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Items: 4

1.

A Temperature-sensitive mutation in the Arabidopsis thaliana phosphomannomutase gene disrupts protein glycosylation and triggers cell death.

Hoeberichts FA, Vaeck E, Kiddle G, Coppens E, van de Cotte B, Adamantidis A, Ormenese S, Foyer CH, Zabeau M, Inzé D, Périlleux C, Van Breusegem F, Vuylsteke M.

J Biol Chem. 2008 Feb 29;283(9):5708-18. Epub 2007 Dec 17.

2.

Molecular basis of carbohydrate-deficient glycoprotein syndromes type I with normal phosphomannomutase activity.

Freeze HH, Aebi M.

Biochim Biophys Acta. 1999 Oct 8;1455(2-3):167-78. Review. Erratum in: Biochim Biophys Acta 2000 Mar 17;1500(3):349.

3.

The prenatal diagnosis of congenital disorders of glycosylation (CDG).

Matthijs G, Schollen E, Van Schaftingen E.

Prenat Diagn. 2004 Feb;24(2):114-6. Review. No abstract available.

PMID:
14974118
4.

Mannose metabolism: more than meets the eye.

Sharma V, Ichikawa M, Freeze HH.

Biochem Biophys Res Commun. 2014 Oct 17;453(2):220-8. doi: 10.1016/j.bbrc.2014.06.021. Epub 2014 Jun 12. Review.

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