| Year |
Citation |
Score |
| 2024 |
Dodd DO, Mechaussier S, Yeyati PL, McPhie F, Anderson JR, Khoo CJ, Shoemark A, Gupta DK, Attard T, Zariwala MA, Legendre M, Bracht D, Wallmeier J, Gui M, Fassad MR, ... ... Escudier E, et al. Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules. Science (New York, N.Y.). 384: eadf5489. PMID 38662826 DOI: 10.1126/science.adf5489 |
0.546 |
|
| 2024 |
Thomas L, Cuisset L, Papon JF, Tamalet A, Pin I, Abou Taam R, Faucon C, Montantin G, Tissier S, Duquesnoy P, Dastot-Le Moal F, Copin B, Carion N, Louis B, Chantot-Bastaraud S, ... ... Escudier E, et al. Skewed X-chromosome inactivation drives the proportion of -defective airway motile cilia and variable expressivity in primary ciliary dyskinesia. Journal of Medical Genetics. PMID 38408845 DOI: 10.1136/jmg-2023-109700 |
0.769 |
|
| 2022 |
Alexandru M, de Boissieu P, Benoudiba F, Moustarhfir M, Kim S, Bequignon É, Honoré I, Garcia G, Mitri-Frangieh R, Legendre M, Crestani B, Taillé C, Escudier E, Maitre B, Papon JF, et al. Otological Manifestations in Adults with Primary Ciliary Dyskinesia: A Controlled Radio-Clinical Study. Journal of Clinical Medicine. 11. PMID 36079093 DOI: 10.3390/jcm11175163 |
0.59 |
|
| 2022 |
Legendre M, Thouvenin G, Taytard J, Baron M, Le Bourgeois M, Tamalet A, Mani R, Jouvion G, Amselem S, Escudier E, Beydon N. High Nasal Nitric Oxide, Cilia Analyses and Genotypes in a Retrospective Cohort of Children with Primary Ciliary Dyskinesia. Annals of the American Thoracic Society. PMID 35622418 DOI: 10.1513/AnnalsATS.202110-1175OC |
0.433 |
|
| 2022 |
Mabrouk I, Al-Harthi N, Mani R, Montantin G, Tissier S, Lagha R, Ben Abdallah F, Hassan MM, Alhomrani M, Gaber A, Alsanie WF, Ouali H, Jambi FA, Almaghamsi TM, Alqarni NA, ... ... Escudier E, et al. Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients. Journal of Human Genetics. PMID 35046476 DOI: 10.1038/s10038-021-01006-9 |
0.575 |
|
| 2021 |
Shoemark A, Rubbo B, Legendre M, Fassad MR, Haarman EG, Best S, Bon ICM, Brandsma J, Burgel PR, Carlsson G, Carr SB, Carroll M, Edwards M, Escudier E, Honoré I, et al. Topological data analysis reveals genotype-phenotype relationships in primary ciliary dyskinesia. The European Respiratory Journal. PMID 33479112 DOI: 10.1183/13993003.02359-2020 |
0.641 |
|
| 2020 |
Bequignon E, Mangin D, Bécaud J, Pasquier J, Angely C, Bottier M, Escudier E, Isabey D, Filoche M, Louis B, Papon JF, Coste A. Pathogenesis of chronic rhinosinusitis with nasal polyps: role of IL-6 in airway epithelial cell dysfunction. Journal of Translational Medicine. 18: 136. PMID 32209102 DOI: 10.1186/S12967-020-02309-9 |
0.723 |
|
| 2020 |
Goutaki M, Papon JF, Boon M, Casaulta C, Eber E, Escudier E, Halbeisen FS, Harris A, Hogg C, Honore I, Jung A, Karadag B, Koerner-Rettberg C, Legendre M, Maitre B, et al. Standardised clinical data from patients with primary ciliary dyskinesia: FOLLOW-PCD. Erj Open Research. 6. PMID 32055632 DOI: 10.1183/23120541.00237-2019 |
0.569 |
|
| 2020 |
Thomas L, Bouhouche K, Whitfield M, Thouvenin G, Coste A, Louis B, Szymanski C, Bequignon E, Papon JF, Castelli M, Lemullois M, Dhalluin X, Drouin-Garraud V, Montantin G, Tissier S, ... ... Escudier E, et al. TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella. American Journal of Human Genetics. PMID 31978331 DOI: 10.1016/J.Ajhg.2019.12.010 |
0.821 |
|
| 2019 |
