Coronavirus-induced CNS disease: a model for virus-induced demyelination.
作者信息
Buchmeier M J, Dalziel R G, Koolen M J
机构信息
Scripps Clinic and Research Foundation, La Jolla, CA 92037.
出版信息
J Neuroimmunol. 1988 Dec;20(2-3):111-6. doi: 10.1016/0165-5728(88)90141-5.
Abstract
摘要
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本文引用的文献
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Coronavirus glycoprotein E1, a new type of viral glycoprotein.冠状病毒糖蛋白E1，一种新型病毒糖蛋白。
J Mol Biol. 1981 Dec 25;153(4):993-1010. doi: 10.1016/0022-2836(81)90463-0.
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The molecular biology of coronaviruses.冠状病毒的分子生物学
Adv Virus Res. 1983;28:35-112. doi: 10.1016/s0065-3527(08)60721-6.
3
Temperature-sensitive mutants of mouse hepatitis virus strain A59: isolation, characterization and neuropathogenic properties.小鼠肝炎病毒A59株温度敏感突变体：分离、特性及神经致病特性
Virology. 1983 Mar;125(2):393-402. doi: 10.1016/0042-6822(83)90211-8.
4
Murine coronaviruses: isolation and characterization of two plaque morphology variants of the JHM neurotropic strain.鼠冠状病毒：JHM嗜神经毒株两种噬斑形态变异株的分离与鉴定
J Gen Virol. 1982 Dec;63(2):265-75. doi: 10.1099/0022-1317-63-2-265.
5
Persistent, slow and latent viral infections.持续性、缓慢和潜伏性病毒感染。
Prog Med Virol. 1982;28:1-43.
6
Monoclonal antibodies to murine hepatitis virus-4 (strain JHM) define the viral glycoprotein responsible for attachment and cell--cell fusion.针对鼠肝炎病毒4型（JHM株）的单克隆抗体确定了负责病毒附着和细胞间融合的病毒糖蛋白。
Virology. 1982 Jun;119(2):358-71. doi: 10.1016/0042-6822(82)90095-2.
7
Mouse hepatitis virus type 4 (JHM strains). induced fatal central nervous system disease. I. genetic control and murine neuron as the susceptible site of disease.4型小鼠肝炎病毒（JHM株）引起致命的中枢神经系统疾病。I. 遗传控制以及小鼠神经元作为疾病的易感部位。
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Isolation of coronavirus envelope glycoproteins and interaction with the viral nucleocapsid.冠状病毒包膜糖蛋白的分离及其与病毒核衣壳的相互作用。
J Virol. 1980 Jan;33(1):449-62. doi: 10.1128/JVI.33.1.449-462.1980.
9
Western and dot immunoblotting analysis of viral antigens and antibodies: application to murine hepatitis virus.病毒抗原和抗体的Western印迹法及斑点免疫印迹分析：应用于小鼠肝炎病毒
J Immunol Methods. 1984 Oct 12;73(1):177-88. doi: 10.1016/0022-1759(84)90043-7.
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Virology. 1984 Jan 30;132(2):261-70. doi: 10.1016/0042-6822(84)90033-3.
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