☰

Jennifer S. Guimbellot, MD PhD - Publications

Affiliations: 
2007 University of Alabama, Birmingham, Birmingham, AL, United States 
Area:
Molecular Biology, Genetics
Tree Info Similar researchers PubMed Report error

12 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Liu Z, Anderson JD, Natt J, Guimbellot JS. Culture and Imaging of Human Nasal Epithelial Organoids. Journal of Visualized Experiments : Jove. PMID 34978285 DOI: 10.3791/63064  0.315
2020 Hoppe JE, Guimbellot J, Martiniano SL, Toprak D, Davis C, Daines CL, Muhlebach MS, Esther CR, Dellon EP. Highlights From the 2019 North American Cystic Fibrosis Conference. Pediatric Pulmonology. PMID 32573948 DOI: 10.1002/Ppul.24919  0.328
2020 Liu Z, Anderson JD, Deng L, Mackay S, Bailey J, Kersh L, Rowe SM, Guimbellot JS. Human Nasal Epithelial Organoids for Therapeutic Development in Cystic Fibrosis. Genes. 11. PMID 32485957 DOI: 10.3390/Genes11060603  0.447
2020 Guimbellot JS, Ryan KJ, Anderson JD, Liu Z, Kersh L, Esther CR, Rowe SM, Acosta EP. Variable cellular ivacaftor concentrations in people with cystic fibrosis on modulator therapy. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 32044246 DOI: 10.1016/J.Jcf.2020.01.011  0.335
2019 Liu Z, Mackay S, Gordon DM, Anderson JD, Haithcock DW, Garson CJ, Tearney GJ, Solomon GM, Pant K, Prabhakarpandian B, Rowe SM, Guimbellot JS. Co-cultured microfluidic model of the airway optimized for microscopy and micro-optical coherence tomography imaging. Biomedical Optics Express. 10: 5414-5430. PMID 31646055 DOI: 10.1364/Boe.10.005414  0.309
2018 Poore TS, Virella-Lowell I, Guimbellot JS. Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosis. Pediatric Pulmonology. PMID 29790674 DOI: 10.1002/Ppul.24043  0.32
2018 Guimbellot J, Solomon GM, Baines A, Heltshe SL, VanDalfsen J, Joseloff E, Sagel SD, Rowe SM. Effectiveness of ivacaftor in cystic fibrosis patients with non-G551D gating mutations. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 29685811 DOI: 10.1016/J.Jcf.2018.04.004  0.357
2017 Guimbellot JS, Leach JM, Chaudhry IG, Quinney NL, Boyles SE, Chua M, Aban I, Jaspers I, Gentzsch M. Nasospheroids permit measurements of CFTR-dependent fluid transport. Jci Insight. 2. PMID 29202459 DOI: 10.1172/Jci.Insight.95734  0.382
2017 Guimbellot J, Sharma J, Rowe SM. Toward inclusive therapy with CFTR modulators: Progress and challenges. Pediatric Pulmonology. PMID 28881097 DOI: 10.1002/Ppul.23773  0.425
2009 Guimbellot JS, Erickson SW, Mehta T, Wen H, Page GP, Sorscher EJ, Hong JS. Correlation of microRNA levels during hypoxia with predicted target mRNAs through genome-wide microarray analysis. Bmc Medical Genomics. 2: 15. PMID 19320992 DOI: 10.1186/1755-8794-2-15  0.46
2008 Guimbellot JS, Fortenberry JA, Siegal GP, Moore B, Wen H, Venglarik C, Chen YF, Oparil S, Sorscher EJ, Hong JS. Role of oxygen availability in CFTR expression and function. American Journal of Respiratory Cell and Molecular Biology. 39: 514-21. PMID 18474670 DOI: 10.1165/Rcmb.2007-0452Oc  0.532
2004 Varga K, Jurkuvenaite A, Wakefield J, Hong JS, Guimbellot JS, Venglarik CJ, Niraj A, Mazur M, Sorscher EJ, Collawn JF, Bebök Z. Efficient intracellular processing of the endogenous cystic fibrosis transmembrane conductance regulator in epithelial cell lines. The Journal of Biological Chemistry. 279: 22578-84. PMID 15066992 DOI: 10.1074/Jbc.M401522200  0.516
Show low-probability matches.