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Editorial for the Genetics of Alzheimer's Disease Special Issue: October 2021.阿尔茨海默病遗传学特刊社论：2021 年 10 月。
Genes (Basel). 2021 Nov 14;12(11):1794. doi: 10.3390/genes12111794.
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Neuronal pentraxin 1 contributes to the neuronal damage evoked by amyloid-beta and is overexpressed in dystrophic neurites in Alzheimer's brain.神经元五聚体蛋白1会导致由β-淀粉样蛋白引发的神经元损伤，并且在阿尔茨海默病大脑的营养不良性神经突中过度表达。
J Neurosci. 2006 Dec 6;26(49):12735-47. doi: 10.1523/JNEUROSCI.0575-06.2006.
3
Familial Alzheimer's disease mutations at position 22 of the amyloid β-peptide sequence differentially affect synaptic loss, tau phosphorylation and neuronal cell death in an ex vivo system.淀粉样β肽序列第 22 位的家族性阿尔茨海默病突变在体外系统中不同程度地影响突触丢失、tau 磷酸化和神经元细胞死亡。
PLoS One. 2020 Sep 23;15(9):e0239584. doi: 10.1371/journal.pone.0239584. eCollection 2020.
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Encephalopathy induced by Alzheimer brain inoculation in a non-human primate.阿尔茨海默病脑接种诱导的非人灵长类动物脑病。
Acta Neuropathol Commun. 2019 Sep 4;7(1):126. doi: 10.1186/s40478-019-0771-x.
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Amyloid-induced neurofibrillary tangle formation in Alzheimer's disease: insight from transgenic mouse and tissue-culture models.淀粉样蛋白诱导的阿尔茨海默病神经原纤维缠结形成：来自转基因小鼠和组织培养模型的见解。
Int J Dev Neurosci. 2004 Nov;22(7):453-65. doi: 10.1016/j.ijdevneu.2004.07.013.
6
Alzheimer's disease.阿尔茨海默病
Subcell Biochem. 2012;65:329-52. doi: 10.1007/978-94-007-5416-4_14.
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Heavy Tau Burden with Subtle Amyloid β Accumulation in the Cerebral Cortex and Cerebellum in a Case of Familial Alzheimer's Disease with APP Osaka Mutation.在一个伴有 APP Osaka 突变的家族性阿尔茨海默病病例中，大脑皮质和小脑存在重度 Tau 负担和轻微的淀粉样β 聚集。
Int J Mol Sci. 2020 Jun 22;21(12):4443. doi: 10.3390/ijms21124443.
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Genetics of β-Amyloid Precursor Protein in Alzheimer's Disease.阿尔茨海默病中β-淀粉样前体蛋白的遗传学
Cold Spring Harb Perspect Med. 2017 Jun 1;7(6):a024539. doi: 10.1101/cshperspect.a024539.
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A three-dimensional human neural cell culture model of Alzheimer's disease.一种阿尔茨海默病的三维人类神经细胞培养模型。
Nature. 2014 Nov 13;515(7526):274-8. doi: 10.1038/nature13800. Epub 2014 Oct 12.
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Brain amyloid-β oligomers in ageing and Alzheimer's disease.脑淀粉样-β寡聚体与衰老和阿尔茨海默病。
Brain. 2013 May;136(Pt 5):1383-98. doi: 10.1093/brain/awt062. Epub 2013 Apr 9.
本文引用的文献
1
Pairwise Correlation Analysis of the Alzheimer's Disease Neuroimaging Initiative (ADNI) Dataset Reveals Significant Feature Correlation.对阿尔茨海默病神经影像学倡议 (ADNI) 数据集的两两相关性分析显示出显著的特征相关性。
Genes (Basel). 2021 Oct 21;12(11):1661. doi: 10.3390/genes12111661.
2
Advances in Genetic and Molecular Understanding of Alzheimer's Disease.阿尔茨海默病的遗传和分子理解的进展。
Genes (Basel). 2021 Aug 15;12(8):1247. doi: 10.3390/genes12081247.
3
Advances with Long Non-Coding RNAs in Alzheimer's Disease as Peripheral Biomarker.长链非编码 RNA 在阿尔茨海默病作为外周生物标志物方面的研究进展。
Genes (Basel). 2021 Jul 24;12(8):1124. doi: 10.3390/genes12081124.
4
Analysis of Genetic Variants Associated with Levels of Immune Modulating Proteins for Impact on Alzheimer's Disease Risk Reveal a Potential Role for SIGLEC14.分析与免疫调节蛋白水平相关的遗传变异对阿尔茨海默病风险的影响，揭示了 SIGLEC14 的潜在作用。
Genes (Basel). 2021 Jun 30;12(7):1008. doi: 10.3390/genes12071008.
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RNA Transcription in Alzheimer's Disease Brain and Its Implication in Mitochondrial Dysfunction.阿尔茨海默病脑中的 RNA 转录及其对线粒体功能障碍的影响。
Genes (Basel). 2021 Jun 6;12(6):871. doi: 10.3390/genes12060871.
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Shared Genetic Etiology between Alzheimer's Disease and Blood Levels of Specific Cytokines and Growth Factors.阿尔茨海默病与特定细胞因子和生长因子的血液水平之间存在共享的遗传病因。
Genes (Basel). 2021 Jun 5;12(6):865. doi: 10.3390/genes12060865.
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The Impact of Complement Genes on the Risk of Late-Onset Alzheimer's Disease.补体基因对迟发性阿尔茨海默病发病风险的影响。
Genes (Basel). 2021 Mar 20;12(3):443. doi: 10.3390/genes12030443.
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Set-Based Rare Variant Expression Quantitative Trait Loci in Blood and Brain from Alzheimer Disease Study Participants.基于集合的罕见变异表达数量性状基因座在阿尔茨海默病研究参与者的血液和大脑中的研究。
Genes (Basel). 2021 Mar 15;12(3):419. doi: 10.3390/genes12030419.
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