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CFTR gene transfer with AAV improves early cystic fibrosis pig phenotypes.
Steines B, Dickey DD, Bergen J, Excoffon KJ, Weinstein JR, Li X, Yan Z, Abou Alaiwa MH, Shah VS, Bouzek DC, Powers LS, Gansemer ND, Ostedgaard LS, Engelhardt JF, Stoltz DA, Welsh MJ, Sinn PL, Schaffer DV, Zabner J. Steines B, et al. Among authors: zabner j. JCI Insight. 2016 Sep 8;1(14):e88728. doi: 10.1172/jci.insight.88728. JCI Insight. 2016. PMID: 27699238 Free PMC article.
Postnatal airway growth in cystic fibrosis piglets.
Adam RJ, Abou Alaiwa MH, Bouzek DC, Cook DP, Gansemer ND, Taft PJ, Powers LS, Stroik MR, Hoegger MJ, McMenimen JD, Hoffman EA, Zabner J, Welsh MJ, Meyerholz DK, Stoltz DA. Adam RJ, et al. Among authors: zabner j. J Appl Physiol (1985). 2017 Sep 1;123(3):526-533. doi: 10.1152/japplphysiol.00263.2017. Epub 2017 Jun 15. J Appl Physiol (1985). 2017. PMID: 28620056 Free PMC article.
Development and Initial Characterization of Pigs with DNAI1 Mutations and Primary Ciliary Dyskinesia.
Abou Alaiwa MA, Hilkin BM, Price MP, Gansemer ND, Rector MR, Stroik MR, Powers LS, Whitworth KM, Samuel MS, Jain A, Ostedgaard LS, Ernst SE, Philibert W, Boyken LD, Moninger TO, Karp PH, Hornick DB, Sinn PL, Fischer AJ, Pezzulo AA, McCray PB Jr, Meyerholz DK, Zabner J, Prather RS, Welsh MJ, Stoltz DA. Abou Alaiwa MA, et al. Among authors: zabner j. bioRxiv [Preprint]. 2024 Aug 21:2024.05.22.594822. doi: 10.1101/2024.05.22.594822. bioRxiv. 2024. PMID: 39229081 Free PMC article. Preprint.
The air-liquid interface and use of primary cell cultures are important to recapitulate the transcriptional profile of in vivo airway epithelia.
Pezzulo AA, Starner TD, Scheetz TE, Traver GL, Tilley AE, Harvey BG, Crystal RG, McCray PB Jr, Zabner J. Pezzulo AA, et al. Among authors: zabner j. Am J Physiol Lung Cell Mol Physiol. 2011 Jan;300(1):L25-31. doi: 10.1152/ajplung.00256.2010. Epub 2010 Oct 22. Am J Physiol Lung Cell Mol Physiol. 2011. PMID: 20971803 Free PMC article.
216 results