影响毛囊的人类疾病的多基因结构

IF 5.7
Anna L Brinks, Carli D Needle, Olivia D Perez, Jerry Shapiro, Kristen I Lo Sicco, Michael A Occidental, Aristotelis Tsirigos, Lynn Petukhova
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引用次数: 0

摘要

影响毛囊(HF)和毛囊皮脂腺单位的疾病给患者带来社会心理和经济负担,并可能预示着其他疾病的风险。人类遗传研究有助于确定控制健康的关键生理机制,并越来越多地用于改进药物开发。GWASs识别人群中常见的遗传变异,并涉及患者之间广泛共享的疾病机制。在这项研究中,我们综合了毛囊皮脂腺单位的生物学知识,这些知识来源于头发相关疾病的GWASs。我们确定了关键的遗传驱动因素,揭示了跨越疾病的基本生物学主题,以确定HF健康的关键调节因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Polygenic Architecture of Human Diseases Affecting the Hair Follicle.

Disorders affecting the hair follicle (HF) and pilosebaceous unit impose psychosocial and financial burdens on patients and may signal risk for other medical conditions. Human genetic studies help to identify key physiological mechanisms that govern health and are increasingly used to improve drug development. GWASs identify genetic variants that are common in the population and implicate disease mechanisms that are widely shared among patients. In this study, we synthesize knowledge about the biology of the pilosebaceous unit that has been derived from GWASs of hair-related diseases. We identify the key genetic drivers and reveal fundamental biological themes that cut across diseases to identify crucial regulators of HF health.

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