Multiple Endocrine Neoplasia Type I Variants and Phenocopies: More than a Nosological Issue?-Reference-Cited by-同舟云学术

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Multiple Endocrine Neoplasia Type I Variants and Phenocopies: More than a Nosological Issue?

Published:2009-05-01 Issue:5 Volume:94 Page:1518-1520
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Falchetti Alberto¹,Brandi Maria Luisa¹²

Affiliation:

1. Regional Centre for Hereditary Endocrine Tumors (A.F., M.L.B.), University of Florence, 50135 Florence, Italy

2. Unit of Metabolic Bone Diseases, Department of Internal Medicine and Spin-off DeGene (M.L.B.), University of Florence, 50135 Florence, Italy

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/94/5/1518/9062896/jcem1518.pdf

Reference19 articles.

1. Proliferation-associated expression of the MEN1 gene as revealed by in situ hybridization: possible role of the menin as a negative regulator of cell proliferation under DNA damage.;Ikeo;Lab Invest,2000

2. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.;Larsson;Nature,1988

3. Loss of heterozygosity at 11q13: analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1.;Dong;J Clin Endocrinol Metab,1997

4. Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.;Simonds;J Clin Endocrinol Metab,2004

5. Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism;Pannett;Clin Endocrinol (Oxf),2003

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1. Endocrinology and Metabolism;Internal Medicine;2023

2. Genetic Basis of ACTH-Secreting Adenomas;International Journal of Molecular Sciences;2022-06-19

3. The role of non-coding RNAs in the pathogenesis of multiple endocrine neoplasia syndrome type 1;Problems of Endocrinology;2020-08-30

4. Current Issues in Terminology and Classification of Hereditary Disorders at Endocrine Cancer;Acta Biomedica Scientifica (East Siberian Biomedical Journal);2019-05-25

5. Deletion of exons 1–3 of the MEN1 gene in a large Italian family causes the loss of menin expression;Familial Cancer;2014-02-13

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