Receptor for advanced glycation end products contributes to postnatal pulmonary development and adult lung maintenance program in mice. (Q45165504)

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17 February 2020

title

Receptor for advanced glycation end products contributes to postnatal pulmonary development and adult lung maintenance program in mice (English)

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17 February 2020

Silvia Fineschi

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17 February 2020

Fabrizio Facchinetti

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17 February 2020

Maurizio Civelli

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17 February 2020

Chiara Carnini

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17 February 2020

Gino Villetti

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17 February 2020

Benedetta Lunghi

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17 February 2020

Stefania Stochino

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17 February 2020

Eleonora Cavarra

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publication date

9 November 2012

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American Journal of Respiratory Cell and Molecular Biology

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published in

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volume

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issue

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page(s)

164-171

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RAGE mediates a novel proinflammatory axis: a central cell surface receptor for S100/calgranulin polypeptides

17 February 2020

cites work

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The receptor for advanced glycation end products (RAGE) is a cellular binding site for amphoterin. Mediation of neurite outgrowth and co-expression of rage and amphoterin in the developing nervous system

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The pattern recognition receptor (RAGE) is a counterreceptor for leukocyte integrins: a novel pathway for inflammatory cell recruitment

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The multiligand receptor RAGE as a progression factor amplifying immune and inflammatory responses

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Identification of genes differentially expressed in rat alveolar type I cells

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Promotion of cell adherence and spreading: a novel function of RAGE, the highly selective differentiation marker of human alveolar epithelial type I cells.

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Association of advanced glycation end products with A549 cells, a human pulmonary epithelial cell line, is mediated by a receptor distinct from the scavenger receptor family and RAGE.

21 January 2018

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Interplay between RAGE, CD44, and focal adhesion molecules in epithelial-mesenchymal transition of alveolar epithelial cells

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Transcriptional control of lung morphogenesis

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RAGE: developmental expression and positive feedback regulation by Egr-1 during cigarette smoke exposure in pulmonary epithelial cells.

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S100P promotes pancreatic cancer growth, survival, and invasion

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The amphoterin (HMGB1)/receptor for advanced glycation end products (RAGE) pair modulates myoblast proliferation, apoptosis, adhesiveness, migration, and invasiveness. Functional inactivation of RAGE in L6 myoblasts results in tumor formation in viv

21 January 2018

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S100A14 Stimulates Cell Proliferation and Induces Cell Apoptosis at Different Concentrations via Receptor for Advanced Glycation End Products (RAGE)

21 January 2018

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Down-regulation of the receptor for advanced glycation end-products (RAGE) supports non-small cell lung carcinoma

21 January 2018

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Pathology of new bronchopulmonary dysplasia

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Lung alveolar septation defects in Ltbp-3-null mice

21 January 2018

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Dysregulation of TGF-beta1 receptor activation leads to abnormal lung development and emphysema-like phenotype in core fucose-deficient mice

21 January 2018

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Conditional overexpression of connective tissue growth factor disrupts postnatal lung development

21 January 2018

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Advanced glycation end products stimulate osteoblast apoptosis via the MAP kinase and cytosolic apoptotic pathways.

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Role of soluble receptor for advanced glycation end products on endotoxin-induced lung injury.

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Effect of high mobility group box-1 protein on apoptosis of peritoneal macrophages

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Advanced glycation end products enhance expression of pro-apoptotic genes and stimulate fibroblast apoptosis through cytoplasmic and mitochondrial pathways

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Advanced glycation endproducts alter functions and promote apoptosis in endothelial progenitor cells through receptor for advanced glycation endproducts mediate overpression of cell oxidant stress

21 January 2018

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Nitric Oxide Inhibits Apoptosis by Preventing Increases in Caspase-3-like Activity via Two Distinct Mechanisms

21 January 2018

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SARPs: A family of secreted apoptosis-related proteins

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Inhibitory effect of receptor for advanced glycation end products (RAGE) on the TGF-β-induced alveolar epithelial to mesenchymal transition

21 January 2018

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21 January 2018

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21 January 2018

Identifiers

DOI

10.1165/RCMB.2012-0111OC

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17 February 2020

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