Blanchon S, Legendre M, Bottier M, Tamalet A, Montantin G, Collot N, Faucon C, Dastot F, Copin B, Clement A, Filoche M, Coste A, Amselem S, Escudier E, Papon JF, et al. Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia. Journal of Medical Genetics. PMID 31772028 DOI: 10.1136/Jmedgenet-2019-106424 |
0.751 |
|
| 2019 |
Bequignon E, Dupuy L, Escabasse V, Zerah-Lancner F, Bassinet L, Honoré I, Legendre M, Devars du Mayne M, Crestani B, Escudier E, Coste A, Papon JF, Maître B. Follow-Up and Management of Chronic Rhinosinusitis in Adults with Primary Ciliary Dyskinesia: Review and Experience of Our Reference Centers. Journal of Clinical Medicine. 8. PMID 31546861 DOI: 10.3390/Jcm8091495 |
0.713 |
|
| 2019 |
Mani R, Belkacem S, Soua Z, Chantot S, Montantin G, Tissier S, Copin B, Bouguila J, Le Gouard NR, Boughamoura L, Ben Ameur S, Hachicha M, Boussoffara R, Boussetta K, Hammouda S, ... ... Escudier E, et al. Primary ciliary dyskinesia gene contribution in Tunisia-identification of a major Mediterranean allele. Human Mutation. PMID 31469207 DOI: 10.1002/Humu.23905 |
0.564 |
|
| 2019 |
Whitfield M, Thomas L, Bequignon E, Schmitt A, Stouvenel L, Montantin G, Tissier S, Duquesnoy P, Copin B, Chantot S, Dastot F, Faucon C, Barbotin AL, Loyens A, Siffroi JP, ... ... Escudier E, et al. Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia. American Journal of Human Genetics. PMID 31178125 DOI: 10.1016/J.Ajhg.2019.04.015 |
0.756 |
|
| 2019 |
Bequignon E, Dupuy L, Zerah-Lancner F, Bassinet L, Honoré I, Legendre M, Devars du Mayne M, Escabasse V, Crestani B, Maître B, Escudier E, Coste A, Papon JF. Critical Evaluation of Sinonasal Disease in 64 Adults with Primary Ciliary Dyskinesia. Journal of Clinical Medicine. 8. PMID 31067752 DOI: 10.3390/Jcm8050619 |
0.704 |
|
| 2019 |
Bequignon E, Dhommée C, Angely C, Thomas L, Bottier M, Escudier E, Isabey D, Coste A, Louis B, Papon JF, Gouilleux-Gruart V. FcRn-Dependent Transcytosis of Monoclonal Antibody in Human Nasal Epithelial Cells In Vitro: A Prerequisite for a New Delivery Route for Therapy? International Journal of Molecular Sciences. 20. PMID 30893823 DOI: 10.3390/Ijms20061379 |
0.725 |
|
| 2019 |
Bustamante-Marin XM, Yin WN, Sears PR, Werner ME, Brotslaw EJ, Mitchell BJ, Jania CM, Zeman KL, Rogers TD, Herring LE, Refabért L, Thomas L, Amselem S, Escudier E, Legendre M, et al. Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance. American Journal of Human Genetics. PMID 30665704 DOI: 10.1016/J.Ajhg.2018.12.009 |
0.613 |
|
| 2018 |
Lorès P, Coutton C, Khouri EE, Stouvenel L, Givelet M, Thomas L, Rode B, Schmitt A, Louis B, Sakheli Z, Chaudhry M, Fernandez-Gonzales A, Mitsialis A, Dacheux D, Wolf JP, ... ... Escudier E, et al. Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia. Human Molecular Genetics. PMID 30517620 DOI: 10.1093/hmg/ddy368 |
0.702 |
|
| 2018 |
Fassad MR, Shoemark A, Legendre M, Hirst RA, Koll F, le Borgne P, Louis B, Daudvohra F, Patel MP, Thomas L, Dixon M, Burgoyne T, Hayes J, Nicholson AG, Cullup T, ... ... Escudier E, et al. Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus. American Journal of Human Genetics. PMID 30471717 DOI: 10.1016/J.Ajhg.2018.10.016 |
0.749 |
|
| 2018 |
Lorès P, Coutton C, El Khouri E, Stouvenel L, Givelet M, Thomas L, Rode B, Schmitt A, Louis B, Sakheli Z, Chaudhry M, Fernandez-Gonzales A, Mitsialis A, Dacheux D, Wolf JP, ... ... Escudier E, et al. Homozygous missense mutation L673P in Adenylate Kinase 7 (AK7) leads to primary male infertility and Multiple Morphological Anomalies of the Flagella but not to Primary Ciliary Dyskinesia. Human Molecular Genetics. PMID 29365104 DOI: 10.1093/Hmg/Ddy034 |
