Year |
Citation |
Score |
2023 |
Illek B, Fischer H, Machen TE, Hari G, Clemons KV, Sass G, Ferreira JAG, Stevens DA. Protective role of CFTR during fungal infection of cystic fibrosis bronchial epithelial cells with . Frontiers in Cellular and Infection Microbiology. 13: 1196581. PMID 37680748 DOI: 10.3389/fcimb.2023.1196581 |
0.582 |
|
2017 |
Sellers ZM, Illek B, Figueira MF, Hari G, Joo NS, Sibley E, Souza-Menezes J, Morales MM, Fischer H, Wine JJ. Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease. Plos One. 12: e0189894. PMID 29281691 DOI: 10.1371/Journal.Pone.0189894 |
0.374 |
|
2016 |
Schwarzer C, Fischer H, Machen TE. Chemotaxis and Binding of Pseudomonas aeruginosa to Scratch-Wounded Human Cystic Fibrosis Airway Epithelial Cells. Plos One. 11: e0150109. PMID 27031335 DOI: 10.1371/Journal.Pone.0150109 |
0.608 |
|
2016 |
Suzuki S, Sargent RG, Illek B, Fischer H, Esmaeili-Shandiz A, Yezzi MJ, Lee A, Yang Y, Kim S, Renz P, Qi Z, Yu J, Muench MO, Beyer AI, Guimarães AO, et al. TALENs Facilitate Single-step Seamless SDF Correction of F508del CFTR in Airway Epithelial Submucosal Gland Cell-derived CF-iPSCs. Molecular Therapy. Nucleic Acids. 5: e273. PMID 26730810 DOI: 10.1038/Mtna.2015.43 |
0.407 |
|
2015 |
Schwagerus E, Sladek S, Buckley ST, Armas-Capote N, de la Rosa DA, Harvey BJ, Fischer H, Illek B, Huwer H, Schneider-Daum N, Lehr CM, Ehrhardt C. Expression and function of the epithelial sodium channel δ-subunit in human respiratory epithelial cells in vitro. Pflugers Archiv : European Journal of Physiology. PMID 25677639 DOI: 10.1007/S00424-015-1693-5 |
0.458 |
|
2014 |
Fischer H. The G551D CFTR chloride channel spurs the development of personalized medicine. The Journal of Physiology. 592: 1907-8. PMID 24786148 DOI: 10.1113/Jphysiol.2014.274464 |
0.358 |
|
2014 |
Schwarzer C, Ravishankar B, Patanwala M, Shuai S, Fu Z, Illek B, Fischer H, Machen TE. Thapsigargin blocks Pseudomonas aeruginosa homoserine lactone-induced apoptosis in airway epithelia. American Journal of Physiology. Cell Physiology. 306: C844-55. PMID 24598360 DOI: 10.1152/Ajpcell.00002.2014 |
0.589 |
|
2011 |
Cho DY, Hwang PH, Illek B, Fischer H. Acid and base secretion in freshly excised nasal tissue from cystic fibrosis patients with ΔF508 mutation International Forum of Allergy and Rhinology. 1: 123-127. PMID 22034590 DOI: 10.1002/Alr.20028 |
0.361 |
|
2011 |
Sweeney RM, Fischer H, McAuley DF. Nasal potential difference to detect Na+ channel dysfunction in acute lung injury. American Journal of Physiology-Lung Cellular and Molecular Physiology. 300. PMID 21112943 DOI: 10.1152/Ajplung.00223.2010 |
0.364 |
|
2010 |
Illek B, Lei D, Fischer H, Gruenert DC. Sensitivity of Chloride Efflux vs. Transepithelial Measurements in Mixed CF and Normal Airway Epithelial Cell Populations Cellular Physiology and Biochemistry. 26: 983-990. PMID 21220929 DOI: 10.1159/000324011 |
0.455 |
|
2010 |
Fischer H, Illek B, Sachs L, Finkbeiner WE, Widdicombe JH. CFTR and calcium-activated chloride channels in primary cultures of human airway gland cells of serous or mucous phenotype. American Journal of Physiology. Lung Cellular and Molecular Physiology. 299: L585-94. PMID 20675434 DOI: 10.1152/Ajplung.00421.2009 |
0.655 |
|
2010 |
Iovannisci D, Illek B, Fischer H. Function of the HVCN1 proton channel in airway epithelia and a naturally occurring mutation, M91T The Journal of General Physiology. 136: 35-46. PMID 20548053 DOI: 10.1085/Jgp.200910379 |
0.402 |
|
2010 |
