Novel association of MEN1 gene mutations with parathyroid carcinoma.

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MEN1 gene mutation with parathyroid carcinoma: first report of a familial case.

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Q47135439-641C4C6D-3E4F-4104-B3D7-4B425185056B

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Novel association of MEN1 gene mutations with parathyroid carcinoma.

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Novel association of MEN1 gene mutations with parathyroid carcinoma.

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Novel association of MEN1 gene mutations with parathyroid carcinoma.

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Novel association of MEN1 gene mutations with parathyroid carcinoma.

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P1476

Novel association of MEN1 gene mutations with parathyroid carcinoma

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Alfredo Scillitani

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Celeste Clemente

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Claudia Battista

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Claudio Marcocci

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David E C Cole

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Elena Pardi

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Eliana Sanpaolo

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Filomena Cetani

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Geoffrey N Hendy

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Leonardo D'Agruma

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P2860

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Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling

The tumor suppressor protein menin interacts with NF-kappaB proteins and inhibits NF-kappaB-mediated transactivation

Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

Positional cloning of the gene for multiple endocrine neoplasia-type 1

The Phyre2 web portal for protein modeling, prediction and analysis

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.

Genetic aspects of adenomatosis of endocrine glands.

Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).

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23-30

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scholarly article

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10.3892/OL.2017.6162

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Angelo Sparaneo

E Maiello

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2017-05-12T00:00:00Z

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28693130

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5494910

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Novel association of MEN1 gene mutations with parathyroid carcinoma.

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P2860

P2860

Novel association of MEN1 gene mutations with parathyroid carcinoma.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932