A novel deletion of theMEN1gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype-Reference-Cited by-同舟云学术

A novel deletion of theMEN1gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype

Published:2011-11-09 Issue:6 Volume:75 Page:791-800
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Raef Hussein,Zou Minjing,Baitei Essa Y.,Al-Rijjal Roua A.,Kaya Namik,Al-Hamed Mohamed,Monies Dorota,Abu-Dheim Nada N.,Al-Hindi Hindi,Al-Ghamdi Mohammed H.,Meyer Brian F.,Shi Yufei

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2011.04134.x/fullpdf

Reference39 articles.

1. Positional cloning of the gene for multiple endocrine neoplasia-type 1;Chandrasekharappa;Science,1997

2. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans;Pellegata;Proceedings of the National Academy of Sciences of the United States of America,2006

3. Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states;Agarwal;Journal of Clinical Endocrinology and Metabolism,2009

4. Molecular and genetic mechanisms of tumorigenesis in multiple endocrine neoplasia type-1;Guo;Molecular Endocrinology,2001

5. Hereditary hormone excess: genes, molecular pathways, and syndromes;Marx;Endocrine Reviews,2005

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Syndromic MEN1 parathyroid adenomas consist of both subclonal nodules and clonally independent tumors;Virchows Archiv;2024-01-20

2. Modeling MEN1 with Patient-Origin iPSCs Reveals GLP-1R Mediated Hypersecretion of Insulin;Cells;2022-08-03

3. Association of Famine Exposure on the Changing Clinical Phenotypes of Primary Hyperparathyroidism in 20 years;Frontiers in Endocrinology;2022-06-17

4. Multiple endocrine neoplasia type 1: a new germline “homozygous” variant (c.201delC) caused by detection errors;Hereditary Cancer in Clinical Practice;2022-03-07

5. Molecular alterations in retinoblastoma beyond RB1;Experimental Eye Research;2021-10