A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance von Anderson, Douglas M., Anderson, Kelly M., Chang, Chi-Lun, Makarewich, Catherine A., Nelson, Benjamin R., McAnally, John R., Kasaragod, Prasad, Shelton, John M., Liou, Jen, Bassel-Duby, Rhonda, Olson, Eric N.

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Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy von Long, Chengzu, Amoasii, Leonela, Mireault, Alex A., McAnally, John R., Li, Hui, Sanchez-Ortiz, Efrain, Bhattacharyya, Samadrita, Shelton, John M., Bassel-Duby, Rhonda, Olson, Eric N.

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Degenerative and regenerative pathways underlying Duchenne muscular dystrophy revealed by single-nucleus RNA sequencing von Chemello, Francesco, Wang, Zhaoning, Li, Hui, McAnally, John R., Liu, Ning, Bassel-Duby, Rhonda, Olson, Eric N.

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Control of muscle formation by the fusogenic micropeptide myomixer von Bi, Pengpeng, Ramirez-Martinez, Andres, Li, Hui, Cannavino, Jessica, McAnally, John R., Shelton, John M., Sánchez-Ortiz, Efrain, Bassel-Duby, Rhonda, Olson, Eric N.

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Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA von Long, Chengzu, McAnally, John R., Shelton, John M., Mireault, Alex A., Bassel-Duby, Rhonda, Olson, Eric N.

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Transcription of the non-coding RNA upperhand controls Hand2 expression and heart development von Anderson, Kelly M., Anderson, Douglas M., McAnally, John R., Shelton, John M., Bassel-Duby, Rhonda, Olson, Eric N.

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A peptide encoded by a transcript annotated as long noncoding RNA enhances SERCA activity in muscle von Nelson, Benjamin R., Makarewich, Catherine A., Anderson, Douglas M., Winders, Benjamin R., Troupes, Constantine D., Wu, Fenfen, Reese, Austin L., McAnally, John R., Chen, Xiongwen, Kavalali, Ege T., Cannon, Stephen C., Houser, Steven R., Bassel-Duby, Rhonda, Olson, Eric N.

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Base editing correction of hypertrophic cardiomyopathy in human cardiomyocytes and humanized mice von Chai, Andreas C., Cui, Miao, Chemello, Francesco, Li, Hui, Chen, Kenian, Tan, Wei, Atmanli, Ayhan, McAnally, John R., Zhang, Yu, Xu, Lin, Liu, Ning, Bassel-Duby, Rhonda, Olson, Eric N.

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Fusogenic micropeptide Myomixer is essential for satellite cell fusion and muscle regeneration von Bi, Pengpeng, McAnally, John R., Shelton, John M., Sánchez-Ortiz, Efrain, Bassel-Duby, Rhonda, Olson, Eric N.

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Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing von Min, Yi-Li, Chemello, Francesco, Li, Hui, Rodriguez-Caycedo, Cristina, Sanchez-Ortiz, Efrain, Mireault, Alex A., McAnally, John R., Shelton, John M., Zhang, Yu, Bassel-Duby, Rhonda, Olson, Eric N.

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Opposing gene regulatory programs governing myofiber development and maturation revealed at single nucleus resolution von Dos Santos, Matthieu, Shah, Akansha M., Zhang, Yichi, Bezprozvannaya, Svetlana, Chen, Kenian, Xu, Lin, Lin, Weichun, McAnally, John R., Bassel-Duby, Rhonda, Liu, Ning, Olson, Eric N.

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MOXI Is a Mitochondrial Micropeptide That Enhances Fatty Acid β-Oxidation von Makarewich, Catherine A., Baskin, Kedryn K., Munir, Amir Z., Bezprozvannaya, Svetlana, Sharma, Gaurav, Khemtong, Chalermchai, Shah, Akansha M., McAnally, John R., Malloy, Craig R., Szweda, Luke I., Bassel-Duby, Rhonda, Olson, Eric N.

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CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice von Zhang, Yu, Long, Chengzu, Li, Hui, McAnally, John R, Baskin, Kedryn K, Shelton, John M, Bassel-Duby, Rhonda, Olson, Eric N

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Hippo pathway effector Yap promotes cardiac regeneration von Xin, Mei, Kim, Yuri, Sutherland, Lillian B., Murakami, Masao, Qi, Xiaoxia, McAnally, John, Porrello, Enzo R., Mahmoud, Ahmed I., Tan, Wei, Shelton, John M., Richardson, James A., Sadek, Hesham A., Bassel-Duby, Rhonda, Olson, Eric N.

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RBPMS regulates cardiomyocyte contraction and cardiac function through RNA alternative splicing von Gan, Peiheng, Wang, Zhaoning, Bezprozvannaya, Svetlana, McAnally, John R, Tan, Wei, Li, Hui, Bassel-Duby, Rhonda, Liu, Ning, Olson, Eric N

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CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells von Min, Yi-Li, Li, Hui, Rodriguez-Caycedo, Cristina, Mireault, Alex A, Huang, Jian, Shelton, John M, McAnally, John R, Amoasii, Leonela, Mammen, Pradeep P A, Bassel-Duby, Rhonda, Olson, Eric N

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Loss of function of the nuclear envelope protein LEMD2 causes DNA damage-dependent cardiomyopathy von Caravia, Xurde M, Ramirez-Martinez, Andres, Gan, Peiheng, Wang, Feng, McAnally, John R, Xu, Lin, Bassel-Duby, Rhonda, Liu, Ning, Olson, Eric N

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Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy von Zhang, Yichi, Ramirez-Martinez, Andres, Chen, Kenian, McAnally, John R, Cai, Chunyu, Durbacz, Mateusz Z, Chemello, Francesco, Wang, Zhaoning, Xu, Lin, Bassel-Duby, Rhonda, Liu, Ning, Olson, Eric N

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A mouse model for adult cardiac-specific gene deletion with CRISPR/Cas9 von Carroll, Kelli J., Makarewich, Catherine A., McAnally, John, Anderson, Douglas M., Zentilin, Lorena, Liu, Ning, Giacca, Mauro, Bassel-Duby, Rhonda, Olson, Eric N.

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In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse von Amoasii, Leonela, Li, Hui, Zhang, Yu, Min, Yi-Li, Sanchez-Ortiz, Efrain, Shelton, John M., Long, Chengzu, Mireault, Alex A., Bhattacharyya, Samadrita, McAnally, John R., Bassel-Duby, Rhonda, Olson, Eric N.

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