ORA - Oxford University Research Archive

1 - 3 of 3

1

Journal article

Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.

Senderek, J, Müller, JS, Dusl, M, et al.
2011-02-05

2

Journal article

Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR.

Zoltowska, K, Webster, R, Finlayson, S, et al.
2013-07-05

3

Journal article

Activation of hexosamine pathway impairs nitric oxide (NO)-dependent arteriolar dilations by increased protein O-GlcNAcylation.

Beleznai, T, Bagi, Z
2012-03-05

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