A Novel Mutation F826L in the Human Androgen Receptor in Partial Androgen Insensitivity Syndrome; Increased NH2-/COOH-terminal Domain Interaction and TIF2 Co-Activation

Molecular and Cellular Endocrinology - Ireland
doi 10.1016/j.mce.2008.06.016
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Elsevier BV

Related search

A Novel Androgen Receptor Mutation Resulting in Complete Androgen Insensitivity Syndrome and Bilateral Leydig Cell Hyperplasia

Journal of Andrology
2006English

Partial Androgen Insensitivity Syndrome – Case Report

Pediatric Endocrinology
2014English

Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient With Androgen Insensitivity Syndrome

Journal of Pediatric and Adolescent Gynecology
Child HealthGynecologyPerinatologyObstetricsMedicinePediatrics
2019English

Androgen Insensitivity Syndrome

2020English

Molecular Analysis of the Androgen-Receptor Gene in a Family With Receptor-Positive Partial Androgen Insensitivity: An Unusual Type of Intronic Mutation

American Journal of Human Genetics
Genetics
1997English

Complete Androgen Insensitivity Syndrome

2020English

Isolated Micropenis Reveals Partial Androgen Insensitivity Syndrome Confirmed by Molecular Analysis

Asian Journal of Andrology
MedicineUrology
2010English

Sintokamide a Is a Novel Antagonist of Androgen Receptor That Uniquely Binds Activation Function-1 in Its Amino-Terminal Domain

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2016English

A Novel insA2933 Causes Premature Termination of Translation and Is Accompanied by Overexpression of Truncated Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome

Journal of Applied Genetics
MedicineGenetics
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy