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Studio della patogenesi della mutazione MYH7 Gly823Glu nella cardiomiopatia ipertrofica familiare utilizzando un modello murino
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03:45 min
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August 08, 2022
DOI:
1Department of Cardiovascular Surgery, Guangdong Provincial Hospital of Traditional Chinese Medicine,the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, 2The Second Clinical College of Guangzhou University of Chinese Medicine, 3Department of Cardiovascular Surgery, The First Affiliated Hospital,Jinan University, 4Guangdong Provincial Key Laboratory of Laboratory Animals,Guangdong Laboratory Animals Monitoring Institute, 5Department of Anesthesiology, Guangdong Provincial Hospital of Chinese Medicine,the Second Affiliated Hospital of Guangzhou University of Chinese Medicine
Summary
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Sulla base della famiglia di cardiomiopatie ereditarie familiari trovata nel nostro lavoro clinico, abbiamo creato un modello murino C57BL / 6N con una mutazione puntiforme (G823E) nel locus MYH7 del topo attraverso l'ingegneria del genoma mediata da CRISPR / Cas9 per verificare questa mutazione.
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Cite this Article
Xia, Y., Hu, J., Li, X., Zheng, S., Wang, G., Tan, S., Zou, Z., Ling, Q., Yang, F., Fan, X. Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model. J. Vis. Exp. (186), e63949, doi:10.3791/63949 (2022).
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