Search alternatives:
teer decrease » greater decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
12 mean » 12 men (Expand Search), 2012 mean (Expand Search)
teer decrease » greater decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
12 mean » 12 men (Expand Search), 2012 mean (Expand Search)
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99441
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99442
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99443
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99444
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99445
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99446
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99447
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99448
Identification of the miR21 deletion in ECs.
Published 2013“…(<b>D</b>) Real-time PCR was performed to determine the level of miR21 from each group described in A. The miR21 expression level of endothelial-specific KO group was significantly decreased. …”
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99449
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99450
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99451
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99452
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99453
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99454
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99455
SOX4 Transcriptionally Regulates Multiple SEMA3/Plexin Family Members and Promotes Tumor Growth in Pancreatic Cancer
Published 2012“…Unlike other epithelial malignancies that often express a small number of specific genes in the Semaphorin/Plexin family, five or more are often expressed in human PDAC. …”
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99456
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99457
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99458
Combined KIX domain and c-Myb haploinsufficiency synergistically affects multiple blood lineages.
Published 2013“…Zero indicates no epistasis or the lack of synergistic interaction between mutations [i.e. equality of the multiplicative phenotype (or additivity of log-transformed phenotype in this case) of the extreme (wild type and <i>p300<sup>+/KIX</sup></i>;<i>CBP<sup>+/KIX</sup></i>;<i>c-Myb<sup>+/-</sup></i>) and intermediate genotypes (<i>c-Myb<sup>+/-</sup></i> and <i>p300<sup>+/KIX</sup></i>;<i>CBP</i><sup>+/KIX</sup>)]. A positive epistasis value indicates a greater than multiplicative increased phenotype for the extreme genotype, a negative epistasis value indicates a greater than multiplicative decreased (aggravated) phenotype for the extreme genotype. …”
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99459
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99460