Related Articles by Review for PMID: 18487356

Year	Number of Results
1995	1
1996	1
1998	2
1999	2
2000	1
2003	1
2005	1
2006	2
2008	2
2011	3
2012	4
2013	3
2014	7
2015	3
2016	9
2017	5
2018	3
2019	2
2020	8
2021	7
2022	10
2023	4
2024	1

1

The porcine lung as a potential model for cystic fibrosis.

Rogers CS, Abraham WM, Brogden KA, Engelhardt JF, Fisher JT, McCray PB Jr, McLennan G, Meyerholz DK, Namati E, Ostedgaard LS, Prather RS, Sabater JR, Stoltz DA, Zabner J, Welsh MJ. Rogers CS, et al. Am J Physiol Lung Cell Mol Physiol. 2008 Aug;295(2):L240-63. doi: 10.1152/ajplung.90203.2008. Epub 2008 May 16. Am J Physiol Lung Cell Mol Physiol. 2008. PMID: 18487356 Free PMC article. Review.

2

Cellular heterogeneity of CFTR expression and function in the lung: implications for gene therapy of cystic fibrosis.

Jiang Q, Engelhardt JF. Jiang Q, et al. Eur J Hum Genet. 1998 Jan;6(1):12-31. doi: 10.1038/sj.ejhg.5200158. Eur J Hum Genet. 1998. PMID: 9781011 Review.

3

Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology.

Olivier AK, Gibson-Corley KN, Meyerholz DK. Olivier AK, et al. Am J Physiol Gastrointest Liver Physiol. 2015 Mar 15;308(6):G459-71. doi: 10.1152/ajpgi.00146.2014. Epub 2015 Jan 15. Am J Physiol Gastrointest Liver Physiol. 2015. PMID: 25591863 Free PMC article. Review.

4

Lessons learned from the cystic fibrosis pig.

Meyerholz DK. Meyerholz DK. Theriogenology. 2016 Jul 1;86(1):427-32. doi: 10.1016/j.theriogenology.2016.04.057. Epub 2016 Apr 21. Theriogenology. 2016. PMID: 27142487 Free PMC article. Review.

5

Advances in gene therapy for cystic fibrosis lung disease.

Yan Z, McCray PB Jr, Engelhardt JF. Yan Z, et al. Hum Mol Genet. 2019 Oct 1;28(R1):R88-R94. doi: 10.1093/hmg/ddz139. Hum Mol Genet. 2019. PMID: 31332440 Free PMC article. Review.

6

Current Treatment Options for Cystic Fibrosis-Related Liver Disease.

Staufer K. Staufer K. Int J Mol Sci. 2020 Nov 14;21(22):8586. doi: 10.3390/ijms21228586. Int J Mol Sci. 2020. PMID: 33202578 Free PMC article. Review.

7

New therapies in cystic fibrosis.

Ratjen F, Grasemann H. Ratjen F, et al. Curr Pharm Des. 2012;18(5):614-27. doi: 10.2174/138161212799315984. Curr Pharm Des. 2012. PMID: 22229570 Review.

8

Understanding how cystic fibrosis mutations disrupt CFTR function: from single molecules to animal models.

Wang Y, Wrennall JA, Cai Z, Li H, Sheppard DN. Wang Y, et al. Int J Biochem Cell Biol. 2014 Jul;52:47-57. doi: 10.1016/j.biocel.2014.04.001. Epub 2014 Apr 13. Int J Biochem Cell Biol. 2014. PMID: 24727426 Review.

9

Molecular modelling approaches for cystic fibrosis transmembrane conductance regulator studies.

Odolczyk N, Zielenkiewicz P. Odolczyk N, et al. Int J Biochem Cell Biol. 2014 Jul;52:39-46. doi: 10.1016/j.biocel.2014.04.004. Epub 2014 Apr 13. Int J Biochem Cell Biol. 2014. PMID: 24735712 Review.

10

Understanding how cystic fibrosis mutations cause a loss of Cl- channel function.

Sheppard DN, Ostedgaard LS. Sheppard DN, et al. Mol Med Today. 1996 Jul;2(7):290-7. doi: 10.1016/1357-4310(96)10028-9. Mol Med Today. 1996. PMID: 8796909 Review.

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