RAGE and amyloid-beta peptide neurotoxicity in Alzheimer's disease (Q24314906)

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X Chen

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J Fu

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M Chen

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H Zhu

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A Roher

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T Slattery

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L Zhao

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M Nagashima

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J Morser

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A Migheli

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D Stern

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A M Schmidt

Tau protein and the neurofibrillary pathology of Alzheimer's disease

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language of work or name

English

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publication date

22 August 1996

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published in

Nature

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volume

382

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page(s)

685-91

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issue

6593

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cites work

1 reference

7 January 2021

The Alzheimer's disease sphinx: a riddle with plaques and tangles

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Amyloid beta-protein as a substrate interacts with extracellular matrix to promote neurite outgrowth

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Neurotrophic and neurotoxic effects of amyloid beta protein: reversal by tachykinin neuropeptides

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The amyloid beta-protein of Alzheimer's disease is chemotactic for mononuclear phagocytes

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Neurodegeneration induced by beta-amyloid peptides in vitro: the role of peptide assembly state

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A model for beta-amyloid aggregation and neurotoxicity based on free radical generation by the peptide: relevance to Alzheimer disease

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Hydrogen peroxide mediates amyloid beta protein toxicity

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Activation of microglial cells by beta-amyloid protein and interferon-gamma.

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Activation of macrophages by Alzheimer beta amyloid peptide.

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β-Amyloid stimulates glial cells in vitro to produce growth factors that accumulate in senile plaques in Alzheimer's disease

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?1-Antichymotrypsin Binding to Alzheimer A? Peptides Is Sequence Specific and Induces Fibril Disaggregation In Vitro

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The cerebrospinal-fluid soluble form of Alzheimer's amyloid beta is complexed to SP-40,40 (apolipoprotein J), an inhibitor of the complement membrane-attack complex

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Amyloid beta-protein activates tachykinin receptors and inositol trisphosphate accumulation by synergy with glutamate

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Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

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Avid binding of beta A amyloid peptide to its own precursor

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Transthyretin sequesters amyloid beta protein and prevents amyloid formation

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Arresting amyloidosis in vivo using small-molecule anionic sulphonates or sulphates: implications for Alzheimer's disease.

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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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Glycated tau protein in Alzheimer disease: a mechanism for induction of oxidant stress

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Non-enzymatically glycated tau in Alzheimer's disease induces neuronal oxidant stress resulting in cytokine gene expression and release of amyloid beta-peptide.

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Direct evidence of oxidative injury produced by the Alzheimer's beta-amyloid peptide (1-40) in cultured hippocampal neurons

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Different amyloidogenic peptides share a similar mechanism of neurotoxicity involving reactive oxygen species and calcium

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beta-Amyloid-mediated vasoactivity and vascular endothelial damage.

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Direct expression cloning of vascular cell adhesion molecule 1, a cytokine-induced endothelial protein that binds to lymphocytes

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Regulation of human mononuclear phagocyte migration by cell surface-binding proteins for advanced glycation end products

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An immortalized cell line expresses properties of activated microglial cells

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Microglia and cytokines in neurological disease, with special reference to AIDS and Alzheimer's disease

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Microglia in degenerative neurological disease.

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Receptor-mediated endothelial cell dysfunction in diabetic vasculopathy. Soluble receptor for advanced glycation end products blocks hyperpermeability in diabetic rats

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Advanced glycation endproducts interacting with their endothelial receptor induce expression of vascular cell adhesion molecule-1 (VCAM-1) in cultured human endothelial cells and in mice. A potential mechanism for the accelerated vasculopathy of dia

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Clinical trial of indomethacin in Alzheimer's disease.

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Inverse association of anti-inflammatory treatments and Alzheimer's disease: initial results of a co-twin control study.

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Attachment and culture of dissociated cells from rat embryo cerebral hemispheres on polylysine-coated surface

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Effect of fatty acid profiles on the susceptibility of cultured rabbit tracheal epithelial cells to hyperoxic injury.

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Identifiers

DOI

10.1038/382685A0

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Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

124759

1012543542

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124759

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference