Kunzelmann K - Search Results

1

Establishment and characterization of a novel polarized MDCK epithelial cellular model for CFTR studies.

Mendes F, Wakefield J, Bachhuber T, Barroso M, Bebok Z, Penque D, Kunzelmann K, Amaral MD. Mendes F, et al. Among authors: kunzelmann k. Cell Physiol Biochem. 2005;16(4-6):281-90. doi: 10.1159/000089857. Cell Physiol Biochem. 2005. PMID: 16301828

2

No evidence for direct activation of the cystic fibrosis transmembrane conductance regulator by 8-cyclopentyl-1,3-dipropylxanthine.

Kunzelmann K, Briel M, Schreiber R, Ricken S, Nitschke R, Greger R. Kunzelmann K, et al. Cell Physiol Biochem. 1998;8(4):185-93. doi: 10.1159/000016281. Cell Physiol Biochem. 1998. PMID: 9694345

3

The cystic fibrosis transmembrane conductance regulator and its function in epithelial transport.

Kunzelmann K. Kunzelmann K. Rev Physiol Biochem Pharmacol. 1999;137:1-70. doi: 10.1007/3-540-65362-7_4. Rev Physiol Biochem Pharmacol. 1999. PMID: 10207304 Review.

4

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M. Hirtz S, et al. Among authors: kunzelmann k. Gastroenterology. 2004 Oct;127(4):1085-95. doi: 10.1053/j.gastro.2004.07.006. Gastroenterology. 2004. PMID: 15480987

5

Purinergic inhibition of the epithelial Na+ transport via hydrolysis of PIP2.

Kunzelmann K, Bachhuber T, Regeer R, Markovich D, Sun J, Schreiber R. Kunzelmann K, et al. FASEB J. 2005 Jan;19(1):142-3. doi: 10.1096/fj.04-2314fje. Epub 2004 Oct 25. FASEB J. 2005. PMID: 15504951

6

Cl- interference with the epithelial Na+ channel ENaC.

Bachhuber T, König J, Voelcker T, Mürle B, Schreiber R, Kunzelmann K. Bachhuber T, et al. Among authors: kunzelmann k. J Biol Chem. 2005 Sep 9;280(36):31587-94. doi: 10.1074/jbc.M504347200. Epub 2005 Jul 18. J Biol Chem. 2005. PMID: 16027156 Free article.

7

Characterization of novel airway submucosal gland cell models for cystic fibrosis studies.

da Paula AC, Ramalho AS, Farinha CM, Cheung J, Maurisse R, Gruenert DC, Ousingsawat J, Kunzelmann K, Amaral MD. da Paula AC, et al. Among authors: kunzelmann k. Cell Physiol Biochem. 2005;15(6):251-62. doi: 10.1159/000087235. Cell Physiol Biochem. 2005. PMID: 16037690

8

An extract from the medicinal plant Phyllanthus acidus and its isolated compounds induce airway chloride secretion: A potential treatment for cystic fibrosis.

Sousa M, Ousingsawat J, Seitz R, Puntheeranurak S, Regalado A, Schmidt A, Grego T, Jansakul C, Amaral MD, Schreiber R, Kunzelmann K. Sousa M, et al. Among authors: kunzelmann k. Mol Pharmacol. 2007 Jan;71(1):366-76. doi: 10.1124/mol.106.025262. Epub 2006 Oct 25. Mol Pharmacol. 2007. PMID: 17065237

9

Molecular targeting of CFTR as a therapeutic approach to cystic fibrosis.

Amaral MD, Kunzelmann K. Amaral MD, et al. Among authors: kunzelmann k. Trends Pharmacol Sci. 2007 Jul;28(7):334-41. doi: 10.1016/j.tips.2007.05.004. Epub 2007 Jun 18. Trends Pharmacol Sci. 2007. PMID: 17573123 Review.

10

Regulation of the epithelial Na+ channel by the protein kinase CK2.

Bachhuber T, Almaça J, Aldehni F, Mehta A, Amaral MD, Schreiber R, Kunzelmann K. Bachhuber T, et al. Among authors: kunzelmann k. J Biol Chem. 2008 May 9;283(19):13225-32. doi: 10.1074/jbc.M704532200. Epub 2008 Feb 28. J Biol Chem. 2008. PMID: 18308722 Free PMC article.

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