| Year |
Citation |
Score |
| 2023 |
Zajac M, Lepissier A, Dréano E, Chevalier B, Hatton A, Kelly-Aubert M, Guidone D, Planelles G, Edelman A, Girodon E, Hinzpeter A, Crambert G, Pranke I, Galietta LJV, Sermet-Gaudelus I. Putting bicarbonate on the spot: pharmacological insights for CFTR correction in the airway epithelium. Frontiers in Pharmacology. 14: 1293578. PMID 38149052 DOI: 10.3389/fphar.2023.1293578 |
0.796 |
|
| 2023 |
Kuzmuk V, Pranke I, Rollason R, Butler M, Ding WY, Beesley M, Waters AM, Coward RJ, Sessions R, Tuffin J, Foster RR, Mollet G, Antignac C, Edelman A, Welsh GI, et al. A small molecule chaperone rescues keratin-8 mediated trafficking of misfolded podocin to correct genetic Nephrotic Syndrome. Kidney International. PMID 37995908 DOI: 10.1016/j.kint.2023.11.006 |
0.319 |
|
| 2023 |
Dreano E, Burgel PR, Hatton A, Bouazza N, Chevalier B, Macey J, Leroy S, Durieu I, Weiss L, Grenet D, Stremler N, Ohlmann C, Reix P, Porzio M, Roux Claude P, ... ... Edelman A, et al. Theratyping Cystic Fibrosis patients to guide Elexacaftor-Tezacaftor-Ivacaftor out of label prescription. The European Respiratory Journal. PMID 37696564 DOI: 10.1183/13993003.00110-2023 |
0.782 |
|
| 2023 |
Orenti A, Pranke I, Faucon C, Varilh J, Hatton A, Golec A, Dehillotte C, Durieu I, Reix P, Burgel PR, Grenet D, Tasset C, Gachelin E, Perisson C, Lepissier A, ... ... Edelman A, et al. Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 37422433 DOI: 10.1016/j.jcf.2023.06.005 |
0.647 |
|
| 2022 |
Ravatin M, Odolczyk N, Servel N, Guijarro JI, Tagat E, Chevalier B, Baatallah N, Corringer PJ, Lukács GL, Edelman A, Zielenkiewicz P, Chambard JM, Hinzpeter A, Faure G. Design of Crotoxin-Based Peptides with Potentiator Activity Targeting the ΔF508NBD1 Cystic Fibrosis Transmembrane Conductance Regulator. Journal of Molecular Biology. 435: 167929. PMID 36566799 DOI: 10.1016/j.jmb.2022.167929 |
0.657 |
|
| 2022 |
Baatallah N, Elbahnsi A, Chevalier B, Castanier S, Mornon JP, Pranke I, Edelman A, Sermet-Gaudelus I, Callebaut I, Hinzpeter A. Acting on the CFTR Membrane-Spanning Domains Interface Rescues Some Misfolded Mutants. International Journal of Molecular Sciences. 23. PMID 36555865 DOI: 10.3390/ijms232416225 |
0.681 |
|
| 2022 |
Lhuillier M, Aoust L, Dreano E, Franco-Montoya ML, Landry-Truchon K, Houde N, Chhun S, Hinzpeter A, Edelman A, Delacourt C, Jeannotte L, Sermet-Gaudelus I, Hadchouel A. Elexacaftor/Tezacaftor/Ivacaftor Disrupts Respiratory Tract Development in a Murine Fetal Lung Explant Model. American Journal of Respiratory Cell and Molecular Biology. 67: 723-726. PMID 36454086 DOI: 10.1165/rcmb.2022-0175LE |
0.601 |
|
| 2022 |
Saha K, Chevalier B, Doly S, Baatallah N, Guilbert T, Pranke I, Scott MGH, Enslen H, Guerrera C, Chuon C, Edelman A, Sermet-Gaudelus I, Hinzpeter A, Marullo S. Pharmacological chaperone-rescued cystic fibrosis CFTR-F508del mutant overcomes PRAF2-gated access to endoplasmic reticulum exit sites. Cellular and Molecular Life Sciences : Cmls. 79: 530. PMID 36167862 DOI: 10.1007/s00018-022-04554-1 |
0.71 |
|
| 2022 |
Pranke IM, Chevalier B, Premchandar A, Baatallah N, Tomaszewski KF, Bitam S, Tondelier D, Golec A, Stolk J, Lukacs GL, Hiemstra PS, Dadlez M, Lomas DA, Irving JA, Delaunay-Moisan A, ... ... Edelman A, et al. Keratin 8 is a scaffolding and regulatory protein of ERAD complexes. Cellular and Molecular Life Sciences : Cmls. 79: 503. PMID 36045259 DOI: 10.1007/s00018-022-04528-3 |
0.791 |
|
| 2022 |
Chevalier B, Baatallah N, Najm M, Castanier S, Jung V, Pranke I, Golec A, Stoven V, Marullo S, Antigny F, Guerrera IC, Sermet-Gaudelus I, Edelman A, Hinzpeter A. Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC Transporters. International Journal of Molecular Sciences. 23. PMID 36012204 DOI: 10.3390/ijms23168937 |
0.683 |
|
| 2022 |
da Cunha MF, Pranke I, Sassi A, Schreiweis C, Moriceau S, Vidovic D, Hatton A, Carlon MS, Creste G, Berhal F, Prestat G, Freund R, Odolczyk N, Jais JP, Gravier-Pelletier C, ... ... Edelman A, et al. Systemic bis-phosphinic acid derivative restores chloride transport in Cystic Fibrosis mice. Scientific Reports. 12: 6132. PMID 35413967 DOI: 10.1038/s41598-022-09678-9 |
0.711 |
|
| 2021 |
