Functional Defects From Endocrine Disease-Associated Mutations in HLXB9 and Its Interacting Partner, NONO.

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Functional Defects From Endocrine Disease-Associated Mutations in HLXB9 and Its Interacting Partner, NONO.

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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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Functional Defects From Endocr ...... Its Interacting Partner, NONO.

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Functional Defects From Endocr ...... Its Interacting Partner, NONO.

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Functional Defects From Endocr ...... Its Interacting Partner, NONO.

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Functional Defects From Endocr ...... Its Interacting Partner, NONO.

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Functional Defects From Endocr ...... Its Interacting Partner, NONO.

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Functional Defects From Endocr ...... Its Interacting Partner, NONO.

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P1476

Functional Defects From Endocr ...... Its Interacting Partner, NONO

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P2093

Sampada S Kharade

http://www.w3.org/2001/XMLSchema#string

Vaishali I Parekh

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P2860

Genome-wide analysis of menin binding provides insights into MEN1 tumorigenesis.

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

A novel human homeobox gene distantly related to proboscipedia is expressed in lymphoid and pancreatic tissues

The 32-kilodalton subunit of replication protein A interacts with menin, the product of the MEN1 tumor suppressor gene

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors

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

Selective agenesis of the dorsal pancreas in mice lacking homeobox gene Hlxb9

Reexpression of oncoprotein MafB in proliferative β-cells and Men1 insulinomas in mouse

Altered MENIN expression disrupts the MAFA differentiation pathway in insulinoma

P304

1199-1212

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P31

scholarly article

P356

10.1210/EN.2017-03155

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P407

English

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P478

159

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P50

Sunita K Agarwal

P577

2018-02-01T00:00:00Z

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P698

29309627

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P932

5793795

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