Genetic background modulates outcome of therapeutic amyloid peptides in treatment of neuroinflammation.
第一作者:
Allison,Kraus
第一单位:
Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA. Electronic address: allison.kraus@nih.gov.
作者:
医学主题词
淀粉样β肽类(Amyloid beta-Peptides);动物(Animals);消炎药(Anti-Inflammatory Agents);细胞, 培养的(Cells, Cultured);疾病模型, 动物(Disease Models, Animal);脑脊髓炎, 自身免疫性, 实验性(Encephalomyelitis, Autoimmune, Experimental);嗜酸细胞(Eosinophils);女(雌)性(Female);基因表达调控(Gene Expression Regulation);白细胞介素4(Interleukin-4);淋巴细胞(Lymphocytes);小鼠(Mice);小鼠, 近交系(Mice, Inbred Strains);小鼠, 转基因(Mice, Transgenic);单核细胞(Monocytes);肽碎片(Peptide Fragments);种特异性(Species Specificity);tau蛋白质类(tau Proteins)
DOI
10.1016/j.jneuroim.2016.06.010
PMID
27609274
发布时间
2017-11-21
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