0.771 |
|
| 2017 |
Vanaken GJ, Bassinet L, Boon M, Mani R, Honoré I, Papon JF, Cuppens H, Jaspers M, Laurent N, Coste A, Escudier E, Amselem S, Maitre B, Legendre M, Christin-Maitre S. Infertility in an adult cohort with primary ciliary dyskinesia: phenotype-gene association. The European Respiratory Journal. 50. PMID 29122913 DOI: 10.1183/13993003.00314-2017 |
0.775 |
|
| 2017 |
Ryan R, Failler M, Reilly ML, Garfa-Traore M, Delous M, Filhol E, Reboul T, Bole-Feysot C, Nitschké P, Baudouin V, Amselem S, Escudier E, Legendre M, Benmerah A, Saunier S. Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathies. Human Molecular Genetics. PMID 29121203 DOI: 10.1093/Hmg/Ddx396 |
0.667 |
|
| 2017 |
Bottier M, Blanchon S, Pelle G, Bequignon E, Isabey D, Coste A, Escudier E, Grotberg JB, Papon JF, Filoche M, Louis B. A new index for characterizing micro-bead motion in a flow induced by ciliary beating: Part I, experimental analysis. Plos Computational Biology. 13: e1005605. PMID 28708889 DOI: 10.1371/Journal.Pcbi.1005605 |
0.691 |
|
| 2017 |
Olcese C, Patel MP, Shoemark A, Kiviluoto S, Legendre M, Williams HJ, Vaughan CK, Hayward J, Goldenberg A, Emes RD, Munye MM, Dyer L, Cahill T, Bevillard J, Gehrig C, ... ... Escudier E, et al. X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3. Nature Communications. 8: 14279. PMID 28176794 DOI: 10.1038/Ncomms14279 |
0.701 |
|
| 2017 |
Frija-Masson J, Bassinet L, Honoré I, Dufeu N, Housset B, Coste A, Papon JF, Escudier E, Burgel PR, Maître B. Clinical characteristics, functional respiratory decline and follow-up in adult patients with primary ciliary dyskinesia. Thorax. 72: 154-160. PMID 27382041 DOI: 10.1136/Thoraxjnl-2015-207891 |
0.72 |
|
| 2017 |
Blanchon S, Legendre M, Bottier M, Tamalet A, Montantin G, Collot N, Tissier S, Faucon C, Dastot F, Copin B, Clement A, Coste A, Amselem S, Escudier E, Papon J, et al. L’analyse quantitative du mouvement ciliaire permet d’identifier le phénotype ultra-structural des dyskinésies ciliaires primitives Revue Des Maladies Respiratoires. 34: A34. DOI: 10.1016/J.Rmr.2016.10.069 |
0.658 |
|
| 2016 |
Lucas JS, Barbato A, Collins SA, Goutaki M, Behan L, Caudri D, Dell S, Eber E, Escudier E, Hirst RA, Hogg C, Jorissen M, Latzin P, Legendre M, Leigh MW, et al. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia. The European Respiratory Journal. PMID 27836958 DOI: 10.1183/13993003.01090-2016 |
0.564 |
|
| 2016 |
El Khouri E, Thomas L, Jeanson L, Bequignon E, Vallette B, Duquesnoy P, Montantin G, Copin B, Dastot-Le Moal F, Blanchon S, Papon JF, Lorès P, Yuan L, Collot N, Tissier S, ... ... Escudier E, et al. Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility. American Journal of Human Genetics. 99: 489-500. PMID 27486783 DOI: 10.1016/J.Ajhg.2016.06.022 |
0.811 |
|
| 2016 |
Jeanson L, Thomas L, Copin B, Coste A, Sermet-Gaudelus I, Moal FD, Duquesnoy P, Montantin G, Collot N, Tissier S, Papon JF, Clement A, Louis B, Escudier E, Amselem S, et al. Mutations in GAS8, A Gene Encoding A Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia With Axonemal Disorganization. Human Mutation. PMID 27120127 DOI: 10.1002/Humu.23005 |
0.814 |
|
| 2016 |
