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Els C. M. Brinkman-Van der Linden

Researcher at Johnson & Johnson

Publications -  15
Citations -  1493

Els C. M. Brinkman-Van der Linden is an academic researcher from Johnson & Johnson. The author has contributed to research in topics: SIGLEC & Sialic acid. The author has an hindex of 12, co-authored 15 publications receiving 1376 citations. Previous affiliations of Els C. M. Brinkman-Van der Linden include University of California, San Diego & Crucell.

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GlycoPEGylation of recombinant therapeutic proteins produced in Escherichia coli.

TL;DR: A novel strategy for site-directed PEGylation using glycosyltransferases to attach PEG to O-glycans is presented, which was applied to three therapeutic polypeptides, granulocyte colony stimulating factor (G-CSF), interferon-alpha2b (IFN- alpha2b), and granulocytes/macrophage colony stimulation factor (GM- CSF), which are currently in clinical use.
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OB-BP1/Siglec-6. a leptin- and sialic acid-binding protein of the immunoglobulin superfamily.

TL;DR: The identification of OB-BP1/Siglec-6 as a Siglec family member, coupled with its restricted expression pattern, suggests that it may mediate cell-cell recognition events by interacting with sialylated glycoprotein ligands expressed on specific cell populations.
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I-type lectins.

TL;DR: The I- type lectins are a subset of the immunoglobulin superfamily that are capable of carbohydrate-protein interactions and there are I-type lectins recognizing sialic acids, other sugars and glycosaminoglycans.
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Human-specific Regulation of α2–6-linked Sialic Acids

TL;DR: Since the last common ancestor with apes, humans underwent a concerted bidirectional switch in α2–6-linked Sia expression between airway epithelial cell surfaces and secreted mucins, showing that Sia linkage expression patterns can be conserved during millions of years of evolution within some vertebrate taxa while undergoing sudden major changes in other closely related ones.
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Loss of N-Glycolylneuraminic Acid in Human Evolution IMPLICATIONS FOR SIALIC ACID RECOGNITION BY SIGLECS

TL;DR: The human loss of Neu5Gc may alter biological processes involving siglec-1, and possibly, sigleC-4a or -5, the myelin-associated glycoprotein, which may have some preference for Neu 5Gc.