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Melissa Baerenfaenger

Radboud University Nijmegen

11

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48

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Loss of the AMD-associated B3GLCT gene affects glycosylation of TSP1 without impairing secretion in retinal pigment epithelial cells

2021 Experimental Eye Research
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Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings.

2021 American Journal of Human Genetics
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Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability

2020 Journal of Human Genetics
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Congenital disorder of glycosylation caused by starting site-specific variant in syntaxin-5

2020 medRxiv
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Dissecting Total Plasma and Protein-Specific Glycosylation Profiles in Congenital Disorders of Glycosylation

2020 International Journal of Molecular Sciences
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Quantitation of Glycopeptides by ESI/MS - size of the peptide part strongly affects the relative proportions and allows discovery of new glycan compositions of Ceruloplasmin

2019 Glycoconjugate Journal
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In silico evaluation of the binding site of fucosyltransferase 8 and first attempts of synthesizing an inhibitor with drug‐like properties

2019 ChemBioChem
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Intact Human Alpha-Acid Glycoprotein Analyzed by ESI-qTOF-MS: Simultaneous Determination of the Glycan Composition of Multiple Glycosylation Sites

2018 Journal of Proteome Research
- Melissa Baerenfaenger
- Bernd Meyer
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Glycan analysis: scope and limitations of different techniques—a case for integrated use of LC-MS(/MS) and NMR techniques

2013 Analytical and Bioanalytical Chemistry
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