Abstract
In contrast to animal-based mutant phenotype assays, recent biochemical and quantitative genetic studies have identified hundreds of potential regulators of known signaling pathways. We discuss the discrepancy between previous models and new data, put forward a different signaling conceptual framework incorporating time-dependent quantitative contributions, and suggest how this new framework can impact our study of human disease.
MeSH terms
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Animals
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Computational Biology / methods
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Computational Biology / trends
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Gene Expression Regulation / genetics
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Gene Regulatory Networks / genetics*
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Genetic Diseases, Inborn / genetics
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Genetic Diseases, Inborn / physiopathology
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Genetic Diseases, Inborn / therapy
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Genetic Testing / methods*
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Genetic Testing / trends
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Humans
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Molecular Biology / methods*
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Molecular Biology / trends
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Neoplasms / therapy
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Signal Transduction / genetics*