Lessons from genes mutated in multiple endocrine neoplasia (MEN) syndromes
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Reference92 articles.
1. Germline mutations of the MENI gene in familial multiple endocrine neoplasia type 1 and related states;Agarwal;Hum Mol Genet,1997
2. Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription;Agarwal;Cell,1999
3. Molecular pathology of the MEN1 gene;Agarwal;Ann N Y Acad Sci,2004
4. Biological effects of the dual phenotypic Janus mutation of ret cosegregating with both multiple endocrine neoplasia type 2 and Hirschsprung's disease;Arighi;Mol Endocrinol,2004
5. Meningiomas may be a component tumor of multiple endocrine neoplasia type 1;Asgharian;Clin Cancer Res,2004
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1. The Multiple Endocrine Neoplasia Syndromes;Neuroendocrine Tumours;2024
2. Patients’ perception on the quality of care for multiple endocrine neoplasia disorders in Europe: an online survey from a patient support group;Endocrine;2021-02-03
3. Phenotypes Associated With MEN1 Syndrome: A Focus on Genotype-Phenotype Correlations;Frontiers in Endocrinology;2020-11-18
4. When should genetic testing be performed in patients with neuroendocrine tumours?;Reviews in Endocrine and Metabolic Disorders;2017-09-30
5. MEN1 in children and adolescents: Data from patients of a regional referral center for hereditary endocrine tumors;Endocrine;2017-05-22
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