Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Philip, Kym"'
Autor:
Kathleen McGuire, Christina Baumgartner, Carey Backus, Rebecca Mathew, Kelly Klinge, Joseph Klahn, Prasanthi Geda, Kyle Halliwill, Jacqueline Aguado, Liang Mu, Ryan Duggan, Cara Hrusch, Elliot Farney, Zhaoming Xiong, Marinka Bulic, Patricia Trusk, Loren Lasko, Hakimeh Ebrahimi-Nik, Kathleen Yates, Robert Manguso, Keith Hamel, Marcia Paddock, Jennifer Frost, Philip Kym
Publikováno v:
Regular and Young Investigator Award Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28878187d896b81f89652a17a3f425f7
https://doi.org/10.1136/jitc-2022-sitc2022.1365
https://doi.org/10.1136/jitc-2022-sitc2022.1365
Autor:
Marc J C, Scanio, Xenia B, Searle, Bo, Liu, John R, Koenig, Robert J, Altenbach, Gregory A, Gfesser, Andrew, Bogdan, Stephen, Greszler, Gang, Zhao, Ashvani, Singh, Yihong, Fan, Andrew M, Swensen, Timothy, Vortherms, Arlene, Manelli, Corina, Balut, Wenqing, Gao, Hong, Yong, Michael, Schrimpf, Chris, Tse, Philip, Kym, Xueqing, Wang
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 72:128843
Cystic fibrosis (CF) is an autosomal recessive disease resulting from mutations on both copies of the CFTR gene. Phenylalanine deletion at position 508 of the CFTR protein (F508del-CFTR) is the most frequent mutation in CF patients. Currently, the mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15a2a884faa7901f5e486831d30b03cd
https://doi.org/10.1016/j.bmcl.2022.128843
https://doi.org/10.1016/j.bmcl.2022.128843
Autor:
Zhi Su, James Limberis, Andrew Souers, Philip Kym, Ann Mikhail, Kathryn Houseman, Gilbert Diaz, Ruth L. Martin, Bryan F. Cox, Gary A. Gintant
Publikováno v:
Biophysical Journal. (3):485a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67ae3746989c082935d3dc5d55df51a0