Targeting menin

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microRNA‑802 promotes lung carcinoma proliferation by targeting the tumor suppressor menin.

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Distribution of menin-occupied regions in chromatin specifies a broad role of menin in transcriptional regulation.

Menin is the protein product of the MEN1 tumor-suppressor gene; one allele of MEN1 is inactivated in the germ line of patients with "multiple endocrine neoplasia type 1" (MEN1) cancer syndrome. Menin interacts with several proteins involved in transcriptional regulation. RNA expression analyses have identified several menin-regulated genes that could represent proximal or distal interaction sit...

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FBP1 Is an Interacting Partner of Menin

Multiple endocrine neoplasia type 1 (MEN1) is a syndrome characterized by tumors in multiple endocrine tissues such as the parathyroid glands, the pituitary gland, and the enteropancreatic neuroendocrine tissues. MEN1 is usually caused by mutations in the MEN1 gene that codes for the protein menin. Menin interacts with proteins that regulate transcription, DNA repair and processing, and mainten...

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MLL1 and menin: not partners in crime?

In this issue of Blood, Li et al report an unexpected but clinically relevant finding. They demonstrate that the mixed lineage leukemia (MLL1) gene acts independently from menin (Men1) in the hematopoietic system.

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ژورنال

عنوان ژورنال: Nature Reviews Drug Discovery

سال: 2012

ISSN: 1474-1776,1474-1784

DOI: 10.1038/nrd3689