Protein O-mannosylation is necessary for normal embryonic development in zebrafish
Author:
Publisher
Oxford University Press (OUP)
Subject
Biochemistry
Link
http://academic.oup.com/glycob/article-pdf/20/9/1089/5849375/cwq069.pdf
Reference47 articles.
1. Mutations of the POMT1 gene found in patients with Walker–Warburg syndrome lead to a defect of protein O-mannosylation
2. Physical and Functional Association of Human Protein O-Mannosyltransferases 1 and 2
3. The zebrafish as a model for muscular dystrophy and congenital myopathy
4. Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo
5. Fukutin-related Protein Associates with the Sarcolemmal Dystrophin-Glycoprotein Complex
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5. Mammalian O-mannosyl glycans: Biochemistry and glycopathology;Proceedings of the Japan Academy, Series B;2019-01-11
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