Hatton A, Bergougnoux A, Zybert K, Chevalier B, Mesbahi M, Altéri JP, Walicka-Serzysko K, Postek M, Taulan-Cadars M, Edelman A, Hinzpeter A, Claustres M, Girodon E, Raynal C, Sermet-Gaudelus I, et al. Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forward. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 34949556 DOI: 10.1016/j.jcf.2021.12.010 |
0.665 |
|
| 2021 |
Noel S, Servel N, Hatton A, Golec A, Rodrat M, Ng DRS, Li H, Pranke I, Hinzpeter A, Edelman A, Sheppard DN, Sermet-Gaudelus I. Correlating genotype with phenotype using CFTR-mediated whole-cell Cl currents in human nasal epithelial cells. The Journal of Physiology. PMID 34761808 DOI: 10.1113/JP282143 |
0.698 |
|
| 2021 |
Baatallah N, Elbahnsi A, Mornon JP, Chevalier B, Pranke I, Servel N, Zelli R, Décout JL, Edelman A, Sermet-Gaudelus I, Callebaut I, Hinzpeter A. Pharmacological chaperones improve intra-domain stability and inter-domain assembly via distinct binding sites to rescue misfolded CFTR. Cellular and Molecular Life Sciences : Cmls. 78: 7813-7829. PMID 34714360 DOI: 10.1007/s00018-021-03994-5 |
0.655 |
|
| 2021 |
Bitam S, Elbahnsi A, Creste G, Pranke I, Chevalier B, Berhal F, Hoffmann B, Servel N, Baatalah N, Tondelier D, Hatton A, Moquereau C, Faria Da Cunha M, Pastor A, Lepissier A, ... ... Edelman A, et al. Author Correction: New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation. Scientific Reports. 11: 18709. PMID 34526640 DOI: 10.1038/s41598-021-98301-4 |
0.76 |
|
| 2021 |
Bitam S, Elbahnsi A, Creste G, Pranke I, Chevalier B, Berhal F, Hoffmann B, Servel N, Tondelier D, Hatton A, Moquereau C, Faria Da Cunha M, Pastor A, Lepissier A, Hinzpeter A, ... ... Edelman A, et al. New insights into structure and function of bis-phosphinic acid derivatives and implications for CFTR modulation. Scientific Reports. 11: 6842. PMID 33767236 DOI: 10.1038/s41598-021-83240-x |
0.792 |
|
| 2020 |
Gauthier S, Pranke I, Jung V, Martignetti L, Stoven V, Nguyen-Khoa T, Semeraro M, Hinzpeter A, Edelman A, Guerrera IC, Sermet-Gaudelus I. Urinary Exosomes of Patients with Cystic Fibrosis Unravel CFTR-Related Renal Disease. International Journal of Molecular Sciences. 21. PMID 32927759 DOI: 10.3390/Ijms21186625 |
0.711 |
|
| 2020 |
Baatallah N, Elbahnsi A, Mornon J, Chevalier B, Pranke I, Servel N, Edelman A, Sermet-Gaudelus I, Callebaut I, Hinzpeter A. WS05.1 AVX-770 binding site within CFTR membrane spanning domain 2 enables ATP-independent channel activation Journal of Cystic Fibrosis. 19: S8. DOI: 10.1016/S1569-1993(20)30189-2 |
0.666 |
|
| 2019 |
Simonin J, Bille E, Crambert G, Noel S, Dreano E, Edwards A, Hatton A, Pranke I, Villeret B, Cottart CH, Vrel JP, Urbach V, Baatallah N, Hinzpeter A, Golec A, ... ... Edelman A, et al. Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis. Scientific Reports. 9: 17535. PMID 31754179 DOI: 10.1038/S41598-019-54253-4 |
0.645 |
|
| 2019 |
Simonin J, Bille E, Crambert G, Noel S, Dreano E, Edwards A, Hatton A, Pranke I, Villeret B, Cottart CH, Vrel JP, Urbach V, Baatallah N, Hinzpeter A, Golec A, ... ... Edelman A, et al. Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis. Scientific Reports. 9: 6516. PMID 31019198 DOI: 10.1038/S41598-019-42751-4 |
0.708 |
|
| 2019 |
Pranke I, Golec A, Hinzpeter A, Edelman A, Sermet-Gaudelus I. Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine. Frontiers in Pharmacology. 10: 121. PMID 30873022 DOI: 10.3389/Fphar.2019.00121 |
0.708 |
|
| 2019 |
Noel S, Servel N, Hatton A, Golec A, Edelman A, Sheppard D, Sermet-Gaudelus I. WS13-2 Whole-cell patch-clamp recordings of CFTR-mediated chloride currents in native and cultured nasal epithelial cells from cystic fibrosis and non-cystic fibrosis subjects Journal of Cystic Fibrosis. 18: S24. DOI: 10.1016/S1569-1993(19)30193-6 |
0.396 |
|
| 2018 |
Masson A, Schneider-Futschik EK, Baatallah N, Nguyen-Khoa T, Girodon E, Hatton A, Flament T, Le Bourgeois M, Chedevergne F, Bailly C, Kyrilli S, Achimastos D, Hinzpeter A, Edelman A, Sermet-Gaudelus I. Predictive factors for lumacaftor/ivacaftor clinical response. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 30595473 DOI: 10.1016/J.Jcf.2018.12.011 |
0.628 |
|
| 2018 |
Pranke I, Hatton A, Masson A, Flament T, Le Bourgeois M, Chedevergne F, Bailly C, Urbach V, Hinzpeter A, Edelman A, Sermet-Gaudelus I. Might Brushed Nasal Cells Be a Surrogate for CFTR Modulator Clinical Response? American Journal of Respiratory and Critical Care Medicine. PMID 30326728 DOI: 10.1164/Rccm.201808-1436Le |
