Transferrin glycosylation analysis from dried blood spot cards and capillary blood samples
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Clinical Biochemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference27 articles.
1. Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome;Jaeken;Clin. Chim. Acta,1984
2. Congenital disorders of glycosylation: review of their molecular bases, clinical presentations and specific therapies;Marquardt;Eur. J. Pediatr.,2003
3. Perspectives on glycosylation and its congenital disorders;Ng;Trends Genet.,2018
4. Congenital disorders of glycosylation (CDG): it's (nearly) all in it!;Jaeken;J. Inherit. Metab. Dis.,2011
5. Clinical diagnostics and therapy monitoring in the congenital disorders of glycosylation;Van Scherpenzeel;Glycoconj. J.,2016
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1. Comparative analysis of transferrin and IgG N-glycosylation in two human populations;Communications Biology;2023-03-23
2. Mass Spectrometry of Transferrin and Apolipoprotein CIII from Dried Blood Spots for Congenital Disorders of Glycosylation;Mass Spectrometry;2022-12-28
3. Congenital Disorders of Glycosylation: What Clinicians Need to Know?;Frontiers in Pediatrics;2021-09-03
4. Translational balancing questioned: Unaltered glycosylation during disulfiram treatment in mannosyl‐oligosaccharide alpha‐1,2‐mannnosidase ‐ congenital disorders of glycosylation (MAN1B1‐CDG);JIMD Reports;2021-03-20
5. Transferrin isoform analysis from dried blood spots and serum samples by gel isoelectric focusing for screening congenital disorders of glycosylation;Acta Biochimica Polonica;2021-03-05
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