Androgen receptor dysfunction as a prevalent manifestation in young male carriers of a FLNA gene mutation-Reference-Cited by-同舟云学术

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Androgen receptor dysfunction as a prevalent manifestation in young male carriers of a FLNA gene mutation

Published:2017-04-21 Issue:6 Volume:173 Page:1710-1713
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Carrera-García Laura¹^ORCID,Rivas-Crespo Maximiliano Francisco²,Fernández García María Soledad³

Affiliation:

1. Pediatric Neurology; Hospital Universitario Central de Asturias; University of Oviedo; Oviedo Spain

2. Endocrinology; Hospital Universitario Central de Asturias; University of Oviedo; Oviedo Spain

3. Pathology; Hospital Universitario Central de Asturias; University of Oviedo; Oviedo Spain

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Androgen-Induced Cell Migration: Role of androgen Receptor/Filamin a association;Castoria;PLoS ONE,2011

2. Role of non-genomic androgen signalling in supressing proliferation of fibroblasts and fibrosarcoma cells;Castoria;Cell Death & Disease,2014

3. Androgen-stimulated DNA synthesis and cytoskeletal changes in fibroblasts by nontranscriptional receptor action;Castoria;Journal of Cell Biology,2003

4. Growth Factors as mediators of androgen action during the development of the male urogenital tract;Cunha;World Journal of Urology,1995

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1. PTPN11 and FLNA variants in a boy with ambiguous genitalia, short stature, and non-specific dysmorphic features;CLIN PEDIATR ENDOCRI;2024

2. <i>PTPN11</i> and <i>FLNA</i> variants in a boy with ambiguous genitalia, short stature, and non-specific dysmorphic features;Clinical Pediatric Endocrinology;2024

3. Whole-Exome Sequencing Identified Rare Genetic Variants Associated with Undervirilized Genitalia in Taiwanese Pediatric Patients;Biomedicines;2023-01-17

4. A classification of genes involved in normal and delayed male puberty;Asian Journal of Andrology;2023

5. Genetic analysis of failed male puberty using whole exome sequencing;Journal of Pediatric Endocrinology and Metabolism;2022-09-15

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