1. Shrimal, Shiteshu, Ng, Bobby G, Losfeld, Marie-Estelle, Gilmore, Reid, Freeze, Hudson H. 2013. Mutations in STT3A and STT3B cause two congenital disorders of glycosylation. In Human molecular genetics, 22, 4638-45. doi:10.1093/hmg/ddt312. https://pubmed.ncbi.nlm.nih.gov/23842455/
2. Shrimal, Shiteshu, Cherepanova, Natalia A, Gilmore, Reid. 2014. Cotranslational and posttranslocational N-glycosylation of proteins in the endoplasmic reticulum. In Seminars in cell & developmental biology, 41, 71-8. doi:10.1016/j.semcdb.2014.11.005. https://pubmed.ncbi.nlm.nih.gov/25460543/
3. Kitajima, Toshihiko, Xue, Wei, Liu, Yi-Shi, Fujita, Morihisa, Gao, Xiao-Dong. 2018. Construction of green fluorescence protein mutant to monitor STT3B-dependent N-glycosylation. In The FEBS journal, 285, 915-928. doi:10.1111/febs.14375. https://pubmed.ncbi.nlm.nih.gov/29282902/
4. Zhu, Shenglin, Wan, Weiwei, Zhang, Yanjun, Zhang, Lei-Ke, Xiao, Gengfu. 2019. Comprehensive Interactome Analysis Reveals that STT3B Is Required for N-Glycosylation of Lassa Virus Glycoprotein. In Journal of virology, 93, . doi:10.1128/JVI.01443-19. https://pubmed.ncbi.nlm.nih.gov/31511384/
5. Prados, María Belén, Sica, Mauricio Pablo, Miranda, Silvia. 2020. Inflammatory conditions promote a switch of oligosaccharyltransferase (OST) catalytic subunit isoform expression. In Archives of biochemistry and biophysics, 693, 108538. doi:10.1016/j.abb.2020.108538. https://pubmed.ncbi.nlm.nih.gov/32810478/
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