Llwytho...
Tumor microenvironment and neurofibromatosis type I: connecting the GAPs
The human disease von Recklinghausen's neurofibromatosis (Nf1) is one of the most common genetic disorders. It is caused by mutations in the NF1 tumor suppressor gene, which encodes a GTPase activating protein (GAP) that negatively regulates p21-RAS signaling. Dermal and plexiform neurofibromas...
Wedi'i Gadw mewn:
| Prif Awduron: | , |
|---|---|
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2007
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2760340/ https://ncbi.nlm.nih.gov/pubmed/17297459 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.onc.1210261 |
| Tagiau: |
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