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Spatial transcriptomics identifies spatially dysregulated expression of GRM3 and USP47 in amyotrophic lateral sclerosis
Neuropathology and Applied Neurobiology ( IF 5 ) Pub Date : 2020-01-24 , DOI: 10.1111/nan.12597
J M Gregory 1, 2, 3 , K McDade 1, 2, 3 , M R Livesey 3, 4 , I Croy 2, 5 , S Marion de Proce 5 , T Aitman 3, 5 , S Chandran 1, 3, 4 , C Smith 1, 2, 3
Affiliation  

The mechanisms underlying the selective degeneration of motor neurones in amyotrophic lateral sclerosis (ALS) are poorly understood. The aim of this study was to implement spatially resolved RNA sequencing in human post mortem cortical tissue from an ALS patient harbouring the C9orf72 hexanucleotide repeat expansion to identify dysregulated transcripts that may account for differential vulnerabilities of distinct (i) cell types and (ii) brain regions in the pathogenesis of ALS.

中文翻译:

空间转录组学鉴定肌萎缩侧索硬化中 GRM3 和 USP47 的空间失调表达

肌萎缩侧索硬化症 (ALS) 中运动神经元选择性变性的潜在机制知之甚少。本研究的目的是在来自携带 C9orf72 六核苷酸重复扩增的 ALS 患者的死后皮层组织中实施空间分辨 RNA 测序,以识别可能导致不同 (i) 细胞类型和 (ii) 大脑的差异脆弱性的失调转录本。 ALS 发病机制中的区域。
更新日期:2020-01-24
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