Rommens J - Search Results

1

SLC6A14, an amino acid transporter, modifies the primary CF defect in fluid secretion.

Ahmadi S, Xia S, Wu YS, Di Paola M, Kissoon R, Luk C, Lin F, Du K, Rommens J, Bear CE. Ahmadi S, et al. Among authors: rommens j. Elife. 2018 Jul 13;7:e37963. doi: 10.7554/eLife.37963. Elife. 2018. PMID: 30004386 Free PMC article.

2

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: rommens jm. Cell. 1991 Feb 22;64(4):681-91. doi: 10.1016/0092-8674(91)90498-n. Cell. 1991. PMID: 1705179

3

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. 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.

4

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: rommens jm. Nat Genet. 1993 Apr;3(4):311-6. doi: 10.1038/ng0493-311. Nat Genet. 1993. PMID: 7526932

5

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: rommens jm. 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.

6

ClC-2 contributes to native chloride secretion by a human intestinal cell line, Caco-2.

Mohammad-Panah R, Gyomorey K, Rommens J, Choudhury M, Li C, Wang Y, Bear CE. Mohammad-Panah R, et al. Among authors: rommens j. J Biol Chem. 2001 Mar 16;276(11):8306-13. doi: 10.1074/jbc.M006764200. Epub 2000 Nov 28. J Biol Chem. 2001. PMID: 11096079 Free article.

7

The chloride channel ClC-4 co-localizes with cystic fibrosis transmembrane conductance regulator and may mediate chloride flux across the apical membrane of intestinal epithelia.

Mohammad-Panah R, Ackerley C, Rommens J, Choudhury M, Wang Y, Bear CE. Mohammad-Panah R, et al. Among authors: rommens j. J Biol Chem. 2002 Jan 4;277(1):566-74. doi: 10.1074/jbc.M106968200. Epub 2001 Oct 23. J Biol Chem. 2002. PMID: 11675385 Free article.

8

Non-CFTR chloride channels likely contribute to secretion in the murine small intestine.

Gyömörey K, Garami E, Galley K, Rommens JM, Bear CE. Gyömörey K, et al. Among authors: rommens jm. Pflugers Arch. 2001;443 Suppl 1:S103-6. doi: 10.1007/s004240100654. Epub 2001 Jul 6. Pflugers Arch. 2001. PMID: 11845313

9

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.

Sun L, Rommens JM, Corvol H, Li W, Li X, Chiang TA, Lin F, Dorfman R, Busson PF, Parekh RV, Zelenika D, Blackman SM, Corey M, Doshi VK, Henderson L, Naughton KM, O'Neal WK, Pace RG, Stonebraker JR, Wood SD, Wright FA, Zielenski J, Clement A, Drumm ML, Boëlle PY, Cutting GR, Knowles MR, Durie PR, Strug LJ. Sun L, et al. Among authors: rommens jm. Nat Genet. 2012 May;44(5):562-9. doi: 10.1038/ng.2221. Nat Genet. 2012. PMID: 22466613 Free PMC article.

10

Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities.

Li W, Soave D, Miller MR, Keenan K, Lin F, Gong J, Chiang T, Stephenson AL, Durie P, Rommens J, Sun L, Strug LJ. Li W, et al. Among authors: rommens j. Hum Genet. 2014 Feb;133(2):151-61. doi: 10.1007/s00439-013-1363-7. Epub 2013 Sep 22. Hum Genet. 2014. PMID: 24057835

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