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Down's syndrome and Alzheimer's disease: dendritic spine counts in the hippocampus.

作者信息

Ferrer I, Gullotta F

机构信息

Departamento Anatomía Patológica, Hospital Príncipes de España, Universidad Barcelona, Spain.

出版信息

Acta Neuropathol. 1990;79(6):680-5. doi: 10.1007/BF00294247.

DOI:10.1007/BF00294247
PMID:2141748
Abstract

Samples of the hippocampus of four patients with Down's syndrome [two men aged 35 and 36 years with no evidence of Alzheimer's disease (AD) and two patients aged 47 and 55 years with associated AD] were obtained at post mortem and processed according to the rapid Golgi method. A significant reduction in the number of dendritic spines (DS) was found in the apical (middle, distal and oblique segments) and basilar (thick and thin segments) dendritic arbors of CA1 and CA2-3 pyramidal neurons in patients with Down's syndrome and no AD when compared to age-matched controls. An additional decrease of DS in every segment occurred in Down's patients with associated AD when compared to age-matched controls and Down's patients with no AD. In Down's syndrome (either associated or not to AD) thin basilar dendrites were the most severely involved; in AD patients CA1 pyramids were more severely affected than pyramidal neurons of the CA2-3 subfield.

摘要

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Spine distribution along the apical dendrites of the pyramidal neurons in Down's syndrome. A quantitative Golgi study.唐氏综合征中锥体神经元顶树突上的脊柱分布。一项定量高尔基研究。
Acta Neuropathol. 1980;50(3):207-10. doi: 10.1007/BF00688755.
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理解唐氏综合征的遗传机制和认知障碍:走向整体方法。
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Dose imbalance of DYRK1A kinase causes systemic progeroid status in Down syndrome by increasing the un-repaired DNA damage and reducing LaminB1 levels.DYRK1A 激酶的剂量失衡通过增加未修复的 DNA 损伤和降低 laminB1 水平导致唐氏综合征的全身性早衰状态。
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From neurodevelopment to neurodegeneration: utilizing human stem cell models to gain insight into Down syndrome.从神经发育到神经退行性变:利用人类干细胞模型深入了解唐氏综合征。
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