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Deep protein methylation profiling by combined chemical and immunoaffinity approaches reveals novel PRMT1 targets
Nicolas G. Hartel, Brandon Chew, Jian Qin, Jian Xu, Nicholas A. Graham
doi: https://doi.org/10.1101/538686
Nicolas G. Hartel
1Mork Family Department of Chemical Engineering and Materials Science, Viterbi School of Engineering Wuhan University, Wuhan, Hubei, China
Brandon Chew
1Mork Family Department of Chemical Engineering and Materials Science, Viterbi School of Engineering Wuhan University, Wuhan, Hubei, China
Jian Qin
2Center for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry Wuhan University, Wuhan, Hubei, China
3Central Laboratory, Renmin Hospital, Wuhan University, Wuhan, Hubei, China
Jian Xu
2Center for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry Wuhan University, Wuhan, Hubei, China
4Department of Biochemistry and Molecular Medicine, University of Southern California, Los Angeles, CA 90089
5Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089
Nicholas A. Graham
1Mork Family Department of Chemical Engineering and Materials Science, Viterbi School of Engineering Wuhan University, Wuhan, Hubei, China
5Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089
Posted February 05, 2019.
Deep protein methylation profiling by combined chemical and immunoaffinity approaches reveals novel PRMT1 targets
Nicolas G. Hartel, Brandon Chew, Jian Qin, Jian Xu, Nicholas A. Graham
bioRxiv 538686; doi: https://doi.org/10.1101/538686
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