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FANCG Is Phosphorylated at Serines 383 and 387 during Mitosis
Fanconi anemia (FA) is an autosomal recessive disease marked by congenital defects, bone marrow failure, and high incidence of leukemia and solid tumors. Eight genes have been cloned, with the accompanying protein products participating in at least two complexes, which appear to be functionally depe...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Microbiology
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC516759/ https://ncbi.nlm.nih.gov/pubmed/15367677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.24.19.8576-8585.2004 |
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