Ballard PL, Lee JW, Fang X, Chapin C, Allen L, Segal MR, Fischer H, Illek B, Gonzales LW, Kolla V, Matthay MA. Regulated gene expression in cultured type II cells of adult human lung. American Journal of Physiology. Lung Cellular and Molecular Physiology. 299: L36-50. PMID 20382749 DOI: 10.1152/Ajplung.00427.2009 |
0.33 |
|
2009 |
Fischer H. Mechanisms and function of DUOX in epithelia of the lung Antioxidants &Amp; Redox Signaling. 11: 2453-2465. PMID 19358684 DOI: 10.1089/Ars.2009.2558 |
0.39 |
|
2008 |
Fischer H, Illek B. Activation of the CFTR Cl- channel by trimethoxyflavone in vitro and in vivo. Cellular Physiology and Biochemistry. 22: 685-692. PMID 19088450 DOI: 10.1159/000185552 |
0.418 |
|
2008 |
Schwarzer C, Fischer H, Kim EJ, Barber KJ, Mills AD, Kurth MJ, Gruenert DC, Suh JH, Machen TE, Illek B. Oxidative stress caused by pyocyanin impairs CFTR Cl(-) transport in human bronchial epithelial cells. Free Radical Biology & Medicine. 45: 1653-62. PMID 18845244 DOI: 10.1016/J.Freeradbiomed.2008.09.011 |
0.684 |
|
2008 |
Illek B, Maurisse R, Wahler L, Kunzelmann K, Fischer H, Gruenert DC. Cl transport in complemented CF bronchial epithelial cells correlates with CFTR mRNA expression levels. Cellular Physiology and Biochemistry. 22: 57-68. PMID 18769032 DOI: 10.1159/000149783 |
0.407 |
|
2008 |
Schwarzer C, Fu Z, Fischer H, Machen TE. Redox-independent activation of NF-kappaB by Pseudomonas aeruginosa pyocyanin in a cystic fibrosis airway epithelial cell line. The Journal of Biological Chemistry. 283: 27144-53. PMID 18682396 DOI: 10.1074/Jbc.M709693200 |
0.575 |
|
2008 |
Rajagopal M, Fischer H, Widdicombe JH. Hormonal and purinergic stimulation of bicarbonate secretion in oviducts of rhesus monkey. American Journal of Physiology. Endocrinology and Metabolism. 295: E55-62. PMID 18430967 DOI: 10.1152/Ajpendo.00714.2007 |
0.566 |
|
2007 |
Schwarzer C, Illek B, Suh JH, Remington SJ, Fischer H, Machen TE. Organelle redox of CF and CFTR-corrected airway epithelia Free Radical Biology and Medicine. 43: 300-316. PMID 17603939 DOI: 10.1016/J.Freeradbiomed.2007.04.015 |
0.637 |
|
2007 |
Fischer H, Gonzales LK, Kolla V, Schwarzer C, Miot F, Illek B, Ballard PL. Developmental regulation of DUOX1 expression and function in human fetal lung epithelial cells. American Journal of Physiology-Lung Cellular and Molecular Physiology. 292. PMID 17337509 DOI: 10.1152/Ajplung.00029.2007 |
0.341 |
|
2007 |
Fischer H, Illek B, Finkbeiner WE, Widdicombe JH. Basolateral Cl channels in primary airway epithelial cultures. American Journal of Physiology. Lung Cellular and Molecular Physiology. 292: L1432-43. PMID 17322286 DOI: 10.1152/Ajplung.00032.2007 |
0.621 |
|
2007 |
Gaggioli V, Schwarzer C, Fischer H. Expression of Nox1 in 3T3 cells increases cellular acid production but not proton conductance. Archives of Biochemistry and Biophysics. 459: 189-196. PMID 17234149 DOI: 10.1016/J.Abb.2006.11.023 |
0.351 |
|
2006 |
Fischer H, Widdicombe JH. Mechanisms of acid and base secretion by the airway epithelium. The Journal of Membrane Biology. 211: 139-50. PMID 17091214 DOI: 10.1007/S00232-006-0861-0 |
0.588 |
|
2006 |
Fischer H, Illek B, Kolla V, Gonzales LW, Ballard PL. 166 Expression And Function Of Dual Oxidase In Fetal Lung Epithelial Cells. Journal of Investigative Medicine. 54. DOI: 10.2310/6650.2005.X0004.165 |
0.414 |
|
2005 |
Schuier M, Sies H, Illek B, Fischer H. Cocoa-related flavonoids inhibit CFTR-mediated chloride transport across T84 human colon epithelia. The Journal of Nutrition. 135: 2320-5. PMID 16177189 DOI: 10.1093/Jn/135.10.2320 |
