Spermatogenesis disorder is associated with mutations in the ligand‐binding domain of an androgen receptor-Reference-Cited by-同舟云学术

Spermatogenesis disorder is associated with mutations in the ligand‐binding domain of an androgen receptor

Published:2019-08-02 Issue:10 Volume:51 Page:
ISSN:0303-4569
Container-title:Andrologia
language:en
Short-container-title:Andrologia

Author:

Hasani Nafiseh¹,Mohseni Meybodi Anahita²^ORCID,Rafaee Alemeh³^ORCID,Sadighi Gilani Mohammad Ali³⁴^ORCID,Mohammadzadeh Reza¹^ORCID,Sabbaghian Marjan³^ORCID

Affiliation:

1. Department of Cell and Molecular Biology, Faculty of Basic Science University of Maragheh Maragheh Iran

2. Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine ACECR Tehran Iran

3. Department of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine ACECR Tehran Iran

4. Department of Urology, Shariati Hospital Tehran University of Medical Sciences Tehran Iran

Publisher

Wiley

Subject

Urology,Endocrinology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/and.13376

Reference35 articles.

1. Predicting Functional Effect of Human Missense Mutations Using PolyPhen‐2

2. Novel (60%) and Recurrent (40%) Androgen Receptor Gene Mutations in a Series of 59 Patients with a 46,XY Disorder of Sex Development

3. A naturally occurring mutation in the human androgen receptor of a subject with complete androgen insensitivity confers binding and transactivation by estradiol

4. The human androgen receptor: Domain structure, genomic organization and regulation of expression

5. Scalable web services for the PSIPRED Protein Analysis Workbench

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