Blanchon S, Legendre M, Bottier M, Tamalet A, Montantin G, Collot N, Tessier S, Escudier E, Papon J, Louis B. Objective videomicroscopy parameters correlate ciliary beating to ultrastructure in primary ciliary dyskinesia European Respiratory Journal. 48. DOI: 10.1183/13993003.Congress-2016.Pa1542 |
0.679 |
|
| 2016 |
Blanchon S, Legendre M, Coste A, Beydon N, Amselem S, Escudier E, Papon J. Dyskinésies ciliaires primitives : actualités diagnostiques Revue FrançAise D'Allergologie. 56: 209-211. DOI: 10.1016/J.Reval.2016.01.014 |
0.628 |
|
| 2015 |
Jeanson L, Copin B, Papon JF, Dastot-Le Moal F, Duquesnoy P, Montantin G, Cadranel J, Corvol H, Coste A, Désir J, Souayah A, Kott E, Collot N, Tissier S, Louis B, ... ... Escudier E, et al. RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes. American Journal of Human Genetics. 97: 153-62. PMID 26073779 DOI: 10.1016/J.Ajhg.2015.05.004 |
0.8 |
|
| 2015 |
Philippe C, Boussadia Y, Prulière-Escabasse V, Papon JF, Clérici C, Isabey D, Coste A, Escudier E, d'Ortho MP. Airway cell involvement in intermittent hypoxia-induced airway inflammation. Sleep & Breathing = Schlaf & Atmung. 19: 297-306. PMID 24993984 DOI: 10.1007/S11325-014-1019-4 |
0.624 |
|
| 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 |
0.769 |
|
| 2013 |
Kott E, Legendre M, Copin B, Papon JF, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, ... ... Escudier E, et al. Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects. American Journal of Human Genetics. 93: 561-70. PMID 23993197 DOI: 10.1016/J.Ajhg.2013.07.013 |
0.809 |
|
| 2013 |
Vallet C, Escudier E, Roudot-Thoraval F, Blanchon S, Fauroux B, Beydon N, Boulé M, Vojtek AM, Amselem S, Clément A, Tamalet A. Primary ciliary dyskinesia presentation in 60 children according to ciliary ultrastructure. European Journal of Pediatrics. 172: 1053-60. PMID 23571820 DOI: 10.1007/S00431-013-1996-5 |
0.555 |
|
| 2013 |
Martin C, Coolen N, Wu Y, Thévenot G, Touqui L, Prulière-Escabasse V, Papon JF, Coste A, Escudier E, Dusser DJ, Fajac I, Burgel PR. CFTR dysfunction induces vascular endothelial growth factor synthesis in airway epithelium. The European Respiratory Journal. 42: 1553-62. PMID 23520314 DOI: 10.1183/09031936.00164212 |
0.708 |
|
| 2012 |
Kott E, Duquesnoy P, Copin B, Legendre M, Dastot-Le Moal F, Montantin G, Jeanson L, Tamalet A, Papon JF, Siffroi JP, Rives N, Mitchell V, de Blic J, Coste A, Clement A, ... ... Escudier E, et al. Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia. American Journal of Human Genetics. 91: 958-64. PMID 23122589 DOI: 10.1016/J.Ajhg.2012.10.003 |
0.804 |
|
| 2012 |
Papon JF, Bassinet L, Cariou-Patron G, Zerah-Lancner F, Vojtek AM, Blanchon S, Crestani B, Amselem S, Coste A, Housset B, Escudier E, Louis B. Quantitative analysis of ciliary beating in primary ciliary dyskinesia: a pilot study. Orphanet Journal of Rare Diseases. 7: 78. PMID 23057704 DOI: 10.1186/2046-2530-1-S1-O3 |
0.752 |
|
| 2012 |
Blanchon S, Legendre M, Copin B, Duquesnoy P, Montantin G, Kott E, Dastot F, Jeanson L, Cachanado M, Rousseau A, Papon JF, Beydon N, Brouard J, Crestani B, Deschildre A, ... ... Escudier E, et al. Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia. Journal of Medical Genetics. 49: 410-6. PMID 22693285 DOI: 10.1186/2046-2530-1-S1-P91 |
0.797 |
|
| 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 |
0.694 |
|
| 2012 |
