Similar articles for PMID: 25124441

Year	Number of Results
1976	1
1993	1
1995	1
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1999	1
2001	1
2002	3
2003	5
2004	5
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2006	6
2007	9
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2012	3
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2015	4
2016	5
2017	6
2018	11
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2020	9
2021	10
2022	16
2023	5
2024	0

1

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

Hoegger MJ, Fischer AJ, McMenimen JD, Ostedgaard LS, Tucker AJ, Awadalla MA, Moninger TO, Michalski AS, Hoffman EA, Zabner J, Stoltz DA, Welsh MJ. Hoegger MJ, et al. Science. 2014 Aug 15;345(6198):818-22. doi: 10.1126/science.1255825. Science. 2014. PMID: 25124441 Free PMC article.

2

Mucociliary Transport in Healthy and Cystic Fibrosis Pig Airways.

Xie Y, Ostedgaard L, Abou Alaiwa MH, Lu L, Fischer AJ, Stoltz DA. Xie Y, et al. Ann Am Thorac Soc. 2018 Nov;15(Suppl 3):S171-S176. doi: 10.1513/AnnalsATS.201805-308AW. Ann Am Thorac Soc. 2018. PMID: 30431346 Free PMC article. Review.

3

Model of mucociliary clearance in cystic fibrosis lungs.

Kurbatova P, Bessonov N, Volpert V, Tiddens HA, Cornu C, Nony P, Caudri D; CRESim Working Group. Kurbatova P, et al. J Theor Biol. 2015 May 7;372:81-8. doi: 10.1016/j.jtbi.2015.02.023. Epub 2015 Mar 5. J Theor Biol. 2015. PMID: 25746843

4

Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.

Joo NS, Cho HJ, Khansaheb M, Wine JJ. Joo NS, et al. J Clin Invest. 2010 Sep;120(9):3161-6. doi: 10.1172/JCI43466. Epub 2010 Aug 25. J Clin Invest. 2010. PMID: 20739758 Free PMC article.

5

Cellular and molecular architecture of submucosal glands in wild-type and cystic fibrosis pigs.

Yu W, Moninger TO, Thurman AL, Xie Y, Jain A, Zarei K, Powers LS, Pezzulo AA, Stoltz DA, Welsh MJ. Yu W, et al. Proc Natl Acad Sci U S A. 2022 Jan 25;119(4):e2119759119. doi: 10.1073/pnas.2119759119. Proc Natl Acad Sci U S A. 2022. PMID: 35046051 Free PMC article.

6

Acid exposure disrupts mucus secretion and impairs mucociliary transport in neonatal piglet airways.

Liao YSJ, Kuan SP, Guevara MV, Collins EN, Atanasova KR, Dadural JS, Vogt K, Schurmann V, Bravo L, Eken E, Sponchiado M, Reznikov LR. Liao YSJ, et al. Am J Physiol Lung Cell Mol Physiol. 2020 May 1;318(5):L873-L887. doi: 10.1152/ajplung.00025.2020. Epub 2020 Mar 11. Am J Physiol Lung Cell Mol Physiol. 2020. PMID: 32160007 Free PMC article.

7

Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis Mucus.

Xie Y, Lu L, Tang XX, Moninger TO, Huang TJ, Stoltz DA, Welsh MJ. Xie Y, et al. Dev Cell. 2020 Aug 24;54(4):488-500.e5. doi: 10.1016/j.devcel.2020.07.002. Epub 2020 Jul 29. Dev Cell. 2020. PMID: 32730755 Free PMC article.

8

Tromethamine improves mucociliary clearance in cystic fibrosis pigs.

Ash JJ, Hilkin BM, Gansemer ND, Hoffman EA, Zabner J, Stoltz DA, Abou Alaiwa MH. Ash JJ, et al. Physiol Rep. 2022 Sep;10(17):e15340. doi: 10.14814/phy2.15340. Physiol Rep. 2022. PMID: 36073059 Free PMC article.

9

Elastic mucus strands impair mucociliary clearance in cystic fibrosis pigs.

Pino-Argumedo MI, Fischer AJ, Hilkin BM, Gansemer ND, Allen PD, Hoffman EA, Stoltz DA, Welsh MJ, Abou Alaiwa MH. Pino-Argumedo MI, et al. Proc Natl Acad Sci U S A. 2022 Mar 29;119(13):e2121731119. doi: 10.1073/pnas.2121731119. Epub 2022 Mar 24. Proc Natl Acad Sci U S A. 2022. PMID: 35324331 Free PMC article.

10

Measurement of fluid secretion from intact airway submucosal glands.

Wine JJ, Joo NS, Choi JY, Cho HJ, Krouse ME, Wu JV, Khansaheb M, Irokawa T, Ianowski J, Hanrahan JW, Cuthbert AW, Tran KV. Wine JJ, et al. Methods Mol Biol. 2011;742:93-112. doi: 10.1007/978-1-61779-120-8_6. Methods Mol Biol. 2011. PMID: 21547728

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