0.4 |
|
2005 |
Maurisse R, Illek B, Cheung J, Shuto T, Kai H, Fischer H, Gruenert DC. 913. Development and Characterization of CF Airway Epithelial Cell Lines Complemented with Wild-Type and |[Delta]|F508 CFTR cDNA Molecular Therapy. 11. DOI: 10.1016/J.Ymthe.2005.07.456 |
0.427 |
|
2004 |
Fischer H, Machen TE, Widdicombe JH, Carlson TJ, King SR, Chow JW, Illek B. A novel extract SB-300 from the stem bark latex of Croton lechleri inhibits CFTR-mediated chloride secretion in human colonic epithelial cells. Journal of Ethnopharmacology. 93: 351-7. PMID 15234776 DOI: 10.1016/J.Jep.2004.04.005 |
0.703 |
|
2004 |
Schwarzer C, Machen TE, Illek B, Fischer H. NADPH oxidase-dependent acid production in airway epithelial cells. The Journal of Biological Chemistry. 279: 36454-61. PMID 15210697 DOI: 10.1074/Jbc.M404983200 |
0.608 |
|
2004 |
Fischer H, Schwarzer C, Illek B. Vitamin C controls the cystic fibrosis transmembrane conductance regulator chloride channel Proceedings of the National Academy of Sciences of the United States of America. 101: 3691-3696. PMID 14993613 DOI: 10.1073/Pnas.0308393100 |
0.38 |
|
2003 |
Howard M, Fischer H, Roux J, Santos BC, Gullans SR, Yancey PH, Welch WJ. Mammalian osmolytes and S-nitrosoglutathione promote Delta F508 cystic fibrosis transmembrane conductance regulator (CFTR) protein maturation and function. The Journal of Biological Chemistry. 278: 35159-67. PMID 12837761 DOI: 10.1074/Jbc.M301924200 |
0.348 |
|
2003 |
Chung NC, Illek B, Widdicombe JH, Fischer H. Measurement of nasal potential difference in mild asthmatics. Chest. 123: 1467-71. PMID 12740262 DOI: 10.1378/Chest.123.5.1467 |
0.507 |
|
2002 |
Fischer H, Widdicombe JH, Illek B. Acid secretion and proton conductance in human airway epithelium. American Journal of Physiology. Cell Physiology. 282: C736-43. PMID 11880261 DOI: 10.1152/Ajpcell.00369.2001 |
0.595 |
|
2001 |
Fischer H, Fukuda N, Barbry P, Illek B, Sartori C, Matthay MA. Partial restoration of defective chloride conductance in ΔF508 CF mice by trimethylamine oxide American Journal of Physiology-Lung Cellular and Molecular Physiology. 281. PMID 11404245 DOI: 10.1152/Ajplung.2001.281.1.L52 |
0.323 |
|
2000 |
Illek B, Lizarzaburu ME, Lee V, Nantz MH, Kurth MJ, Fischer H. Structural determinants for activation and block of CFTR-mediated chloride currents by apigenin. American Journal of Physiology. Cell Physiology. 279: C1838-46. PMID 11078699 DOI: 10.1152/Ajpcell.2000.279.6.C1838 |
0.655 |
|
2000 |
Liu Q, Fischer H, Welch WJ, Harris HW. Increased susceptibility of pancreatic acinar cells to hyperstimulatory stress in ∆F508 cystic fibrosis transmembrane conductance regulator (CFTR) heterozygous mice Gastroenterology. 118. DOI: 10.1016/S0016-5085(00)86313-1 |
0.341 |
|
1999 |
Illek B, Zhang L, Lewis NC, Moss RB, Dong JY, Fischer H. Defective function of the cystic fibrosis-causing missense mutation G551D is recovered by genistein. The American Journal of Physiology. 277: C833-9. PMID 10516113 DOI: 10.1152/Ajpcell.1999.277.4.C833 |
0.434 |
|
1999 |
Wang D, Fischer H, Zhang L, Fan P, Ding RX, Dong J. Efficient CFTR expression from AAV vectors packaged with promoters--the second generation. Gene Therapy. 6: 667-675. PMID 10476227 DOI: 10.1038/Sj.Gt.3300856 |
0.332 |
|
1999 |
Illek B, Tam AWK, Fischer H, Machen TE. Anion selectivity of apical membrane conductance of Calu 3 human airway epithelium Pflugers Archiv European Journal of Physiology. 437: 812-822. PMID 10370058 DOI: 10.1007/S004240050850 |
