CLINICAL, BIOLOGICAL AND PHARMACOLOGICAL INVESTIGATION OF A NEDD4L POLYMORPHISM (RS4149601) IN NORMOTENSIVE HEALTHY SUBJECTS

被引:0
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作者
Wuerzner, G. [1 ]
Blanchard, A. [1 ]
Frank, M. [1 ]
Peyrard, S. [1 ]
Burnichon, N. [1 ]
Azizi, M. [1 ]
Jeunemaitre, X. [1 ]
机构
[1] Georges Pompidou European Hosp, Paris, France
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R6 [外科学];
学科分类号
1002 ; 100210 ;
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页码:S166 / S166
页数:1
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  • [1] Clinical, biological and pharmacological investigation of a NEDD4L polymorphism (rs4149601) in normotensive healthy subjects
    Blanchard, A.
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    Frank, M.
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    [J]. FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2010, 24 : 44 - 44
  • [2] Genetic variation in NEDD4L, salt sensitivity, and hypertension: human NEDD4L rs4149601 G allele generates evolutionary new isoform I with C2 domain
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    Araki, Naomi
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    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
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    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
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    [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
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    Hirawa, Nobuhito
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    Uchino, Kazuaki
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    [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
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    [J]. 临床军医杂志, 2015, 43 (11) : 788 - 790