Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas-Reference-Cited by-同舟云学术

Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas

Published:2016-04-02 Issue:2 Volume:55 Page:386-397
ISSN:1355-008X
Container-title:Endocrine
language:en
Short-container-title:Endocrine

Author:

Borsari Simona,Pardi Elena,Pellegata Natalia S.,Lee Misu,Saponaro Federica,Torregrossa Liborio,Basolo Fulvio,Paltrinieri Elena,Zatelli Maria Chiara,Materazzi Gabriele,Miccoli Paolo,Marcocci Claudio,Cetani Filomena

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/s12020-016-0941-6.pdf

Reference61 articles.

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3. M.C. Lemos, R.V. Thakker, Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene. Hum. Mutat. 29, 22–32 (2008)

4. E. Pardi, C. Marcocci, S. Borsari, F. Saponaro, L. Torregrossa, M. Tancredi, B. Raspini, F. Basolo, F. Cetani, Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas. J. Clin. Endocrinol. Metab. 98, 2800–2810 (2013)

5. M.K. Cromer, L.F. Starker, M. Choi, R. Udelsman, C. Nelson-Williams, R.P. Lifton, T. Carling, Identification of somatic mutations in parathyroid tumors using whole-exome sequencing. J. Clin. Endocrinol. Metab. 97, E1774–E1781 (2012)

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