Mass spectrometric analysis of glycans in elucidating the pathogenesis of CDG type IIx . (Q30972875)

27 June 2017

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title

Mass spectrometric analysis of glycans in elucidating the pathogenesis of CDG type IIx . (English)

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27 June 2017

Peter Theodore Clayton

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ORCID Public Data File 2021

author name string

Mills PB

1

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27 June 2017

Mills K

2

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27 June 2017

Mian N

3

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27 June 2017

Winchester BG

4

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27 June 2017

Clayton PT

5

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27 June 2017

1 January 2003

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Journal of Inherited Metabolic Disease

27 June 2017

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27 June 2017

26

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27 June 2017

119-134

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27 June 2017

2-3

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Identification of protein-bound carbohydrates by mass spectrometry

27 June 2017

1 reference

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Protein glycosylation: nature, distribution, enzymatic formation, and disease implications of glycopeptide bonds

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Biological roles of oligosaccharides: all of the theories are correct

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A novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency

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Fast sequencing of oligosaccharides: the reagent-array analysis method

1 reference

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Capillary electrophoresis/electrospray ion trap mass spectrometry for the analysis of negatively charged derivatized and underivatized glycans

1 reference

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The joys of HexNAc. The synthesis and function of N- and O-glycan branches

1 reference

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Structural determination of N-linked carbohydrates by matrix-assisted laser desorption/ionization-mass spectrometry following enzymatic release within sodium dodecyl sulphate-polyacrylamide electrophoresis gels: application to species-specific glyco

1 reference

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Electrospray mass spectrometry and fragmentation of N-linked carbohydrates derivatized at the reducing terminus

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Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase

1 reference

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Mass Spectrometric Sequencing of Proteins from Silver-Stained Polyacrylamide Gels

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Selective inhibition of beta-1,4- and alpha-1,3-galactosyltransferases: donor sugar-nucleotide based approach

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Negative-ion electrospray mass spectrometry of neutral underivatized oligosaccharides

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A new type of carbohydrate-deficient glycoprotein syndrome due to a decreased import of GDP-fucose into the golgi

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Ultrasensitive profiling and sequencing of N-linked oligosaccharides using standard DNA-sequencing equipment.

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F.A.B.-mass spectrometry of carbohydrates

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Protein glycosylation in development and disease

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On the frequency of protein glycosylation, as deduced from analysis of the SWISS-PROT database

1 reference

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Matrix-assisted laser desorption/ionization mass spectrometry of carbohydrates

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Electrospray ionization-mass spectrometric analysis of serum transferrin isoforms in patients with carbohydrate-deficient glycoprotein syndrome

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Defective galactosylation of serum transferrin in galactosemia

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Sequential deglycosylation and utilization of the N-linked, complex-type glycans of human alpha1-acid glycoprotein mediates growth of Streptococcus oralis

1 reference

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A calculation of all possible oligosaccharide isomers both branched and linear yields 1.05 x 10(12) structures for a reducing hexasaccharide: the Isomer Barrier to development of single-method saccharide sequencing or synthesis systems

1 reference

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Glycoscreening by on-line sheathless capillary electrophoresis/electrospray ionization-quadrupole time of flight-tandem mass spectrometry

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Analysis of acidic oligosaccharides and glycopeptides by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

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ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg

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HEMPAS. Hereditary erythroblastic multinuclearity with positive acidified serum lysis test

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Determination of glycan structures and molecular masses of the glycovariants of serum transferrin from a patient with carbohydrate deficient syndrome type II

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Congenital disorders of glycosylation: genetic model systems lead the way.

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Structural investigations of glycoconjugates at high sensitivity

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Structural analysis of oligosaccharides by atmospheric pressure matrix-assisted laser desorption/ionisation quadrupole ion trap mass spectrometry

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Carbohydrate-deficient glycoprotein syndromes: inborn errors of protein glycosylation

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Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.

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Highly enhanced fucosylation of serum glycoproteins in patients with hepatocellular carcinoma

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Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylation

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12 December 2020

Molecular cloning and expression of cDNAs encoding human alpha-mannosidase II and a previously unrecognized alpha-mannosidase IIx isozyme

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Congenital disorders of glycosylation

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12 December 2020

Facile sequencing of oligosaccharides by matrix-assisted laser desorption/ionisation on a hybrid quadrupole orthogonal acceleration time-of-flight mass spectrometer

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Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technology

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12 December 2020

Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1

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Glycoprotein structure determination by mass spectrometry

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12 December 2020

A general approach to desalting oligosaccharides released from glycoproteins

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12 December 2020

Glycosylation and rheumatic disease

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Intracellular functions of N-linked glycans

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12 December 2020

Carbohydrate-based measurements on alpha-fetoprotein in the early diagnosis of hepatocellular carcinoma

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Initial sequencing and analysis of the human genome

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12 December 2020

Identifiers

DOI

10.1023/A:1024476915278

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Dimensions Publication ID

27 June 2017

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