0.629 |
|
| 2018 |
Veit G, Xu H, Dreano E, Avramescu RG, Bagdany M, Beitel LK, Roldan A, Hancock MA, Lay C, Li W, Morin K, Gao S, Mak PA, Ainscow E, Orth AP, ... ... Edelman A, et al. Structure-guided combination therapy to potently improve the function of mutant CFTRs. Nature Medicine. PMID 30297908 DOI: 10.1038/s41591-018-0200-x |
0.354 |
|
| 2018 |
Rollet-Cohen V, Bourderioux M, Lipecka J, Chhuon C, Jung VA, Mesbahi M, Nguyen-Khoa T, Guérin-Pfyffer S, Schmitt A, Edelman A, Sermet-Gaudelus I, Guerrera IC. Comparative proteomics of respiratory exosomes in cystic fibrosis, primary ciliary dyskinesia and asthma. Journal of Proteomics. 185: 1-7. PMID 30032860 DOI: 10.1016/J.Jprot.2018.07.001 |
0.411 |
|
| 2018 |
Pranke I, Bidou L, Martin N, Blanchet S, Hatton A, Karri S, Cornu D, Costes B, Chevalier B, Tondelier D, Girodon E, Coupet M, Edelman A, Fanen P, Namy O, et al. Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons. Erj Open Research. 4. PMID 29497617 DOI: 10.1183/23120541.00080-2017 |
0.673 |
|
| 2017 |
Baatallah N, Bitam S, Martin N, Servel N, Costes B, Mekki C, Chevalier B, Pranke I, Simonin J, Girodon E, Hoffmann B, Mornon JP, Callebaut I, Sermet-Gaudelus I, Fanen P, ... Edelman A, et al. Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules. Human Mutation. PMID 29271547 DOI: 10.1002/Humu.23389 |
0.776 |
|
| 2017 |
Pranke IM, Hatton A, Simonin J, Jais JP, Le Pimpec-Barthes F, Carsin A, Bonnette P, Fayon M, Stremler-Le Bel N, Grenet D, Thumerel M, Mazenq J, Urbach V, Mesbahi M, Girodon-Boulandet E, ... ... Edelman A, et al. Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators. Scientific Reports. 7: 7375. PMID 28785019 DOI: 10.1038/S41598-017-07504-1 |
0.733 |
|
| 2016 |
Premchandar A, Kupniewska A, Bonna A, Faure G, Fraczyk T, Roldan A, Hoffmann B, Faria da Cunha M, Herrmann H, Lukacs GL, Edelman A, Dadlez M. New insights into interactions between the nucleotide-binding domain of CFTR and keratin 8. Protein Science : a Publication of the Protein Society. PMID 27870250 DOI: 10.1002/Pro.3086 |
0.374 |
|
| 2016 |
Cunha MF, Simonin J, Sassi A, Freund R, Hatton A, Cottart CH, Elganfoud N, Zoubairi R, Dragu C, Jais JP, Hinzpeter A, Edelman A, Sermet-Gaudelus I. Analysis of nasal potential in murine cystic fibrosis models. The International Journal of Biochemistry & Cell Biology. PMID 27717840 DOI: 10.1016/J.Biocel.2016.10.001 |
0.703 |
|
| 2016 |
Chhuon C, Pranke I, Borot F, Tondelier D, Lipecka J, Fritsch J, Chanson M, Edelman A, Ollero M, Guerrera IC. Dataset of differential lipid raft and global proteomes of SILAC-labeled cystic fibrosis cells upon TNF -α stimulation. Data in Brief. 9: 51-6. PMID 27626054 DOI: 10.1016/j.dib.2016.08.012 |
0.352 |
|
| 2016 |
Faure G, Bakouh N, Lourdel S, Odolczyk N, Premchandar A, Servel N, Hatton A, Ostrowski MK, Xu H, Saul FA, Moquereau C, Bitam S, Pranke I, Planelles G, Teulon J, ... ... Edelman A, et al. Rattlesnake Phospholipase A2 increases CFTR-chloride channel current and corrects ∆F508CFTR dysfunction: impact in Cystic Fibrosis. Journal of Molecular Biology. PMID 27241308 DOI: 10.1016/J.Jmb.2016.05.016 |
0.824 |
|
| 2016 |
Le Henaff C, Da Cunha MF, Hatton A, Tondelier D, Marty C, Collet C, Zarka M, Geoffroy V, Zatloukal K, Laplantine E, Edelman A, Sermet-Gaudelus I, Marie PJ. Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosis. Human Molecular Genetics. PMID 26769674 DOI: 10.1093/Hmg/Ddw009 |
0.335 |
|
| 2015 |
Bitam S, Pranke I, Hollenhorst M, Servel N, Moquereau C, Tondelier D, Hatton A, Urbach V, Sermet-Gaudelus I, Hinzpeter A, Edelman A. An unexpected effect of TNF-α on F508del-CFTR maturation and function. F1000research. 4: 218. PMID 26594334 DOI: 10.12688/F1000Research.6683.2 |
0.828 |
|
| 2015 |
Vidović D, Carlon MS, F da Cunha M, Dekkers JF, Hollenhorst MI, Bijvelds MJ, Ramalho AS, Van den Haute C, Ferrante M, Baekelandt V, Janssens HM, De Boeck K, Sermet-Gaudelus I, de Jonge HR, Gijsbers R, ... ... Edelman A, et al. rAAV-CFTRΔR Rescues the Cystic Fibrosis Phenotype in Human Intestinal Organoids and CF Mice. American Journal of Respiratory and Critical Care Medicine. PMID 26509335 DOI: 10.1164/Rccm.201505-0914Oc |
0.386 |
|
| 2015 |
