Robert Tarran - Publications

Affiliations: 
Cell & Molecular Physiology University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Physiology Biology, Cell Biology

106 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
2023 Cholon DM, Greenwald MA, Higgs MG, Quinney NL, Boyles SE, Meinig SL, Minges JT, Chaubal A, Tarran R, Ribeiro CMP, Wolfgang MC, Gentzsch M. A Novel Co-Culture Model Reveals Enhanced CFTR Rescue in Primary Cystic Fibrosis Airway Epithelial Cultures with Persistent Infection. Cells. 12. PMID 37998353 DOI: 10.3390/cells12222618  0.366
2023 Ghosh A, Coakley RD, Alexis NE, Tarran R. Vaping-Induced Proteolysis Causes Airway Surface Dehydration. International Journal of Molecular Sciences. 24. PMID 37895029 DOI: 10.3390/ijms242015348  0.423
2023 Woodall M, Tarran R, Lee R, Anfishi H, Prins S, Counsell J, Vergani P, Hart S, Baines D. Expression of gain-of-function CFTR in cystic fibrosis airway cells restores epithelial function better than wild-type or codon-optimized CFTR. Molecular Therapy. Methods & Clinical Development. 30: 593-605. PMID 37701179 DOI: 10.1016/j.omtm.2023.08.006  0.346
2023 Wu T, Wrennall JA, Dang H, Baines DL, Tarran R. Passaging Primary Human Bronchial Epithelia Reduces CFTR-Mediated Fluid Transport and Alters mRNA Expression. Cells. 12. PMID 37048070 DOI: 10.3390/cells12070997  0.337
2022 Goriounova AS, Gilmore RC, Wrennall JA, Tarran R. Super resolution microscopy analysis reveals increased Orai1 activity in asthma and cystic fibrosis lungs. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 35961837 DOI: 10.1016/j.jcf.2022.07.003  0.355
2021 Woodall M, Reidel B, Kesimer M, Tarran R, Baines DL. Culture with apically applied healthy or disease sputum alters the airway surface liquid proteome and ion transport across human bronchial epithelial cells. American Journal of Physiology. Cell Physiology. 321: C954-C963. PMID 34613844 DOI: 10.1152/ajpcell.00234.2021  0.37
2021 Giorgetti M, Klymiuk N, Bähr A, Hemmerling M, Jinton L, Tarran R, Malmgren A, Åstrand A, Hansson GC, Ermund A. New generation ENaC inhibitors detach cystic fibrosis airway mucus bundles via sodium/hydrogen exchanger inhibition. European Journal of Pharmacology. 904: 174123. PMID 33974881 DOI: 10.1016/j.ejphar.2021.174123  0.354
2021 Khanal S, Webster M, Niu N, Zielonka J, Nunez M, Chupp G, Slade MD, Cohn L, Sauler M, Gomez JL, Tarran R, Sharma L, Dela Cruz CS, Egan M, Laguna T, et al. SPLUNC1: a novel marker of cystic fibrosis exacerbations. The European Respiratory Journal. PMID 33958427 DOI: 10.1183/13993003.00507-2020  0.306
2020 Abdelwahab SH, Reidel B, Martin JR, Ghosh A, Keating JE, Haridass P, Carpenter J, Glish GL, Tarran R, Doerschuk CM, Kesimer M. Cigarillos Compromise the Mucosal Barrier and Protein Expression in Airway Epithelia. American Journal of Respiratory Cell and Molecular Biology. PMID 32877614 DOI: 10.1165/Rcmb.2019-0085Oc  0.346
2020 Ahmad S, Kim CSK, Tarran R. The SPLUNC1-βENaC complex prevents Burkholderia cenocepacia invasion in normal airway epithelia. Respiratory Research. 21: 190. PMID 32680508 DOI: 10.1186/S12931-020-01454-5  0.39
2020 Herman M, Tarran R. E-cigarettes, nicotine, the lung and the brain: multi-level cascading pathophysiology. The Journal of Physiology. PMID 32515030 DOI: 10.1113/Jp278388  0.339
2020 Lee RE, Miller SM, Mascenik TM, Lewis CA, Dang H, Boggs ZH, Tarran R, Randell SH. Assessing Human Airway Epithelial Progenitor Cells for Cystic Fibrosis Cell Therapy. American Journal of Respiratory Cell and Molecular Biology. PMID 32437238 DOI: 10.1165/Rcmb.2019-0384Oc  0.371
2020 Crotty Alexander LE, Ware LB, Calfee CS, Callahan SJ, Eissenberg T, Farver C, Goniewicz ML, Jaspers I, Kheradmand F, King TE, Meyer NJ, Mikheev V, Shields PG, Shihadeh A, Strongin R, ... Tarran R, et al. NIH Workshop Report: E-cigarette or Vaping Product Use Associated Lung Injury (EVALI): Developing a Research Agenda. American Journal of Respiratory and Critical Care Medicine. PMID 32243764 DOI: 10.1164/Rccm.201912-2332Ws  0.342
