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新生儿坏死性小肠结肠炎的单核苷酸多态性。

Single Nucleotide Polymorphisms in Neonatal Necrotizing Enterocolitis.

机构信息

Department of Pediatrics, University of South Florida Health Morsani College of Medicine, Tampa, FL, USA.

Poole Hospital NHS Foundation Trust and Bournemouth University, Poole, United Kingdom.

出版信息

Curr Pediatr Rev. 2022;18(3):197-209. doi: 10.2174/1573396318666220117091621.

Abstract

The etiopathogenesis of necrotizing enterocolitis (NEC) remains unclear, but increasing information suggests that the risk and severity of NEC may be influenced by single nucleotide polymorphisms in many genes. In this article, we have reviewed gene variations that have either been specifically identified in NEC or have been noted in other inflammatory bowel disorders with similar histopathological abnormalities. We present evidence from our own peer-reviewed laboratory studies and data from an extensive literature search in the databases PubMed, EMBASE, and Scopus. To avoid bias in the identification of existing studies, search keywords were short-listed both from our own studies and from PubMed's Medical Subject Heading (MeSH) thesaurus.

摘要

坏死性小肠结肠炎(NEC)的发病机制仍不清楚,但越来越多的信息表明,NEC 的风险和严重程度可能受到许多基因中单核苷酸多态性的影响。本文综述了已在 NEC 中明确鉴定或在具有相似组织病理学异常的其他炎症性肠病中注意到的基因变异。我们提供了来自我们自己同行评议的实验室研究的证据和来自 PubMed、EMBASE 和 Scopus 数据库的广泛文献检索的数据。为了避免在确定现有研究时出现偏差,搜索关键字是从我们自己的研究和 PubMed 的医学主题词(MeSH)词库中筛选出来的。

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