Ahmadi S - Search Results

1

Activity of a novel antimicrobial peptide against Pseudomonas aeruginosa biofilms.

Beaudoin T, Stone TA, Glibowicka M, Adams C, Yau Y, Ahmadi S, Bear CE, Grasemann H, Waters V, Deber CM. Beaudoin T, et al. Among authors: ahmadi s. Sci Rep. 2018 Oct 3;8(1):14728. doi: 10.1038/s41598-018-33016-7. Sci Rep. 2018. PMID: 30283025 Free PMC article.

2

SLC6A14 Is a Genetic Modifier of Cystic Fibrosis That Regulates Pseudomonas aeruginosa Attachment to Human Bronchial Epithelial Cells.

Di Paola M, Park AJ, Ahmadi S, Roach EJ, Wu YS, Struder-Kypke M, Lam JS, Bear CE, Khursigara CM. Di Paola M, et al. Among authors: ahmadi s. mBio. 2017 Dec 19;8(6):e02073-17. doi: 10.1128/mBio.02073-17. mBio. 2017. PMID: 29259090 Free PMC article.

3

Conversion of human and mouse fibroblasts into lung-like epithelial cells.

Wong AP, Shojaie S, Liang Q, Xia S, Di Paola M, Ahmadi S, Bilodeau C, Garner J, Post M, Duchesneau P, Waddell TK, Bear CE, Nagy A, Rossant J. Wong AP, et al. Among authors: ahmadi s. Sci Rep. 2019 Jun 21;9(1):9027. doi: 10.1038/s41598-019-45195-y. Sci Rep. 2019. PMID: 31227724 Free PMC article.

4

Facilitating Structure-Function Studies of CFTR Modulator Sites with Efficiencies in Mutagenesis and Functional Screening.

Molinski SV, Ahmadi S, Hung M, Bear CE. Molinski SV, et al. Among authors: ahmadi s. J Biomol Screen. 2015 Dec;20(10):1204-17. doi: 10.1177/1087057115605834. Epub 2015 Sep 18. J Biomol Screen. 2015. PMID: 26385858

5

Augmentation of Cystic Fibrosis Transmembrane Conductance Regulator Function in Human Bronchial Epithelial Cells via SLC6A14-Dependent Amino Acid Uptake. Implications for Treatment of Cystic Fibrosis.

Ahmadi S, Wu YS, Li M, Ip W, Lloyd-Kuzik A, Di Paola M, Du K, Xia S, Lew A, Bozoky Z, Forman-Kay J, Bear CE, Gonska T. Ahmadi S, et al. Am J Respir Cell Mol Biol. 2019 Dec;61(6):755-764. doi: 10.1165/rcmb.2019-0094OC. Am J Respir Cell Mol Biol. 2019. PMID: 31189070

6

Conformational defects underlie proteasomal degradation of Dent's disease-causing mutants of ClC-5.

D'Antonio C, Molinski S, Ahmadi S, Huan LJ, Wellhauser L, Bear CE. D'Antonio C, et al. Among authors: ahmadi s. Biochem J. 2013 Jun 15;452(3):391-400. doi: 10.1042/BJ20121848. Biochem J. 2013. PMID: 23566014

7

Eckford PD, Ramjeesingh M, Molinski S, Pasyk S, Dekkers JF, Li C, Ahmadi S, Ip W, Chung TE, Du K, Yeger H, Beekman J, Gonska T, Bear CE. Eckford PD, et al. Among authors: ahmadi s. Chem Biol. 2014 May 22;21(5):666-78. doi: 10.1016/j.chembiol.2014.02.021. Epub 2014 Apr 10. Chem Biol. 2014. PMID: 24726831

8

Orkambi® and amplifier co-therapy improves function from a rare CFTR mutation in gene-edited cells and patient tissue.

Molinski SV, Ahmadi S, Ip W, Ouyang H, Villella A, Miller JP, Lee PS, Kulleperuma K, Du K, Di Paola M, Eckford PD, Laselva O, Huan LJ, Wellhauser L, Li E, Ray PN, Pomès R, Moraes TJ, Gonska T, Ratjen F, Bear CE. Molinski SV, et al. Among authors: ahmadi s. EMBO Mol Med. 2017 Sep;9(9):1224-1243. doi: 10.15252/emmm.201607137. EMBO Mol Med. 2017. PMID: 28667089 Free PMC article.

9

SLC6A14, an amino acid transporter, modifies the primary CF defect in fluid secretion.

Ahmadi S, Xia S, Wu YS, Di Paola M, Kissoon R, Luk C, Lin F, Du K, Rommens J, Bear CE. Ahmadi S, et al. Elife. 2018 Jul 13;7:e37963. doi: 10.7554/eLife.37963. Elife. 2018. PMID: 30004386 Free PMC article.

10

Lipophilicity of the Cystic Fibrosis Drug, Ivacaftor (VX-770), and Its Destabilizing Effect on the Major CF-causing Mutation: F508del.

Chin S, Hung M, Won A, Wu YS, Ahmadi S, Yang D, Elmallah S, Toutah K, Hamilton CM, Young RN, Viirre RD, Yip CM, Bear CE. Chin S, et al. Among authors: ahmadi s. Mol Pharmacol. 2018 Aug;94(2):917-925. doi: 10.1124/mol.118.112177. Epub 2018 Jun 14. Mol Pharmacol. 2018. PMID: 29903751

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