Bear CE - Search Results

1

Generation of functional ciliated cholangiocytes from human pluripotent stem cells.

Ogawa M, Jiang JX, Xia S, Yang D, Ding A, Laselva O, Hernandez M, Cui C, Higuchi Y, Suemizu H, Dorrell C, Grompe M, Bear CE, Ogawa S. Ogawa M, et al. Among authors: bear ce. Nat Commun. 2021 Nov 11;12(1):6504. doi: 10.1038/s41467-021-26764-0. Nat Commun. 2021. PMID: 34764255 Free PMC article.

2

Regulation of CFTR expression and function during differentiation of intestinal epithelial cells.

Sood R, Bear C, Auerbach W, Reyes E, Jensen T, Kartner N, Riordan JR, Buchwald M. Sood R, et al. EMBO J. 1992 Jul;11(7):2487-94. doi: 10.1002/j.1460-2075.1992.tb05313.x. EMBO J. 1992. PMID: 1378393 Free PMC article.

3

The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.

Li C, Ramjeesingh M, Reyes E, Jensen T, Chang X, Rommens JM, Bear CE. Li C, et al. Among authors: bear ce. Nat Genet. 1993 Apr;3(4):311-6. doi: 10.1038/ng0493-311. Nat Genet. 1993. PMID: 7526932

4

The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells.

Lukacs GL, Chang XB, Bear C, Kartner N, Mohamed A, Riordan JR, Grinstein S. Lukacs GL, et al. J Biol Chem. 1993 Oct 15;268(29):21592-8. J Biol Chem. 1993. PMID: 7691813 Free article.

5

Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor.

Rozmahel R, Wilschanski M, Matin A, Plyte S, Oliver M, Auerbach W, Moore A, Forstner J, Durie P, Nadeau J, Bear C, Tsui LC. Rozmahel R, et al. Nat Genet. 1996 Mar;12(3):280-7. doi: 10.1038/ng0396-280. Nat Genet. 1996. PMID: 8589719

6

In vivo measurements of ion transport in long-living CF mice.

Wilschanski MA, Rozmahel R, Beharry S, Kent G, Li C, Tsui LC, Durie P, Bear CE. Wilschanski MA, et al. Among authors: bear ce. Biochem Biophys Res Commun. 1996 Feb 27;219(3):753-9. doi: 10.1006/bbrc.1996.0306. Biochem Biophys Res Commun. 1996. PMID: 8645253

7

Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel.

Li C, Ramjeesingh M, Bear CE. Li C, et al. Among authors: bear ce. J Biol Chem. 1996 May 17;271(20):11623-6. doi: 10.1074/jbc.271.20.11623. J Biol Chem. 1996. PMID: 8662751 Free article.

8

Coupling of ATP hydrolysis with channel gating by purified, reconstituted CFTR.

Bear CE, Li C, Galley K, Wang Y, Garami E, Ramjeesingh M. Bear CE, et al. J Bioenerg Biomembr. 1997 Oct;29(5):465-73. doi: 10.1023/a:1022435007193. J Bioenerg Biomembr. 1997. PMID: 9511931 Review.

9

ATPase assay of purified, reconstituted CFTR protein.

Kogan I, Ramjeesingh M, Bear CE. Kogan I, et al. Among authors: bear ce. J Cyst Fibros. 2004 Aug;3 Suppl 2:133-4. doi: 10.1016/j.jcf.2004.05.028. J Cyst Fibros. 2004. PMID: 15463945 Free article.

10

A small-molecule modulator interacts directly with deltaPhe508-CFTR to modify its ATPase activity and conformational stability.

Wellhauser L, Kim Chiaw P, Pasyk S, Li C, Ramjeesingh M, Bear CE. Wellhauser L, et al. Among authors: bear ce. Mol Pharmacol. 2009 Jun;75(6):1430-8. doi: 10.1124/mol.109.055608. Epub 2009 Apr 1. Mol Pharmacol. 2009. PMID: 19339490

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