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靶向修饰炎症性肠病易感基因的新型大鼠模型的突变分析。

Mutational analyses of novel rat models with targeted modifications in inflammatory bowel disease susceptibility genes.

机构信息

Rat Resource and Research Center, University of Missouri, Columbia, MO, 65201, USA.

Department of Veterinary Pathobiology, University of Missouri, Columbia, MO, 65201, USA.

出版信息

Mamm Genome. 2021 Jun;32(3):173-182. doi: 10.1007/s00335-021-09868-2. Epub 2021 Apr 11.

Abstract

Mutations and single base pair polymorphisms in various genes have been associated with increased susceptibility to inflammatory bowel disease (IBD). We have created a series of rat strains carrying targeted genetic alterations within three IBD susceptibility genes: Nod2, Atg16l1, and Il23r, using CRISPR/Cas9 genome editing technology. Knock-out alleles and alleles with known human susceptibility polymorphisms were generated on three different genetic backgrounds: Fischer, Lewis and Sprague Dawley. The availability of these rat models will contribute to our understanding of the basic biological roles of these three genes as well as provide new potential IBD animal models.

摘要

各种基因的突变和单碱基对多态性与炎症性肠病(IBD)的易感性增加有关。我们使用 CRISPR/Cas9 基因组编辑技术在三个 IBD 易感性基因:Nod2、Atg16l1 和 Il23r 内创建了一系列携带靶向遗传改变的大鼠品系。在三个不同的遗传背景(Fisher、Lewis 和 Sprague Dawley)上生成了敲除等位基因和具有已知人类易感性多态性的等位基因。这些大鼠模型的出现将有助于我们理解这三个基因的基本生物学作用,并为新的潜在 IBD 动物模型提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86c6/8128796/ab62d5484c34/335_2021_9868_Fig1_HTML.jpg

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