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Cited by 436

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Protein Glycation: A Firm Link to Endothelial Cell Dysfunction

Wautier, Jean-Luc, Schmidt, Ann Marie·2004·Circulation Research

Abstract

The advanced glycation end products (AGEs) are a heterogeneous class of molecules, including the following main subgroups: bis(lysyl)imidazolium cross-links, hydroimidazolones, 3-deoxyglucosone derivatives, and monolysyl adducts. AGEs are increased in diabetes, renal failure, and aging. Microvascular lesions correlate with the accumulation of AGEs, as demonstrated in diabetic retinopathy or renal glomerulosclerosis. On endothelial cells, ligation of receptor for AGE (RAGE) by AGEs induces the expression of cell adhesion molecules, tissue factor, cytokines such as interleukin-6, and monocyte chemoattractant protein-1. A chief means by which AGEs via RAGE exert their effects is by generation of reactive oxygen species, at least in part via stimulation of NADPH oxidase. Diabetes-associated vascular dysfunction in vivo can be prevented by blockade of RAGE. Thus, agents that limit AGE formation, increase the catabolism of these species, or antagonize their binding to RAGE may provide new targets for vascular protection in diabetes.

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Metadata

Authors
Wautier, J.-L., & Schmidt, A. M.
Venue
Circulation Research
Published
2004-08-06
Volume
95
Issue
3
Pages
233-238
ISSN
  • 0009-7330 (ISSN-L)
  • 1524-4571
OpenAlex
W2163647109
Cited by
436
References
6
FWCI
17.02
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Protein Glycation: A Firm Link to Endothelial Cell Dysfunction. https://app.cochat.ai/papers/10.1161/01.res.0000137876.28454.64
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Wautier, J.-L., & Schmidt, A. M. (2004). Protein Glycation: A Firm Link to Endothelial Cell Dysfunction. Circulation Research. https://doi.org/10.1161/01.res.0000137876.28454.64

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

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.