2020 Biggart MGS, Ling X, Simpson N, Gani J, Wrobel J, Hilpert K, Chen X, Tarran R, Baines D. Identification Of A Novel Histone Derived Antimicrobial Peptide In Airway Surface Liquid. The Faseb Journal. 34: 1-1. DOI: 10.1096/Fasebj.2020.34.S1.02889  0.306
2019 Rowell TR, Keating JE, Zorn BT, Glish GL, Shears SB, Tarran R. Flavored E-liquids Increase Cytoplasmic Ca Levels in Airway Epithelia. American Journal of Physiology. Lung Cellular and Molecular Physiology. PMID 31693394 DOI: 10.1152/Ajplung.00123.2019  0.309
2019 Gotts JE, Jordt SE, McConnell R, Tarran R. What are the respiratory effects of e-cigarettes? Bmj (Clinical Research Ed.). 366: l5275. PMID 31570493 DOI: 10.1136/Bmj.L5275  0.349
2019 Marklew AJ, Patel W, Moore PJ, Tan CD, Smith AJ, Sassano MF, Gray MA, Tarran R. Cigarette Smoke Exposure Induces Retrograde Trafficking of CFTR to the Endoplasmic Reticulum. Scientific Reports. 9: 13655. PMID 31541117 DOI: 10.1038/S41598-019-49544-9  0.494
2019 Ghosh A, Coakley RD, Ghio AJ, Muhlebach MS, Esther CR, Alexis NE, Tarran R. Chronic E-Cigarette Use Increases Neutrophil Elastase and Matrix Metalloprotease Levels in the Lung. American Journal of Respiratory and Critical Care Medicine. PMID 31390877 DOI: 10.1164/Rccm.201903-0615Oc  0.395
2019 Couroux P, Farias P, Rizvi L, Griffin K, Hudson C, Crowder T, Tarran R, Tullis E. First clinical trials of novel ENaC targeting therapy, SPX-101, in healthy volunteers and adults with cystic fibrosis. Pulmonary Pharmacology & Therapeutics. 101819. PMID 31302339 DOI: 10.1016/J.Pupt.2019.101819  0.312
2019 Moore PJ, Sesma J, Alexis NE, Tarran R. Tobacco exposure inhibits SPLUNC1-dependent antimicrobial activity. Respiratory Research. 20: 94. PMID 31113421 DOI: 10.1186/S12931-019-1066-2  0.341
2019 Ahmad S, Gilmore RC, Alexis NE, Tarran R. SPLUNC1 Loses its Antimicrobial Activity in Acidic Cystic Fibrosis Airway Secretions. American Journal of Respiratory and Critical Care Medicine. PMID 31013116 DOI: 10.1164/Rccm.201812-2303Le  0.384
2018 Patel W, Moore PJ, Sassano MF, Lopes-Pacheco M, Aleksandrov AA, Amaral MD, Tarran R, Gray MA. Increases in cytosolic Ca induce dynamin- and calcineurin-dependent internalisation of CFTR. Cellular and Molecular Life Sciences : Cmls. PMID 30547226 DOI: 10.1007/S00018-018-2989-3  0.376
2018 Hill DB, Long RF, Kissner WJ, Atieh E, Garbarine IC, Markovetz MR, Fontana NC, Christy M, Habibpour M, Tarran R, Gregory Forest M, Boucher RC, Button B. Pathological Mucus and Impaired Mucus Clearance in Cystic Fibrosis Patients Results from Increased Concentration, not altered pH. The European Respiratory Journal. PMID 30361244 DOI: 10.1183/13993003.01297-2018  0.451
2018 Webster MJ, Tarran R. Slippery When Wet: Airway Surface Liquid Homeostasis and Mucus Hydration. Current Topics in Membranes. 81: 293-335. PMID 30243435 DOI: 10.1016/Bs.Ctm.2018.08.004  0.461
2018 Webster MJ, Reidel B, Tan CD, Ghosh A, Alexis NE, Donaldson SH, Kesimer M, Ribeiro CMP, Tarran R. SPLUNC1 Degradation by the Cystic Fibrosis Mucosal Environment Drives Airway Surface Liquid Dehydration. The European Respiratory Journal. PMID 30190268 DOI: 10.1183/13993003.00668-2018  0.498
2018 Tarran R, Ghosh A, Alexis N. Reply to: Electronic Cigarettes and the Lung Proteome. American Journal of Respiratory and Critical Care Medicine. PMID 30153039 DOI: 10.1164/Rccm.201807-1336Le  0.343
2018 Moore PJ, Tarran R. The epithelial sodium channel (ENaC) as a therapeutic target for cystic fibrosis lung disease. Expert Opinion On Therapeutic Targets. PMID 30028216 DOI: 10.1080/14728222.2018.1501361  0.496
