INT46350
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
This is curious, because acLDL is endocytosed by MSR-A, as is oxLDL. | |||||||||||||||
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The SR-A receptors occur in two different forms that are generated by alternative splicing of the primary transcript: SR-AI and SR-AII. | |||||||||||||||
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This shows that the lack of SR-A receptors does not affect the establishment of a protective immune response against RAS. | |||||||||||||||
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SR-AI and II receptors are expressed by both activated macrophages and glial cells. | |||||||||||||||
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The initial targeting of sporozoites to the liver involves close interactions with sinusoidal endothelial cells and Kupffer cells [2], both of which express SR-AI and SR-AII receptors. | |||||||||||||||
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The initial targeting of sporozoites to the liver involves close interactions with sinusoidal endothelial cells and Kupffer cells [2], both of which express SR-AI and SR-AII receptors. | |||||||||||||||
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The SR-A receptors occur in two different forms that are generated by alternative splicing of the primary transcript: SR-AI and SR-AII. | |||||||||||||||
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The SR-A receptors occur in two different forms that are generated by alternative splicing of the primary transcript: SR-AI and SR-AII. | |||||||||||||||
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Msr proteins are highly expressed in liver and kidney tissues, suggesting their overall importance in detoxification and therefore maintenance of cellular resistance to oxidative protein damage (Moskovitz et al. 2001; Moskovitz 2005). | |||||||||||||||
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The 5-HT precursor l-5-hydroxytryptophan (L-5-HTP) depressed MSR in the spinal cord injured rats but not in normal rats. | |||||||||||||||
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In the present study, a series of SR141716A analogs were synthesized and were tested for CB(1) binding affinity and in a battery of in vivo tests, including hypomobility, antinociception, and hypothermia in mice. | |||||||||||||||
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Synthesis of an antagonist, SR141716A, that selectively binds to brain cannabinoid (CB(1)) receptors without producing cannabimimetic activity in vivo, suggests that recognition and activation of cannabinoid receptors are separable events. | |||||||||||||||
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Transgenic (Tg) DN MSR RAGE and Tg DN PPET RAGE mice were prepared and characterized as previously described (20,22). | |||||||||||||||
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We observed that in diabetic RAGE KO, Tg DN PPET RAGE, and Tg DN MSR RAGE mice hearts, protection from injury due to I/R was also associated with reductions in caspase-3 activation and cytochrome c release. | |||||||||||||||
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We examined the levels of specific AGEs, CML, pentosidine, and furosine (glycated lysine) in diabetic wild-type, RAGE-KO, Tg DN PPET RAGE, and Tg DN MSR RAGE heart under baseline conditions and after I/R (Table 2). | |||||||||||||||
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Interestingly, after I/R, CML levels were significantly greater in diabetic WT hearts in comparison with diabetic RAGE-KO, Tg DN PPET RAGE, and Tg DN MSR RAGE hearts (Table 2). | |||||||||||||||
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The initial targeting of sporozoites to the liver involves close interactions with sinusoidal endothelial cells and Kupffer cells [2], both of which express SR-AI and SR-AII receptors. | |||||||||||||||
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The initial targeting of sporozoites to the liver involves close interactions with sinusoidal endothelial cells and Kupffer cells [2], both of which express SR-AI and SR-AII receptors. | |||||||||||||||
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SR-AI and II receptors are expressed by both activated macrophages and glial cells. | |||||||||||||||
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Where clinical doubt exists, the value of nerve biopsy in distinguishing HSN types I and II is emphasized. | |||||||||||||||
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General Comments
This test has worked.