New splicing mutation of MEN1 gene affecting the translocation of menin to the nucleous
, 2006 Multiple endocrine neoplasia type 1 (MEN1) is a syndrome inherited in an autosomal dominant trait caused by the inactivation of the tumor suppressor gene MEN1.
Campino, C. +8 more
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Turning Points in Cross-Disciplinary Perspective of Primary Hyperparathyroidism and Pancreas Involvements: Hypercalcemia-Induced Pancreatitis, MEN1 Gene-Related Tumors, and Insulin Resistance. [PDF]
Int J Mol SciCarsote M +7 more
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Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease. [PDF]
Clin Endocrinol (Oxf), 2018 Makri A +11 more
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Clinical features of MEN1 in children, adolescents, and young adults: a single-center study. [PDF]
Front Endocrinol (Lausanne)Della Valentina S +13 more
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Genetic factors associated with thymic tumors in patients with MEN1: a nested case-control study in the GTE/AFCE cohort. [PDF]
J Endocr SocJourné A +7 more
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Long-term survival and molecular heterogeneity of sporadic multifocal non-functional pancreatic neuroendocrine tumors. [PDF]
iSciencePeng Y +11 more
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Multidisciplinary Management of the Rare Coexistence of Multiple Endocrine Neoplasia Type 1 and Chronic Thromboembolic Pulmonary Hypertension: A Case Report. [PDF]
CureusDeb G +4 more
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The tumor suppressor menin is a key scaffold mediator for homologous recombination repair. [PDF]
Nucleic Acids ResLian A +8 more
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