Verkman AS, Edelman A, Amaral M, Mall MA, Beekman JM, Meiners T, Galietta LJ, Bear CE. Finding new drugs to enhance anion secretion in cystic fibrosis: Toward suitable systems for better drug screening. Report on the pre-conference meeting to the 12th ECFS Basic Science Conference, Albufeira, 25-28 March 2015. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 14: 700-5. PMID 26474804 DOI: 10.1016/J.Jcf.2015.10.001 |
0.444 |
|
| 2015 |
Premchandar A, Kupniewska A, Tarnowski K, Mücke N, Mauermann M, Kaus-Drobek M, Edelman A, Herrmann H, Dadlez M. Analysis of distinct molecular assembly complexes of keratin K8 and K18 by hydrogen-deuterium exchange. Journal of Structural Biology. 192: 426-40. PMID 26434626 DOI: 10.1016/J.Jsb.2015.10.001 |
0.303 |
|
| 2015 |
Chatin B, Mével M, Devallière J, Dallet L, Haudebourg T, Peuziat P, Colombani T, Berchel M, Lambert O, Edelman A, Pitard B. Liposome-based Formulation for Intracellular Delivery of Functional Proteins. Molecular Therapy. Nucleic Acids. 4: e244. PMID 26102064 DOI: 10.1038/Mtna.2015.17 |
0.33 |
|
| 2015 |
Carlon M, Vidovic D, Dekkers J, da Cunha MF, Hollenhorst M, Bijvelds M, Van den Haute C, Baekelandt V, de Jonge H, De Boeck K, Gijsbers R, Sermet-Gaudelus I, Edelman A, Beekman J, Debyser Z. WS01.1 rAAV2/5 encoding a truncated CFTR rescues the CF phenotype in intestinal organoids and a CF mouse model Journal of Cystic Fibrosis. 14: S1. DOI: 10.1016/S1569-1993(15)30001-1 |
0.442 |
|
| 2015 |
Pranke I, Tomaszewski K, Bitam S, Faure G, Chevet E, Sermet-Gaudelus I, Edelman A. The role of cytokeratin 8 in alpha-1-antitrypsin secretion and/or degradation Revue Des Maladies Respiratoires. 32: 319-320. DOI: 10.1016/j.rmr.2015.02.040 |
0.749 |
|
| 2014 |
Jeanson L, Guerrera IC, Papon JF, Chhuon C, Zadigue P, Prulière-Escabasse V, Amselem S, Escudier E, Coste A, Edelman A. Proteomic analysis of nasal epithelial cells from cystic fibrosis patients. Plos One. 9: e108671. PMID 25268127 DOI: 10.1371/Journal.Pone.0108671 |
0.342 |
|
| 2014 |
Edelman A, Sallenave JM. Cystic fibrosis, a multi-systemic mucosal disease: 25 years after the discovery of CFTR. The International Journal of Biochemistry & Cell Biology. 52: 2-4. PMID 24735713 DOI: 10.1016/J.Biocel.2014.04.006 |
0.337 |
|
| 2014 |
Edelman A. Cytoskeleton and CFTR. The International Journal of Biochemistry & Cell Biology. 52: 68-72. PMID 24685681 DOI: 10.1016/J.Biocel.2014.03.018 |
0.492 |
|
| 2014 |
Sermet-Gaudelus I, de Blic J, LeBourgeois M, Pranke I, Edelman A, Ramsey BW. Potentiating and correcting mutant CFTR in patients with cystic fibrosis European Respiratory Monograph. 64: 129-149. DOI: 10.1183/1025448X.10009513 |
0.416 |
|
| 2013 |
Bakouh N, Bienvenu T, Thomas A, Ehrenfeld J, Liote H, Roussel D, Duquesnoy P, Farman N, Viel M, Cherif-Zahar B, Amselem S, Taam RA, Edelman A, Planelles G, Sermet-Gaudelus I. Characterization of SLC26A9 in patients with CF-like lung disease. Human Mutation. 34: 1404-14. PMID 24272871 DOI: 10.1002/Humu.22382 |
0.345 |
|
| 2013 |
Odolczyk N, Fritsch J, Norez C, Servel N, da Cunha MF, Bitam S, Kupniewska A, Wiszniewski L, Colas J, Tarnowski K, Tondelier D, Roldan A, Saussereau EL, Melin-Heschel P, Wieczorek G, ... ... Edelman A, et al. Discovery of novel potent ΔF508-CFTR correctors that target the nucleotide binding domain. Embo Molecular Medicine. 5: 1484-501. PMID 23982976 DOI: 10.1002/emmm.201302699 |
0.813 |
|
| 2013 |
Saussereau EL, Roussel D, Diallo S, Debarbieux L, Edelman A, Sermet-Gaudelus I. Characterization of nasal potential difference in cftr knockout and F508del-CFTR mice. Plos One. 8: e57317. PMID 23505426 DOI: 10.1371/Journal.Pone.0057317 |
0.419 |
|
| 2013 |
Le Gars M, Descamps D, Roussel D, Saussereau E, Guillot L, Ruffin M, Tabary O, Hong SS, Boulanger P, Paulais M, Malleret L, Belaaouaj A, Edelman A, Huerre M, Chignard M, et al. Neutrophil elastase degrades cystic fibrosis transmembrane conductance regulator via calpains and disables channel function in vitro and in vivo. American Journal of Respiratory and Critical Care Medicine. 187: 170-9. PMID 23220915 DOI: 10.1164/rccm.201205-0875OC |
0.335 |
|
| 2012 |
Bakouh N, Chérif-Zahar B, Hulin P, Prié D, Friedlander G, Edelman A, Planelles G. Functional interaction between CFTR and the sodium-phosphate co-transport type 2a in Xenopus laevis oocytes. Plos One. 7: e34879. PMID 22514683 DOI: 10.1371/journal.pone.0034879 |
0.333 |
|
| 2012 |
