Weber WM - Search Results

1

Chitosan as a non-viral co-transfection system in a cystic fibrosis cell line.

Fernández Fernández E, Santos-Carballal B, Weber WM, Goycoolea FM. Fernández Fernández E, et al. Among authors: weber wm. Int J Pharm. 2016 Apr 11;502(1-2):1-9. doi: 10.1016/j.ijpharm.2016.01.083. Epub 2016 Feb 11. Int J Pharm. 2016. PMID: 26875537 Free article.

2

Cystic fibrosis transmembrane conductance regulator-mRNA delivery: a novel alternative for cystic fibrosis gene therapy.

Bangel-Ruland N, Tomczak K, Fernández Fernández E, Leier G, Leciejewski B, Rudolph C, Rosenecker J, Weber WM. Bangel-Ruland N, et al. Among authors: weber wm. J Gene Med. 2013 Nov-Dec;15(11-12):414-26. doi: 10.1002/jgm.2748. J Gene Med. 2013. PMID: 24123772

3

Chitosan Nanocomplexes for the Delivery of ENaC Antisense Oligonucleotides to Airway Epithelial Cells.

Kolonko AK, Bangel-Ruland N, Goycoolea FM, Weber WM. Kolonko AK, et al. Among authors: weber wm. Biomolecules. 2020 Apr 5;10(4):553. doi: 10.3390/biom10040553. Biomolecules. 2020. PMID: 32260534 Free PMC article.

4

Capsaicin-Loaded Chitosan Nanocapsules for wtCFTR-mRNA Delivery to a Cystic Fibrosis Cell Line.

Kolonko AK, Efing J, González-Espinosa Y, Bangel-Ruland N, van Driessche W, Goycoolea FM, Weber WM. Kolonko AK, et al. Among authors: weber wm. Biomedicines. 2020 Sep 20;8(9):364. doi: 10.3390/biomedicines8090364. Biomedicines. 2020. PMID: 32962254 Free PMC article.

5

Targeting ENaC as a Molecular Suspect in Cystic Fibrosis.

Bangel-Ruland N, Tomczak K, Weber WM. Bangel-Ruland N, et al. Among authors: weber wm. Curr Drug Targets. 2015;16(9):951-7. doi: 10.2174/1389450116666141212101626. Curr Drug Targets. 2015. PMID: 25544019 Review.

6

Targeted Integration of a Super-Exon into the CFTR Locus Leads to Functional Correction of a Cystic Fibrosis Cell Line Model.

Bednarski C, Tomczak K, Vom Hövel B, Weber WM, Cathomen T. Bednarski C, et al. Among authors: weber wm. PLoS One. 2016 Aug 15;11(8):e0161072. doi: 10.1371/journal.pone.0161072. eCollection 2016. PLoS One. 2016. PMID: 27526025 Free PMC article.

7

Specific inhibition of epithelial Na+ channels by antisense oligonucleotides for the treatment of Na+ hyperabsorption in cystic fibrosis.

Sobczak K, Segal A, Bangel-Ruland N, Semmler J, Van Driessche W, Lindemann H, Heermann R, Weber WM. Sobczak K, et al. Among authors: weber wm. J Gene Med. 2009 Sep;11(9):813-23. doi: 10.1002/jgm.1363. J Gene Med. 2009. PMID: 19533590

8

Sildenafil acts as potentiator and corrector of CFTR but might be not suitable for the treatment of CF lung disease.

Leier G, Bangel-Ruland N, Sobczak K, Knieper Y, Weber WM. Leier G, et al. Among authors: weber wm. Cell Physiol Biochem. 2012;29(5-6):775-90. doi: 10.1159/000265129. Epub 2012 May 11. Cell Physiol Biochem. 2012. PMID: 22613978

9

Expression of ENaC and other transport proteins in Xenopus oocytes is modulated by intracellular Na+.

Kusche-Vihrog K, Segal A, Grygorczyk R, Bangel-Ruland N, Van Driessche W, Weber WM. Kusche-Vihrog K, et al. Among authors: weber wm. Cell Physiol Biochem. 2009;23(1-3):9-24. doi: 10.1159/000204076. Epub 2009 Feb 18. Cell Physiol Biochem. 2009. PMID: 19255496

10

Upregulated expression of ENaC in human CF nasal epithelium.

Bangel N, Dahlhoff C, Sobczak K, Weber WM, Kusche-Vihrog K. Bangel N, et al. Among authors: weber wm. J Cyst Fibros. 2008 May;7(3):197-205. doi: 10.1016/j.jcf.2007.07.012. Epub 2007 Sep 4. J Cyst Fibros. 2008. PMID: 17766193 Free article.

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