Reference40 articles.
1. Agarwal SK, Guru SC, Heppner C, et al. Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription. Cell 1999;84:730–735.
2. Agarwal SK, Kester MB, Deblenko LV, et al. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum Mol Genet 1997;6:1169-1175.
3. Bassett JH, Rashbass P, Harding B, Forbes SA, Pannett AA, Thakker RV. Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, MEN1. J Bone Miner Res 1999;14:3–10.
4. Bassett JHD, Forbes SA, Pannett AAJ, et al. Characterisation of mutations in patients with multiple endocrine neoplasia type 1 (MEN1). Am J Hum Genet 1998;62:232–244.
5. Bertolino P, Radovanovic I, Casse H, Aguzzi A, Wang Z-Q, Zhang C-X. Genetic ablation of the tumor suppressor menin causes lethality at mid-gestation with defects in multiple organs. Mech Dev 2003;120: 549–560.
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