Characterization of a novel androgen receptor gene variant identified in an Iranian family with complete androgen insensitivity syndrome (CAIS): a molecular dynamics simulation study-Reference-Cited by-同舟云学术

Characterization of a novel androgen receptor gene variant identified in an Iranian family with complete androgen insensitivity syndrome (CAIS): a molecular dynamics simulation study

Published:2022-11-21 Issue: Volume: Page:1-15
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Aghaei Shahrzad¹^ORCID,Parvizpour Sepideh²³^ORCID,Farrokhi Effat¹^ORCID,Molavi Newsha⁴^ORCID,Hoseinzadeh Marziyeh⁴^ORCID,Tabatabaiefar Mohammad Amin⁴⁵^ORCID

Affiliation:

1. Department of Molecular Medicine, School of Advanced Technologies, Shahrekord University of Medical Sciences, Shahrekord, Iran

2. Research center for Pharmaceutical Nanotechnology, Biomedicine Institute Tabriz University of Medical Sciences, Tabriz, Iran

3. Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran

4. Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

5. Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Noncommunicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran

Funder

Shahrekord University of Medical Sciences

Isfahan University of Medical Sciences

Publisher

Informa UK Limited

Subject

Molecular Biology,General Medicine,Structural Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/07391102.2022.2148125

Reference34 articles.

1. Identification of the Underlying Androgen Receptor Defect in the Dallas Reifenstein Family

2. The Universal Protein Resource (UniProt)

3. Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome

4. Wide variation in androgen receptor dysfunction in complete androgen insensitivity syndrome

5. GenotypeVersusPhenotype in Families with Androgen Insensitivity Syndrome

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