Bear CE - Search Results

1

Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis.

Birimberg-Schwartz L, Ip W, Bartlett C, Avolio J, Vonk AM, Gunawardena T, Du K, Esmaeili M, Beekman JM, Rommens J, Strug L, Bear CE, Moraes TJ, Gonska T. Birimberg-Schwartz L, et al. Among authors: bear ce. Life Sci Alliance. 2023 Apr 5;6(6):e202201857. doi: 10.26508/lsa.202201857. Print 2023 Jun. Life Sci Alliance. 2023. PMID: 37024122 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

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance.

Kartner N, Hanrahan JW, Jensen TJ, Naismith AL, Sun SZ, Ackerley CA, Reyes EF, Tsui LC, Rommens JM, Bear CE, et al. Kartner N, et al. Among authors: bear ce. Cell. 1991 Feb 22;64(4):681-91. doi: 10.1016/0092-8674(91)90498-n. Cell. 1991. PMID: 1705179

4

cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator.

Rommens JM, Dho S, Bear CE, Kartner N, Kennedy D, Riordan JR, Tsui LC, Foskett JK. Rommens JM, et al. Among authors: bear ce. Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7500-4. doi: 10.1073/pnas.88.17.7500. Proc Natl Acad Sci U S A. 1991. PMID: 1715567 Free PMC article.

5

Cl- channel activity in Xenopus oocytes expressing the cystic fibrosis gene.

Bear CE, Duguay F, Naismith AL, Kartner N, Hanrahan JW, Riordan JR. Bear CE, et al. J Biol Chem. 1991 Oct 15;266(29):19142-5. J Biol Chem. 1991. PMID: 1717461 Free article.

6

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

7

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.

8

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

9

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.

10

ATPase activity of the cystic fibrosis transmembrane conductance regulator.

Li C, Ramjeesingh M, Wang W, Garami E, Hewryk M, Lee D, Rommens JM, Galley K, Bear CE. Li C, et al. Among authors: bear ce. J Biol Chem. 1996 Nov 8;271(45):28463-8. doi: 10.1074/jbc.271.45.28463. J Biol Chem. 1996. PMID: 8910473 Free article.

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