N-glycosylation site occupancy in serum glycoproteins using multiple reaction monitoring liquid chromatography-mass spectrometry. (Q54184910)

26 May 2018

title

N-glycosylation site occupancy in serum glycoproteins using multiple reaction monitoring liquid chromatography-mass spectrometry. (English)

1 reference

26 May 2018

1 reference

Andreas J Hülsmeier

1 reference

26 May 2018

Patricie Paesold-Burda

series ordinal

1 reference

26 May 2018

Thierry Hennet

series ordinal

1 reference

26 May 2018

publication date

6 September 2007

1 reference

26 May 2018

Molecular & Cellular Proteomics

published in

1 reference

26 May 2018

volume

1 reference

26 May 2018

issue

1 reference

26 May 2018

page(s)

2132-2138

1 reference

26 May 2018

Glycosylation in cellular mechanisms of health and disease

cites work

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Altered glycan structures: the molecular basis of congenital disorders of glycosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Congenital disorders of glycosylation: a rapidly expanding disease family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Diagnosis of congenital disorders of glycosylation type-I using protein chip technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Mass spectrometry for congenital disorders of glycosylation, CDG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Mass spectrometry and protein analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

N-glycosylation site mapping of human serotransferrin by serial lectin affinity chromatography, fast atom bombardment-mass spectrometry, and 1H nuclear magnetic resonance spectroscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Identification of carbohydrate deficient transferrin forms by MALDI-TOF mass spectrometry and lectin ELISABiochim Biophys Acta 1998 Aug 24;1381(3):356.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Absolute quantification of proteins and phosphoproteins from cell lysates by tandem MS

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

18O-labeling of N-glycosylation sites to improve the identification of gel-separated glycoproteins using peptide mass mapping and database searching.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Lectin affinity capture, isotope-coded tagging and mass spectrometry to identify N-linked glycoproteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Triple quadrupole linear ion trap mass spectrometer for the analysis of small molecules and macromolecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

The molecular basis of coupling of translocation and N-glycosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FMCP.M700361-MCP200

10.1074/MCP.M700361-MCP200

21 January 2018

Identifiers

DOI

1 reference

26 May 2018

release_x25jzztz5bckzle4hsasem5x5i

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/x25jzztz5bckzle4hsasem5x5i

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

26 May 2018