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Structural requirements for Arabidopsis beta1,2-xylosyltransferase activity and targeting to the Golgi.

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Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis.

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Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and III.

British journal of haematology·2001

Tissues of the clawed frog Xenopus laevis contain two closely related forms of UDP-GlcNAc:alpha3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I.

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Congenital disorders involving defective N-glycosylation of proteins.

Cellular and molecular life sciences : CMLS·2001

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Postgraduate medicine·2026

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Postgraduate medicine·2026

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Postgraduate medicine·2026

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Anti-cancer agents in medicinal chemistry·2026

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Journal of surgical oncology·2026

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Stroke·2026

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Metabolomic and inflammatory signatures in congenital hypothyroidism: a longitudinal analysis of levothyroxine response.

Frontiers in endocrinology·2026

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Cureus·2026

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Structural requirements for Arabidopsis beta1,2-xylosyltransferase activity and targeting to the Golgi.

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