0.655 |
|
1998 |
Illek B, Fischer H, Machen TE. Genetic disorders of membrane transport. II. Regulation of CFTR by small molecules including HCO 3/ - American Journal of Physiology - Gastrointestinal and Liver Physiology. 275: G1221-G1226. PMID 9843756 DOI: 10.1152/Ajpgi.1998.275.6.G1221 |
0.637 |
|
1998 |
Illek B, Fischer H. Flavonoids stimulate Cl conductance of human airway epithelium in vitro and in vivo. American Journal of Physiology-Lung Cellular and Molecular Physiology. 275. PMID 9815107 DOI: 10.1152/Ajplung.1998.275.5.L902 |
0.431 |
|
1998 |
Zhang L, Wang D, Fischer H, Fan PD, Widdicombe JH, Kan YW, Dong JY. Efficient expression of CFTR function with adeno-associated virus vectors that carry shortened CFTR genes. Proceedings of the National Academy of Sciences of the United States of America. 95: 10158-63. PMID 9707617 DOI: 10.1073/Pnas.95.17.10158 |
0.531 |
|
1998 |
Fischer H, Illek B, Machen TE. Regulation of CFTR by protein phosphatase 2B and protein kinase C Pflugers Archiv European Journal of Physiology. 436: 175-181. PMID 9594016 DOI: 10.1007/S004240050620 |
0.66 |
|
1998 |
Illek B, Machen T, Widdicombe J, Fischer H. Stimulation of cystic fibrosis transmembrane conductance regulator (CFTR) chloride channels by flavonoids Expert Opinion On Therapeutic Targets. 2: 1-4. DOI: 10.1517/14728222.2.1.1 |
0.7 |
|
1996 |
Fischer H, Machen TE. The tyrosine kinase p60(c-src) regulates the fast gate of the cystic fibrosis transmembrane conductance regulator chloride channel Biophysical Journal. 71: 3073-3082. PMID 8968578 DOI: 10.1016/S0006-3495(96)79501-2 |
0.608 |
|
1996 |
Illek B, Fischer H, Machen TE. Alternate stimulation of apical CFTR by genistein in epithelia American Journal of Physiology - Cell Physiology. 270: C265-C275. PMID 8772453 DOI: 10.1152/Ajpcell.1996.270.1.C265 |
0.667 |
|
1995 |
Fischer H, Illek B, Machen TE. The actin filament disrupter cytochalasin D activates the recombinant cystic fibrosis transmembrane conductance regulator Cl- channel in mouse 3T3 fibroblasts Journal of Physiology. 489: 745-754. PMID 8788939 DOI: 10.1113/Jphysiol.1995.Sp021088 |
0.617 |
|
1995 |
Illek B, Fischer H, Santos GF, Widdicombe JH, Machen TE, Reenstra WW. cAMP-independent activation of CFTR Cl channels by the tyrosine kinase inhibitor genistein American Journal of Physiology - Cell Physiology. 268: C886-C893. PMID 7537452 DOI: 10.1152/Ajpcell.1995.268.4.C886 |
0.701 |
|
1994 |
Fischer H, Machen TE. CFTR displays voltage dependence and two gating modes during stimulation Journal of General Physiology. 104: 541-566. PMID 7528783 DOI: 10.1085/Jgp.104.3.541 |
0.598 |
|
1994 |
Poulsen JH, Fischer H, Illek B, Machen TE. Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator Proceedings of the National Academy of Sciences of the United States of America. 91: 5340-5344. PMID 7515498 DOI: 10.1073/Pnas.91.12.5340 |
0.657 |
|
1992 |
Illek B, Fischer H, Machen TE. Intracellular Ca2+ signalling is modulated by K+ channel blockers in colonie epithelial cells (HT-29/B6) PflüGers Archiv European Journal of Physiology. 422: 48-54. PMID 1437524 DOI: 10.1007/Bf00381512 |
0.603 |
|
1992 |
Fischer H, Illek B, Negulescu PA, Clauss W, Machen TE. Carbachol-activated calcium entry into HT-29 cells is regulated by both membrane potential and cell volume Proceedings of the National Academy of Sciences of the United States of America. 89: 1438-1442. PMID 1311099 DOI: 10.1073/Pnas.89.4.1438 |
0.695 |
|
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