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Gilliam, T. Conrad
One or more keywords matched the following items that are connected to Gilliam, T. Conrad
Item TypeName
Concept Hepatolenticular Degeneration
Academic Article Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.
Academic Article Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.
Academic Article Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions.
Academic Article Arm tremor secondary to Wilson's disease.
Academic Article An international symposium on Wilson's and Menkes' diseases.
Academic Article Genetic disorders of copper metabolism.
Academic Article Heterologous expression of the metal-binding domains of human copper-transporting ATPases (P1-ATPases).
Academic Article Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice.
Academic Article Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments.
Academic Article Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice
Academic Article The Wilson disease gene is a copper transporting ATPase with homology to the Menkes Disease gene
Academic Article Physical mapping, cloning, and genetic characterization of the Wilson disease locus
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  • Hepatolenticular Degeneration