Li C - Search Results

1

Studies of the molecular basis for cystic fibrosis using purified reconstituted CFTR protein.

Kogan I, Ramjeesingh M, Li C, Bear CE. Kogan I, et al. Among authors: li c. Methods Mol Med. 2002;70:143-57. doi: 10.1385/1-59259-187-6:143. Methods Mol Med. 2002. PMID: 11917519 No abstract available.

2

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR).

Bear CE, Li CH, Kartner N, Bridges RJ, Jensen TJ, Ramjeesingh M, Riordan JR. Bear CE, et al. Among authors: li ch. Cell. 1992 Feb 21;68(4):809-18. doi: 10.1016/0092-8674(92)90155-6. Cell. 1992. PMID: 1371239

3

Calcium-permeable channels in rat hepatoma cells are activated by extracellular nucleotides.

Bear CE, Li CH. Bear CE, et al. Among authors: li ch. Am J Physiol. 1991 Dec;261(6 Pt 1):C1018-24. doi: 10.1152/ajpcell.1991.261.6.C1018. Am J Physiol. 1991. PMID: 1662901

4

CFTR directly mediates nucleotide-regulated glutathione flux.

Kogan I, Ramjeesingh M, Li C, Kidd JF, Wang Y, Leslie EM, Cole SP, Bear CE. Kogan I, et al. Among authors: li c. EMBO J. 2003 May 1;22(9):1981-9. doi: 10.1093/emboj/cdg194. EMBO J. 2003. PMID: 12727866 Free PMC article.

5

Stable dimeric assembly of the second membrane-spanning domain of CFTR (cystic fibrosis transmembrane conductance regulator) reconstitutes a chloride-selective pore.

Ramjeesingh M, Ugwu F, Li C, Dhani S, Huan LJ, Wang Y, Bear CE. Ramjeesingh M, et al. Among authors: li c. Biochem J. 2003 Nov 1;375(Pt 3):633-41. doi: 10.1042/BJ20030774. Biochem J. 2003. PMID: 12892562 Free PMC article.

6

Phosphorylation-induced conformational changes of cystic fibrosis transmembrane conductance regulator monitored by attenuated total reflection-Fourier transform IR spectroscopy and fluorescence spectroscopy.

Grimard V, Li C, Ramjeesingh M, Bear CE, Goormaghtigh E, Ruysschaert JM. Grimard V, et al. Among authors: li c. J Biol Chem. 2004 Feb 13;279(7):5528-36. doi: 10.1074/jbc.M311014200. Epub 2003 Dec 2. J Biol Chem. 2004. PMID: 14660584 Free article.

7

Methods to study CFTR protein in vitro.

Benos DJ, Berdiev BK, Ismailov II, Ostedgaard LS, Kogan I, Li C, Ramjeesingh M, Bear CE. Benos DJ, et al. Among authors: li c. J Cyst Fibros. 2004 Aug;3 Suppl 2:79-83. doi: 10.1016/j.jcf.2004.05.018. J Cyst Fibros. 2004. PMID: 15463933 Free article. Review.

8

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. Among authors: li c, li h. 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.

9

Determination of CFTR chloride channel activity and pharmacology using radiotracer flux methods.

Norez C, Heda GD, Jensen T, Kogan I, Hughes LK, Auzanneau C, Dérand R, Bulteau-Pignoux L, Li C, Ramjeesingh M, Li H, Sheppard DN, Bear CE, Riordan JR, Becq F. Norez C, et al. Among authors: li c, li h. J Cyst Fibros. 2004 Aug;3 Suppl 2:119-21. doi: 10.1016/j.jcf.2004.05.025. J Cyst Fibros. 2004. PMID: 15463942 Free article. Review.

10

Evaluation of the membrane-spanning domain of ClC-2.

Ramjeesingh M, Li C, She YM, Bear CE. Ramjeesingh M, et al. Among authors: li c. Biochem J. 2006 Jun 15;396(3):449-60. doi: 10.1042/BJ20060043. Biochem J. 2006. PMID: 16526942 Free PMC article.

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