Multiple endocrine neoplasia type I variants and phenocopies: more than a nosological issue?

Suppr

超能文献

作者信息

Falchetti Alberto, Brandi Maria Luisa

出版信息

J Clin Endocrinol Metab. 2009 May;94(5):1518-20. doi: 10.1210/jc.2009-0494.

DOI:10.1210/jc.2009-0494

PMID:19420274

Abstract

摘要

相似文献

Multiple endocrine neoplasia type I variants and phenocopies: more than a nosological issue?

J Clin Endocrinol Metab. 2009 May;94(5):1518-20. doi: 10.1210/jc.2009-0494.

Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.

J Clin Endocrinol Metab. 2007 Aug;92(8):3321-5. doi: 10.1210/jc.2006-2843. Epub 2007 May 22.

Germline mutations in the CDKN1B gene encoding p27 Kip1 are a rare cause of multiple endocrine neoplasia type 1.

Clin Endocrinol (Oxf). 2009 Mar;70(3):499-500. doi: 10.1111/j.1365-2265.2008.03363.x. Epub 2008 Jul 31.

Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain.

Clin Endocrinol (Oxf). 2012 May;76(5):719-24. doi: 10.1111/j.1365-2265.2011.04269.x.

Haploinsufficient and predominant expression of multiple endocrine neoplasia type 1 (MEN1)-related genes, MLL, p27Kip1 and p18Ink4C in endocrine organs.

Biochem Biophys Res Commun. 2011 Nov 18;415(2):378-83. doi: 10.1016/j.bbrc.2011.10.077. Epub 2011 Oct 21.

Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds.

Endocr Relat Cancer. 2012 May 3;19(3):233-41. doi: 10.1530/ERC-11-0362. Print 2012 Jun.

Multiple endocrine neoplasia, the old and the new: a mini review.

G Chir. 2012 Nov-Dec;33(11-12):370-3.

[MEN1].

Nihon Rinsho. 2011 Mar;69 Suppl 2:686-9.

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans.

Proc Natl Acad Sci U S A. 2006 Oct 17;103(42):15558-63. doi: 10.1073/pnas.0603877103. Epub 2006 Oct 9.

[Multiple endocrine neoplasia type 1 variants and phenocopies].

Ter Arkh. 2014;86(10):87-91.

引用本文的文献

Genetic Basis of ACTH-Secreting Adenomas.

Int J Mol Sci. 2022 Jun 19;23(12):6824. doi: 10.3390/ijms23126824.

Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expression.

Fam Cancer. 2014 Jun;13(2):273-80. doi: 10.1007/s10689-014-9702-y.

A differential diagnosis of inherited endocrine tumors and their tumor counterparts.

Clinics (Sao Paulo). 2013 Jul;68(7):1039-56. doi: 10.6061/clinics/2013(07)24.

Total parathyroidectomy in a large cohort of cases with hyperparathyroidism associated with multiple endocrine neoplasia type 1: experience from a single academic center.

Clinics (Sao Paulo). 2012;67 Suppl 1(Suppl 1):131-9. doi: 10.6061/clinics/2012(sup01)22.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验