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There are 8566 results for: content related to: Early activation of sperm by HCO 3 − is regulated hormonally in the murine uterus

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    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

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    Revertant mutants modify, but do not rescue, the gating defect of the cystic fibrosis mutant G551D-CFTR

    The Journal of Physiology

    Volume 592, Issue 9, 1 May 2014, Pages: 1931–1947, Zhe Xu, Luísa S. Pissarra, Carlos M. Farinha, Jia Liu, Zhiwei Cai, Patrick H. Thibodeau, Margarida D. Amaral and David N. Sheppard

    Version of Record online : 27 MAR 2014, DOI: 10.1113/jphysiol.2014.271817

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    Impact of the F508del mutation on ovine CFTR, a Cl channel with enhanced conductance and ATP-dependent gating

    The Journal of Physiology

    Volume 593, Issue 11, 1 June 2015, Pages: 2427–2446, Zhiwei Cai, Timea Palmai-Pallag, Pissared Khuituan, Michael J. Mutolo, Clément Boinot, Beihui Liu, Toby S. Scott-Ward, Isabelle Callebaut, Ann Harris and David N. Sheppard

    Version of Record online : 9 APR 2015, DOI: 10.1113/JP270227

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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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    Optical imaging of Ca2+-evoked fluid secretion by murine nasal submucosal gland serous acinar cells

    The Journal of Physiology

    Volume 582, Issue 3, August 2007, Pages: 1099–1124, Robert J. Lee, Maria P. Limberis, Michael F. Hennessy, James M. Wilson and J. Kevin Foskett

    Version of Record online : 21 JUL 2007, DOI: 10.1113/jphysiol.2007.131995

  6. SLC26A9 stimulates CFTR expression and function in human bronchial cell lines

    Journal of Cellular Physiology

    Volume 226, Issue 1, January 2011, Pages: 212–223, Martine Avella, Céline Loriol, Kim Boulukos, Franck Borgese and Jordi Ehrenfeld

    Version of Record online : 23 JUL 2010, DOI: 10.1002/jcp.22328

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    CFTR Cl channel and CFTR-associated ATP channel: distinct pores regulated by common gates

    The EMBO Journal

    Volume 17, Issue 4, February 15, 1998, Pages: 898–908, Makoto Sugita, Yun Yue and J.Kevin Foskett

    Version of Record online : 15 FEB 1998, DOI: 10.1093/emboj/17.4.898

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    Prolonged treatment of cells with genistein modulates the expression and function of the cystic fibrosis transmembrane conductance regulator

    British Journal of Pharmacology

    Volume 153, Issue 6, March 2008, Pages: 1311–1323, A Schmidt, L K Hughes, Z Cai, F Mendes, H Li, D N Sheppard and M D Amaral

    Version of Record online : 29 JAN 2009, DOI: 10.1038/sj.bjp.0707663

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    The Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis

    The EMBO Journal

    Volume 18, Issue 6, March 15, 1999, Pages: 1492–1505, Geoffrey C. Meacham, Zhen Lu, Scott King, Eric Sorscher, Albert Tousson and Douglas M. Cyr

    Version of Record online : 15 MAR 1999, DOI: 10.1093/emboj/18.6.1492

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    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

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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

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    Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels

    The Journal of Physiology

    Volume 524, Issue 3, May 2000, Pages: 637–648, Fei Wang, Shawn Zeltwanger, Shenghui Hu and Tzyh-Chang Hwang

    Version of Record online : 13 AUG 2004, DOI: 10.1111/j.1469-7793.2000.00637.x

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    The cystic fibrosis transmembrane conductance regulator in reproductive health and disease

    The Journal of Physiology

    Volume 587, Issue 10, May 2009, Pages: 2187–2195, Hsiao Chang Chan, Ye Chun Ruan, Qiong He, Min Hui Chen, Hui Chen, Wen Ming Xu, Wen Ying Chen, Chen Xie, Xiao Hu Zhang and Zhen Zhou

    Version of Record online : 14 MAY 2009, DOI: 10.1113/jphysiol.2008.164970

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    Traffic Pattern of Cystic Fibrosis Transmembrane Regulator through the Early Exocytic Pathway

    Traffic

    Volume 1, Issue 11, November 2000, Pages: 852–870, Sergei I. Bannykh, Galina I. Bannykh, Kenneth N. Fish, Bryan D. Moyer, John R. Riordan and William E. Balch

    Version of Record online : 3 SEP 2008, DOI: 10.1034/j.1600-0854.2000.011105.x

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    HEK-293 cells expressing the cystic fibrosis transmembrane conductance regulator (CFTR): a model for studying regulation of Cl transport

    Physiological Reports

    Volume 2, Issue 9, September 2014, Jada C. Domingue, Mei Ao, Jayashree Sarathy, Alvin George, Waddah A. Alrefai, Deborah J. Nelson and Mrinalini C. Rao

    Version of Record online : 28 SEP 2014, DOI: 10.14814/phy2.12158

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    Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers

    The Journal of Physiology

    Volume 588, Issue 8, April 2010, Pages: 1195–1209, Pierre LeSimple, Jie Liao, Renaud Robert, Dieter C. Gruenert and John W. Hanrahan

    Version of Record online : 14 APR 2010, DOI: 10.1113/jphysiol.2009.182246

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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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    Failure of cAMP agonists to activate rescued ΔF508 CFTR in CFBE41o airway epithelial monolayers

    The Journal of Physiology

    Volume 569, Issue 2, December 2005, Pages: 601–615, Zsuzsa Bebok, James F. Collawn, John Wakefield, William Parker, Yao Li, Karoly Varga, Eric J. Sorscher and J. P. Clancy

    Version of Record online : 24 NOV 2005, DOI: 10.1113/jphysiol.2005.096669

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    Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl channels expressed in murine cell line

    The Journal of Physiology

    Volume 524, Issue 2, April 2000, Pages: 317–330, K. A. Lansdell, Z. Cai, J. F. Kidd and D. N. Sheppard

    Version of Record online : 13 AUG 2004, DOI: 10.1111/j.1469-7793.2000.t01-1-00317.x