MEN1 protein, human

Known as: menin, menin protein, human, multiple endocrine neoplasia I protein, human 
 
National Institutes of Health

Papers overview

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2013
2013
Multiple endocrine neoplasia type 1 (MEN1) is an inherited tumor syndrome that includes susceptibility to pancreatic islet tumors… (More)
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Highly Cited
2008
Highly Cited
2008
Menin displays the unique ability to either promote oncogenic function in the hematopoietic lineage or suppress tumorigenesis in… (More)
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Highly Cited
2005
Highly Cited
2005
Mutations in the MEN1 gene are associated with the multiple endocrine neoplasia syndrome type 1 (MEN1), which is characterized by… (More)
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Highly Cited
2005
Highly Cited
2005
Menin, the product of the Men1 gene mutated in familial multiple endocrine neoplasia type 1 (MEN1), regulates transcription in… (More)
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Review
2003
Review
2003
Multiple endocrine neoplasia type 1 (MEN1) is a familial cancer syndrome characterized mostly by tumors of the parathyroids… (More)
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Highly Cited
2003
Highly Cited
2003
Menin, a gene product of multiple endocrine neoplasia type I (MEN1), is known to act as a tumor suppressor to repress JunD… (More)
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2002
2002
Recently the multiple endocrine neoplasia type 1 (MEN1) tumor suppressor gene was cloned. Its protein product, called menin, has… (More)
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2001
2001
The tumour suppressor gene causing multiple endocrine neoplasia type 1 (MEN1) encodes a 610 amino acid protein, menin. In order… (More)
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Highly Cited
1999
Highly Cited
1999
MEN1 is a tumor suppressor gene that encodes a 610 amino acid nuclear protein (menin) of previously unknown function. Using a… (More)
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1999
1999
Although there is indirect genetic evidence that MEN1, the gene for multiple endocrine neoplasia type 1, is a tumor suppressor… (More)
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