Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG. (Q35763317)

10 August 2017

Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG. (English)

1 reference

10 August 2017

0 references

4

1 reference

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1 June 2020

Hudson H. Freeze

5

1 reference

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1 June 2020

author name string

Per Bengtson

1

1 reference

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1 June 2020

Bobby G Ng

2

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1 June 2020

Jaak Jaeken

3

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1 June 2020

Erik A Eklund

6

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1 June 2020

language of work or name

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3 September 2015

1 reference

Journal of Inherited Metabolic Disease

10 August 2017

1 reference

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1 June 2020

volume

39

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1 June 2020

page(s)

107-114

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1 June 2020

issue

1

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https://scigraph.springernature.com/pub.10.1007/s10545-015-9884-y

1 June 2020

exact match

0 references

cites work

A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9

1 reference

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Neurological aspects of human glycosylation disorders

2 October 2017

1 reference

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Clinical utility gene card for: ALG1 defective congenital disorder of glycosylation

2 October 2017

1 reference

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29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype

2 October 2017

1 reference

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Congenital disorders of glycosylation: new defects and still counting

2 October 2017

1 reference

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Solving glycosylation disorders: fundamental approaches reveal complicated pathways

2 October 2017

1 reference

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ALG1-CDG: a new case with early fatal outcome

2 October 2017

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Neurology of inherited glycosylation disorders

2 October 2017

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Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient

2 October 2017

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The congenital disorders of glycosylation: a multifaceted group of syndromes

2 October 2017

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Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I

2 October 2017

1 reference

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Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.

2 October 2017

1 reference

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Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.

2 October 2017

1 reference

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A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation

2 October 2017

1 reference

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Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutations

12 July 2018

1 reference

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Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations

12 July 2018

1 reference

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Characterizing protein glycosylation sites through higher-energy C-trap dissociation

25 September 2018

1 reference

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Rapid determination of transferrin isoforms by immunoaffinity liquid chromatography and electrospray mass spectrometry

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26335155

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10545-015-9884-Y

1 reference

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1 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26335155%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

1 reference

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