Ngā hua rapu - Chen, Jeng‐Haur

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  1. 1
    Protein kinase A phosphorylation potentiates cystic fibrosis transmembrane conductance regulator gating by relieving autoinhibition on the stimulatory C terminus of the regulatory domain

    Protein kinase A phosphorylation potentiates cystic fibrosis transmembrane conductance regulator gating by relieving autoinhibition on the stimulatory C terminus of the regulatory... mā Chen, Jeng-Haur

    I whakaputaina 2020
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  2. 2
    Direct Sensing of Intracellular pH by the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Cl(−) Channel

    Direct Sensing of Intracellular pH by the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Cl(−) Channel mā Chen, Jeng-Haur, Cai, Zhiwei, Sheppard, David N.

    I whakaputaina 2009
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  3. 3
    Altering intracellular pH reveals the kinetic basis of intraburst gating in the CFTR Cl(−) channel

    Altering intracellular pH reveals the kinetic basis of intraburst gating in the CFTR Cl(−) channel mā Chen, Jeng‐Haur, Xu, Weiyi, Sheppard, David N.

    I whakaputaina 2017
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  4. 4
    Acute inhibition of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl(−) channel by thyroid hormones involves multiple mechanisms

    Acute inhibition of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl(−) channel by thyroid hormones involves multiple mechanisms mā Cai, Zhiwei, Li, Hongyu, Chen, Jeng-Haur, Sheppard, David N.

    I whakaputaina 2013
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  5. 5
    Human cystic fibrosis airway epithelia have reduced Cl(−) conductance but not increased Na(+) conductance

    Human cystic fibrosis airway epithelia have reduced Cl(−) conductance but not increased Na(+) conductance mā Itani, Omar A., Chen, Jeng-Haur, Karp, Philip H., Ernst, Sarah, Keshavjee, Shaf, Parekh, Kalpaj, Klesney-Tait, Julia, Zabner, Joseph, Welsh, Michael J.

    I whakaputaina 2011
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  6. 6
    Inhibition of Protein Kinase CK2 Closes the CFTR Cl(−) Channel, but has no Effect on the Cystic Fibrosis Mutant ΔF508-CFTR

    Inhibition of Protein Kinase CK2 Closes the CFTR Cl(−) Channel, but has no Effect on the Cystic Fibrosis Mutant ΔF508-CFTR mā Treharne, Kate J., Xu, Zhe, Chen, Jeng-Haur, Best, O. Giles, Cassidy, Diane M., Gruenert, Dieter C., Hegyi, Péter, Gray, Michael A., Sheppard, David N., Kunzelmann, Karl, Mehta, Anil

    I whakaputaina 2009
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  7. 7
    Protein kinase CK2, cystic fibrosis transmembrane conductance regulator, and the ΔF508 mutation. F508 deletion disrupts a kinase-binding site. VOLUME 282 (2007) PAGES 10804-10813

    Protein kinase CK2, cystic fibrosis transmembrane conductance regulator, and the ΔF508 mutation. F508 deletion disrupts a kinase-binding site. VOLUME 282 (2007) PAGES 10804-10813 mā Treharne, Kate J., Crawford, Russell M., Xu, Zhe, Chen, Jeng-Haur, Best, O. Giles, Schulte, Eva A., Gruenert, Dieter C., Wilson, Stuart M., Sheppard, David N., Kunzelmann, Kar, Mehta, Anil

    I whakaputaina 2008
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  8. 8
    CFTR-deficient pigs display peripheral nervous system defects at birth

    CFTR-deficient pigs display peripheral nervous system defects at birth mā Reznikov, Leah R., Dong, Qian, Chen, Jeng-Haur, Moninger, Thomas O., Park, Jung Min, Zhang, Yuzhou, Du, Jianyang, Hildebrand, Michael S., Smith, Richard J. H., Randak, Christoph O., Stoltz, David A., Welsh, Michael J.

    I whakaputaina 2013
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  9. 9
    Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia

    Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia mā Chen, Jeng-Haur, Stoltz, David A., Karp, Philip H., Ernst, Sarah E., Pezzulo, Alejandro A., Moninger, Thomas O., Rector, Michael V., Reznikov, Leah R., Launspach, Janice L., Chaloner, Kathryn, Zabner, Joseph, Welsh, Michael J.

    I whakaputaina 2010
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  10. 10
    CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis

    CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis mā Leung, Gordon K. C., Ying, Dingge, Mak, Christopher C. Y., Chen, Xin‐Ying, Xu, Weiyi, Yeung, Kit‐San, Wong, Wai‐Lap, Chu, Yoyo W. Y., Mok, Gary T. K., Chau, Christy S. K., McLuskey, Jenna, Ong, Winnie P. T., Leong, Huey‐Yin, Chan, Kelvin Y. K., Yang, Wanling, Chen, Jeng‐Haur, Li, Albert M., Sham, Pak C., Lau, Yu‐Lung, Chung, Brian H. Y., Lee, So‐Lun

    I whakaputaina 2016
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  11. 11
    The ΔF508 Mutation Causes CFTR Misprocessing and Cystic Fibrosis-Like Disease in Pigs

    The ΔF508 Mutation Causes CFTR Misprocessing and Cystic Fibrosis-Like Disease in Pigs mā Ostedgaard, Lynda S, Meyerholz, David K, Chen, Jeng-Haur, Pezzulo, Alejandro A, Karp, Philip H, Rokhlina, Tatiana, Ernst, Sarah E, Hanfland, Robert A, Reznikov, Leah R, Ludwig, Paula S, Rogan, Mark P, Davis, Greg J, Dohrn, Cassie L, Wohlford-Lenane, Christine, Taft, Peter J, Rector, Michael V, Hornick, Emma, Nassar, Boulos S, Samuel, Melissa, Zhang, Yuping, Richter, Sandra S, Uc, Aliye, Shilyansky, Joel, Prather, Randall S, McCray, Paul B, Zabner, Joseph, Welsh, Michael J, Stoltz, David A

    I whakaputaina 2011
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  12. 12
    Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs

    Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs mā Stoltz, David A., Rokhlina, Tatiana, Ernst, Sarah E., Pezzulo, Alejandro A., Ostedgaard, Lynda S., Karp, Philip H., Samuel, Melissa S., Reznikov, Leah R., Rector, Michael V., Gansemer, Nicholas D., Bouzek, Drake C., Alaiwa, Mahmoud H. Abou, Hoegger, Mark J., Ludwig, Paula S., Taft, Peter J., Wallen, Tanner J., Wohlford-Lenane, Christine, McMenimen, James D., Chen, Jeng-Haur, Bogan, Katrina L., Adam, Ryan J., Hornick, Emma E., Nelson, George A., Hoffman, Eric A., Chang, Eugene H., Zabner, Joseph, McCray, Paul B., Prather, Randall S., Meyerholz, David K., Welsh, Michael J.

    I whakaputaina 2013
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