Publications

Zhang, Y., Long, C., Li, H., McAnally, J.R., Baskin, K., Shelton, J.M., Bassel-Duby, R., and Olson, E. “CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice”. Science Advances, Apr 2017, Vol. 3, no. 4.

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Long, C., Amoasii, L., Bassel-Duby, R., and Olson, E.N. (2016). Genome Editing of Monogenic Neuromuscular Diseases. JAMA Neurology. 73 1349-1355.

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Long, C., Amoasii, L., Mireault, A.A., McAnally, J.R., Li, H., Sanchez-Ortiz, E., Bhattacharyya, S., Shelton, J.M., Bassel-Duby, R., and Olson, E.N. (2016). Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy. Science 351, 400–403.

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Long, C., McAnally, J.R., Shelton, J.M., Mireault, A.A., Bassel-Duby, R., and Olson, E.N. (2014). Prevention of muscular dystrophy in mice by CRISPR/Cas9-mediated editing of germline DNA. Science 345, 1184–1188.

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