Results 201 to 210 of about 55,722 (248)
Some of the next articles are maybe not open access.
Ageing Research Reviews, 2015
Danger molecules are the first signals released from dying tissue after stroke. These danger signals bind to receptors on immune cells that will result in their activation and the release of inflammatory and neurotoxic mediators, resulting in amplification of the immune response and subsequent enlargement of the damaged brain volume.
Mathias Gelderblom +2 more
exaly +3 more sources
Danger molecules are the first signals released from dying tissue after stroke. These danger signals bind to receptors on immune cells that will result in their activation and the release of inflammatory and neurotoxic mediators, resulting in amplification of the immune response and subsequent enlargement of the damaged brain volume.
Mathias Gelderblom +2 more
exaly +3 more sources
Editorial: Endogenous danger signals in cancer immunology and immunotherapy [PDF]
Frontiers in ImmunologyXiubao Ren, Ren Xiubao, Gao Jinming
exaly +2 more sources
The innate signaling of dangers and the dangers of innate signaling
Nature Immunology, 2006The innate immune system of mammals has been forged by coevolution with microbes in response to the double constraint of preserving a symbiotic interaction with commensal flora and eliminating intrusion of those commensals or invasion by pathogens. Thus, a 'sensing' network, accompanied by or lacking inflammatory responses, is controlled by elaborate ...
openaire +2 more sources
Science Signaling, 2016
The glycolytic enzyme hexokinase is a pattern recognition receptor for the NLRP3 inflammasome.
openaire +1 more source
The glycolytic enzyme hexokinase is a pattern recognition receptor for the NLRP3 inflammasome.
openaire +1 more source
Journal of the American Medical Association, 1914
To the Editor: —The wide-spread interest in this question, among both the medical profession and the public at large, is my excuse for referring once more to Dr. Patterson's article, which you discussed in an editorial (Nov. 8, 1913, p. 1724). I have also seen comments on the same article in a number of our popular magazines.
openaire +1 more source
To the Editor: —The wide-spread interest in this question, among both the medical profession and the public at large, is my excuse for referring once more to Dr. Patterson's article, which you discussed in an editorial (Nov. 8, 1913, p. 1724). I have also seen comments on the same article in a number of our popular magazines.
openaire +1 more source
Science, 2018
Structural Immunology In the classical complement pathway, the C1 initiation complex binds to danger patterns on the surface of microbes or damaged host cells and triggers an immune response. Immunoglobulin G (IgG) antibodies form hexamers on cell surfaces that have high avidity for the C1 complex.
openaire +1 more source
Structural Immunology In the classical complement pathway, the C1 initiation complex binds to danger patterns on the surface of microbes or damaged host cells and triggers an immune response. Immunoglobulin G (IgG) antibodies form hexamers on cell surfaces that have high avidity for the C1 complex.
openaire +1 more source