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该基因在原发性和继发性淋巴水肿中的可能作用:文献复习与两种罕见致病变异的遗传研究。

Possible Role of the Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants.

机构信息

Department of Vascular Rehabilitation, San Giovanni Battista Hospital, Rome, Italy.

Rehabilitative Medicine, University Hospital, Ospedali Riuniti of Ancona, Torrette, Italy.

出版信息

Lymphat Res Biol. 2021 Apr;19(2):129-133. doi: 10.1089/lrb.2020.0030. Epub 2020 Sep 22.

Abstract

RAR-related Orphan Receptor C (RORC) is a DNA-binding transcription factor and the key transcription factor responsible for differentiation of T helper 17 cells. The gene plays a role in lymphoid organogenesis, thymopoiesis, and lymph node organogenesis. The aim of our study was to determine the possible role of in the development of lymphatic system malformations by combining data from the scientific literature and next-generation sequencing of in lymphedema patients negative for known causative genes. We sequenced in 235 lymphedema patients negative for known lymphedema-associated genes. We found two probands carrying nonsense variants. We show that is important for normal function of the lymphatic system and that a rare variant with a possible causative effect may imply predisposition for lymphedema.

摘要

RAR 相关孤儿受体 C(RORC)是一种 DNA 结合转录因子,也是负责辅助性 T 细胞 17 分化的关键转录因子。该基因在淋巴器官发生、胸腺生成和淋巴结发生中发挥作用。我们的研究目的是通过将科学文献中的数据与淋巴水肿患者中已知致病基因阴性的下一代测序相结合,确定 在淋巴管畸形发育中的可能作用。我们对 235 名已知淋巴水肿相关基因阴性的淋巴水肿患者进行了测序。我们发现两名先证者携带无意义的 变异。我们表明, 对于淋巴系统的正常功能很重要,而具有可能致病作用的罕见变异可能意味着易患淋巴水肿。

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