Baudouin-Legros M, Colas J, Moriceau S, Kelly M, Planelles G, Edelman A, Ollero M. Long-term CFTR inhibition modulates 15d-prostaglandin J2 in human pulmonary cells. The International Journal of Biochemistry & Cell Biology. 44: 1009-18. PMID 22481026 DOI: 10.1016/J.Biocel.2012.03.010 |
0.37 |
|
| 2012 |
Jeanson L, Kelly M, Coste A, Guerrera IC, Fritsch J, Nguyen-Khoa T, Baudouin-Legros M, Papon JF, Zadigue P, Prulière-Escabasse V, Amselem S, Escudier E, Edelman A. Oxidative stress induces unfolding protein response and inflammation in nasal polyposis. Allergy. 67: 403-12. PMID 22188019 DOI: 10.1111/J.1398-9995.2011.02769.X |
0.313 |
|
| 2012 |
Colas J, Faure G, Saussereau E, Trudel S, Rabeh WM, Bitam S, Guerrera IC, Fritsch J, Sermet-Gaudelus I, Davezac N, Brouillard F, Lukacs GL, Herrmann H, Ollero M, Edelman A. Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect. Human Molecular Genetics. 21: 623-34. PMID 22038833 DOI: 10.1093/Hmg/Ddr496 |
0.79 |
|
| 2012 |
Siwiak M, Edelman A, Zielenkiewicz P. Structural models of CFTR-AMPK and CFTR-PKA interactions: R-domain flexibility is a key factor in CFTR regulation. Journal of Molecular Modeling. 18: 83-90. PMID 21455600 DOI: 10.1007/S00894-011-1029-0 |
0.412 |
|
| 2011 |
Ollero M, Guerrera IC, Astarita G, Piomelli D, Edelman A. New lipidomic approaches in cystic fibrosis. Methods in Molecular Biology (Clifton, N.J.). 742: 265-78. PMID 21547738 DOI: 10.1007/978-1-61779-120-8_16 |
0.341 |
|
| 2011 |
Guerrera IC, Ollero M, Vieu DL, Edelman A. Quantitative differential proteomics of cystic fibrosis cell models by SILAC (stable isotope labelling in cell culture). Methods in Molecular Biology (Clifton, N.J.). 742: 213-25. PMID 21547735 DOI: 10.1007/978-1-61779-120-8_13 |
0.379 |
|
| 2011 |
Kelly-Aubert M, Trudel S, Fritsch J, Nguyen-Khoa T, Baudouin-Legros M, Moriceau S, Jeanson L, Djouadi F, Matar C, Conti M, Ollero M, Brouillard F, Edelman A. GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models. Human Molecular Genetics. 20: 2745-59. PMID 21518732 DOI: 10.1093/Hmg/Ddr173 |
0.798 |
|
| 2011 |
Hamdaoui N, Baudoin-Legros M, Kelly M, Aissat A, Moriceau S, Vieu DL, Colas J, Fritsch J, Edelman A, Planelles G. Resveratrol rescues cAMP-dependent anionic transport in the cystic fibrosis pancreatic cell line CFPAC1. British Journal of Pharmacology. 163: 876-86. PMID 21366549 DOI: 10.1111/j.1476-5381.2011.01289.x |
0.4 |
|
| 2011 |
Ollero M, Astarita G, Guerrera IC, Sermet-Gaudelus I, Trudel S, Piomelli D, Edelman A. Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients. Journal of Lipid Research. 52: 1011-22. PMID 21335323 DOI: 10.1194/Jlr.P013722 |
0.638 |
|
| 2010 |
Dalli J, Rosignoli G, Hayhoe RP, Edelman A, Perretti M. CFTR inhibition provokes an inflammatory response associated with an imbalance of the annexin A1 pathway. The American Journal of Pathology. 177: 176-86. PMID 20489160 DOI: 10.2353/Ajpath.2010.091149 |
0.453 |
|
| 2010 |
Kelly M, Trudel S, Brouillard F, Bouillaud F, Colas J, Nguyen-Khoa T, Ollero M, Edelman A, Fritsch J. Cystic fibrosis transmembrane regulator inhibitors CFTR(inh)-172 and GlyH-101 target mitochondrial functions, independently of chloride channel inhibition. The Journal of Pharmacology and Experimental Therapeutics. 333: 60-9. PMID 20051483 DOI: 10.1124/Jpet.109.162032 |
0.709 |
|
| 2009 |
Guerrera IC, Astarita G, Jais JP, Sands D, Nowakowska A, Colas J, Sermet-Gaudelus I, Schuerenberg M, Piomelli D, Edelman A, Ollero M. A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patients. Plos One. 4: e7735. PMID 19893743 DOI: 10.1371/Journal.Pone.0007735 |
0.361 |
|
| 2009 |
Borot F, Vieu DL, Faure G, Fritsch J, Colas J, Moriceau S, Baudouin-Legros M, Brouillard F, Ayala-Sanmartin J, Touqui L, Chanson M, Edelman A, Ollero M. Eicosanoid release is increased by membrane destabilization and CFTR inhibition in Calu-3 cells. Plos One. 4: e7116. PMID 19847291 DOI: 10.1371/Journal.Pone.0007116 |
0.416 |
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| 2009 |
Trudel S, Kelly M, Fritsch J, Nguyen-Khoa T, Thérond P, Couturier M, Dadlez M, Debski J, Touqui L, Vallée B, Ollero M, Edelman A, Brouillard F. Peroxiredoxin 6 fails to limit phospholipid peroxidation in lung from Cftr-knockout mice subjected to oxidative challenge. Plos One. 4: e6075. PMID 19562038 DOI: 10.1371/Journal.Pone.0006075 |
0.69 |
