Retention in the endoplasmic reticulum is the underlying mechanism of some hereditary haemorrhagic telangiectasia type 2 ALK1 missense mutations. [electronic resource]
Producer: 20130531Description: 247-57 p. digitalISSN:- 1573-4919
- Activin Receptors, Type II -- genetics
- Calnexin -- metabolism
- Endoplasmic Reticulum -- enzymology
- Green Fluorescent Proteins -- genetics
- HeLa Cells
- Humans
- Microscopy, Fluorescence
- Mutation, Missense
- Protein Transport
- Recombinant Fusion Proteins -- genetics
- Telangiectasia, Hereditary Hemorrhagic -- enzymology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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