Thomas PJ - Search Results

1

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene.

Sosnay PR, Siklosi KR, Van Goor F, Kaniecki K, Yu H, Sharma N, Ramalho AS, Amaral MD, Dorfman R, Zielenski J, Masica DL, Karchin R, Millen L, Thomas PJ, Patrinos GP, Corey M, Lewis MH, Rommens JM, Castellani C, Penland CM, Cutting GR. Sosnay PR, et al. Among authors: thomas pj. Nat Genet. 2013 Oct;45(10):1160-7. doi: 10.1038/ng.2745. Epub 2013 Aug 25. Nat Genet. 2013. PMID: 23974870 Free PMC article.

2

The cystic fibrosis transmembrane conductance regulator. Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide.

Thomas PJ, Shenbagamurthi P, Sondek J, Hullihen JM, Pedersen PL. Thomas PJ, et al. J Biol Chem. 1992 Mar 25;267(9):5727-30. J Biol Chem. 1992. PMID: 1372891 Free article.

3

Altered protein folding may be the molecular basis of most cases of cystic fibrosis.

Thomas PJ, Ko YH, Pedersen PL. Thomas PJ, et al. FEBS Lett. 1992 Nov 2;312(1):7-9. doi: 10.1016/0014-5793(92)81399-7. FEBS Lett. 1992. PMID: 1385213 Free article. Review.

4

Cystic fibrosis transmembrane conductance regulator: nucleotide binding to a synthetic peptide.

Thomas PJ, Shenbagamurthi P, Ysern X, Pedersen PL. Thomas PJ, et al. Science. 1991 Feb 1;251(4993):555-7. doi: 10.1126/science.1703660. Science. 1991. PMID: 1703660

5

The cystic fibrosis transmembrane conductance regulator. Nucleotide binding to a synthetic peptide segment from the second predicted nucleotide binding fold.

Ko YH, Thomas PJ, Pedersen PL. Ko YH, et al. Among authors: thomas pj. J Biol Chem. 1994 May 20;269(20):14584-8. J Biol Chem. 1994. PMID: 7514174 Free article.

6

The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein.

Ko YH, Thomas PJ, Delannoy MR, Pedersen PL. Ko YH, et al. Among authors: thomas pj. J Biol Chem. 1993 Nov 15;268(32):24330-8. J Biol Chem. 1993. PMID: 7693699 Free article.

7

The molecular chaperone Hsc70 assists the in vitro folding of the N-terminal nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator.

Strickland E, Qu BH, Millen L, Thomas PJ. Strickland E, et al. Among authors: thomas pj. J Biol Chem. 1997 Oct 10;272(41):25421-4. doi: 10.1074/jbc.272.41.25421. J Biol Chem. 1997. PMID: 9325249 Free article.

8

Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis.

Choi JY, Muallem D, Kiselyov K, Lee MG, Thomas PJ, Muallem S. Choi JY, et al. Among authors: thomas pj. Nature. 2001 Mar 1;410(6824):94-7. doi: 10.1038/35065099. Nature. 2001. PMID: 11242048 Free PMC article.

9

Organic solutes rescue the functional defect in delta F508 cystic fibrosis transmembrane conductance regulator.

Zhang XM, Wang XT, Yue H, Leung SW, Thibodeau PH, Thomas PJ, Guggino SE. Zhang XM, et al. Among authors: thomas pj. J Biol Chem. 2003 Dec 19;278(51):51232-42. doi: 10.1074/jbc.M309076200. Epub 2003 Oct 7. J Biol Chem. 2003. PMID: 14532265 Free article.

10

Gating of CFTR by the STAS domain of SLC26 transporters.

Ko SB, Zeng W, Dorwart MR, Luo X, Kim KH, Millen L, Goto H, Naruse S, Soyombo A, Thomas PJ, Muallem S. Ko SB, et al. Among authors: thomas pj. Nat Cell Biol. 2004 Apr;6(4):343-50. doi: 10.1038/ncb1115. Epub 2004 Mar 28. Nat Cell Biol. 2004. PMID: 15048129 Free PMC article.

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