2018 Figueira MF, Webster MJ, Tarran R. CrossTalk proposal: mucosal acidification drives early progressive lung disease in cystic fibrosis. The Journal of Physiology. PMID 30014571 DOI: 10.1113/Jp275425  0.4
2018 Moore PJ, Reidel B, Ghosh A, Sesma J, Kesimer M, Tarran R. Cigarette smoke modifies and inactivates SPLUNC1, leading to airway dehydration. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201800345R. PMID 29890087 DOI: 10.1096/Fj.201800345R  0.467
2018 Ghosh A, Coakley RC, Mascenik T, Rowell TR, Davis ES, Rogers K, Webster MJ, Dang H, Herring LE, Sassano MF, Livraghi-Butrico A, Van Buren SK, Graves LM, Herman MA, Randell SH, ... ... Tarran R, et al. Chronic E-cigarette Exposure Alters the Human Bronchial Epithelial Proteome. American Journal of Respiratory and Critical Care Medicine. PMID 29481290 DOI: 10.1164/Rccm.201710-2033Oc  0.357
2018 Kim CS, Ahmad S, Wu T, Walton WG, Redinbo MR, Tarran R. SPLUNC1 is an allosteric modulator of the epithelial sodium channel. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 29295861 DOI: 10.1096/Fj.201701126R  0.438
2018 Wu T, Tarran R. Lung Epithelial Derived SPLUNC1 Regulates Th2 inflammation in Allergic Asthma The Journal of Allergy and Clinical Immunology. 141. DOI: 10.1016/J.Jaci.2017.12.346  0.376
2017 Abdullah LH, Coakley R, Webster MJ, Zhu Y, Tarran R, Radicioni G, Kesimer M, Boucher RC, Davis CW, Ribeiro CMP. Mucin Production and Hydration Responses to Mucopurulent Materials in Normal vs. CF Airway Epithelia. American Journal of Respiratory and Critical Care Medicine. PMID 29099608 DOI: 10.1164/Rccm.201706-1139Oc  0.469
2017 Terryah ST, Fellner RC, Ahmad S, Moore PJ, Reidel B, Sesma JI, Kim CS, Garland AL, Scott DW, Sabater JR, Carpenter J, Randell SH, Kesimer M, Abraham WM, Arendshorst WJ, ... Tarran R, et al. Evaluation of a SPLUNC1-Derived Peptide for the Treatment of Cystic Fibrosis Lung Disease. American Journal of Physiology. Lung Cellular and Molecular Physiology. ajplung.00546.2016. PMID 28982737 DOI: 10.1152/Ajplung.00546.2016  0.443
2017 Ghosh A, Nethery RC, Herring AH, Tarran R. Flavored little cigar smoke induces cytotoxicity and apoptosis in airway epithelia. Cell Death Discovery. 3: 17019. PMID 28496992 DOI: 10.1038/Cddiscovery.2017.19  0.363
2017 Scott DW, Walker MP, Sesma J, Wu B, Stuhlmiller TJ, Sabater JR, Abraham WM, Crowder TM, Christensen DJ, Tarran R. SPX-101 is a Novel ENaC-targeted Therapeutic for Cystic Fibrosis that Restores Mucus Transport. American Journal of Respiratory and Critical Care Medicine. PMID 28481660 DOI: 10.1164/Rccm.201612-2445Oc  0.395
2017 Ghosh A, Abdelwahab SH, Reeber SL, Reidel B, Marklew AJ, Garrison AJ, Lee S, Dang H, Herring AH, Glish GL, Kesimer M, Tarran R. Little Cigars are More Toxic than Cigarettes and Uniquely Change the Airway Gene and Protein Expression. Scientific Reports. 7: 46239. PMID 28447619 DOI: 10.1038/Srep46239  0.38
2017 Rowell TR, Reeber SL, Lee SL, Harris RA, Nethery RC, Herring AH, Glish GL, Tarran R. Flavored E-cigarette Liquids Reduce Proliferation and Viability in the CALU3 Airway Epithelial Cell Line. American Journal of Physiology. Lung Cellular and Molecular Physiology. ajplung.00392.2016. PMID 28428175 DOI: 10.1152/Ajplung.00392.2016  0.359
2017 Wu T, Huang J, Moore PJ, Little MS, Walton WG, Fellner RC, Alexis NE, Peter Di Y, Redinbo MR, Tilley SL, Tarran R. Identification of BPIFA1/SPLUNC1 as an epithelium-derived smooth muscle relaxing factor. Nature Communications. 8: 14118. PMID 28165446 DOI: 10.1038/Ncomms14118  0.382
2016 Garnett JP, Kalsi KK, Sobotta M, Bearham J, Carr G, Powell J, Brodlie M, Ward C, Tarran R, Baines DL. Hyperglycaemia and Pseudomonas aeruginosa acidify cystic fibrosis airway surface liquid by elevating epithelial monocarboxylate transporter 2 dependent lactate-H(+) secretion. Scientific Reports. 6: 37955. PMID 27897253 DOI: 10.1038/Srep37955  0.461
