Education
Ph.D of Biochemistry and Molecular Biology, Harvard University, USA
Current position
Professor, Department of Genetics, Stanford University School of Medicine, Stanford, California, USA
Publications (since 2011)
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Farruggio, A. P., Bhakta, M. S., du Bois, H., Ma, J. and M, P. C. (2017). Genomic integration of the full-length dystrophin coding sequence in Duchenne muscular dystrophy induced pluripotent stem cells. Biotechnol J.
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Calos, M. P. (2017). Genome Editing Techniques and Their Therapeutic Applications. Clin Pharmacol Ther 101(1): 42-51.
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Calos, M. P. (2016). The CRISPR Way to Think about Duchenne's. N Engl J Med 374(17): 1684-1686.
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Turan, S., Farruggio, A. P., Srifa, W., Day, J. W. and Calos, M. P. (2016). Precise Correction of Disease Mutations in Induced Pluripotent Stem Cells Derived From Patients With Limb Girdle Muscular Dystrophy. Mol Ther 24(4): 685-696.
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Calos, M. P. (2016). Phage integrases for genome editing. In Cathomen, T., Hirsch, M. and Porteus, M. (Eds). Genome Editing: The Next Step in Gene Therapy. Springer, 895: 81-91.
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Geisinger, J. M., Turan, S., Hernandez, S., Spector, L. P. and Calos, M. P. (2016). In vivo blunt-end cloning through CRISPR/Cas9-facilitated non-homologous end-joining. Nucleic Acids Res 44(8): e76.
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Woodard, L. E. and Calos, M. P. (2015). Nonviral genome modification strategies for gene therapy: Transposon, integrase, and nuclease systems. In: Templeton, N. S. (Ed). Gene and Cell Therapy Therapeutic Mechanisms and Strategies, Fourth Edition. CRC Press, 675-700.
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Geisinger, J. M. and Calos, M. P. (2015). Using phage integrases in a site-specific dual integrase cassette exchange strategy. Methods Mol Biol 1239: 29-38.
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Farruggio, A. P. and Calos, M. P. (2014). Serine integrase chimeras with activity in E. coli and HeLa cells. Biol Open 3(10): 895-903.
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Zhao, C., Farruggio, A. P., Bjornson, C. R., Chavez, C. L., Geisinger, J. M., Neal, T. L., Karow, M. and Calos, M. P. (2014). Recombinase-mediated reprogramming and dystrophin gene addition in mdx mouse induced pluripotent stem cells. PLoS One 9(4): e96279.
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Zhu, F., Gamboa, M., Farruggio, A. P., Hippenmeyer, S., Tasic, B., Schule, B., Chen-Tsai, Y. and Calos, M. P. (2014). DICE, an efficient system for iterative genomic editing in human pluripotent stem cells. Nucleic Acids Res 42(5): e34.
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Tremblay, J. P., Xiao, X., Aartsma-Rus, A., Barbas, C., Blau, H. M., Bogdanove, A. J., Boycott, K., Braun, S., Breakefield, X. O., Bueren, J. A., Buschmann, M., Byrne, B. J., Calos, M., Cathomen, T., Chamberlain, J., Chuah, M., Cornetta, K., Davies, K. E., Dickson, J. G., Duchateau, P., Flotte, T. R., Gaudet, D., Gersbach, C. A., Gilbert, R., Glorioso, J., Herzog, R. W., High, K. A., Huang, W., Huard, J., Joung, J. K., Liu, D., Liu, D., Lochmuller, H., Lustig, L., Martens, J., Massie, B., Mavilio, F., Mendell, J. R., Nathwani, A., Ponder, K., Porteus, M., Puymirat, J., Samulski, J., Takeda, S., Thrasher, A., VandenDriessche, T., Wei, Y., Wilson, J. M., Wilton, S. D., Wolfe, J. H. and Gao, G. (2013). Translating the genomics revolution: the need for an international gene therapy consortium for monogenic diseases. Mol Ther 21(2): 266-268.
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Geisinger, J. M. and Calos, M. P. (2013). Site-specific recombination using phiC31 integrase. In: Renault, S. and Duchateau, P. (Eds). Site-directed insertion of transgenes. Springer, 211 - 239.
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Farruggio, A. P., Chavez, C. L., Mikell, C. L. and Calos, M. P. (2012). Efficient reversal of phiC31 integrase recombination in mammalian cells. Biotechnol J 7(11): 1332-1336.
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Lan, F., Liu, J., Narsinh, K. H., Hu, S., Han, L., Lee, A. S., Karow, M., Nguyen, P. K., Nag, D., Calos, M. P., Robbins, R. C. and Wu, J. C. (2012). Safe genetic modification of cardiac stem cells using a site-specific integration technique. Circulation 126(11 Suppl 1): S20-28.
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Hillman, R. T. and Calos, M. P. (2012). Site-specific integration with bacteriophage PhiC31 integrase. Cold Spring Harb Protoc 2012(5).
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Chavez, C. L., Keravala, A., Chu, J. N., Farruggio, A. P., Cuellar, V. E., Voorberg, J. and Calos, M. P. (2012). Long-term expression of human coagulation factor VIII in a tolerant mouse model using the phiC31 integrase system. Hum Gene Ther 23(4): 390-398.
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Karow, M., Chavez, C. L., Farruggio, A. P., Geisinger, J. M., Keravala, A., Jung, W. E., Lan, F., Wu, J. C., Chen-Tsai, Y. and Calos, M. P. (2011). Site-specific recombinase strategy to create induced pluripotent stem cells efficiently with plasmid DNA. Stem Cells 29(11): 1696-1704.
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Chavez, C. L. and Calos, M. P. (2011). Therapeutic applications of the PhiC31 integrase system. Curr Gene Ther 11(5): 375-381.
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Karow, M. and Calos, M. P. (2011). The therapeutic potential of PhiC31 integrase as a gene therapy system. Expert Opin Biol Ther 11(10): 1287-1296.
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Keravala, A., Chavez, C. L., Hu, G., Woodard, L. E., Monahan, P. E. and Calos, M. P. (2011). Long-term phenotypic correction in factor IX knockout mice by using PhiC31 integrase-mediated gene therapy. Gene Ther 18(8): 842-848.
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Ito, M., Yamanouchi, K., Naito, K., Calos, M. P. and Tojo, H. (2011). Site-specific integration of transgene targeting an endogenous lox-like site in early mouse embryos. J Appl Genet 52(1): 89-94.