|
| 2009 |
Trudel S, Kelly M, Thérond P, Nguyen-Khoa T, Dadlez M, Ollero M, Roussel D, Fritsch J, Edelman A, Brouillard F. Evaluation of oxidant and antioxidant status in CFTR-KO mice: role of Peroxiredoxin 6 Journal of Cystic Fibrosis. 8: S53. DOI: 10.1016/S1569-1993(09)60212-5 |
0.633 |
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| 2009 |
Kelly M, Trudel S, Nguyen-Khoa T, Fritsch J, Djouadi F, Edelman A, Brouillard F. Mitochondrial glutathione and decreased complex I activity in cystic fibrosis models Journal of Cystic Fibrosis. 8: S23. DOI: 10.1016/S1569-1993(09)60097-7 |
0.67 |
|
| 2009 |
Jeanson L, Guerrera C, Baudouin-Legros M, Amselem S, Coste A, Escudier E, Edelman A. Expression of Unfolded Protein Response (UPR) protein markers are increased in primary and cystic fibrosis (CF) nasal polyposis (NP) Journal of Cystic Fibrosis. 8: S22. DOI: 10.1016/S1569-1993(09)60090-4 |
0.407 |
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| 2009 |
Baudouin-Legros M, Kelly M, Ollero M, Edelman A. Pharmacological inhibition of CFTR modifies cyclooxygenase-1 and -2 expression and PGD2 production in Calu-3 cells Journal of Cystic Fibrosis. 8: S21. DOI: 10.1016/S1569-1993(09)60089-8 |
0.323 |
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| 2009 |
Colas J, Faure G, Trudel S, Fritsch J, Guerrera C, Davezac N, Brouillard F, Herrmann H, Ollero M, Edelman A. Increased interaction of F508del-CFTR with K8/K18 cytokeratin network by direct binding of K8 to NBD1 Journal of Cystic Fibrosis. 8: S21. DOI: 10.1016/S1569-1993(09)60087-4 |
0.636 |
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| 2009 |
Hamdaoui N, Vieu D, Baudouin-Legros M, Edelman A, Planelles G. Estrogen and phytoestrogens increase the CFTR and F508del CFTR expression and function Journal of Cystic Fibrosis. 8: S18. DOI: 10.1016/S1569-1993(09)60077-1 |
0.368 |
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| 2009 |
Guerrera C, Colas J, Sands D, Vieu D, Sermet-Gaudelus I, Astarita G, Piomelli D, Edelman A, Ollero M. Revealing potential plasma lipid biomarkers of cystic fibrosis by mass spectrometry Journal of Cystic Fibrosis. 8: S9. DOI: 10.1016/S1569-1993(09)60041-2 |
0.327 |
|
| 2008 |
Baudouin-Legros M, Hamdaoui N, Borot F, Fritsch J, Ollero M, Planelles G, Edelman A. Control of basal CFTR gene expression by bicarbonate-sensitive adenylyl cyclase in human pulmonary cells. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 21: 75-86. PMID 18209474 DOI: 10.1159/000113749 |
0.337 |
|
| 2008 |
Zoonens M, Bensalem N, Masscheleyn S, Mozo J, Vallée B, Brouillard F, Trudel S, Ricquier D, Edelman A, Guerrera IC, Miroux B. S16.5 High sensitivity identification of membrane proteins by MALDI TOF-mass spectrometry using polystyrene beads Biochimica Et Biophysica Acta. 1777. DOI: 10.1016/J.Bbabio.2008.05.420 |
0.761 |
|
| 2007 |
Edelman A, Sermet-Gaudelus I, Rousset JP. Genetic testing to provide targeted treatment for cystic fibrosis patients. Pharmacogenomics. 8: 1101-4. PMID 17924824 DOI: 10.2217/14622416.8.9.1101 |
0.314 |
|
| 2007 |
Sermet-Gaudelus I, Renouil M, Fajac A, Bidou L, Parbaille B, Pierrot S, Davy N, Bismuth E, Reinert P, Lenoir G, Lesure JF, Rousset JP, Edelman A. In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: A pilot study Bmc Medicine. 5. PMID 17394637 DOI: 10.1186/1741-7015-5-5 |
0.321 |
|
| 2007 |
Bensalem N, Masscheleyn S, Mozo J, Vallée B, Brouillard F, Trudel S, Ricquier D, Edelman A, Guerrera IC, Miroux B. High sensitivity identification of membrane proteins by MALDI TOF-MASS spectrometry using polystyrene beads. Journal of Proteome Research. 6: 1595-602. PMID 17355127 DOI: 10.1021/Pr0606272 |
0.772 |
|
| 2007 |
Hinzpeter A, Fritsch J, Borot F, Trudel S, Vieu DL, Brouillard F, Baudouin-Legros M, Clain J, Edelman A, Ollero M. Membrane cholesterol content modulates ClC-2 gating and sensitivity to oxidative stress. The Journal of Biological Chemistry. 282: 2423-32. PMID 17110372 DOI: 10.1074/Jbc.M608251200 |
0.763 |
|
| 2006 |
Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A. The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening. Bmc Pediatrics. 6: 25. PMID 17018149 DOI: 10.1186/1471-2431-6-25 |
0.338 |
|
| 2006 |
Ollero M, Brouillard F, Edelman A. Cystic fibrosis enters the proteomics scene: new answers to old questions. Proteomics. 6: 4084-99. PMID 16791827 DOI: 10.1002/pmic.200600028 |
