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Role of CFTR in autosomal recessive polycystic kidney disease.
Nakanishi K, Sweeney WE Jr, Macrae Dell K, Cotton CU, Avner ED. Nakanishi K, et al. Among authors: cotton cu. J Am Soc Nephrol. 2001 Apr;12(4):719-725. doi: 10.1681/ASN.V124719. J Am Soc Nephrol. 2001. PMID: 11274233
Role of kidney chloride channels in health and disease.
Veizis IE, Cotton CU. Veizis IE, et al. Among authors: cotton cu. Pediatr Nephrol. 2007 Jun;22(6):770-7. doi: 10.1007/s00467-006-0355-4. Epub 2006 Nov 16. Pediatr Nephrol. 2007. PMID: 17109136 Review.
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
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 article.
74 results