The receptor for advanced glycation end-products (RAGE) is only present in mammals, and belongs to a family of cell adhesion molecules (CAMs). (Q41862027)

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scientific article published on 27 January 2014

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English	The receptor for advanced glycation end-products (RAGE) is only present in mammals, and belongs to a family of cell adhesion molecules (CAMs).	scientific article published on 27 January 2014

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6 March 2020

The receptor for advanced glycation end-products (RAGE) is only present in mammals, and belongs to a family of cell adhesion molecules (CAMs) (English)

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6 March 2020

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Giulio Pompilio

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Marco E. Bianchi

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Antonella Antonelli

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Michael Koch

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Luca Sessa

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Elena Gatti

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Filippo Zeni

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Alessandro Catucci

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Angela Raucci

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27 January 2014

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e86903

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Creative Commons Attribution 4.0 International

27 January 2014

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Structural insights into the oligomerization mode of the human receptor for advanced glycation end-products

1 reference

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Structural basis for pattern recognition by the receptor for advanced glycation end products (RAGE).

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Advanced glycation end products (AGEs) and their involvement in liver disease

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RAGE and its ligands in retinal disease

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RAGE in diabetic nephropathy

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V domain of RAGE interacts with AGEs on prostate carcinoma cells.

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A role for the receptor for advanced glycation end products in idiopathic pulmonary fibrosis

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Vascular and inflammatory stresses mediate atherosclerosis via RAGE and its ligands in apoE-/- mice

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Receptor for advanced glycation endproducts and atherosclerosis: From basic mechanisms to clinical implications.

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1 reference

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1 reference

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1 reference

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1 reference

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RAGE and ICAM-1 cooperate in mediating leukocyte recruitment during acute inflammation in vivo

1 reference

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12 December 2020

based on heuristic

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RAGE: a single receptor fits multiple ligands

1 reference

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Receptor for advanced glycation endproducts mediates neutrophil migration across intestinal epithelium

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12 December 2020

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The Immunoglobulin Fold

1 reference

https://pubmed.ncbi.nlm.nih.gov/24475194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0086903

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6 March 2020

2014PLoSO...986903S

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1 reference

Europe PubMed Central

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6 March 2020

1 reference

Europe PubMed Central

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6 March 2020

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