Glucose-dependent insulinotropic peptide receptor overexpression in adrenocortical hyperplasia in MEN1 syndrome without loss of heterozygosity at the 11q13 locus
BACKGROUND: The molecular mechanisms involved in the genesis of the adrenocortical lesions seen in MEN1 syndrome (ACL-MEN1) remain poorly understood; loss of heterozygosity at 11q13 and somatic mutations of MEN1 are not usually found in these lesions. Thus, additional genes must be involved in MEN1...
Main Authors: | Marcia Helena Soares Costa, Sorahia Domenice, Rodrigo Almeida Toledo, Delmar Muniz L. Junior, Ana Claudia Latronico, Emilia Modolo Pinto, Sergio Pereira Almeida Toledo, Berenice Bilharinho Mendonca, Maria Candida Barisson Villares Fragoso |
---|---|
Format: | Article |
Language: | English |
Published: |
Faculdade de Medicina / USP
2011-01-01
|
Series: | Clinics |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322011000400002 |
Similar Items
-
Untreated Congenital Adrenal Hyperplasia with 17-α Hydroxylase/17,20-Lyase Deficiency Presenting as Massive Adrenocortical Tumor
by: Su Jin Lee, et al.
Published: (2015-09-01) -
Glucose-dependent insulinotropic polypeptide (GIP) and GIP receptor (GIPR) genes: An association analysis of polymorphisms and bone in young and elderly women
by: Gaurav Garg, et al.
Published: (2016-06-01) -
Long-term Results after CT-Guided Percutaneous Ethanol Ablation for the Treatment of Hyperfunctioning Adrenal Disorders
by: Nathan Elie Frenk, et al. -
Genotype analysis of the human endostatin variant p.D104N in benign and malignant adrenocortical tumors
by: Beatriz Marinho de Paula Mariani, et al.
Published: (2012-01-01) -
Role of ACTH receptor in adrenocortical tumor formation
by: A.C. Latronico
Published: (2000-10-01)