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Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B(12)) absorption in vivo

Amnionless (AMN) and cubilin gene products appear to be essential functional subunits of an endocytic receptor called cubam. Mutation of either gene causes autosomal recessive Imerslund-Gräsbeck syndrome (I-GS, OMIM no. 261100) in humans, a disorder characterized by selective intestinal malabsorptio...

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Main Authors: He, Qianchuan, Madsen, Mette, Kilkenney, Adam, Gregory, Brittany, Christensen, Erik I., Vorum, Henrik, Højrup, Peter, Schäffer, Alejandro A., Kirkness, Ewen F., Tanner, Stephan M., de la Chapelle, Albert, Giger, Urs, Moestrup, Søren K., Fyfe, John C.
Formato: Artigo
Idioma:Inglês
Publicado: The American Society of Hematology 2005
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1895201/
https://ncbi.nlm.nih.gov/pubmed/15845892
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2005-03-1197
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