Search Results

There are 71420 results for: content related to: Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis

  1. You have free access to this content
    Poster Session Abstracts

    Pediatric Pulmonology

    Volume 50, Issue S41, October 2015, Pages: S193–S453,

    Version of Record online : 4 SEP 2015, DOI: 10.1002/ppul.23297

    Corrected by:

    Errata: Errata

    Vol. 50, Issue 12, 1175, Version of Record online: 9 NOV 2015

  2. You have free access to this content
    Poster Session Abstracts

    Pediatric Pulmonology

    Volume 51, Issue S45, October 2016, Pages: S194–S485,

    Version of Record online : 21 SEP 2016, DOI: 10.1002/ppul.23576

  3. You have free access to this content
    Disrupted posttranscriptional regulation of the cystic fibrosis transmembrane conductance regulator (CFTR) by a 5′UTR mutation is associated with a cftr-related disease

    Human Mutation

    Volume 32, Issue 10, October 2011, Pages: E2266–E2282, Samuel W. Lukowski, Cristina Bombieri and Ann E. O. Trezise

    Version of Record online : 19 SEP 2011, DOI: 10.1002/humu.21545

  4. You have free access to this content
    Symposium Summaries

    Pediatric Pulmonology

    Volume 51, Issue S45, October 2016, Pages: S115–S193,

    Version of Record online : 21 SEP 2016, DOI: 10.1002/ppul.23575

  5. You have free access to this content
    Symposium Summaries

    Pediatric Pulmonology

    Volume 50, Issue S41, October 2015, Pages: S108–S192,

    Version of Record online : 4 SEP 2015, DOI: 10.1002/ppul.23296

  6. You have free access to this content
    Congenital tracheal malformation in cystic fibrosis transmembrane conductance regulator-deficient mice

    The Journal of Physiology

    Volume 586, Issue 13, July 2008, Pages: 3231–3243, Elise Bonvin, Philippe Le Rouzic, Jean-François Bernaudin, Charles-Henry Cottart, Clarisse Vandebrouck, Antoine Crié, Teresinha Leal, Annick Clement and Monique Bonora

    Version of Record online : 28 JUN 2008, DOI: 10.1113/jphysiol.2008.150763

  7. Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens

    Human Mutation

    Volume 32, Issue 8, August 2011, Pages: 912–920, Bernhard Steiner, Jonas Rosendahl, Heiko Witt, Niels Teich, Volker Keim, Hans-Ulrich Schulz, Roland Pfützer, Matthias Lühr, Thomas M. Gress, Renate Nickel, Olfert Landt, Monika Koudova, Milan Macek Jr, Antoni Farre, Teresa Casals, Marie-Claire Desax, Sabina Gallati, Macarena Gomez-Lira, Marie Pierre Audrezet, Claude Férec, Marie des Georges, Mireille Claustres and Kaspar Truninger

    Version of Record online : 7 JUN 2011, DOI: 10.1002/humu.21511

    Corrected by:

    Errata: Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens

    Vol. 33, Issue 2, 456, Version of Record online: 12 JAN 2012

  8. You have free access to this content
    Genetic Investigations of CFTR Mutations in Congenital Absence of Vas Deferens, Uterus, and Vagina as a Cause of Infertility

    Journal of Andrology

    Volume 29, Issue 5, September-October 2008, Pages: 506–513, Ramin Radpour, Hamid Gourabi, Ahmad Vosough Dizaj, Wolfgang Holzgreve and Xiao Yan Zhong

    Version of Record online : 2 JAN 2013, DOI: 10.2164/jandrol.108.005074

  9. CFTR-France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variants

    Human Mutation

    Mireille Claustres, Corinne Thèze, Marie des Georges, David Baux, Emmanuelle Girodon, Thierry Bienvenu, Marie-Pierre Audrezet, Ingrid Dugueperoux, Claude Férec, Guy Lalau, Adrien Pagin, Alain Kitzis, Vincent Thoreau, Véronique Gaston, Eric Bieth, Marie-Claire Malinge, Marie-Pierre Reboul, Patricia Fergelot, Lydie Lemonnier, Chadia Mekki, Pascale Fanen, Anne Bergougnoux, Souphatta Sasorith, Caroline Raynal and Corinne Bareil

    Version of Record online : 28 JUN 2017, DOI: 10.1002/humu.23276

  10. You have full text access to this OnlineOpen article
    Abnormal tracheal smooth muscle function in the CF mouse

    Physiological Reports

    Volume 1, Issue 6, November 2013, Helen L. Wallace, Kevin W. Southern, Marilyn G. Connell, Susan Wray and Theodor Burdyga

    Version of Record online : 5 NOV 2013, DOI: 10.1002/phy2.138

  11. CFTR mutations and polymorphisms in male infertility

    International Journal of Andrology

    Volume 27, Issue 5, October 2004, Pages: 251–256, Harry Cuppens and Jean-Jacques Cassiman

