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Modeling psychiatric disorders: from genomic findings to cellular phenotypes

机译:精神疾病建模:从基因组发现到细胞表型

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Major programs in psychiatric genetics have identified >150 risk loci for psychiatric disorders. These loci converge on a small number of functional pathways, which span conventional diagnostic criteria, suggesting a partly common biology underlying schizophrenia, autism and other psychiatric disorders. Nevertheless, the cellular phenotypes that capture the fundamental features of psychiatric disorders have not yet been determined. Recent advances in genetics and stem cell biology offer new prospects for cell-based modeling of psychiatric disorders. The advent of cell reprogramming and induced pluripotent stem cells (iPSC) provides an opportunity to translate genetic findings into patient-specific in vitro models. iPSC technology is less than a decade old but holds great promise for bridging the gaps between patients, genetics and biology. Despite many obvious advantages, iPSC studies still present multiple challenges. In this expert review, we critically review the challenges for modeling of psychiatric disorders, potential solutions and how iPSC technology can be used to develop an analytical framework for the evaluation and therapeutic manipulation of fundamental disease processes.
机译:精神病学遗传学的重大计划已经确定了> 150个精神病学疾病的风险基因座。这些基因座集中在跨越常规诊断标准的少数功能途径上,这表明精神分裂症,自闭症和其他精神疾病的部分生物学生物学基础。然而,还没有确定捕获精神疾病基本特征的细胞表型。遗传学和干细胞生物学的最新进展为基于精神病的细胞建模提供了新的前景。细胞重编程和诱导多能干细胞(iPSC)的出现提供了将遗传学发现转化为患者特异性体外模型的机会。 iPSC技术还不到十年的历史,但有望弥合患者,遗传学和生物学之间的鸿沟。尽管有许多明显的优势,但iPSC研究仍然提出了许多挑战。在此专家审查中,我们严格审查了精神疾病建模的挑战,潜在的解决方案以及如何使用iPSC技术来开发用于评估和治疗基本疾病过程的分析框架。

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