Deletion of the Wilson's disease gene in hereditary hepatitis LEC rats.
Author:
Affiliation:
1. Chromosome Research Unit, Faculty of Science
2. Laboratory of Cytogenetics, Division of Bioscience, Graduate School of Environmental Earth Science, Hokkaido University
3. AISIN COSMOS R & D CO., LTD
Publisher
Genetics Society of Japan
Subject
Genetics,General Medicine
Link
http://www.jstage.jst.go.jp/article/jjg/70/1/70_1_25/_pdf
Reference25 articles.
1. Genetic and biochemical aspects of Wilson's disease
2. The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
3. Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.
4. Histochemical demonstration of copper in LEC rat liver
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1. Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes;Journal of Medical Genetics;2007-08-23
2. Role of tumor necrosis factor-α in the development of spontaneous hepatic toxicity in Long-Evans Cinnamon rats;Toxicology and Applied Pharmacology;2004-10
3. Storage of lipid droplets in and production of extracellular matrix by hepatic stellate cells (vitamin A-storing cells) in Long-Evans cinnamon-like colored (LEC) rats;The Anatomical Record;2000-04-01
4. Report on rat chromosome 16;Journal of Experimental Animal Science;1999-12
5. Molecular Genetics of Menkes Disease;Metals and Genetics;1999
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