Three-dimensional microCT imaging of mouse heart development from early post-implantation to late fetal stages.

IF 2.7 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mammalian Genome Pub Date : 2023-06-01 Epub Date: 2023-01-03 DOI:10.1007/s00335-022-09976-7
Nanbing Li-Villarreal, Tara L Rasmussen, Audrey E Christiansen, Mary E Dickinson, Chih-Wei Hsu
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引用次数: 0

Abstract

Comprehensive detailed characterization of new mouse models can be challenging due to the individual focus involved in developing these models. Often models are engineered to test a specific hypothesis in a limited number of tissues, stages, and/or other contexts. Whether or not the model produces the desired phenotypes, phenotyping beyond the desired context can be extremely work intensive and these studies are often not undertaken. However, the general information resulting from broader phenotyping can be invaluable to the wider scientific community. The International Mouse Phenotyping Consortium (IMPC) and its subsidiaries, like the Knockout Mouse Project (KOMP), has made great strides in streamlining this process. In particular, the use of microCT has been an invaluable resource in examining internal organ systems throughout fetal/developmental stages. Here, we provide several novel vignettes demonstrating the utility of microCT in uncovering cardiac phenotypes both based on human disease correlations and those that are unpredicted.

Abstract Image

小鼠心脏从植入后早期到胎儿晚期发育的三维显微ct成像。
由于开发这些模型所涉及的个体焦点,对新小鼠模型进行全面详细的表征可能具有挑战性。通常,设计模型是为了在有限数量的组织、阶段和/或其他环境中测试特定的假设。无论模型是否产生期望的表型,超出期望环境的表型可能是非常繁重的工作,这些研究通常不会进行。然而,从更广泛的表型中得到的一般信息对更广泛的科学界来说是无价的。国际小鼠表型联盟(IMPC)及其子公司,如敲除小鼠项目(KOMP),在简化这一过程方面取得了巨大进展。特别是,在整个胎儿/发育阶段,使用微ct检查内脏系统是一种宝贵的资源。在这里,我们提供了几个新的小片段,展示了microCT在揭示基于人类疾病相关性和不可预测的心脏表型方面的效用。
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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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