Cotton CU - Search Results

1

Linaclotide improves gastrointestinal transit in cystic fibrosis mice by inhibiting sodium/hydrogen exchanger 3.

McHugh DR, Cotton CU, Moss FJ, Vitko M, Valerio DM, Kelley TJ, Hao S, Jafri A, Drumm ML, Boron WF, Stern RC, McBennett K, Hodges CA. McHugh DR, et al. Among authors: cotton cu. Am J Physiol Gastrointest Liver Physiol. 2018 Nov 1;315(5):G868-G878. doi: 10.1152/ajpgi.00261.2017. Epub 2018 Aug 17. Am J Physiol Gastrointest Liver Physiol. 2018. PMID: 30118317 Free PMC article.

2

Activation of endogenous deltaF508 cystic fibrosis transmembrane conductance regulator by phosphodiesterase inhibition.

Kelley TJ, Al-Nakkash L, Cotton CU, Drumm ML. Kelley TJ, et al. Among authors: cotton cu. J Clin Invest. 1996 Jul 15;98(2):513-20. doi: 10.1172/JCI118819. J Clin Invest. 1996. PMID: 8755664 Free PMC article.

3

In vivo activation of CFTR-dependent chloride transport in murine airway epithelium by CNP.

Kelley TJ, Cotton CU, Drumm ML. Kelley TJ, et al. Among authors: cotton cu. Am J Physiol. 1997 Nov;273(5):L1065-72. doi: 10.1152/ajplung.1997.273.5.L1065. Am J Physiol. 1997. PMID: 9374736

4

Regulation of amiloride-sensitive sodium absorption in murine airway epithelium by C-type natriuretic peptide.

Kelley TJ, Cotton CU, Drumm ML. Kelley TJ, et al. Among authors: cotton cu. Am J Physiol. 1998 Jun;274(6):L990-6. doi: 10.1152/ajplung.1998.274.6.L990. Am J Physiol. 1998. PMID: 9609738

5

CFTR inhibition mimics the cystic fibrosis inflammatory profile.

Perez A, Issler AC, Cotton CU, Kelley TJ, Verkman AS, Davis PB. Perez A, et al. Among authors: cotton cu. Am J Physiol Lung Cell Mol Physiol. 2007 Feb;292(2):L383-95. doi: 10.1152/ajplung.00403.2005. Epub 2006 Aug 18. Am J Physiol Lung Cell Mol Physiol. 2007. PMID: 16920886 Free article.

6

Generation of a conditional null allele for Cftr in mice.

Hodges CA, Cotton CU, Palmert MR, Drumm ML. Hodges CA, et al. Among authors: cotton cu. Genesis. 2008 Oct;46(10):546-52. doi: 10.1002/dvg.20433. Genesis. 2008. PMID: 18802965 Free PMC article.

7

Dysfunction of Nrf-2 in CF epithelia leads to excess intracellular H2O2 and inflammatory cytokine production.

Chen J, Kinter M, Shank S, Cotton C, Kelley TJ, Ziady AG. Chen J, et al. PLoS One. 2008;3(10):e3367. doi: 10.1371/journal.pone.0003367. Epub 2008 Oct 10. PLoS One. 2008. PMID: 18846238 Free PMC article.

8

Cystic fibrosis growth retardation is not correlated with loss of Cftr in the intestinal epithelium.

Hodges CA, Grady BR, Mishra K, Cotton CU, Drumm ML. Hodges CA, et al. Among authors: cotton cu. Am J Physiol Gastrointest Liver Physiol. 2011 Sep;301(3):G528-36. doi: 10.1152/ajpgi.00052.2011. Epub 2011 Jun 9. Am J Physiol Gastrointest Liver Physiol. 2011. PMID: 21659619 Free PMC article.

9

Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection.

Bonfield TL, Hodges CA, Cotton CU, Drumm ML. Bonfield TL, et al. Among authors: cotton cu. J Leukoc Biol. 2012 Nov;92(5):1111-22. doi: 10.1189/jlb.0412188. Epub 2012 Aug 2. J Leukoc Biol. 2012. PMID: 22859830 Free PMC article.

10

Role of Exchange Protein Activated by cAMP 1 in Regulating Rates of Microtubule Formation in Cystic Fibrosis Epithelial Cells.

Rymut SM, Ivy T, Corey DA, Cotton CU, Burgess JD, Kelley TJ. Rymut SM, et al. Among authors: cotton cu. Am J Respir Cell Mol Biol. 2015 Dec;53(6):853-62. doi: 10.1165/rcmb.2014-0462OC. Am J Respir Cell Mol Biol. 2015. PMID: 25955407 Free PMC article.

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