    Version of Record online : 17 SEP 2004, DOI: 10.1111/j.1365-2605.2004.00485.x

  12. You have free access to this content
    Disruption of CFTR chloride channel alters mechanical properties and cAMP-dependent Cl transport of mouse aortic smooth muscle cells

    The Journal of Physiology

    Volume 568, Issue 2, October 2005, Pages: 483–495, Renaud Robert, Caroline Norez and Frédéric Becq

    Version of Record online : 24 OCT 2005, DOI: 10.1113/jphysiol.2005.085019

  13. You have free access to this content
    Cftr and ENaC ion channels mediate NaCl absorption in the mouse submandibular gland

    The Journal of Physiology

    Volume 588, Issue 4, February 2010, Pages: 713–724, Marcelo A. Catalán, Tetsuji Nakamoto, Mireya Gonzalez-Begne, Jean M. Camden, Susan M. Wall, Lane L. Clarke and James E. Melvin

    Version of Record online : 12 FEB 2010, DOI: 10.1113/jphysiol.2009.183541

  14. You have free access to this content
    Insertion of natural intron 6a-6b into a human cDNA-derived gene therapy vector for cystic fibrosis improves plasmid stability and permits facile RNA/DNA discrimination

    The Journal of Gene Medicine

    Volume 1, Issue 5, September/October 1999, Pages: 312–321, A. Christopher Boyd, Friedrich Popp, Uwe Michaelis, Heather Davidson, Hazel Davidson-Smith, Ann Doherty, Gerry McLachlan, David J. Porteous and Stefan Seeber

    Version of Record online : 23 NOV 1999, DOI: 10.1002/(SICI)1521-2254(199909/10)1:5<312::AID-JGM55>3.0.CO;2-#

  15. You have free access to this content
    The Phenotypic Consequences of CFTR Mutations

    Annals of Human Genetics

    Volume 67, Issue 5, September 2003, Pages: 471–485, Rebecca K. Rowntree and Ann Harris

    Version of Record online : 27 AUG 2003, DOI: 10.1046/j.1469-1809.2003.00028.x

  16. You have free access to this content
    Altered ion transport by thyroid epithelia from CFTR−/− pigs suggests mechanisms for hypothyroidism in cystic fibrosis

    Experimental Physiology

    Volume 95, Issue 12, December 2010, Pages: 1132–1144, Hui Li, Suhasini Ganta and Peying Fong

    Version of Record online : 20 SEP 2010, DOI: 10.1113/expphysiol.2010.054700

  17. Identification of a Novel 5′ Alternative CFTR mRNA Isoform in a Patient with Nasal Polyposis and CFTR Mutations

    Human Mutation

    Volume 35, Issue 7, July 2014, Pages: 805–808, Alexandre Hinzpeter, Alix de Becdelièvre, Eric Bieth, Christine Gameiro, François Brémont, Natacha Martin, Bruno Costes, Catherine Costa, Abdel Aissat, Aurélie Lorot, Virginie Prulière-Escabasse, Michel Goossens, Pascale Fanen and Emmanuelle Girodon

    Version of Record online : 9 APR 2014, DOI: 10.1002/humu.22548

  18. Characterization of SLC26A9 in Patients with CF-Like Lung Disease

    Human Mutation

    Volume 34, Issue 10, October 2013, Pages: 1404–1414, Naziha Bakouh, Thierry Bienvenu, Annick Thomas, Jordi Ehrenfeld, Huguette Liote, Delphine Roussel, Philippe Duquesnoy, Nicolette Farman, Marion Viel, Baya Cherif-Zahar, Serge Amselem, Rola Abou Taam, Aleksander Edelman, Gabrielle Planelles and Isabelle Sermet-Gaudelus

    Version of Record online : 13 AUG 2013, DOI: 10.1002/humu.22382

  19. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for Ivacaftor Therapy in the Context of CFTR Genotype

    Clinical Pharmacology & Therapeutics

    Volume 95, Issue 6, June 2014, Pages: 592–597, J P Clancy, S G Johnson, S W Yee, E M McDonagh, K E Caudle, T E Klein, M Cannavo and K M Giacomini

    Version of Record online : 5 MAR 2014, DOI: 10.1038/clpt.2014.54

  20. You have full text access to this OnlineOpen article
    Orkambi® and amplifier co-therapy improves function from a rare CFTR mutation in gene-edited cells and patient tissue

    EMBO Molecular Medicine

    Steven V Molinski, Saumel Ahmadi, Wan Ip, Hong Ouyang, Adriana Villella, John P Miller, Po-Shun Lee, Kethika Kulleperuma, Kai Du, Michelle Di Paola, Paul DW Eckford, Onofrio Laselva, Ling Jun Huan, Leigh Wellhauser, Ellen Li, Peter N Ray, Régis Pomès, Theo J Moraes, Tanja Gonska, Felix Ratjen and Christine E Bear

    Version of Record online : 30 JUN 2017, DOI: 10.15252/emmm.201607137