MALDI-TOF MS applied to apoC-III glycoforms of patients with congenital disorders affecting O-glycosylation. Comparison with two-dimensional electrophoresis
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Title
MALDI-TOF MS applied to apoC-III glycoforms of patients with congenital disorders affecting O-glycosylation. Comparison with two-dimensional electrophoresis
Authors
Keywords
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Journal
Proteomics Clinical Applications
Volume 9, Issue 7-8, Pages 787-793
Publisher
Wiley
Online
2015-01-12
DOI
10.1002/prca.201400187
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Note: Only part of the references are listed.- MappingO-glycosylation of apolipoprotein C-III in MALDI-FT-ICR protein profiles
- (2013) Simone Nicolardi et al. PROTEOMICS
- Site-specific protein O-glycosylation modulates proprotein processing — Deciphering specific functions of the large polypeptide GalNAc-transferase gene family
- (2012) Katrine T.-B.G. Schjoldager et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- Mass spectrometry of apolipoprotein C-III, a simple analytical method for mucin-type O-glycosylation and its application to an autosomal recessive cutis laxa type-2 (ARCL2) patient
- (2012) Yoshinao Wada et al. GLYCOBIOLOGY
- Glycosylation disorders of membrane trafficking
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- Vertebrate protein glycosylation: diversity, synthesis and function
- (2012) Kelley W. Moremen et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Re‘COG’nition at the Golgi
- (2012) Victoria J. Miller et al. TRAFFIC
- Golgi pH, its regulation and roles in human disease
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- Functional Organization of GolgiN- andO-Glycosylation Pathways Involves pH-dependent Complex Formation That Is Impaired in Cancer Cells
- (2011) Antti Hassinen et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Congenital disorders of glycosylation (CDG): it’s (nearly) all in it!
- (2011) Jaak Jaeken JOURNAL OF INHERITED METABOLIC DISEASE
- Location, location, location: new insights into O-GalNAc protein glycosylation
- (2010) David J. Gill et al. TRENDS IN CELL BIOLOGY
- Vacuolar H+-ATPase meets glycosylation in patients with cutis laxa
- (2009) Mailys Guillard et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Autosomal recessive cutis laxa syndrome revisited
- (2009) Éva Morava et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Comparison of Methods for ProfilingO-Glycosylation
- (2009) Yoshinao Wada et al. MOLECULAR & CELLULAR PROTEOMICS
- O-Glycoside Biomarker of Apolipoprotein C3: Responsiveness to Obesity, Bariatric Surgery, and Therapy with Metformin, to Chronic or Severe Liver Disease and to Mortality in Severe Sepsis and Graft vs Host Disease
- (2008) Stephen B. Harvey et al. JOURNAL OF PROTEOME RESEARCH
- Two dimensional gel electrophoresis of apolipoprotein C-III and MALDI-TOF MS are complementary techniques for the study of combined defects in N- and mucin type O-glycan biosynthesis
- (2008) Arnaud Bruneel et al. Proteomics Clinical Applications
- Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation
- (2007) Renate Zeevaert et al. MOLECULAR GENETICS AND METABOLISM
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