Alzheimer's disease and prion proteins: a meeting made in muscle.
作者信息
Gambetti P, Perry G
机构信息
Division of Neuropathology, Case Western Reserve School of Medicine, Cleveland, Ohio 44106.
出版信息
Am J Pathol. 1994 Dec;145(6):1261-4.
Abstract
摘要
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Neuroreport. 1993 Jun;4(6):815-8. doi: 10.1097/00001756-199306000-00055.
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A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.A68是印第安纳家族型格斯特曼-施特劳斯勒-谢inker病成对螺旋丝的一个组成部分。
Brain Res. 1993 Jul 9;616(1-2):325-9. doi: 10.1016/0006-8993(93)90226-d.
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Identification and transport of full-length amyloid precursor proteins in rat peripheral nervous system.大鼠外周神经系统中全长淀粉样前体蛋白的鉴定与转运
J Neurosci. 1993 Jul;13(7):3136-42. doi: 10.1523/JNEUROSCI.13-07-03136.1993.
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Prion protein is strongly immunolocalized at the postsynaptic domain of human normal neuromuscular junctions.朊病毒蛋白在人类正常神经肌肉接头的突触后区域有强烈的免疫定位。
Neurosci Lett. 1993 Sep 3;159(1-2):111-4. doi: 10.1016/0304-3940(93)90811-x.
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Normal and abnormal biology of the beta-amyloid precursor protein.β-淀粉样前体蛋白的正常与异常生物学特性
Annu Rev Neurosci. 1994;17:489-517. doi: 10.1146/annurev.ne.17.030194.002421.
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Prion diseases and neurodegeneration.朊病毒病与神经退行性变。
Annu Rev Neurosci. 1994;17:311-39. doi: 10.1146/annurev.ne.17.030194.001523.
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Soluble beta-amyloid induction of Alzheimer's phenotype for human fibroblast K+ channels.可溶性β淀粉样蛋白诱导人成纤维细胞K+通道出现阿尔茨海默病表型。
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New advances in inclusion-body myositis.
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Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.β-淀粉样前体蛋白参与印第安纳家族性格斯特曼-施特劳斯勒-谢inker病的朊蛋白淀粉样斑块形成。
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