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Cited by 311

The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.

Gangliosides in cell recognition and membrane protein regulation

Open access
Lopez, Pablo HH, Schnaar, Ronald L·2009·Current Opinion in Structural Biology

Abstract

Summary Gangliosides, sialic acid-bearing glycosphingolipids, are expressed on all vertebrate cells, and are the major glycans on nerve cells. They are anchored to the plasma membrane through their ceramide lipids with their varied glycans extending into the extracellular space. Through sugar-specific interactions with glycan binding proteins on apposing cells, gangliosides function as receptors in cell-cell recognition, regulating natural killer cell cytotoxicity via Siglec-7 binding, myelin-axon interactions via Siglec-4 (myelin-associated glycoprotein) binding, and inflammation via E-selectin binding. Gangliosides also interact laterally in their own membranes, regulating the responsiveness of signaling proteins including the insulin, epidermal growth factor and vascular endothelial growth factor receptors. In these ways, gangliosides act as regulatory elements in the immune system, in the nervous system, in metabolic regulation and in cancer progression.

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Crossref · 10.1016/j.sbi.2009.06.001

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Metadata

Authors
Lopez, P. H., & Schnaar, R. L.
Venue
Current Opinion in Structural Biology
Publisher
Elsevier BV
Published
2009-10
Volume
19
Issue
5
Pages
549-557
ISSN
0959-440X (ISSN-L)
OpenAlex
W2006073788
Cited by
311
References
54
FWCI
8.40
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Gangliosides in cell recognition and membrane protein regulation. https://app.cochat.ai/papers/10.1016/j.sbi.2009.06.001
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Lopez, P. H., & Schnaar, R. L. (2009). Gangliosides in cell recognition and membrane protein regulation. Current Opinion in Structural Biology. https://doi.org/10.1016/j.sbi.2009.06.001

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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