(Q34093285)

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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip

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scholarly article

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Europe PubMed Central

PubMed publication ID

31 July 2017

A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

congenital disorder

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congenital disorder of glycosylation Ip

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1 reference

based on heuristic

inferred from title

metabolic disease

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based on heuristic

inferred from title

congenital disorder

1 reference

based on heuristic

inferred from title

author name string

Nina Rind

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Verena Schmeiser

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Christian Thiel

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Birgit Absmanner

4

1 reference

Europe PubMed Central

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31 July 2017

Jürgen Lübbehusen

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Julia Hocks

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Neophytos Apeshiotis

7

1 reference

Europe PubMed Central

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31 July 2017

Ekkehard Wilichowski

8

1 reference

Europe PubMed Central

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31 July 2017

Ludwig Lehle

9

1 reference

Europe PubMed Central

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31 July 2017

Christian Körner

10

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31 July 2017

publication date

15 January 2010

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31 July 2017

Human Molecular Genetics

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31 July 2017

19

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31 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1413-1424

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Human RFT1 deficiency leads to a disorder of N-linked glycosylation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Congenital disorders of glycosylation: a rapidly expanding disease family

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Congenital Disorders of Glycosylation: CDG-I, CDG-II, and beyond

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Biochemical characterization and membrane topology of Alg2 from Saccharomyces cerevisiae as a bifunctional alpha1,3- and 1,6-mannosyltransferase involved in lipid-linked oligosaccharide biosynthesis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Physical interactions between the Alg1, Alg2, and Alg11 mannosyltransferases of the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

The yeast ALG11 gene specifies addition of the terminal alpha 1,2-Man to the Man5GlcNAc2-PP-dolichol N-glycosylation intermediate formed on the cytosolic side of the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

On the nomenclature of congenital disorders of glycosylation (CDG).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Free oligosaccharide regulation during mammalian protein N-glycosylation.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Structures and mechanisms of glycosyltransferases

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

The oligosaccharyltransferase complex from Saccharomyces cerevisiae. Isolation of the OST6 gene, its synthetic interaction with OST3, and analysis of the native complex

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

A new type of congenital disorders of glycosylation (CDG-Ii) provides new insights into the early steps of dolichol-linked oligosaccharide biosynthesis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ016

21 January 2018

Identifiers

10.1093/HMG/DDQ016

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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