317 AW1282X mouse model for cystic fibrosis and in vitro correction of the phenotype by pharmacologics and gene editing by Michicich, M., Traylor, Z., Steele, M., Conlon, R., Cotton, C., Kelley, T., Drumm, M., Hodges, C.

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661: W1282X cystic fibrosis mouse models for examining in vivo nonsense mutation correction by Michicich, M., Traylor, Z., LePage, D., Mann, R., Jiang, W., Kelley, T., Conlon, R., Drumm, M., Hodges, C.

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640 The cystic fibrosis mouse model resource center by Conlon, R., Corey, D., Wilson, M., Mansbach, S., Rosenjack, J., Duesler, L., Wilson, A., Davis, S., Michicich, M., Schneider, M., Traylor, Z., Jiang, W., LePage, D., Mann, R., Kelley, T., Hodges, C.

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Consumer acceptance, consumption and sensory attributes of spreads made from designer fats by Michicich, M, Vickers, Z, Martini, M.C, Labat, J.B

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A W1282X cystic fibrosis mouse allows the study of pharmacological and gene-editing therapeutics to restore CFTR function by Michicich, Margaret, Traylor, Zachary, McCoy, Caitlan, Valerio, Dana M., Wilson, Alma, Schneider, Molly, Davis, Sakeena, Barabas, Amanda, Mann, Rachel J., LePage, David F., Jiang, Weihong, Drumm, Mitchell L., Kelley, Thomas J., Conlon, Ronald A., Hodges, Craig A.

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Epidemiology of psychiatric care of patients with severe mental disorders in Italy : Rationale and design of a prospective study, and characteristics of the cohort by TERZIAN, E, STERNAI, E, BARBATO, A, TOGNONI, G, SARACENO, B

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