Blanchon S, Bassinet L, Beydon N, Clément A, Escudier E, Papon J, Tamalet A. Diagnostic algorithm for Primary Ciliary Dyskinesia: recommendations of the French National Centre for Rare Respiratory Diseases Cilia. 1: 5. DOI: 10.1186/2046-2530-1-S1-P5 |
0.627 |
|
| 2012 |
Blanchon S, Bassinet L, Clément A, Coste A, Escudier E, Thumerelle C. Diagnostic of Primary Ciliary Dyskinesia: guidelines to obtain appropriate ciliate cell samples Cilia. 1: 4. DOI: 10.1186/2046-2530-1-S1-P4 |
0.6 |
|
| 2011 |
Merveille AC, Davis EE, Becker-Heck A, Legendre M, Amirav I, Bataille G, Belmont J, Beydon N, Billen F, Clément A, Clercx C, Coste A, Crosbie R, de Blic J, Deleuze S, ... ... Escudier E, et al. CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nature Genetics. 43: 72-8. PMID 21131972 DOI: 10.1038/Ng.726 |
0.811 |
|
| 2010 |
Prulière-Escabasse V, Coste A, Chauvin P, Fauroux B, Tamalet A, Garabedian EN, Escudier E, Roger G. Otologic features in children with primary ciliary dyskinesia. Archives of Otolaryngology--Head & Neck Surgery. 136: 1121-6. PMID 21079168 DOI: 10.1001/Archoto.2010.183 |
0.523 |
|
| 2010 |
Prulière-Escabasse V, Clerici C, Vuagniaux G, Coste A, Escudier E, Planès C. Effect of neutrophil elastase and its inhibitor EPI-hNE4 on transepithelial sodium transport across normal and cystic fibrosis human nasal epithelial cells. Respiratory Research. 11: 141. PMID 20932306 DOI: 10.1186/1465-9921-11-141 |
0.599 |
|
| 2010 |
Prulière-Escabasse V, Gomez-Roca C, Escudier E, Coste A, Besse B, Massard C, Soria JC. Rhinitis in patients treated with a combination of an mTOR inhibitor and an EGFR inhibitor. Onkologie. 33: 401-2. PMID 20631489 DOI: 10.1159/000315757 |
0.459 |
|
| 2009 |
Duquesnoy P, Escudier E, Vincensini L, Freshour J, Bridoux AM, Coste A, Deschildre A, de Blic J, Legendre M, Montantin G, Tenreiro H, Vojtek AM, Loussert C, Clément A, Escalier D, et al. Loss-of-function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia. American Journal of Human Genetics. 85: 890-6. PMID 19944405 DOI: 10.1016/J.Ajhg.2009.11.008 |
0.752 |
|
| 2009 |
Papon JF, Coste A, Roudot-Thoraval F, Boucherat M, Roger G, Tamalet A, Vojtek AM, Amselem S, Escudier E. A 20-year experience of electron microscopy in the diagnosis of primary ciliary dyskinesia. The European Respiratory Journal. 35: 1057-63. PMID 19840971 DOI: 10.1183/09031936.00046209 |
0.702 |
|
| 2009 |
Mougou-Zerelli S, Thomas S, Szenker E, Audollent S, Elkhartoufi N, Babarit C, Romano S, Salomon R, Amiel J, Esculpavit C, Gonzales M, Escudier E, Leheup B, Loget P, Odent S, et al. CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation. Human Mutation. 30: 1574-82. PMID 19777577 DOI: 10.1002/Humu.21116 |
0.309 |
|
| 2009 |
Escudier E, Duquesnoy P, Papon JF, Amselem S. Ciliary defects and genetics of primary ciliary dyskinesia. Paediatric Respiratory Reviews. 10: 51-4. PMID 19410201 DOI: 10.1016/J.Prrv.2009.02.001 |
0.757 |
|
| 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 |
0.529 |
|
| 2008 |
Botterel F, Gross K, Ibrahim-Granet O, Khoufache K, Escabasse V, Coste A, Cordonnier C, Escudier E, Bretagne S. Phagocytosis of Aspergillus fumigatus conidia by primary nasal epithelial cells in vitro. Bmc Microbiology. 8: 97. PMID 18564423 DOI: 10.1186/1471-2180-8-97 |
0.564 |
|
| 2007 |
Prulière-Escabasse V, Planès C, Escudier E, Fanen P, Coste A, Clerici C. Modulation of epithelial sodium channel trafficking and function by sodium 4-phenylbutyrate in human nasal epithelial cells. The Journal of Biological Chemistry. 282: 34048-57. PMID 17890229 DOI: 10.1074/Jbc.M702384200 |
