LE WE PMID CA
ATP7B5236ATP7B

ATP7A

ATP7B

Cisplatin

Copper

Ctr1

CTR2

Menkes s disease

Transporter (Copper)

Wilson s disease

1998  
1
Physiologic function of the Wilson disease gene product, ATP7B.
[9587140] Am J Clin Nutr 67(5 Suppl): 982S-987S (1998)
2010  
2
Mammalian copper-transporting P-type ATPases, ATP7A and ATP7B: emerging roles.
[19922814] Int J Biochem Cell Biol 42(2): 206-9 (2010)
2002  
3
Molecular mechanism of copper transport in Wilson disease.
[12426114] Environ Health Perspect 110 Suppl 5(-): 695-8 (2002)
2007  
4
Biochemical basis of regulation of human copper-transporting ATPases.
[17562324] Arch Biochem Biophys 463(2): 134-48 (2007)
2009  
5
Human copper transporters: mechanism, role in human diseases and therapeutic potential.
[20454597] Future Med Chem 1(6): 1125-42 (2009)
2007  
6
Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.
[17717039] J Med Genet 44(11): 673-88 (2007)
PMC   
7
Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B.
[24706876] Proc Natl Acad Sci U S A 111(14):E1364-73 (2014)

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  • ATP7B

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