MEN1 gene

Known as: MENIN, Multiple Endocrine Neoplasia 1 Gene, MEN1 
This gene is involved in transcriptional regulation and has tumor suppressor activity.
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… (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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Highly Cited
2005
Highly Cited
2005
Multiple endocrine neoplasia type I (MEN1) is a familial cancer syndrome characterized primarily by tumors of multiple endocrine… (More)
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Highly Cited
2005
Highly Cited
2005
service Email alerting top right corner of the article Receive free email alerts when new articles cite this article sign up in… (More)
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Highly Cited
2005
Highly Cited
2005
The Mixed-Lineage Leukemia (MLL) protein is a histone methyltransferase that is mutated in clinically and biologically… (More)
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Highly Cited
2004
Highly Cited
2004
MLL (for mixed-lineage leukemia) is a proto-oncogene that is mutated in a variety of human leukemias. Its product, a homolog of… (More)
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Highly Cited
2004
Highly Cited
2004
The cellular function of the menin tumor suppressor protein, product of the MEN1 gene mutated in familial multiple endocrine… (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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Highly Cited
1998
Highly Cited
1998
The MEN1 gene, mutations in which are responsible for multiple endocrine neoplasia type 1 (MEN1), encodes a 610-amino acid… (More)
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Highly Cited
1997
Highly Cited
1997
Familial multiple endocrine neoplasia type 1 (FMEN1) is an autosomal dominant trait characterized by tumors of the parathyroids… (More)
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