0.346 |
|
| 2006 |
Lipecka J, Norez C, Bensalem N, Baudouin-Legros M, Planelles G, Becq F, Edelman A, Davezac N. Rescue of DeltaF508-CFTR (cystic fibrosis transmembrane conductance regulator) by curcumin: involvement of the keratin 18 network. The Journal of Pharmacology and Experimental Therapeutics. 317: 500-5. PMID 16424149 DOI: 10.1124/Jpet.105.097667 |
0.821 |
|
| 2006 |
Hinzpeter A, Lipecka J, Brouillard F, Baudoin-Legros M, Dadlez M, Edelman A, Fritsch J. Association between Hsp90 and the ClC-2 chloride channel upregulates channel function. American Journal of Physiology. Cell Physiology. 290: C45-56. PMID 16049054 DOI: 10.1152/Ajpcell.00209.2005 |
0.683 |
|
| 2006 |
Moriceau S, Brouillard E, Tondeher D, Sermet-Gaudelus I, DeVillartay P, Lenoir G, Edelman A, Witko-Sarsat V. 171 Investigation of neutrophil apoptosis in Cystic Fibrosis children using a proteomic approach Journal of Cystic Fibrosis. 5. DOI: 10.1016/S1569-1993(06)80153-0 |
0.302 |
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| 2006 |
Lipecka J, Norez C, Bensalem N, Baudouin-Legros M, Planelles G, Becq E, Edelman A, Davezac N. 28 Curcumin rescues deltaF508-CFTR via the keratin 18 network Journal of Cystic Fibrosis. 5: S6. DOI: 10.1016/S1569-1993(06)80025-1 |
0.757 |
|
| 2005 |
Brouillard F, Bensalem N, Hinzpeter A, Tondelier D, Trudel S, Gruber AD, Ollero M, Edelman A. Blue native/SDS-PAGE analysis reveals reduced expression of the mClCA3 protein in cystic fibrosis knock-out mice. Molecular & Cellular Proteomics : McP. 4: 1762-75. PMID 16099848 DOI: 10.1074/Mcp.M500098-Mcp200 |
0.805 |
|
| 2005 |
Bensalem N, Ventura AP, Vallée B, Lipecka J, Tondelier D, Davezac N, Dos Santos A, Perretti M, Fajac A, Sermet-Gaudelus I, Renouil M, Lesure JF, Halgand F, Laprévote O, Edelman A. Down-regulation of the anti-inflammatory protein annexin A1 in cystic fibrosis knock-out mice and patients. Molecular & Cellular Proteomics : McP. 4: 1591-601. PMID 16014420 DOI: 10.1074/Mcp.M500019-Mcp200 |
0.817 |
|
| 2005 |
Baudouin-Legros M, Hinzpeter A, Jaulmes A, Brouillard F, Costes B, Fanen P, Edelman A. Cell-specific posttranscriptional regulation of CFTR gene expression via influence of MAPK cascades on 3'UTR part of transcripts. American Journal of Physiology. Cell Physiology. 289: C1240-50. PMID 15944206 DOI: 10.1152/Ajpcell.00595.2004 |
0.66 |
|
| 2005 |
Flis K, Hinzpeter A, Edelman A, Kurlandzka A. The functioning of mammalian ClC-2 chloride channel in Saccharomyces cerevisiae cells requires an increased level of Kha1p. The Biochemical Journal. 390: 655-64. PMID 15926887 DOI: 10.1042/Bj20050480 |
0.706 |
|
| 2005 |
Clain J, Lehmann-Che J, Duguépéroux I, Arous N, Girodon E, Legendre M, Goossens M, Edelman A, de Braekeleer M, Teulon J, Fanen P. Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype. Human Mutation. 25: 360-71. PMID 15776432 DOI: 10.1002/Humu.20156 |
0.325 |
|
| 2005 |
Clain J, Lehmann-Che J, Girodon E, Lipecka J, Edelman A, Goossens M, Fanen P. A neutral variant involved in a complex CFTR allele contributes to a severe cystic fibrosis phenotype. Human Genetics. 116: 454-60. PMID 15744523 DOI: 10.1007/s00439-004-1246-z |
0.306 |
|
| 2005 |
Sermet-Gaudelus I, Déchaux M, Vallée B, Fajac A, Girodon E, Nguyen-Khoa T, Marianovski R, Hurbain I, Bresson JL, Lenoir G, Edelman A. Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes. American Journal of Respiratory and Critical Care Medicine. 171: 1026-31. PMID 15709055 DOI: 10.1164/Rccm.200406-740Oc |
0.461 |
|
| 2005 |
Borot F, Hinzpeter A, Brouillard F, Bensalem N, Tondelier D, Fritsch J, Edelman A, Ollero M. 035 Localisation du CFTR dans les microdomaines lipidiques membranaires de cellules Calu3 Revue Des Maladies Respiratoires. 22: 861. DOI: 10.1016/S0761-8425(05)92447-9 |
0.629 |
|
| 2004 |
Davezac N, Tondelier D, Lipecka J, Fanen P, Demaugre F, Debski J, Dadlez M, Schrattenholz A, Cahill MA, Edelman A. Global proteomic approach unmasks involvement of keratins 8 and 18 in the delivery of cystic fibrosis transmembrane conductance regulator (CFTR)/deltaF508-CFTR to the plasma membrane. Proteomics. 4: 3833-44. PMID 15529338 DOI: 10.1002/pmic.200400850 |
0.391 |
|
| 2004 |
