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We noticed that the molecular network for cell cycle entry was partially re-activated by VC (Fig. 4B and 4C).
The first step of NTPGE is to construct the integrated molecular network for a given organism comprising protein physical, metabolic and transcriptional regulation interactions.
TCGA contains somatic mutations, copy number variation, mRNA expression, miRNA expression, protein expression, and histology slides, and aims to develop an integrated landscape of complex molecular network for approximately 7000 human tumors.
A comprehensive analysis will help to determine the entire molecular network for L. pneumophila pathogensis.
The molecular network for these cellular activities remains to be elucidated.
Our data therefore identifies a molecular network for nephron patterning.
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Molecular networks for transcriptional regulation could explain partly the carcinogenic effect seen in mice with over-expression of the c-Myc oncogene.
Engineering strategies aimed at gaining stress tolerance have focused on overexpression of endogenous genes belonging to molecular networks for stress perception or responses.
This resource allows visualization of the dynamic interactions in the transcriptome, proteome, and metabolome within known molecular networks (for example, metabolic or signaling pathways).
Next, we constructed molecular networks for the two diseases.
Large-scale interactome data have provided maps of molecular networks for several organisms (4 7).
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