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斑马鱼作为生物医学研究的动物模型。

Zebrafish as an animal model for biomedical research.

机构信息

Department of Pathology, Digestive Disease Research Institute, Wonkwang University, Iksan, Jeonbuk, 54538, Republic of Korea.

Department of Biomedical Science, Graduate School, Wonkwang University, Iksan, Jeonbuk, 54538, Republic of Korea.

出版信息

Exp Mol Med. 2021 Mar;53(3):310-317. doi: 10.1038/s12276-021-00571-5. Epub 2021 Mar 1.

DOI:10.1038/s12276-021-00571-5
PMID:33649498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8080808/
Abstract

Zebrafish have several advantages compared to other vertebrate models used in modeling human diseases, particularly for large-scale genetic mutant and therapeutic compound screenings, and other biomedical research applications. With the impactful developments of CRISPR and next-generation sequencing technology, disease modeling in zebrafish is accelerating the understanding of the molecular mechanisms of human genetic diseases. These efforts are fundamental for the future of precision medicine because they provide new diagnostic and therapeutic solutions. This review focuses on zebrafish disease models for biomedical research, mainly in developmental disorders, mental disorders, and metabolic diseases.

摘要

斑马鱼相对于其他用于人类疾病建模的脊椎动物模型具有许多优势,特别是在大规模遗传突变体和治疗化合物筛选以及其他生物医学研究应用方面。随着 CRISPR 和下一代测序技术的发展,斑马鱼疾病模型正在加速理解人类遗传疾病的分子机制。这些努力对于精准医学的未来至关重要,因为它们提供了新的诊断和治疗解决方案。本综述重点介绍了用于生物医学研究的斑马鱼疾病模型,主要涉及发育障碍、精神障碍和代谢疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/8080808/b3188335f903/12276_2021_571_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/8080808/266f46b8f79e/12276_2021_571_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/8080808/b84da8c3ca46/12276_2021_571_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/8080808/b3188335f903/12276_2021_571_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/8080808/266f46b8f79e/12276_2021_571_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/8080808/b84da8c3ca46/12276_2021_571_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/8080808/b3188335f903/12276_2021_571_Fig3_HTML.jpg

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Neurosci Bull. 2020 Dec;36(12):1500-1512. doi: 10.1007/s12264-020-00600-9. Epub 2020 Oct 29.
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Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy.FAM50A 突变提示 Armfield X-连锁智力障碍综合征是一种剪接体病。
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Mitochondria, mitophagy, and metabolic disease: towards assembling the puzzle.
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