2016 Ahmad S, Tyrrell J, Walton WG, Tripathy A, Redinbo MR, Tarran R. SPLUNC1 has Antimicrobial and Antibiofilm Activity against Burkholderia cepacia Complex. Antimicrobial Agents and Chemotherapy. PMID 27458217 DOI: 10.1128/Aac.00975-16  0.416
2016 Watson MJ, Lee SL, Marklew AJ, Gilmore RC, Gentzsch M, Sassano MF, Gray MA, Tarran R. The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Uses its C-Terminus to Regulate the A2B Adenosine Receptor. Scientific Reports. 6: 27390. PMID 27278076 DOI: 10.1038/Srep27390  0.411
2016 Behrsing H, Raabe H, Manuppello J, Bombick B, Curren R, Sullivan K, Sethi S, Phipps R, Tesfaigzi Y, Yan S, D'Ruiz C, Tarran R, Constant S, Phillips G, Gaça M, et al. Assessment of in vitro COPD models for tobacco regulatory science: Workshop proceedings, conclusions and paths forward for in vitro model use. Alternatives to Laboratory Animals : Atla. 44: 129-66. PMID 27256455 DOI: 10.1177/026119291604400206  0.356
2016 Walton WG, Ahmad S, Little MR, Kim CS, Tyrrell JS, Lin Q, Di YP, Tarran R, Redinbo MR. Structural Features Essential to the Antimicrobial Functions of Human SPLUNC1. Biochemistry. PMID 27145151 DOI: 10.1021/Acs.Biochem.6B00271  0.325
2016 Fellner RC, Terryah ST, Tarran R. Inhaled protein/peptide-based therapies for respiratory disease. Molecular and Cellular Pediatrics. 3: 16. PMID 27098663 DOI: 10.1186/S40348-016-0044-8  0.409
2015 Turner MJ, Saint-Criq V, Patel W, Ibrahim SH, Verdon B, Ward C, Garnett JP, Tarran R, Cann MJ, Gray MA. Hypercapnia modulates cAMP signalling and cystic fibrosis transmembrane conductance regulator-dependent anion and fluid secretion in airway epithelia. The Journal of Physiology. PMID 26574187 DOI: 10.1113/Jp271309  0.458
2015 Rowell TR, Tarran R. Will chronic e-cigarette use cause lung disease? American Journal of Physiology. Lung Cellular and Molecular Physiology. 309: L1398-409. PMID 26408554 DOI: 10.1152/Ajplung.00272.2015  0.371
2015 Kicic A, Ling K, Martinovich K, Garratt L, Looi K, Kicic-Starcevich E, Iosifidis T, Sutanto E, Tarran R, Cmielewski P, Donnelley M, Parsons D, Stick S, Moodley Y. Corrective effects on airway epithelial function by human amniotic epithelial cells (HAEC) when treating cystic fibrosis Pediatric Pulmonology. 50: 274-274. PMID 26340478 DOI: 10.1002/Ppul.23294  0.415
2015 Manzanares D, Krick S, Baumlin N, Dennis JS, Tyrrell J, Tarran R, Salathe M. Airway Surface Dehydration by Growth Factor TGF-β in Cystic Fibrosis is Due to Decreased Function of a Voltage-dependent Potassium Channel and Can Be Rescued by the Drug Pirfenidone. The Journal of Biological Chemistry. PMID 26338706 DOI: 10.1074/Jbc.M115.670885  0.348
2015 Ghosh A, Boucher RC, Tarran R. Airway hydration and COPD. Cellular and Molecular Life Sciences : Cmls. 72: 3637-52. PMID 26068443 DOI: 10.1007/S00018-015-1946-7  0.436
2015 Choi HC, Kim CS, Tarran R. Automated acquisition and analysis of airway surface liquid height by confocal microscopy. American Journal of Physiology. Lung Cellular and Molecular Physiology. 309: L109-18. PMID 26001773 DOI: 10.1152/Ajplung.00027.2015  0.404
2015 Tyrrell J, Qian X, Freire J, Tarran R. Roflumilast combined with adenosine increases mucosal hydration in human airway epithelial cultures after cigarette smoke exposure. American Journal of Physiology. Lung Cellular and Molecular Physiology. 308: L1068-77. PMID 25795727 DOI: 10.1152/Ajplung.00395.2014  0.392
2015 Xu X, Balsiger R, Tyrrell J, Boyaka PN, Tarran R, Cormet-Boyaka E. Cigarette smoke exposure reveals a novel role for the MEK/ERK1/2 MAPK pathway in regulation of CFTR. Biochimica Et Biophysica Acta. 1850: 1224-32. PMID 25697727 DOI: 10.1016/J.Bbagen.2015.02.004  0.384
