{"title":"利用MultiVINE-seq揭示神经血管疾病的风险。","authors":"Lynn van Olst, David Gate","doi":"10.1016/j.neuron.2025.09.016","DOIUrl":null,"url":null,"abstract":"<p><p>In this issue of Neuron, Reid et al. introduce MultiVINE-seq, a single-nucleus multi-omic platform for profiling human cerebrovascular and perivascular cells for paired transcriptomic and epigenomic profiling.<sup>1</sup> By integrating genome-wide association data, they map neurodegenerative and cerebrovascular disease risk variants to specific vascular and immune cell types, uncovering distinct and convergent pathogenic pathways.</p>","PeriodicalId":19313,"journal":{"name":"Neuron","volume":"113 19","pages":"3065-3067"},"PeriodicalIF":15.0000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unraveling neurovascular disease risk with MultiVINE-seq.\",\"authors\":\"Lynn van Olst, David Gate\",\"doi\":\"10.1016/j.neuron.2025.09.016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In this issue of Neuron, Reid et al. introduce MultiVINE-seq, a single-nucleus multi-omic platform for profiling human cerebrovascular and perivascular cells for paired transcriptomic and epigenomic profiling.<sup>1</sup> By integrating genome-wide association data, they map neurodegenerative and cerebrovascular disease risk variants to specific vascular and immune cell types, uncovering distinct and convergent pathogenic pathways.</p>\",\"PeriodicalId\":19313,\"journal\":{\"name\":\"Neuron\",\"volume\":\"113 19\",\"pages\":\"3065-3067\"},\"PeriodicalIF\":15.0000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neuron\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.neuron.2025.09.016\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuron","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.neuron.2025.09.016","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Unraveling neurovascular disease risk with MultiVINE-seq.
In this issue of Neuron, Reid et al. introduce MultiVINE-seq, a single-nucleus multi-omic platform for profiling human cerebrovascular and perivascular cells for paired transcriptomic and epigenomic profiling.1 By integrating genome-wide association data, they map neurodegenerative and cerebrovascular disease risk variants to specific vascular and immune cell types, uncovering distinct and convergent pathogenic pathways.
期刊介绍:
Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.