0.529 |
|
| 2007 |
Zhang Z, Zariwala MA, Mahadevan MM, Caballero-Campo P, Shen X, Escudier E, Duriez B, Bridoux AM, Leigh M, Gerton GL, Kennedy M, Amselem S, Knowles MR, Strauss JF. A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axoneme Biology of Reproduction. 77: 864-871. PMID 17699735 DOI: 10.1095/Biolreprod.107.063206 |
0.555 |
|
| 2007 |
Duriez B, Duquesnoy P, Escudier E, Bridoux AM, Escalier D, Rayet I, Marcos E, Vojtek AM, Bercher JF, Amselem S. A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia. Proceedings of the National Academy of Sciences of the United States of America. 104: 3336-41. PMID 17360648 DOI: 10.1073/Pnas.0611405104 |
0.597 |
|
| 2007 |
Lazard DS, Prulière-Escabasse V, Papon JF, Escudier E, Coste A. [Injury and epithelial wound healing: a pathophysiologic hypothesis for nasal and sinus polyposis]. Presse Medicale (Paris, France : 1983). 36: 1104-8. PMID 17306500 DOI: 10.1016/J.Lpm.2007.01.021 |
0.71 |
|
| 2007 |
Khoufache K, Puel O, Loiseau N, Delaforge M, Rivollet D, Coste A, Cordonnier C, Escudier E, Botterel F, Bretagne S. Verruculogen associated with Aspergillus fumigatus hyphae and conidia modifies the electrophysiological properties of human nasal epithelial cells. Bmc Microbiology. 7: 5. PMID 17244350 DOI: 10.1186/1471-2180-7-5 |
0.611 |
|
| 2007 |
Martin C, Shao M, Danel S, Escudier E, Coste A, Fajac I, Dusser D, Nadel J, Burgel P. 071 Les facteurs de virulence de Pseudomonas aeruginosa (PA) induisent la synthèse de VEGF-A par activation d’une cascade de mécanismes à la surface de l’épithélium respiratoire Revue Des Maladies Respiratoires. 24: 1226. DOI: 10.1016/S0761-8425(07)74362-0 |
0.518 |
|
| 2006 |
Zariwala MA, Leigh MW, Ceppa F, Kennedy MP, Noone PG, Carson JL, Hazucha MJ, Lori A, Horvath J, Olbrich H, Loges NT, Bridoux AM, Pennarun G, Duriez B, Escudier E, et al. Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation. American Journal of Respiratory and Critical Care Medicine. 174: 858-66. PMID 16858015 DOI: 10.1164/Rccm.200603-370Oc |
0.573 |
|
| 2006 |
Lechapt-Zalcman E, Prulière-Escabasse V, Advenier D, Galiacy S, Charrière-Bertrand C, Coste A, Harf A, d'Ortho MP, Escudier E. Transforming growth factor-beta1 increases airway wound repair via MMP-2 upregulation: a new pathway for epithelial wound repair? American Journal of Physiology. Lung Cellular and Molecular Physiology. 290: L1277-82. PMID 16414983 DOI: 10.1152/Ajplung.00149.2005 |
0.701 |
|
| 2006 |
Mahut B, Escudier E, de Blic J, Zerah-Lancner F, Coste A, Harf A, Delclaux C. Impairment of nitric oxide output of conducting airways in primary ciliary dyskinesia. Pediatric Pulmonology. 41: 158-63. PMID 16353174 DOI: 10.1002/Ppul.20329 |
0.511 |
|
| 2006 |
Prulière-Escabasse V, Planès C, Fanen P, Coste S, Escudier E, Clerici C. 31 Sodium 4-phenylbutyrate increases CFTR function but also enhances ENaC expression and function in human nasal epithelial cells Journal of Cystic Fibrosis. 5: S7. DOI: 10.1016/S1569-1993(06)80028-7 |
0.327 |
|
| 2006 |
Martin C, Danel S, Escudier E, Coste A, Dusser D, Fajac I, Burgel P. 120 Régulation de la synthèse de VEGF165 dans l’épithélium respiratoire par le LPS de Pseudomonas aeruginosa : Rôle du récepteur de l’EGF Revue Des Maladies Respiratoires. 23: 575. DOI: 10.1016/S0761-8425(06)71948-9 |
0.517 |
|
| 2006 |
