|1.||Chen, Chen: 1 article (07/2015)|
|2.||Shen, Bo: 1 article (07/2015)|
|3.||Duff Canning, Sarah Jane: 1 article (07/2015)|
|4.||Wu, Rong: 1 article (07/2015)|
|5.||Wang, Xiao-Ping: 1 article (07/2015)|
|6.||Xiao, Jia-Jia: 1 article (07/2015)|
|7.||Pardasani, Vibhor: 1 article (12/2010)|
|8.||Behari, Madhuri: 1 article (12/2010)|
|9.||Turecky, L: 1 article (01/2008)|
|10.||Szantova, M: 1 article (01/2008)|
|1.||Hepatolenticular Degeneration (Wilson's Disease)
12/01/2004 - "ATP7B is the gene product of the Wilson disease gene located on chromosome 13 and resides in hepatocytes in the trans-Golgi network, transporting copper into the secretory pathway for incorporation into apoceruloplasmin and excretion into the bile. "
08/20/1999 - "Significantly, the developmental expression pattern of sCP was closely correlated with that of the sheep Wilson disease gene (sATP7B), suggesting that the expression of the two genes may be coordinated to ensure that copper is supplied to apoceruloplasmin. "
10/01/1974 - "Determination of apoceruloplasmin by radioimmunoassay in nutritional copper deficiency, Menkes' kinky hair syndrome, Wilson's disease, and umbilical cord blood."
12/01/2010 - "Wilson's disease is a rare autosomal recessive disorder of copper transport due to mutations in the ATP7B gene, responsible for transport of copper into bile from hepatocytes and its incorporation into apoceruloplasmin to form ceruloplasmin resulting in excessive accumulation of copper in the liver and extrahepatic tissues. "
|2.||Whooping Cough (Pertussis)
|3.||Vitamin A Deficiency
|5.||Liver Diseases (Liver Disease)
07/05/2015 - "Decreased biliary copper excretion and reduced incorporation of copper into apoceruloplasmin caused by defunctionalization of ATP7B protein lead to accumulation of copper in many tissues and organs, including liver, brain, and cornea, finally resulting in liver disease and extrapyramidal symptoms. "
|3.||Vitamin A (Retinol)