Progressive aggregation despite chaperone associations of a mutant SOD1-YFP in transgenic mice that develop ALS.
第一作者:
Jiou,Wang
第一单位:
Howard Hughes Medical Institute, Department of Genetics, Section of Comparative Medicine, and Department of Neurosurgery, Yale University School of Medicine, New Haven, CT 06510, USA.
作者:
主题词
肌萎缩侧索硬化(Amyotrophic Lateral Sclerosis);动物(Animals);神经胶质原纤维酸性蛋白质(Glial Fibrillary Acidic Protein);发光蛋白质类(Luminescent Proteins);小鼠(Mice);小鼠, 转基因(Mice, Transgenic);分子伴侣(Molecular Chaperones);运动神经元(Motor Neurons);核酸杂交(Nucleic Acid Hybridization);溶解度(Solubility);脊髓(Spinal Cord);超氧化物歧化酶(Superoxide Dismutase);泛素(Ubiquitin)
DOI
10.1073/pnas.0813045106
PMID
19171884
发布时间
2022-03-09
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