Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

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Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

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Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

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Item

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Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

@en

Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

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Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

@en

Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

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P1476

Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives.

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P2093

Fatemeh Khatami

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Seyed Mohammad Tavangar

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P2860

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

Molecular modeling of the extracellular domain of the RET receptor tyrosine kinase reveals multiple cadherin-like domains and a calcium-binding site

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

Menin is required for bone morphogenetic protein 2- and transforming growth factor beta-regulated osteoblastic differentiation through interaction with Smads and Runx2

Menin uncouples Elk-1, JunD and c-Jun phosphorylation from MAP kinase activation

Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B

Menin suppresses osteoblast differentiation by antagonizing the AP-1 factor, JunD

Lung cancer cell migration is regulated via repressing growth factor PTN/RPTP β/ζ signaling by menin

Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

P304

1177271918785129

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P31

scholarly article

P356

10.1177/1177271918785129

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P478

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P577

2018-07-02T00:00:00Z

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P698

30013307

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P932

6043927

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