2015 Ã…strand AB, Hemmerling M, Root J, Wingren C, Pesic J, Johansson E, Garland AL, Ghosh A, Tarran R. Linking increased airway hydration, ciliary beating, and mucociliary clearance through ENaC inhibition. American Journal of Physiology. Lung Cellular and Molecular Physiology. 308: L22-32. PMID 25361567 DOI: 10.1152/Ajplung.00163.2014  0.443
2014 Tan CD, Hobbs C, Sameni M, Sloane BF, Stutts MJ, Tarran R. Cathepsin B contributes to Na+ hyperabsorption in cystic fibrosis airway epithelial cultures. The Journal of Physiology. 592: 5251-68. PMID 25260629 DOI: 10.1113/Jphysiol.2013.267286  0.484
2014 Tyrrell J, Tarran R. Gaining the Upper Hand on Pulmonary Drug Delivery. Journal of Pharmacovigilance. 2: 118. PMID 25126589 DOI: 10.4172/2329-6887.1000118  0.397
2014 Hassan F, Xu X, Nuovo G, Killilea DW, Tyrrell J, Da Tan C, Tarran R, Diaz P, Jee J, Knoell D, Boyaka PN, Cormet-Boyaka E. Accumulation of metals in GOLD4 COPD lungs is associated with decreased CFTR levels. Respiratory Research. 15: 69. PMID 24957904 DOI: 10.1186/1465-9921-15-69  0.496
2014 Tarran R, Redinbo MR. Mammalian short palate lung and nasal epithelial clone 1 (SPLUNC1) in pH-dependent airway hydration. The International Journal of Biochemistry & Cell Biology. 52: 130-5. PMID 24631954 DOI: 10.1016/J.Biocel.2014.03.002  0.464
2014 Rasmussen JE, Sheridan JT, Polk W, Davies CM, Tarran R. Cigarette smoke-induced Ca2+ release leads to cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction. The Journal of Biological Chemistry. 289: 7671-81. PMID 24448802 DOI: 10.1074/Jbc.M113.545137  0.446
2014 Kimple AJ, Garland AL, Cohen SP, Setola V, Willard FS, Zielinski T, Lowery RG, Tarran R, Siderovski DP. RGS21, a regulator of taste and mucociliary clearance? The Laryngoscope. 124: E56-63. PMID 23908053 DOI: 10.1002/Lary.24326  0.303
2013 Garnett JP, Gray MA, Tarran R, Brodlie M, Ward C, Baker EH, Baines DL. Elevated paracellular glucose flux across cystic fibrosis airway epithelial monolayers is an important factor for Pseudomonas aeruginosa growth. Plos One. 8: e76283. PMID 24124542 DOI: 10.1371/Journal.Pone.0076283  0.388
2013 Hobbs CA, Blanchard MG, Alijevic O, Tan CD, Kellenberger S, Bencharit S, Cao R, Kesimer M, Walton WG, Henderson AG, Redinbo MR, Stutts MJ, Tarran R. Identification of the SPLUNC1 ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airway epithelial cultures. American Journal of Physiology. Lung Cellular and Molecular Physiology. 305: L990-L1001. PMID 24124190 DOI: 10.1152/Ajplung.00103.2013  0.476
2013 Sheridan JT, Gilmore RC, Watson MJ, Archer CB, Tarran R. 17β-Estradiol inhibits phosphorylation of stromal interaction molecule 1 (STIM1) protein: implication for store-operated calcium entry and chronic lung diseases. The Journal of Biological Chemistry. 288: 33509-18. PMID 24114840 DOI: 10.1074/Jbc.M113.486662  0.406
2013 Garland AL, Walton WG, Coakley RD, Tan CD, Gilmore RC, Hobbs CA, Tripathy A, Clunes LA, Bencharit S, Stutts MJ, Betts L, Redinbo MR, Tarran R. Molecular basis for pH-dependent mucosal dehydration in cystic fibrosis airways. Proceedings of the National Academy of Sciences of the United States of America. 110: 15973-8. PMID 24043776 DOI: 10.1073/Pnas.1311999110  0.477
2013 Hobbs CA, Da Tan C, Tarran R. Does epithelial sodium channel hyperactivity contribute to cystic fibrosis lung disease? The Journal of Physiology. 591: 4377-87. PMID 23878362 DOI: 10.1113/Jphysiol.2012.240861  0.5
2013 Hobbs CA, Blanchard MG, Kellenberger S, Bencharit S, Cao R, Kesimer M, Walton WG, Redinbo MR, Stutts MJ, Tarran R. Erratum: Identification of SPLUNC1's ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airways (FASEB Journal (2012) 26 (4348-4359) doi:10.1096/fj.12-207431) The Faseb Journal. 27. PMID 23632283 DOI: 10.1096/Fj.12-207431Ret  0.361
