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MEN1 protein, human

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

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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… Expand
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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… Expand
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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… Expand
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Review
2005
Review
2005
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disease predisposed by heterozygous germline mutations in the… Expand
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Highly Cited
2004
Highly Cited
2004
Menin, the product of the multiple endocrine neoplasia type 1 (MEN1) gene, is required for commitment of multipotential… Expand
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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… Expand
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Highly Cited
2003
Highly Cited
2003
Multiple endocrine neoplasia type I (MEN1) is an inherited tumor syndrome characterized by tumors in multiple endocrine organs… Expand
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Highly Cited
2001
Highly Cited
2001
Multiple endocrine neoplasia type 1 is an autosomal dominant tumor syndrome. Manifestations include neoplasms of the parathyroid… Expand
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Highly Cited
2001
Highly Cited
2001
The tumour suppressor gene causing multiple endocrine neoplasia type 1 (MEN1) encodes a 610 amino acid protein, menin. In order… Expand
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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… Expand
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