INFRAFRONTIER: mouse model resources for modelling human diseases.

IF 2.7 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Asrar Ali Khan, Gema Valera Vazquez, Montse Gustems, Rafaele Matteoni, Fei Song, Philipp Gormanns, Sabine Fessele, Michael Raess, Martin Hrabĕ de Angelis
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引用次数: 0

Abstract

Over the last decade, INFRAFRONTIER has positioned itself as a world-class Research Infrastructure for the generation, phenotyping, archiving, and distribution of mouse models in Europe. The INFRAFRONTIER network consists of 22 partners from 15 countries, and is continuously enhancing and broadening its portfolio of resources and services that are offered to the research community on a non-profit basis. By bringing together European rodent model expertise and providing valuable disease model services to the biomedical research community, INFRAFRONTIER strives to push the accessibility of cutting-edge human disease modelling technologies across the European research landscape. This article highlights the latest INFRAFRONTIER developments and informs the research community about its extensively utilised services, resources, and technical developments, specifically the intricacies of the INFRAFRONTIER database, use of Curated Disease Models, overview of the INFRAFRONTIER Cancer and Rare Disease resources, and information about its main state-of-the-art services.

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INFRAFRONTIER:用于人类疾病建模的小鼠模型资源。
在过去的十年中,INFRAFRONTIER已经将自己定位为欧洲小鼠模型的生成,表型,存档和分发的世界级研究基础设施。INFRAFRONTIER网络由来自15个国家的22个合作伙伴组成,并在非营利基础上不断加强和扩大其向研究界提供的资源和服务组合。通过汇集欧洲啮齿动物模型专业知识并为生物医学研究界提供有价值的疾病模型服务,INFRAFRONTIER致力于推动欧洲研究领域尖端人类疾病建模技术的可及性。本文重点介绍了INFRAFRONTIER的最新发展,并向研究界介绍了其广泛使用的服务、资源和技术发展,特别是INFRAFRONTIER数据库的复杂性、策展疾病模型的使用、INFRAFRONTIER癌症和罕见疾病资源的概述,以及有关其主要最先进服务的信息。
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来源期刊
Mammalian Genome
Mammalian Genome 生物-生化与分子生物学
CiteScore
4.00
自引率
0.00%
发文量
33
审稿时长
6-12 weeks
期刊介绍: Mammalian Genome focuses on the experimental, theoretical and technical aspects of genetics, genomics, epigenetics and systems biology in mouse, human and other mammalian species, with an emphasis on the relationship between genotype and phenotype, elucidation of biological and disease pathways as well as experimental aspects of interventions, therapeutics, and precision medicine. The journal aims to publish high quality original papers that present novel findings in all areas of mammalian genetic research as well as review articles on areas of topical interest. The journal will also feature commentaries and editorials to inform readers of breakthrough discoveries as well as issues of research standards, policies and ethics.
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