Immunohistochemical assessment of parafibromin in mouse and human tissues

Parafibromin is a protein encoded by the HRPT2 oncosuppressor gene, whose mutation causes the hyperparathyroidism–jaw tumour syndrome, characterized by the occurrence of parathyroid adenoma or carcinoma, fibro-osseous jaw tumours, and renal neoplastic and non-neoplastic abnormalities. Non-morphologi...

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Autores principales: Porzionato, Andrea, Macchi, Veronica, Barzon, Luisa, Masi, Giulia, Iacobone, Maurizio, Parenti, Anna, Palù, Giorgio, De Caro, Raffaele
Formato: Artigo
Lenguaje:Inglês
Publicado: Blackwell Science Inc 2006
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2048996/
https://ncbi.nlm.nih.gov/pubmed/17118068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-7580.2006.00657.x
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