Resultados da pesquisa - Shengxin Xu

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  1. 1
    In Primary Aldosteronism, Mineralocorticoids Influence Exosomal Sodium-Chloride Cotransporter Abundance

    In Primary Aldosteronism, Mineralocorticoids Influence Exosomal Sodium-Chloride Cotransporter Abundance Por Martin Wolley, Wu A, Shengxin Xu, Richard D. Gordon, Robert A. Fenton, Michael Stowasser

    Publicado em 2016
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  2. 2
    Seated Saline Suppression Testing For The Diagnosis Of Primary Aldosteronism: A Preliminary Study

    Seated Saline Suppression Testing For The Diagnosis Of Primary Aldosteronism: A Preliminary Study Por Ashraf Ahmed, Diane Cowley, Martin Wolley, Richard D. Gordon, Shengxin Xu, Paul J. Taylor, Michael Stowasser

    Publicado em 2014
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  3. 3
    Role for Germline Mutations and a Rare Coding Single Nucleotide Polymorphism Within the KCNJ5 Potassium Channel in a Large Cohort of Sporadic Cases of Primary Aldosteronism

    Role for Germline Mutations and a Rare Coding Single Nucleotide Polymorphism Within the KCNJ5 Potassium Channel in a Large Cohort of Sporadic Cases of Primary Aldosteronism Por Meena Murthy, Shengxin Xu, Gianmichele Massimo, Martin Wolley, Richard D. Gordon, Michael Stowasser, Kevin M. O’Shaughnessy

    Publicado em 2014
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  4. 4
    Somatic Mutations Affecting the Selectivity Filter of KCNJ5 Are Frequent in 2 Large Unselected Collections of Adrenal Aldosteronomas

    Somatic Mutations Affecting the Selectivity Filter of KCNJ5 Are Frequent in 2 Large Unselected Collections of Adrenal Aldosteronomas Por Elena Azizan, Meena Murthy, Michael Stowasser, Richard D. Gordon, Bartosz Kowalski, Shengxin Xu, Matthew A. Brown, Kevin M. O’Shaughnessy

    Publicado em 2012
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  5. 5
    Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo

    Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo Por Yunqing Ren, Sen Yang, Shengxin Xu, Min Gao, Wei Huang, Tianwen Gao, Qiaoyun Fang, Cheng Quan, Chi Zhang, Liangdan Sun, Yanhua Liang, Jianwen Han, Zhimin Wang, Fengyu Zhang, Youwen Zhou, Jianjun Liu, Xuejun Zhang

    Publicado em 2009
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  6. 6
    Detection of mutations in <i>KLHL3</i> and <i>CUL3</i> in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)

    Detection of mutations in <i>KLHL3</i> and <i>CUL3</i> in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome) Por Mark Glover, James S. Ware, Amanda P. Henry, Martin Wolley, Roddy Walsh, Louise V. Wain, Shengxin Xu, William G. van’t Hoff, Martin D. Tobin, Ian P. Hall, Stuart A. Cook, Richard D. Gordon, Michael Stowasser, Kevin M. O’Shaughnessy

    Publicado em 2013
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  7. 7
    CLCN2 chloride channel mutations in familial hyperaldosteronism type II

    CLCN2 chloride channel mutations in familial hyperaldosteronism type II Por Ute I. Scholl, Gabriel Stölting, Julia Schewe, Anne Thiel, Hua Tan, Carol Nelson‐Williams, Alfred A. Vichot, Sheng Chih Jin, Erin Loring, Verena Untiet, Taekyeong Yoo, Jungmin Choi, Shengxin Xu, Wu A, Marieluise Kirchner, Philipp Mertins, Lars Christian Rump, Ali Mirza Onder, Cory Gamble, Daniel W. McKenney, Robert W. Lash, Deborah P. Jones, G. Chune, Priscila Gagliardi, Murim Choi, Richard D. Gordon, Michael Stowasser, Christoph Fahlke, Richard P. Lifton

    Publicado em 2018
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