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中文摘要
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在过去的一年里,我们的研究核心与NIH的十个研究单位合作,产生了新的胚胎干细胞系和新的小鼠模型(8个项目,包括6个CRISPR/Cas9合子注射)。本研究包括建立免疫系统信号通路相互作用、T细胞发育、造血、干细胞生物学、早期胚胎表观遗传、基因组稳定性调控机制、RNA代谢、基因调控和增强子功能、铁代谢与疟疾风险等方面的模型。我们还进行了专门的手术,包括胸腺植入,以支持免疫功能的研究。
英文摘要
During the last year our research core has worked with ten NIH research units to generate novel embryonic stem cell lines and new mouse models (8 projects, including 6 CRISPR/Cas9 Zygote injections). This research included establishment of models to study signal pathway interactions in the immune system, T cell development, hematopoiesis, stem cell biology, epigenetic inheritance in the early embryo, mechanisms regulating genomic stability, RNA metabolis, gene regulation and enhancer function, and iron methabolism and malaria risk. We also performed specialized surgeries including thymus implants to support research on immune function.
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Analysis of Imprinting on Mouse Distal Chromosome 7
Analysis Of Imprinting On Mouse Distal Chromosome 7
Epigenetic mechanisms regulating the Igf2/H19 and Kcnq1 locus
Generating new mouse models
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