mar J, Camakaris J.

Biochem Biophys Res Commun. 2003 Feb 7;301(2):488-94.

PMID:
12565888
18.

Copper transporting P-type ATPases and human disease.

Cox DW, Moore SD.

J Bioenerg Biomembr. 2002 Oct;34(5):333-8. Review.

PMID:
12539960
19.

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. Review.

PMID:
9890194
20.

Biochemical characterization of CopA, the Escherichia coli Cu(I)-translocating P-type ATPase.

Fan B, Rosen BP.

J Biol Chem. 2002 Dec 6;277(49):46987-92. Epub 2002 Sep 25.

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