Escudier E, Tamalet A, Prulière-Escabasse V, Roger G, Coste A. Primary ciliary dyskinesia Revue Francaise D'Allergologie Et D'Immunologie Clinique. 46: 530-537. DOI: 10.1016/j.allerg.2006.08.010 |
0.61 |
|
| 2005 |
Moore A, Escudier E, Roger G, Tamalet A, Pelosse B, Marlin S, Clément A, Geremek M, Delaisi B, Bridoux AM, Coste A, Witt M, Duriez B, Amselem S. RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa. Journal of Medical Genetics. 43: 326-33. PMID 16055928 DOI: 10.1136/Jmg.2005.034868 |
0.709 |
|
| 2005 |
Prulière-Escabasse V, Fanen P, Dazy AC, Lechapt-Zalcman E, Rideau D, Edelman A, Escudier E, Coste A. TGF-beta 1 downregulates CFTR expression and function in nasal polyps of non-CF patients. American Journal of Physiology. Lung Cellular and Molecular Physiology. 288: L77-83. PMID 15361357 DOI: 10.1152/Ajplung.00048.2004 |
0.726 |
|
| 2005 |
Moore A, Amselem S, Duriez B, Escudier E. [Molecular basis of the primary ciliary dyskinesias]. Revue Des Maladies Respiratoires. 21: 521-6. PMID 15292844 DOI: 10.1016/S0761-8425(04)71356-X |
0.575 |
|
| 2004 |
Escudier E, Roger G, Coste A. Nasal ciliary investigations for the diagnosis of primary ciliary dyskinesia in children Archives De Pediatrie. 11: 390-393. PMID 15051102 DOI: 10.1016/j.arcped.2003.11.030 |
0.571 |
|
| 2003 |
Botterel F, Cordonnier C, Barbier V, Wingerstmann L, Liance M, Coste A, Escudier E, Bretagne S. Aspergillus fumigatus causes in vitro electrophysiological and morphological modifications in human nasal epithelial cells. Histology and Histopathology. 17: 1095-101. PMID 12371137 DOI: 10.14670/Hh-17.1095 |
0.609 |
|
| 2002 |
Papon JF, Coste A, Gendron MC, Cordonnier C, Wingerstmann L, Peynègre R, Escudier E. HLA-DR and ICAM-1 expression and modulation in epithelial cells from nasal polyps. The Laryngoscope. 112: 2067-75. PMID 12439183 DOI: 10.1097/00005537-200211000-00030 |
0.714 |
|
| 2002 |
Escudier E, Couprie M, Duriez B, Roudot-Thoraval F, Millepied MC, Prulière-Escabasse V, Labatte L, Coste A. Computer-assisted analysis helps detect inner dynein arm abnormalities. American Journal of Respiratory and Critical Care Medicine. 166: 1257-62. PMID 12403696 DOI: 10.1164/Rccm.2111070 |
0.559 |
|
| 2002 |
Pennarun G, Bridoux AM, Escudier E, Dastot-Le Moal F, Cacheux V, Amselem S, Duriez B. Isolation and expression of the human hPF20 gene orthologous to Chlamydomonas PF20: evaluation as a candidate for axonemal defects of respiratory cilia and sperm flagella. American Journal of Respiratory Cell and Molecular Biology. 26: 362-70. PMID 11867345 DOI: 10.1165/Ajrcmb.26.3.4738 |
0.601 |
|
| 2001 |
Tamalet A, Clement A, Roudot-Thoraval F, Desmarquest P, Roger G, Boulé M, Millepied MC, Baculard TA, Escudier E. Abnormal central complex is a marker of severity in the presence of partial ciliary defect. Pediatrics. 108: E86. PMID 11694670 DOI: 10.1542/Peds.108.5.E86 |
0.376 |
|
| 2000 |
Pennarun G, Chapelin C, Escudier E, Bridoux AM, Dastot F, Cacheux V, Goossens M, Amselem S, Duriez B. The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia. Human Genetics. 107: 642-9. PMID 11153919 DOI: 10.1007/S004390000427 |
0.81 |
|
| 2000 |
Burgel PR, Escudier E, Coste A, Dao-Pick T, Ueki IF, Takeyama K, Shim JJ, Murr AH, Nadel JA. Relation of epidermal growth factor receptor expression to goblet cell hyperplasia in nasal polyps Journal of Allergy and Clinical Immunology. 106: 705-712. PMID 11031341 DOI: 10.1067/Mai.2000.109823 |
0.565 |
|
| 2000 |
