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JoVE Journal Genetics
Undersøgelse af patogenesen af MYH7-mutationen Gly823Glu i familiær hypertrofisk kardiomyopati ved hjælp af en musemodel
 
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Undersøgelse af patogenesen af MYH7-mutationen Gly823Glu i familiær hypertrofisk kardiomyopati ved hjælp af en musemodel

Article DOI: 10.3791/63949-v • 03:45 min • August 8th, 2022
August 8th, 2022 •
*1,2, *3, 4, 4, 1,2, 1,2, 1,2, 2,5, 4, 1,2
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
* These authors contributed equally

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Baseret på den familiære arvelige kardiomyopatifamilie, der findes i vores kliniske arbejde, skabte vi en C57BL/6N-musemodel med en punktmutation (G823E) ved musen MYH7-locus gennem CRISPR/Cas9-medieret genomteknik for at verificere denne mutation.

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