(Q43580839)

24 November 2017

Increased alpha3-fucosylation of alpha(1)-acid glycoprotein in patients with congenital disorder of glycosylation type IA (CDG-Ia). (English)

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congenital disorder of glycosylation type Ia

24 November 2017

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Van Dijk W

1

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24 November 2017

Koeleman C

2

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24 November 2017

Van het Hof B

3

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24 November 2017

Poland D

4

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24 November 2017

Jakobs C

5

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24 November 2017

Jaeken J

6

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24 November 2017

language of work or name

English

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publication date

1 April 2001

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24 November 2017

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24 November 2017

494

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24 November 2017

3

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24 November 2017

232-235

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Synthesis of GDP-L-fucose by the human FX protein

24 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

A missense mutation in the FUT6 gene results in total absence of alpha3-fucosylation of human alpha1-acid glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Inflammation-induced expression of sialyl Lewis X-containing glycan structures on alpha 1-acid glycoprotein (orosomucoid) in human sera

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Acceptor specificity of GDP-Fuc:Gal beta 1-->4GlcNAc-R alpha 3-fucosyltransferase VI (FucT VI) expressed in insect cells as soluble, secreted enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Modulation of sialyl Lewis X dependent binding to E-selectin by glycoforms of alpha-1-acid glycoprotein expressed in rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Study of the conversion of GDP-mannose into GDP-fucose in Nereids: a biochemical marker of oocyte maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

The degree of branching of the glycans of alpha(1)-acid glycoprotein in asthma. A correlation with lung function and inflammatory parameters

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Glycosylation of three molecular forms of human alpha1-acid glycoprotein having different interactions with concanavalin A. Variations in the occurrence of di-, tri-, and tetraantennary glycans and the degree of sialylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

Glycosylation of alpha1-acid glycoprotein in inflammatory disease: analysis by high-pH anion-exchange chromatography and concanavalin A crossed affinity immunoelectrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2801%2902349-3

10.1016/S0014-5793(01)02349-3

21 January 2018

Identifiers

DOI

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24 November 2017

1 reference