Coste A, Brugel L, Maître B, Boussat S, Papon JF, Wingerstmann L, Peynègre R, Escudier E. Inflammatory cells as well as epithelial cells in nasal polyps express vascular endothelial growth factor. The European Respiratory Journal. 15: 367-72. PMID 10706506 DOI: 10.1034/J.1399-3003.2000.15B24.X |
0.504 |
|
| 1999 |
Pennarun G, Escudier E, Chapelin C, Bridoux AM, Cacheux V, Roger G, Clément A, Goossens M, Amselem S, Duriez B. Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. American Journal of Human Genetics. 65: 1508-19. PMID 10577904 DOI: 10.1086/302683 |
0.821 |
|
| 1999 |
Coste A, Lefaucheur JP, Wang QP, Lesprit E, Poron F, Peynegre R, Escudier E. Expression of the transforming growth factor beta isoforms in inflammatory cells of nasal polyps. Archives of Otolaryngology--Head & Neck Surgery. 124: 1361-6. PMID 9865759 DOI: 10.1001/Archotol.124.12.1361 |
0.479 |
|
| 1998 |
Dohrman A, Miyata S, Gallup M, Li JD, Chapelin C, Coste A, Escudier E, Nadel J, Basbaum C. Mucin gene (MUC 2 and MUC 5AC) upregulation by Gram-positive and Gram-negative bacteria. Biochimica Et Biophysica Acta. 1406: 251-9. PMID 9630659 DOI: 10.1016/S0925-4439(98)00010-6 |
0.779 |
|
| 1997 |
Chapelin C, Coste A, Reinert P, Boucherat M, Millepied MC, Poron F, Escudier E. Incidence of primary ciliary dyskinesia in children with recurrent respiratory diseases. The Annals of Otology, Rhinology, and Laryngology. 106: 854-8. PMID 9342982 DOI: 10.1177/000348949710601008 |
0.778 |
|
| 1997 |
Chapelin C, Duriez B, Magnino F, Goossens M, Escudier E, Amselem S. Isolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment. Febs Letters. 412: 325-30. PMID 9256245 DOI: 10.1016/S0014-5793(97)00800-4 |
0.776 |
|
| 1997 |
Calvet JH, Coste A, Levame M, Harf A, Macquin-Mavier I, Escudier E. Airway epithelial damage induced by sulfur mustard in guinea pigs, effects of glucocorticoids. Human & Experimental Toxicology. 15: 964-71. PMID 8981100 DOI: 10.1177/096032719601501204 |
0.565 |
|
| 1996 |
Chapelin C, Coste A, Gilain L, Poron F, Verra F, Escudier E. Modified epithelial cell distribution in chronic airways inflammation. The European Respiratory Journal. 9: 2474-8. PMID 8980956 DOI: 10.1183/09031936.96.09122474 |
0.781 |
|
| 1996 |
Coste A, Wang QP, Roudot-Thoraval F, Chapelin C, Bedbeder P, Poron F, Peynègre R, Escudier E. Epithelial cell proliferation in nasal polyps could be up-regulated by platelet-derived growth factor. The Laryngoscope. 106: 578-83. PMID 8628084 DOI: 10.1097/00005537-199605000-00011 |
0.767 |
|
| 1996 |
Coste A, Rateau JG, Roudot-Thoraval F, Chapelin C, Gilain L, Poron F, Peynegre R, Bernaudin JF, Escudier E. Increased epithelial cell proliferation in nasal polyps. Archives of Otolaryngology--Head & Neck Surgery. 122: 432-6. PMID 8600930 DOI: 10.1001/Archotol.1996.01890160072013 |
0.787 |
|
| 1994 |
Cordonnier C, Escudier E, Verra F, Brochard L, Bernaudin JF, Fleury-Feith J. Bronchoalveolar lavage during neutropenic episodes: diagnostic yield and cellular pattern. The European Respiratory Journal. 7: 114-20. PMID 8143809 DOI: 10.1183/09031936.94.07010114 |
0.316 |
|
| 1986 |
Escudier E, Fleury J, Cordonnier C, Vernant JP, Bernaudin JF. Large granular lymphocytes in bronchoalveolar lavage fluids from immunocompromised patients with cytomegalovirus pneumonitis. American Journal of Clinical Pathology. 86: 641-5. PMID 3022575 DOI: 10.1093/Ajcp/86.5.641 |
0.301 |
|
| Show low-probability matches. |