2013 Tarran R, Sabater JR, Clarke TC, Tan CD, Davies CM, Liu J, Yeung A, Garland AL, Stutts MJ, Abraham WM, Phillips G, Baker WR, Wright CD, Wilbert S. Nonantibiotic macrolides prevent human neutrophil elastase-induced mucus stasis and airway surface liquid volume depletion. American Journal of Physiology. Lung Cellular and Molecular Physiology. 304: L746-56. PMID 23542952 DOI: 10.1152/Ajplung.00292.2012  0.475
2013 Herschlag G, Garcia GJ, Button B, Tarran R, Lindley B, Reinhardt B, Elston TC, Forest MG. A mechanochemical model for auto-regulation of lung airway surface layer volume. Journal of Theoretical Biology. 325: 42-51. PMID 23415939 DOI: 10.1016/J.Jtbi.2013.01.023  0.388
2012 Cohen SP, Buckley BK, Kosloff M, Garland AL, Bosch DE, Cheng G, Radhakrishna H, Brown MD, Willard FS, Arshavsky VY, Tarran R, Siderovski DP, Kimple AJ. Regulator of G-protein signaling-21 (RGS21) is an inhibitor of bitter gustatory signaling found in lingual and airway epithelia. The Journal of Biological Chemistry. 287: 41706-19. PMID 23095746 DOI: 10.1074/Jbc.M112.423806  0.311
2012 Hobbs CA, Blanchard MG, Kellenberger S, Bencharit S, Cao R, Kesimer M, Walton WG, Redinbo MR, Stutts MJ, Tarran R. Identification of SPLUNC1's ENaC-inhibitory domain yields novel strategies to treat sodium hyperabsorption in cystic fibrosis airways. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 26: 4348-59. PMID 22798424 DOI: 10.1096/Fj.12-207431  0.408
2012 Clunes LA, Davies CM, Coakley RD, Aleksandrov AA, Henderson AG, Zeman KL, Worthington EN, Gentzsch M, Kreda SM, Cholon D, Bennett WD, Riordan JR, Boucher RC, Tarran R. Cigarette smoke exposure induces CFTR internalization and insolubility, leading to airway surface liquid dehydration. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 26: 533-45. PMID 21990373 DOI: 10.1096/Fj.11-192377  0.469
2011 Watson MJ, Worthington EN, Clunes LA, Rasmussen JE, Jones L, Tarran R. Defective adenosine-stimulated cAMP production in cystic fibrosis airway epithelia: a novel role for CFTR in cell signaling. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 2996-3003. PMID 21628448 DOI: 10.1096/Fj.11-186080  0.418
2011 Schmid A, Clunes LA, Salathe M, Verdugo P, Dietl P, Davis CW, Tarran R. Nucleotide-mediated airway clearance. Sub-Cellular Biochemistry. 55: 95-138. PMID 21560046 DOI: 10.1007/978-94-007-1217-1_5  0.44
2011 Worthington EN, Tarran R. Methods for ASL measurements and mucus transport rates in cell cultures. Methods in Molecular Biology (Clifton, N.J.). 742: 77-92. PMID 21547727 DOI: 10.1007/978-1-61779-120-8_5  0.404
2011 Harvey PR, Tarran R, Garoff S, Myerburg MM. Measurement of the airway surface liquid volume with simple light refraction microscopy. American Journal of Respiratory Cell and Molecular Biology. 45: 592-9. PMID 21239602 DOI: 10.1165/Rcmb.2010-0484Oc  0.454
2011 Sheridan JT, Worthington EN, Yu K, Gabriel SE, Hartzell HC, Tarran R. Characterization of the oligomeric structure of the Ca(2+)-activated Cl- channel Ano1/TMEM16A. The Journal of Biological Chemistry. 286: 1381-8. PMID 21056985 DOI: 10.1074/Jbc.M110.174847  0.367
2010 Rollins BM, Garcia-Caballero A, Stutts MJ, Tarran R. SPLUNC1 expression reduces surface levels of the epithelial sodium channel (ENaC) in Xenopus laevis oocytes. Channels (Austin, Tex.). 4: 255-9. PMID 20519934 DOI: 10.4161/Chan.4.4.12255  0.485
2010 Gaillard EA, Kota P, Gentzsch M, Dokholyan NV, Stutts MJ, Tarran R. Regulation of the epithelial Na+ channel and airway surface liquid volume by serine proteases. PflüGers Archiv : European Journal of Physiology. 460: 1-17. PMID 20401730 DOI: 10.1007/S00424-010-0827-Z  0.457
2009 Garcia-Caballero A, Rasmussen JE, Gaillard E, Watson MJ, Olsen JC, Donaldson SH, Stutts MJ, Tarran R. SPLUNC1 regulates airway surface liquid volume by protecting ENaC from proteolytic cleavage. Proceedings of the National Academy of Sciences of the United States of America. 106: 11412-7. PMID 19541605 DOI: 10.1073/Pnas.0903609106  0.437
