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The full-length human tau protein formed complex with PrP and some GSS- and fCJD-related PrP mutants
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  • 相关项目：CTMPrP引起细胞依赖微管运输障碍的研究
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CTMPrP引起细胞依赖微管运输障碍的研究
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一种基于链霉素沉淀的PrPSc检测方法的建立.
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重组人Doppel蛋白通过诱导凋亡抑制人神经母细胞瘤SH-SY5Y细胞生长.
A Chinese Creutzfeldt-Jakob disease with a novel seven extra-repeat insertion in PRNP.
The N-terminus of PrP is responsible for interacting with tubulin and fCJD related PrP mutants posse
Treatment of scrapie agent 263K with tetracycline partially abolishes the protease-resistant activit
Removal of the Glycosylation of Prion Protein Provoke Apoptosis in SF126.
Sensitive detection of PrPSc by Western blot assay based on streptomycin sulfate precipitation.
HPV-2 isolates from the patients with huge verrucae vulgaris possess stronger promoter activities.
Generation of Genetic Engineering Monoclonal Antibodies against Prion Protein.
Establishment of a Stable PrP^Sc Panel from Brain Tissues of Experimental Hamsters with Scrapie Strain 263K
Casein kinase Ⅱ interacts with prion protein in vitro and forms complex with native prion protein in vivo
α-Synuclein与14-3-3蛋白在体外分子间相互作用的鉴定
Recombinant Neural Protein PrP Can Bind with Both Recombinant and Native Apolipoprotein E In Vitro
Doppel-induced cytotoxicity in human neuronal SH-SY5Y cells is antagonized by the prion protein
朊病毒病实验动物脑组织PrP^Sc样本库的建立
Tau融合蛋白及其缺失突变体与朊蛋白的体外作用分析