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Defective protein folding as a basis of human disease.
Thomas PJ, Qu BH, Pedersen PL. Thomas PJ, et al. Trends Biochem Sci. 1995 Nov;20(11):456-9. doi: 10.1016/s0968-0004(00)89100-8. Trends Biochem Sci. 1995. PMID: 8578588 Review.
Dynamic association of proteasomal machinery with the centrosome.
Wigley WC, Fabunmi RP, Lee MG, Marino CR, Muallem S, DeMartino GN, Thomas PJ. Wigley WC, et al. Among authors: thomas pj. J Cell Biol. 1999 May 3;145(3):481-90. doi: 10.1083/jcb.145.3.481. J Cell Biol. 1999. PMID: 10225950 Free PMC article.
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.
Protein solubility and folding monitored in vivo by structural complementation of a genetic marker protein.
Wigley WC, Stidham RD, Smith NM, Hunt JF, Thomas PJ. Wigley WC, et al. Among authors: thomas pj. Nat Biotechnol. 2001 Feb;19(2):131-6. doi: 10.1038/84389. Nat Biotechnol. 2001. PMID: 11175726
Recognition of misfolding proteins by PA700, the regulatory subcomplex of the 26 S proteasome.
Strickland E, Hakala K, Thomas PJ, DeMartino GN. Strickland E, et al. Among authors: thomas pj. J Biol Chem. 2000 Feb 25;275(8):5565-72. doi: 10.1074/jbc.275.8.5565. J Biol Chem. 2000. PMID: 10681537
Regulation of Cl-/ HCO3- exchange by cystic fibrosis transmembrane conductance regulator expressed in NIH 3T3 and HEK 293 cells.
Lee MG, Wigley WC, Zeng W, Noel LE, Marino CR, Thomas PJ, Muallem S. Lee MG, et al. Among authors: thomas pj. J Biol Chem. 1999 Feb 5;274(6):3414-21. doi: 10.1074/jbc.274.6.3414. J Biol Chem. 1999. PMID: 9920885
Cystic fibrosis: a disease of altered protein folding.
Qu BH, Strickland E, Thomas PJ. Qu BH, et al. Among authors: thomas pj. J Bioenerg Biomembr. 1997 Oct;29(5):483-90. doi: 10.1023/a:1022439108101. J Bioenerg Biomembr. 1997. PMID: 9511933 Review.
Transmembrane domain of cystic fibrosis transmembrane conductance regulator: design, characterization, and secondary structure of synthetic peptides m1-m6.
Wigley WC, Vijayakumar S, Jones JD, Slaughter C, Thomas PJ. Wigley WC, et al. Among authors: thomas pj. Biochemistry. 1998 Jan 20;37(3):844-53. doi: 10.1021/bi972293n. Biochemistry. 1998. PMID: 9454574
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
., and Thomas, P. J. (1996) J. Biol. Chem. 271, 7261-7264). Here we provide evidence that the molecular chaperone Hsc70 productively interacts with NBD1 to increase the folding yield of the domain and inhibit off-pathway associations leading to the formation of high molecu …
., and Thomas, P. J. (1996) J. Biol. Chem. 271, 7261-7264). Here we provide evidence that the molecular chaperone Hsc70 productively …
Localization and suppression of a kinetic defect in cystic fibrosis transmembrane conductance regulator folding.
Qu BH, Strickland EH, Thomas PJ. Qu BH, et al. Among authors: thomas pj. J Biol Chem. 1997 Jun 20;272(25):15739-44. doi: 10.1074/jbc.272.25.15739. J Biol Chem. 1997. PMID: 9188468
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