Sheppard DN - Search Results

1

Two rare variants that affect the same amino acid in CFTR have distinct responses to ivacaftor.

Li H, Rodrat M, Al-Salmani MK, Veselu DF, Han ST, Raraigh KS, Cutting GR, Sheppard DN. Li H, et al. Among authors: sheppard dn. J Physiol. 2024 Jan;602(2):333-354. doi: 10.1113/JP285727. Epub 2024 Jan 7. J Physiol. 2024. PMID: 38186087

2

Direct block of the cystic fibrosis transmembrane conductance regulator Cl(-) channel by niflumic acid.

Scott-Ward TS, Li H, Schmidt A, Cai Z, Sheppard DN. Scott-Ward TS, et al. Among authors: sheppard dn. Mol Membr Biol. 2004 Jan-Feb;21(1):27-38. doi: 10.1080/09687680310001597758. Mol Membr Biol. 2004. PMID: 14668136

3

The patch-clamp and planar lipid bilayer techniques: powerful and versatile tools to investigate the CFTR Cl- channel.

Sheppard DN, Gray MA, Gong X, Sohma Y, Kogan I, Benos DJ, Scott-Ward TS, Chen JH, Li H, Cai Z, Gupta J, Li C, Ramjeesingh M, Berdiev BK, Ismailov II, Bear CE, Hwang TC, Linsdell P, Hug MJ. Sheppard DN, et al. J Cyst Fibros. 2004 Aug;3 Suppl 2:101-8. doi: 10.1016/j.jcf.2004.05.046. J Cyst Fibros. 2004. PMID: 15463939 Free article. Review.

4

Transepithelial electrical measurements with the Ussing chamber.

Li H, Sheppard DN, Hug MJ. Li H, et al. Among authors: sheppard dn. J Cyst Fibros. 2004 Aug;3 Suppl 2:123-6. doi: 10.1016/j.jcf.2004.05.026. J Cyst Fibros. 2004. PMID: 15463943 Free article. Review.

5

Strategies to investigate the mechanism of action of CFTR modulators.

Cai Z, Scott-Ward TS, Li H, Schmidt A, Sheppard DN. Cai Z, et al. Among authors: sheppard dn. J Cyst Fibros. 2004 Aug;3 Suppl 2:141-7. doi: 10.1016/j.jcf.2004.05.030. J Cyst Fibros. 2004. PMID: 15463947 Free article. Review.

6

The relationship between cell proliferation, Cl- secretion, and renal cyst growth: a study using CFTR inhibitors.

Li H, Findlay IA, Sheppard DN. Li H, et al. Among authors: sheppard dn. Kidney Int. 2004 Nov;66(5):1926-38. doi: 10.1111/j.1523-1755.2004.00967.x. Kidney Int. 2004. PMID: 15496164 Free article.

7

The cystic fibrosis transmembrane conductance regulator Cl⁻ channel: a versatile engine for transepithelial ion transport.

Li H, Cai Z, Chen JH, Ju M, Xu Z, Sheppard DN. Li H, et al. Among authors: sheppard dn. Sheng Li Xue Bao. 2007 Aug 25;59(4):416-30. Sheng Li Xue Bao. 2007. PMID: 17700962 Free article.

8

Therapeutic potential of cystic fibrosis transmembrane conductance regulator (CFTR) inhibitors in polycystic kidney disease.

Li H, Sheppard DN. Li H, et al. Among authors: sheppard dn. BioDrugs. 2009;23(4):203-16. doi: 10.2165/11313570-000000000-00000. BioDrugs. 2009. PMID: 19697963 Review.

9

Targeting F508del-CFTR to develop rational new therapies for cystic fibrosis.

Cai ZW, Liu J, Li HY, Sheppard DN. Cai ZW, et al. Among authors: sheppard dn. Acta Pharmacol Sin. 2011 Jun;32(6):693-701. doi: 10.1038/aps.2011.71. Acta Pharmacol Sin. 2011. PMID: 21642944 Free PMC article. Review.

10

Recommendations for the classification of diseases as CFTR-related disorders.

Bombieri C, Claustres M, De Boeck K, Derichs N, Dodge J, Girodon E, Sermet I, Schwarz M, Tzetis M, Wilschanski M, Bareil C, Bilton D, Castellani C, Cuppens H, Cutting GR, Drevínek P, Farrell P, Elborn JS, Jarvi K, Kerem B, Kerem E, Knowles M, Macek M Jr, Munck A, Radojkovic D, Seia M, Sheppard DN, Southern KW, Stuhrmann M, Tullis E, Zielenski J, Pignatti PF, Ferec C. Bombieri C, et al. Among authors: sheppard dn. J Cyst Fibros. 2011 Jun;10 Suppl 2:S86-102. doi: 10.1016/S1569-1993(11)60014-3. J Cyst Fibros. 2011. PMID: 21658649 Free article.

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