Schüler D, Sermet-Gaudelus I, Wilschanski M, Ballmann M, Dechaux M, Edelman A, Hug M, Leal T, Lebacq J, Lebecque P, Lenoir G, Stanke F, Wallemacq P, Tümmler B, Knowles MR. Basic protocol for transepithelial nasal potential difference measurements. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 3: 151-5. PMID 15463949 DOI: 10.1016/J.Jcf.2004.05.032 |
0.371 |
|
| 2004 |
Roxo-Rosa M, Davezac N, Bensalem N, Majumder M, Heda GD, Simas A, Penque D, Amaral MD, Lukacs GL, Edelman A. Proteomics techniques for cystic fibrosis research. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 3: 85-9. PMID 15463934 DOI: 10.1016/J.Jcf.2004.05.019 |
0.821 |
|
| 2004 |
Farinha CM, Penque D, Roxo-Rosa M, Lukacs G, Dormer R, McPherson M, Pereira M, Bot AG, Jorna H, Willemsen R, Dejonge H, Heda GD, Marino CR, Fanen P, Hinzpeter A, ... ... Edelman A, et al. Biochemical methods to assess CFTR expression and membrane localization. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 3: 73-7. PMID 15463932 DOI: 10.1016/J.Jcf.2004.05.017 |
0.678 |
|
| 2004 |
Mendes F, Doucet L, Hinzpeter A, Férec C, Lipecka J, Fritsch J, Edelman A, Jorna H, Willemsen R, Bot AG, De Jonge HR, Hinnrasky J, Castillon N, Taouil K, Puchelle E, et al. Immunohistochemistry of CFTR in native tissues and primary epithelial cell cultures. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 3: 37-41. PMID 15463923 DOI: 10.1016/J.Jcf.2004.05.008 |
0.659 |
|
| 2004 |
Edelman A, Amaral MD. General introduction to section C: Biochemistry and Biophysics of CFTR Journal of Cystic Fibrosis. 3: 67. DOI: 10.1016/J.Jcf.2004.05.015 |
0.376 |
|
| 2003 |
Hurbain I, Sermet-Gaudelus I, Vallee B, Feuillet MN, Lenoir G, Bernaudin JF, Edelman A, Fajac A. Evaluation of MRP1-5 gene expression in cystic fibrosis patients homozygous for the delta F508 mutation. Pediatric Research. 54: 627-34. PMID 12930913 DOI: 10.1203/01.PDR.0000090926.16166.3F |
0.358 |
|
| 2003 |
Baudouin-Legros M, Brouillard F, Tondelier D, Hinzpeter A, Edelman A. Effect of ouabain on CFTR gene expression in human Calu-3 cells. American Journal of Physiology. Cell Physiology. 284: C620-6. PMID 12556359 DOI: 10.1152/Ajpcell.00457.2002 |
0.674 |
|
| 2002 |
Sermet-Gaudelus I, Vallée B, Urbin I, Torossi T, Marianovski R, Fajac A, Feuillet MN, Bresson JL, Lenoir G, Bernaudin JF, Edelman A. Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation. Pediatric Research. 52: 628-35. PMID 12409506 DOI: 10.1203/00006450-200211000-00005 |
0.313 |
|
| 2002 |
Lipecka J, Bali M, Thomas A, Fanen P, Edelman A, Fritsch J. Distribution of ClC-2 chloride channel in rat and human epithelial tissues. American Journal of Physiology. Cell Physiology. 282: C805-16. PMID 11880269 DOI: 10.1152/ajpcell.00291.2001 |
0.539 |
|
| 2001 |
Bali M, Lipecka J, Edelman A, Fritsch J. Regulation of ClC-2 chloride channels in T84 cells by TGF-alpha. American Journal of Physiology. Cell Physiology. 280: C1588-98. PMID 11350754 DOI: 10.1152/AJPCELL.2001.280.6.C1588 |
0.512 |
|
| 2001 |
Clain J, Fritsch J, Lehmann-Che J, Bali M, Arous N, Goossens M, Edelman A, Fanen P. Two mild cystic fibrosis-associated mutations result in severe cystic fibrosis when combined in cis and reveal a residue important for cystic fibrosis transmembrane conductance regulator processing and function. The Journal of Biological Chemistry. 276: 9045-9. PMID 11118444 DOI: 10.1074/jbc.M008979200 |
0.622 |
|
| 2000 |
Costa de Beauregard MA, Edelman A, Chesnoy-Marchais D, Tondelier D, Lapillonne A, El Marjou F, Robine S, Louvard D. Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells. European Journal of Cell Biology. 79: 795-802. PMID 11139142 DOI: 10.1078/0171-9335-00116 |
0.375 |
|
| 1999 |
Fanen P, Clain J, Labarthe R, Hulin P, Girodon E, Pagesy P, Goossens M, Edelman A. Structure-function analysis of a double-mutant cystic fibrosis transmembrane conductance regulator protein occurring in disorders related to cystic fibrosis. Febs Letters. 452: 371-4. PMID 10386624 DOI: 10.1016/S0014-5793(99)00647-X |
0.367 |
|
| 1997 |
Fanen P, Labarthe R, Garnier F, Benharouga M, Goossens M, Edelman A. Cystic fibrosis phenotype associated with pancreatic insufficiency does not always reflect the cAMP-dependent chloride conductive pathway defect. Analysis of C225R-CFTR and R1066C-CFTR. The Journal of Biological Chemistry. 272: 30563-6. PMID 9374552 DOI: 10.1074/Jbc.272.48.30563 |
0.726 |
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