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Identification of Intercellular Cell Adhesion Molecule 1 (ICAM-1) as a Hypoglycosylation Marker in Congenital Disorders of Glycosylation Cells

Many human inherited disorders cause protein N-glycosylation defects, but there are few cellular markers to test gene complementation for such defects. Plasma membrane glycoproteins are potential biomarkers because they may be reduced or even absent in plasma membranes of glycosylation-deficient cel...

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Библиографические подробности
Главные авторы: He, Ping, Ng, Bobby G., Losfeld, Marie-Estelle, Zhu, Wenhong, Freeze, Hudson H.
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Biochemistry and Molecular Biology 2012
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3365753/
https://ncbi.nlm.nih.gov/pubmed/22496445
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M112.355677
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