T. Conrad Gilliam to Copper
This is a "connection" page, showing publications T. Conrad Gilliam has written about Copper.
Connection Strength
0.426
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Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. Hum Mol Genet. 1999 Sep; 8(9):1665-71.
Score: 0.174
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Genetic disorders of copper metabolism. Curr Opin Pediatr. 1994 Dec; 6(6):698-701.
Score: 0.125
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Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice. Am J Pathol. 2006 Feb; 168(2):423-34.
Score: 0.068
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Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions. Hum Mol Genet. 1994 Sep; 3(9):1647-56.
Score: 0.031
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Heterologous expression of the metal-binding domains of human copper-transporting ATPases (P1-ATPases). Ann N Y Acad Sci. 1997 Nov 03; 834:155-7.
Score: 0.010
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Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments. Biochem J. 1997 Sep 15; 326 ( Pt 3):897-902.
Score: 0.009
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An international symposium on Wilson's and Menkes' diseases. Hepatology. 1996 Oct; 24(4):952-8.
Score: 0.009