Rommens J - 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: rommens j. 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

Expression of cystic fibrosis lung disease modifier genes in human airway models.

He G, Panjwani N, Avolio J, Ouyang H, Keshavjee S, Rommens JM, Gonska T, Moraes TJ, Strug LJ. He G, et al. Among authors: rommens jm. J Cyst Fibros. 2022 Jul;21(4):616-622. doi: 10.1016/j.jcf.2022.02.007. Epub 2022 Feb 18. J Cyst Fibros. 2022. PMID: 35190293 Free article.

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

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.

6

Evidence for a causal relationship between early exocrine pancreatic disease and cystic fibrosis-related diabetes: a Mendelian randomization study.

Soave D, Miller MR, Keenan K, Li W, Gong J, Ip W, Accurso F, Sun L, Rommens JM, Sontag M, Durie PR, Strug LJ. Soave D, et al. Among authors: rommens jm. Diabetes. 2014 Jun;63(6):2114-9. doi: 10.2337/db13-1464. Epub 2014 Feb 18. Diabetes. 2014. PMID: 24550193 Free PMC article.

7

Prevalence of meconium ileus marks the severity of mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene.

Dupuis A, Keenan K, Ooi CY, Dorfman R, Sontag MK, Naehrlich L, Castellani C, Strug LJ, Rommens JM, Gonska T. Dupuis A, et al. Among authors: rommens jm. Genet Med. 2016 Apr;18(4):333-40. doi: 10.1038/gim.2015.79. Epub 2015 Jun 18. Genet Med. 2016. PMID: 26087176 Free article.

8

Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics.

Strug LJ, Gonska T, He G, Keenan K, Ip W, Boëlle PY, Lin F, Panjwani N, Gong J, Li W, Soave D, Xiao B, Tullis E, Rabin H, Parkins MD, Price A, Zuberbuhler PC, Corvol H, Ratjen F, Sun L, Bear CE, Rommens JM. Strug LJ, et al. Among authors: rommens jm. Hum Mol Genet. 2016 Oct 15;25(20):4590-4600. doi: 10.1093/hmg/ddw290. Hum Mol Genet. 2016. PMID: 28171547 Free PMC article.

9

Phenotypic profiling of CFTR modulators in patient-derived respiratory epithelia.

Ahmadi S, Bozoky Z, Di Paola M, Xia S, Li C, Wong AP, Wellhauser L, Molinski SV, Ip W, Ouyang H, Avolio J, Forman-Kay JD, Ratjen F, Hirota JA, Rommens J, Rossant J, Gonska T, Moraes TJ, Bear CE. Ahmadi S, et al. Among authors: rommens j. NPJ Genom Med. 2017 Apr 14;2:12. doi: 10.1038/s41525-017-0015-6. NPJ Genom Med. 2017. PMID: 28649446 Free PMC article.

10

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.

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