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患者来源的细胞——研究运动障碍中基因外显率降低的不可替代工具。

Patient-derived cells - an irreplaceable tool for research of reduced penetrance in movement disorders.

作者信息

Seibler Philip, Rakovic Aleksandar

机构信息

Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.

出版信息

Med Genet. 2022 Aug 12;34(2):125-130. doi: 10.1515/medgen-2022-2133. eCollection 2022 Jun.

Abstract

Movement disorders comprise a clinically, pathologically, and genetically heterogeneous group of diseases associated with the phenomenon of reduced penetrance. Penetrance refers to the likelihood that a clinical condition will occur when a particular genotype is present. Elucidating the cause of reduced penetrance may contribute to more personalized medicine by identifying genetic factors that may prevent individuals from developing disease. Therefore, patient material becomes an irreplaceable resource in this approach. It is needed to identify genetic modifiers of the disease in the first place and to subsequently elucidate underlying mechanisms in endogenous human cell models that provide the entire genetic background.

摘要

运动障碍包括一组在临床、病理和遗传方面具有异质性的疾病,这些疾病与外显率降低现象相关。外显率是指当存在特定基因型时临床病症出现的可能性。阐明外显率降低的原因,通过识别可能阻止个体发病的遗传因素,可能有助于实现更个性化的医疗。因此,患者材料在这种方法中成为一种不可替代的资源。首先需要识别疾病的遗传修饰因子,随后在内源性人类细胞模型中阐明潜在机制,这些模型提供完整的遗传背景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/187a/11006347/57180213b8cd/j_medgen-2022-2133_fig_001.jpg

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