Identification and Functional Investigation of Novel Heterozygous HELQ Mutations in Patients with Sertoli Cell-only Syndrome
Author:
Affiliation:
1. The first affiliated hospital of USTC, Division of Reproduction and Genetics, Hefei National Laboratory for Physical Sciences at Microscale, School of Basic Medical Sciences, University of Science and Technology of China, Hefei, China.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical),General Medicine
Link
https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2021.0104
Reference19 articles.
1. HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis
2. Novel mutation in USP26 associated with azoospermia in a Sertoli cell‐only syndrome patient
3. Human Globozoospermia-Related Gene Spata16 Is Required for Sperm Formation Revealed by CRISPR/Cas9-Mediated Mouse Models
4. Clinical genetic testing for male factor infertility: current applications and future directions
5. Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. HELQ deficiency impairs the induction of primordial germ cell‐like cells;FEBS Open Bio;2024-05-08
2. HELQ as a DNA helicase: Its novel role in normal cell function and tumorigenesis (Review);Oncology Reports;2023-11-02
3. Sertoli cell-only syndrome: advances, challenges, and perspectives in genetics and mechanisms;Cellular and Molecular Life Sciences;2023-02-23
4. Identification of pathogenic mutations from nonobstructive azoospermia patients;Biology of Reproduction;2022-05-09
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