Sheikh, M.O., Venzke, D., Anderson, M.E., Yoshida-Moriguchi, T., Glushka, J.N., Nairn, A.V., Galizzi, M., Moremen, K.W., Campbell, K. P., Wells, L. (2020). HNK-1 Sulfotransferase Modulates α-Dystroglycan Glycosylation by 3-O-sulfation of Glucuronic acid on Matriglycan. Glycobiology. (in press)

Ware, B.C., Sullivan, B.M., LaVergne, S., Marro, B., Egashira, T., Campbell, K.P., Elder, J., Oldstone, M.B.A. (2019). A unique variant of lymphocytic choriomeningitis virus that induces pheromone binding protein MUP: Critical role for CTL. Proc. Natl. Acad. Sci. USA, 116(36):18001-18008. doi:10.1073/pnas.1907070116 PMID:31427525 [PDF]

de Greef, J.C., Slϋtter, B., Anderson, M.E., Hamlyn, R., O’Campo Landa, R., McNutt, E.J., Hara, Y., Pewe, L.L., Venzke, D., Matsumura, K., Saito, F., Harty, J.T., Campbell, K.P. (2019). Protective role for the N-terminal domain of α-dystroglycan in Influenza A virus proliferation. Proc. Natl. Acad. Sci. USA., 116(23). doi:10.1073/pnas.1904493116 PMID:31097590 PMCID: PMC6561248 [PDF]

Beltrán, D, Anderson, M.E., Bharathy, N., Settelmeyer, T.P., Svalina, M.N., Bajwa, Z., Shern, J.F., Gultekin, S.H., Cuellar, M., Yonekawa, T., Keller, C., Campbell, K.P. (2019). Exogenous Expression of the Glycosyltransferase LARGE1 Restores α-Dystroglycan Matriglycan and Laminin Binding in Rhabdomyosarcoma. Skelet. Muscle, 9(1). doi:10.1186/s13395-019-0195-0 PMID:31054580 PMCID: PMC6500046 [PDF]

Chakravorty, S., Berger, K., Arafat, D., Nallamilli, B.R.R., Subramanian H.P., Joseph, S., Anderson, M.E., Campbell, K.P., Glass, J., Gibson, G., Hegde, M. (2019). Clinical Utility of RNA Sequencing to Resolve Unusual GNE Myopathy with a Novel Promoter Deletion. Muscle Nerve, 60(1):98-103. doi: 10.1002/mus.26486 PMID:30990900 [PDF]

Herrador, A., Fedeli, C., Radulovic, E., Campbell, K.P., Moreno, H., Gerold, G., Kunz, S. (2019). Dynamic Dystroglycan Complexes Mediate Cell Entry of Lassa Virus.  mBio, 10(2). doi: 10.1128/mBio.02869-18 PMID:30914516 PMCID: PMC6437060 [PDF]

González Coraspe, J.A.,Weis, J., Anderson, M.E., Münchberg, U., Lorenz, K., Buchkremer, S., Carr, S., Zahedi, R.P., Brauers, E., Michels, H., Sunada, Y., Lochmüller, H., Campbell, K.P., Freier, E., Hathazi, D., Roos, A. (2018). Biochemical and Pathological Changes Result from Mutated Caveolin-3 in Muscle.  Skelet. Muscle, 8(28). doi: 10.1186/s13395-018-0173-y PMID:30153853 PMCID: PMC6114045 [PDF]

Brun, B.N., Willer, T., Darbro, B.W., Gonorazky, H.D., Naumenko, S., Dowling, J.J., Campbell, K.P., Moore, S.A., Mathews, K.D. (2018). Uniparental Disomy Unveils a Novel Recessive Mutation in POMT2.  Neuromuscular Disorders, 28(7), 592-596. doi:10.1016/j.nmd.2018.04.003 PMID: 29759639 PMCID: PMC6115279 [PDF]

Cox, M.L., Evans, J.M., Davis, A.G., Guo, L.T., Levy, J.R., Starr-Moss, A.N., Salmela, E.T., Hytӧnen, M.K., Lohi, H., Campbell, K.P., Clark, L.A., Shelton, G.D. (2017). Exome Sequencing Reveals Independent SGCD Deletions Causing Limb Girdle Muscular Dystrophy in Boston Terriers.  Skeletal Muscle, 7(1):15. doi: 10.1186/s13395-017-0131-0 PMID: 28697784 PMCID: PMC5506588 [PDF]

Clements, R., Turk, R., Campbell, K.P., Wright, K.M. (2017). Dystroglycan Maintains Inner Limiting Membrane Integrity to Coordinate Retinal Development.  Journal of Neuroscience, 30;37(35): 8559-8574. doi: 10.1523/JNEUROSCI.0946-17.2017 PMID: 28760865 PMCID: PMC5577860 [PDF]