In skeletal muscle advanced glycation end products (AGEs) inhibit insulin action and induce the formation of multimolecular complexes including the receptor for AGEs. (Q37142827)

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scientific article published on 27 October 2008

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English	In skeletal muscle advanced glycation end products (AGEs) inhibit insulin action and induce the formation of multimolecular complexes including the receptor for AGEs.	scientific article published on 27 October 2008

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25 December 2019

In skeletal muscle advanced glycation end products (AGEs) inhibit insulin action and induce the formation of multimolecular complexes including the receptor for AGEs (English)

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25 December 2019

Pietro Formisano

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Angela Cassese

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Iolanda Esposito

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Francesca Fiory

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Alessia P M Barbagallo

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Flora Paturzo

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Paola Mirra

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Luca Ulianich

7

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Ferdinando Giacco

8

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Claudia Iadicicco

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Angela Lombardi

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Francesco Oriente

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Emmanuel Van Obberghen

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Francesco Beguinot

13

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Claudia Miele

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27 October 2008

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25 December 2019

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Journal of Biological Chemistry

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25 December 2019

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25 December 2019

36088-36099

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25 December 2019

52

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25 December 2019

Atypical protein kinase C in glucose metabolism

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6 September 2017

The receptor for advanced glycation end-products (RAGE) directly binds to ERK by a D-domain-like docking site

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Activation mechanisms of protein kinase C: maturation, catalytic activation, and targeting

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Regulation of vascular endothelial growth factor expression by advanced glycation end products

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6 September 2017

The role of protein kinase C isoforms in insulin action

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Selective attenuation of metabolic branch of insulin receptor down-signaling by high glucose in a hepatoma cell line, HepG2 cells

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6 September 2017

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

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Receptor for advanced glycation end products (RAGE)-mediated neurite outgrowth and activation of NF-kappaB require the cytoplasmic domain of the receptor but different downstream signaling pathways

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Cell activation by glycated proteins. AGE receptors, receptor recognition factors and functional classification of AGEs

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Orally absorbed reactive glycation products (glycotoxins): an environmental risk factor in diabetic nephropathy

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Advanced glycation endproducts and diabetic nephropathy

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29 September 2017

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27 June 2018

Hyperglycemia-induced activation of nuclear transcription factor kappaB in vascular smooth muscle cells

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Long-term effects of aminoguanidine on insulin release and biosynthesis: evidence that the formation of advanced glycosylation end products inhibits B cell function

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27 June 2018

Key role of Src kinase in S100B-induced activation of the receptor for advanced glycation end products in vascular smooth muscle cells

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Functional interaction of protein kinase Calpha with the tyrosine kinases Syk and Src in human platelets.

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3 September 2018

Human glycated albumin affects glucose metabolism in L6 skeletal muscle cells by impairing insulin-induced insulin receptor substrate (IRS) signaling through a protein kinase C alpha-mediated mechanism

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3 September 2018

Advanced glycation end products induce choroidal endothelial cell proliferation, matrix metalloproteinase-2 and VEGF upregulation in vitro

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3 September 2018

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3 September 2018

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3 September 2018

Overexpression of protein kinase C isoenzymes alpha, beta I, gamma, and epsilon in cells overexpressing the insulin receptor. Effects on receptor phosphorylation and signaling.

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3 September 2018

Impaired glucose transport in skeletal muscle but normal GLUT-4 tissue distribution in glucose-infused rats

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3 September 2018

Blockade of RAGE–amphoterin signalling suppresses tumour growth and metastases

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21 January 2018

STAT5 activation induced by diabetic LDL depends on LDL glycation and occurs via src kinase activity

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12 December 2020

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Growth modulation of retinal microvascular cells by early and advanced glycation products

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12 December 2020

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Dietary glycotoxins: inhibition of reactive products by aminoguanidine facilitates renal clearance and reduces tissue sequestration

1 reference

https://pubmed.ncbi.nlm.nih.gov/18955497

12 December 2020

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10.1074/JBC.M801698200

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25 December 2019

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25 December 2019

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25 December 2019

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