Torthaí cuardaigh - Alexandre Hinzpeter

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  1. 1
    Genetics of cystic fibrosis: CFTR mutation classifications toward genotype-based CF therapies

    Genetics of cystic fibrosis: CFTR mutation classifications toward genotype-based CF therapies de réir Pascale Fanen, Adeline Wohlhuter‐Haddad, Alexandre Hinzpeter

    Foilsithe / Cruthaithe 2014
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  2. 2
    Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine

    Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine de réir Iwona Pranke, Anita Golec, Alexandre Hinzpeter, Aleksander Edelman, Isabelle Sermet‐Gaudelus

    Foilsithe / Cruthaithe 2019
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  3. 3
    COMMD1-Mediated Ubiquitination Regulates CFTR Trafficking

    COMMD1-Mediated Ubiquitination Regulates CFTR Trafficking de réir Loïc Drévillon, Gaëlle Tanguy, Alexandre Hinzpeter, N. Arous, Alix de Becdelièvre, Abdel Aissat, Agathe Tarze, Michel Goossens, Pascale Fanen

    Foilsithe / Cruthaithe 2011
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    Artigo
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  4. 4
    Evidence for direct CFTR inhibition by CFTRinh-172 based on Arg347 mutagenesis

    Evidence for direct CFTR inhibition by CFTRinh-172 based on Arg347 mutagenesis de réir Emanuela Caci, Antonella Caputo, Alexandre Hinzpeter, N. Arous, Pascale Fanen, Nitin D. Sonawane, A. S. Verkman, Roberto Ravazzolo, Olga Zegarra‐Moran, Luis J. V. Galietta

    Foilsithe / Cruthaithe 2008
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    Artigo
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  5. 5
    Modulators of CFTR. Updates on clinical development and future directions

    Modulators of CFTR. Updates on clinical development and future directions de réir Emmanuelle Bardin, Alexandra Pastor, Michaëla Semeraro, Anita Golec, Kate Hayes, B. Chevalier, Farouk Berhal, Guillaume Prestat, Alexandre Hinzpeter, Christine Gravier‐Pelletier, Iwona Pranke, Isabelle Sermet‐Gaudelus

    Foilsithe / Cruthaithe 2021
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  6. 6
    Pharmacological chaperones improve intra-domain stability and inter-domain assembly via distinct binding sites to rescue misfolded CFTR

    Pharmacological chaperones improve intra-domain stability and inter-domain assembly via distinct binding sites to rescue misfolded CFTR de réir Nesrine Baatallah, Ahmad Elbahnsi, Jean‐Paul Mornon, B. Chevalier, Iwona Pranke, Nathalie Servel, Renaud Zelli, Jean‐Luc Décout, Aleksander Edelman, Isabelle Sermet‐Gaudelus, Isabelle Callebaut, Alexandre Hinzpeter

    Foilsithe / Cruthaithe 2021
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    Artigo
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  7. 7
    Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier

    Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier de réir Alexandre Hinzpeter, Abdel Aissat, Elvira Sondo, Cathérine Costa, N. Arous, Christine Gameiro, Natacha Martin, Agathe Tarze, Laurence Weiss, Alix de Becdelièvre, Bruno Costes, Michel Goossens, Luis J. V. Galietta, Emmanuelle Girodon, Pascale Fanen

    Foilsithe / Cruthaithe 2010
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    Artigo
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  8. 8
    Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons

    Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons de réir Iwona Pranke, Laure Bidou, Natacha Martin, Sandra Blanchet, Aurélie Hatton, Sabrina Karri, David Cornu, Bruno Costes, B. Chevalier, Danielle Tondelier, Emmanuelle Girodon, Matthieu Coupet, Aleksander Edelman, Pascale Fanen, Olivier Namy, Isabelle Sermet‐Gaudelus, Alexandre Hinzpeter

    Foilsithe / Cruthaithe 2018
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    Artigo
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  9. 9
    Predictive factors for lumacaftor/ivacaftor clinical response

    Predictive factors for lumacaftor/ivacaftor clinical response de réir Alexandra Masson, Elena K. Schneider‐Futschik, Nesrine Baatallah, Thao Nguyen‐Khoa, Emmanuelle Girodon, Aurélie Hatton, Thomas Flament, M. Le Bourgeois, F. Chedevergne, Céline Bailly, Sylvia Kyrilli, D. Achimastos, Alexandre Hinzpeter, Aleksander Edelman, Isabelle Sermet‐Gaudelus

    Foilsithe / Cruthaithe 2018
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    Artigo
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  10. 10
    Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators

    Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators de réir Iwona Pranke, Aurélie Hatton, Juliette Simonin, Jean Philippe Jaïs, Françoise Le Pimpec‐Barthes, A. Carsin, P. Bonnette, Michaël Fayon, Nathalie Stremler-Le Bel, Dominique Grenet, Matthieu Thumerel, Julie Mazenq, Valérie Urbach, Myriam Mesbahi, Emanuelle Girodon-Boulandet, Alexandre Hinzpeter, Aleksander Edelman, Isabelle Sermet‐Gaudelus

    Foilsithe / Cruthaithe 2017
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  11. 11
    Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis

    Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis de réir Juliette Simonin, Emmanuelle Bille, Gilles Crambert, Sabrina Noël, Elise Dréano, Aurélie Edwards, Aurélie Hatton, Iwona Pranke, Bérengère Villeret, Charles‐Henry Cottart, Jean-Patrick Vrel, Valérie Urbach, Nesrine Baatallah, Alexandre Hinzpeter, Anita Golec, Lhousseine Touqui, Xavier Nassif, Luis J. V. Galietta, Gabrielle Planelles, Jean‐Michel Sallenave, Aleksander Edelman, Isabelle Sermet‐Gaudelus

    Foilsithe / Cruthaithe 2019
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