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Gain and loss of phosphorylation sites in human cancer
Motivation: Coding-region mutations in human genes are responsible for a diverse spectrum of diseases and phenotypes. Among lesions that have been studied extensively, there are insights into several of the biochemical functions disrupted by disease-causing mutations. Currently, there are more than...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2732209/ https://ncbi.nlm.nih.gov/pubmed/18689832 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btn267 |
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