Clinical, biological and pharmacological investigation of a NEDD4L polymorphism (rs4149601) in normotensive healthy subjects

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Blanchard, A.
Wuerzner, G.
Frank, M.
Peyrard, S.
Burnichon, N.
Jeunemaitre, X.
Azizi, M.
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R9 [药学];
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1007 ;
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页码:44 / 44
页数:1
相关论文
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  • [1] CLINICAL, BIOLOGICAL AND PHARMACOLOGICAL INVESTIGATION OF A NEDD4L POLYMORPHISM (RS4149601) IN NORMOTENSIVE HEALTHY SUBJECTS
    Wuerzner, G.
    Blanchard, A.
    Frank, M.
    Peyrard, S.
    Burnichon, N.
    Azizi, M.
    Jeunemaitre, X.
    [J]. JOURNAL OF HYPERTENSION, 2009, 27 : S166 - S166
  • [2] Genetic variation in NEDD4L, salt sensitivity, and hypertension: human NEDD4L rs4149601 G allele generates evolutionary new isoform I with C2 domain
    Ishigami, Tomoaki
    Araki, Naomi
    Minegishi, Shintaro
    Umemura, Masanari
    Umemura, Satoshi
    [J]. JOURNAL OF HYPERTENSION, 2014, 32 (09) : 1905 - 1905
  • [3] Human Nedd4L rs4149601 G Allele Generates Evolutionary New Isoform I With C2 Domain
    Ishigami, Tomoaki
    Araki, Naomi
    Umemura, Satoshi
    [J]. HYPERTENSION, 2010, 55 (02) : E10 - E10
  • [4] Response to Human Nedd4L rs4149601 G Allele Generates Evolutionary New Isoform I With C2 Domain
    Luo, Fang
    Hui, Rutai
    [J]. HYPERTENSION, 2010, 55 (02) : E11 - E11
  • [5] NEDD4L protein truncating variant (v13[G/A]: rs4149601) is associated with essential hypertension in a sample of the Japanese population
    Ishigami, Tomoaki
    Umemura, Masanari
    Araki, Naomi
    Hirawa, Nobuhito
    Tamura, Koichi
    Uchino, Kazuaki
    Umemura, Satoshi
    Rohrwasser, Andreas
    Lalouel, Jean-Marc
    [J]. GERIATRICS & GERONTOLOGY INTERNATIONAL, 2007, 7 (02) : 114 - 117
  • [6] NEDD4L基因Rs4149601位点变异与心脏介入术并发低血压的相关性分析
    刘颖
    栗印军
    [J]. 临床军医杂志, 2015, 43 (11) : 788 - 790