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Primary pigmented nodular adrenocortical disease reveals insulin-like growth factor binding protein-2 regulation by protein kinase A
OBJECTIVE: Primary Pigmented Nodular Adrenocortical Disease (PPNAD) can occur as an isolated trait or part of Carney complex, a familial lentiginosis-multiple endocrine neoplasia syndrome frequently caused by mutations in PRKAR1A, which encodes the 1α regulatory subunit of protein kinase A (PKA). Be...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2577759/ https://ncbi.nlm.nih.gov/pubmed/17280861 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ghir.2006.12.004 |
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