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Titlebook: GeNeDis 2022; Molecular, Chemical, Panagiotis Vlamos Conference proceedings 2023 The Editor(s) (if applicable) and The Author(s), under exc

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发表于 2025-3-21 18:41:13 | 显示全部楼层 |阅读模式
书目名称GeNeDis 2022
副标题Molecular, Chemical,
编辑Panagiotis Vlamos
视频video
概述Proceedings of the 5th World Congress on Genetics, Geriatrics and Neurodegenerative Disease Research (GeNeDis).Covers the new drug targets, the development of novel biomarkers, new imaging techniques,
丛书名称Advances in Experimental Medicine and Biology
图书封面Titlebook: GeNeDis 2022; Molecular, Chemical, Panagiotis Vlamos Conference proceedings 2023 The Editor(s) (if applicable) and The Author(s), under exc
描述The 5.th. World Congress on Genetics, Geriatrics and Neurodegenerative Diseases Research (GeNeDis 2022) focuses on the latest major challenges in scientific research, new drug targets, the development of novel biomarkers, new imaging techniques, novel protocols for early diagnosis of neurodegenerative diseases, and several other scientific advances, with the aim of better, safer, and healthier aging. This volume focuses on the sessions from the conference on Molecular Biology, Chemical Biology, and Cellular Biology.
出版日期Conference proceedings 2023
关键词conference proceedings; brain disorders; geriatrics; informatics; computational neuroscience; Neuroeducat
版次1
doihttps://doi.org/10.1007/978-3-031-31978-5
isbn_softcover978-3-031-31980-8
isbn_ebook978-3-031-31978-5Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerl
The information of publication is updating

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Structural Connectivity Changes After Fornix Transection in Macaques Using Probabilistic Diffusion strongly associated with learning and memory in humans and nonhuman primates (NHPs). Here, we sought to investigate alterations in structural connectivity across key cortical and subcortical regions after fornix transection in NHPs. We collected diffusion-weighted MRI (dMRI) data from three macaque
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Protein Structure Prediction for Disease-Related Insertions/Deletions in Presenilin 1 Gene,’s disease (AD) with an early onset. PSEN1 mutations are thought to be responsible for approximately 80% of cases of monogenic AD, which are characterized by complete penetrance and an early age of onset. It is still unknown exactly how mutations in the presenilin 1 gene can cause dementia and neuro
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