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A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy
N-glycosylation mediates many biological functions. Genetic defects in the N-glycosylation pathway cause >35 inherited human disorders called congenital disorders of glycosylation (CDGs). As a result, some N-glycosylation sites are unoccupied. Serum transferrin is a diagnostic marker for these pa...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Federation of American Societies for Experimental Biology
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3448770/ https://ncbi.nlm.nih.gov/pubmed/22691915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.12-211656 |
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