2009 Garcia-Caballero A, Rasmussen JE, Gaillard E, Watson MJ, Olsen JC, Donaldson SH, Stutts MJ, Tarran R. SPLUNC1 regulates airway surface liquid volume by protecting ENaC from proteolytic cleavage (Proceedings of the National Academy of Sciences of the United States of America (2009) 106, 27, (11412-11417) DOI: 10.1073/pnas. 0903609106) Proceedings of the National Academy of Sciences of the United States of America. 106: 15091. DOI: 10.1073/Pnas.0908688106  0.336
2008 Coakley RD, Sun H, Clunes LA, Rasmussen JE, Stackhouse JR, Okada SF, Fricks I, Young SL, Tarran R. 17beta-Estradiol inhibits Ca2+-dependent homeostasis of airway surface liquid volume in human cystic fibrosis airway epithelia. The Journal of Clinical Investigation. 118: 4025-35. PMID 19033671 DOI: 10.1172/Jci33893  0.463
2008 Clunes LA, Bridges A, Alexis N, Tarran R. In vivo versus in vitro airway surface liquid nicotine levels following cigarette smoke exposure. Journal of Analytical Toxicology. 32: 201-7. PMID 18397571 DOI: 10.1093/Jat/32.3.201  0.345
2008 Rollins BM, Burn M, Coakley RD, Chambers LA, Hirsh AJ, Clunes MT, Lethem MI, Donaldson SH, Tarran R. A2B adenosine receptors regulate the mucus clearance component of the lung's innate defense system American Journal of Respiratory Cell and Molecular Biology. 39: 190-197. PMID 18367727 DOI: 10.1165/Rcmb.2007-0450Oc  0.398
2007 Chambers LA, Rollins BM, Tarran R. Liquid movement across the surface epithelium of large airways. Respiratory Physiology & Neurobiology. 159: 256-70. PMID 17692578 DOI: 10.1016/J.Resp.2007.06.005  0.345
2007 Tarran R, Donaldson S, Boucher RC. Rationale for hypertonic saline therapy for cystic fibrosis lung disease. Seminars in Respiratory and Critical Care Medicine. 28: 295-302. PMID 17562499 DOI: 10.1055/S-2007-981650  0.487
2006 Tarran R, Trout L, Donaldson SH, Boucher RC. Soluble mediators, not cilia, determine airway surface liquid volume in normal and cystic fibrosis superficial airway epithelia. The Journal of General Physiology. 127: 591-604. PMID 16636206 DOI: 10.1085/Jgp.200509468  0.461
2006 Tarran R, Button B, Boucher RC. Regulation of normal and cystic fibrosis airway surface liquid volume by phasic shear stress. Annual Review of Physiology. 68: 543-61. PMID 16460283 DOI: 10.1146/Annurev.Physiol.68.072304.112754  0.49
2006 Donaldson SH, Bennett WD, Zeman KL, Knowles MR, Tarran R, Boucher RC. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. The New England Journal of Medicine. 354: 241-50. PMID 16421365 DOI: 10.1056/Nejmoa043891  0.468
2005 Thelin WR, Kesimer M, Tarran R, Kreda SM, Grubb BR, Sheehan JK, Stutts MJ, Milgram SL. The cystic fibrosis transmembrane conductance regulator is regulated by a direct interaction with the protein phosphatase 2A. The Journal of Biological Chemistry. 280: 41512-20. PMID 16239222 DOI: 10.1074/Jbc.M507308200  0.421
2005 Tarran R, Button B, Picher M, Paradiso AM, Ribeiro CM, Lazarowski ER, Zhang L, Collins PL, Pickles RJ, Fredberg JJ, Boucher RC. Normal and cystic fibrosis airway surface liquid homeostasis. The effects of phasic shear stress and viral infections. The Journal of Biological Chemistry. 280: 35751-9. PMID 16087672 DOI: 10.1074/Jbc.M505832200  0.466
2004 Tarran R. Regulation of airway surface liquid volume and mucus transport by active ion transport. Proceedings of the American Thoracic Society. 1: 42-6. PMID 16113411 DOI: 10.1513/pats.2306014  0.309
2004 Roomans GM, Kozlova I, Nilsson H, Vanthanouvong V, Button B, Tarran R. Measurements of airway surface liquid height and mucus transport by fluorescence microscopy, and of ion composition by X-ray microanalysis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 3: 135-9. PMID 15463946 DOI: 10.1016/J.Jcf.2004.05.029  0.366
