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There are 19380 results for: content related to: Spectrum of mutations and variants/haplotypes of CFTR and genotype–phenotype correlation in idiopathic chronic pancreatitis and controls in Chinese by complete analysis

  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. Composition of mineralizing incisor enamel in cystic fibrosis transmembrane conductance regulator-deficient mice

    European Journal of Oral Sciences

    Volume 123, Issue 1, February 2015, Pages: 9–16, Antonius L.J.J. Bronckers, Don M. Lyaruu, Jing Guo, Marcel J.C. Bijvelds, Theodore J.M. Bervoets, Behrouz Zandieh-Doulabi, Juan F. Medina, Zhu Li, Yan Zhang and Pamela K. DenBesten

    Version of Record online : 30 DEC 2014, DOI: 10.1111/eos.12163

  3. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles

    Clinical Genetics

    Volume 72, Issue 3, September 2007, Pages: 218–223, FR Faucz, J Gimenez, MD Ramos, L Pereira-Ferrari, X Estivill, S Raskin, T Casals and L Culpi

    Version of Record online : 27 JUL 2007, DOI: 10.1111/j.1399-0004.2007.00854.x

  4. First prenatal exclusion of cystic fibrosis in East Asia

    Pediatrics International

    Volume 49, Issue 5, October 2007, Pages: 686–687, LEE-JUN C. WONG, 1 MEI-HUI LEE, 2 MING CHEN, 2,3 ÖZGÜL M. ALPER, 1, LONG-YEN TSAO and 2 BAO-TYAN WANG 2,4,

    Version of Record online : 14 SEP 2007, DOI: 10.1111/j.1442-200X.2007.02437.x

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    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

  6. 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

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    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-#

  8. CFTR: The CF Gene and Its Regulation in Physiology and Disease

    Standard Article

    eLS

    Wayne IL Davies

    Published Online : 8 DEC 2013, DOI: 10.1002/9780470015902.a0022929

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    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

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    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

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    Molecular mechanisms controlling CFTR gene expression in the airway

    Journal of Cellular and Molecular Medicine

    Volume 16, Issue 6, June 2012, Pages: 1321–1330, Zhaolin Zhang, Christopher J. Ott, Marzena A. Lewandowska, Shih-Hsing Leir and Ann Harris

    Version of Record online : 28 MAY 2012, DOI: 10.1111/j.1582-4934.2011.01439.x

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    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

  13. 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

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    UMD-CFTR: A database dedicated to CF and CFTR-related disorders

    Human Mutation

    Volume 31, Issue 9, September 2010, Pages: 1011–1019, Corinne Bareil, Corinne Thèze, Christophe Béroud, Dalil Hamroun, Caroline Guittard, Céline René, Damien Paulet, Marie des Georges and Mireille Claustres

    Version of Record online : 6 JUL 2010, DOI: 10.1002/humu.21316

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    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

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    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

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    Complementation of null CF mice with a human CFTR YAC transgene

    The EMBO Journal

    Volume 16, Issue 14, July 15, 1997, Pages: 4238–4249, Ania L. Manson, Ann E. O. Trezise, Lesley J. MacVinish, Kristin D. Kasschau, Nina Birchall, Vasso Episkopou, Georges Vassaux, Martin J. Evans, William H. Colledge, Alan W. Cuthbert and Clare Huxley

    Version of Record online : 15 JUL 1997, DOI: 10.1093/emboj/16.14.4238

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    Correlation between genito-urinary anomalies, semen analysis and CFTR genotype in patients with congenital bilateral absence of the vas deferens

    British Journal of Urology

    Volume 81, Issue 4, April 1998, Pages: 614–619, De La Taille, Rigot, Mahe, Vankemmel, Gervais, Dumur, Lemaitre and Mazeman

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1464-410x.1998.00589.x

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    CFTR potentiators partially restore channel function to A561E-CFTR, a cystic fibrosis mutant with a similar mechanism of dysfunction as F508del-CFTR

    British Journal of Pharmacology

    Volume 171, Issue 19, October 2014, Pages: 4490–4503, Yiting Wang, Jia Liu, Avgi Loizidou, Luc A Bugeja, Ross Warner, Bethan R Hawley, Zhiwei Cai, Ashley M Toye, David N Sheppard and Hongyu Li

    Version of Record online : 5 SEP 2014, DOI: 10.1111/bph.12791

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    Analysis of a DNase I hypersensitive site located −20.9 kb upstream of the CFTR gene

    European Journal of Biochemistry

    Volume 266, Issue 2, December 1999, Pages: 431–443, Hugh N. Nuthall, Georges Vassaux, Clare Huxley and Ann Harris

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1432-1327.1999.00872.x