2004 Davidson DJ, Gray MA, Kilanowski FM, Tarran R, Randell SH, Sheppard DN, Argent BE, Dorin JR. Murine epithelial cells: isolation and culture. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 3: 59-62. PMID 15463928 DOI: 10.1016/J.Jcf.2004.05.013  0.362
2004 Lazarowski ER, Tarran R, Grubb BR, Van Heusden CA, Okada S, Boucher RC. Nucleotide release provides a mechanism for airway surface liquid homeostasis Journal of Biological Chemistry. 279: 36855-36864. PMID 15210701 DOI: 10.1074/Jbc.M405367200  0.419
2002 Tarran R, Loewen ME, Paradiso AM, Olsen JC, Gray MA, Argent BE, Boucher RC, Gabriel SE. Regulation of murine airway surface liquid volume by CFTR and Ca2+-activated Cl- conductances. The Journal of General Physiology. 120: 407-18. PMID 12198094 DOI: 10.1085/Jgp.20028599  0.47
2002 Tarran R, Boucher RC. Thin-film measurements of airway surface liquid volume/composition and mucus transport rates in vitro. Methods in Molecular Medicine. 70: 479-92. PMID 11917544 DOI: 10.1385/1-59259-187-6:479  0.336
2002 Worlitzsch D, Tarran R, Ulrich M, Schwab U, Cekici A, Meyer KC, Birrer P, Bellon G, Berger J, Weiss T, Botzenhart K, Yankaskas JR, Randell S, Boucher RC, Döring G. Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients. The Journal of Clinical Investigation. 109: 317-25. PMID 11827991 DOI: 10.1172/Jci13870  0.442
2002 Caldwell RA, Grubb BR, Tarran R, Boucher RC, Knowles MR, Barker PM. In vivo airway surface liquid Cl- analysis with solid-state electrodes. The Journal of General Physiology. 119: 3-14. PMID 11773234 DOI: 10.1085/Jgp.119.1.3  0.386
2001 Huang P, Lazarowski ER, Tarran R, Milgram SL, Boucher RC, Stutts MJ. Compartmentalized autocrine signaling to cystic fibrosis transmembrane conductance regulator at the apical membrane of airway epithelial cells. Proceedings of the National Academy of Sciences of the United States of America. 98: 14120-5. PMID 11707576 DOI: 10.1073/Pnas.241318498  0.411
2001 Tarran R, Grubb BR, Parsons D, Picher M, Hirsh AJ, Davis CW, Boucher RC. The CF salt controversy: in vivo observations and therapeutic approaches. Molecular Cell. 8: 149-58. PMID 11511368 DOI: 10.1016/S1097-2765(01)00286-6  0.441
2001 Tarran R, Grubb BR, Gatzy JT, Davis CW, Boucher RC. The relative roles of passive surface forces and active ion transport in the modulation of airway surface liquid volume and composition. The Journal of General Physiology. 118: 223-36. PMID 11479349 DOI: 10.1085/Jgp.118.2.223  0.383
2000 Matsui H, Davis CW, Tarran R, Boucher RC. Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epithelia. The Journal of Clinical Investigation. 105: 1419-27. PMID 10811849 DOI: 10.1172/Jci4546  0.406
2000 Tarran R, Argent BE, Gray MA. Regulation of a hyperpolarization-activated chloride current in murine respiratory ciliated cells Journal of Physiology. 524: 353-364. PMID 10766917 DOI: 10.1111/J.1469-7793.2000.00353.X  0.349
1999 Becq F, Mettey Y, Gray MA, Galietta LJ, Dormer RL, Merten M, Métayé T, Chappe V, Marvingt-Mounir C, Zegarra-Moran O, Tarran R, Bulteau L, Dérand R, Pereira MM, McPherson MA, et al. Development of substituted Benzo[c]quinolizinium compounds as novel activators of the cystic fibrosis chloride channel. The Journal of Biological Chemistry. 274: 27415-25. PMID 10488073 DOI: 10.1074/Jbc.274.39.27415  0.365
1998 Matsui H, Grubb BR, Tarran R, Randell SH, Gatzy JT, Davis CW, Boucher RC. Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease. Cell. 95: 1005-15. PMID 9875854 DOI: 10.1016/S0092-8674(00)81724-9  0.492
1998 Tarran R, Gray MA, Evans MJ, Colledge WH, Ratcliff R, Argent BE. Basal chloride currents in murine airway epithelial cells: modulation by CFTR. The American Journal of Physiology. 274: C904-13. PMID 9575786 DOI: 10.1152/Ajpcell.1998.274.4.C904  0.359
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