Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans-Reference-Cited by-同舟云学术

Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans

Published:2023-07 Issue:7 Volume:26 Page:107193
ISSN:2589-0042
Container-title:iScience
language:en
Short-container-title:iScience

Author:

Liu Junyan,Rahim Fazal^ORCID,Zhou Jianteng,Fan Suixing,Jiang Hanwei,Yu Changping,Chen Jing,Xu Jianze,Yang Gang,Shah Wasim,Zubair Muhammad,Khan Asad^ORCID,Li Yang^ORCID,Shah Basit,Zhao Daren,Iqbal Furhan,Jiang Xiaohua,Guo Tonghang,Xu Peng,Xu Bo,Wu Limin,Ma Hui,Zhang Yuanwei,Zhang Huan,Shi Qinghua^ORCID

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference64 articles.

1. Medical management of non-obstructive azoospermia;Kumar;Clinics,2013

2. Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives;Kasak;Hum. Genet.,2021

3. The biology of infertility: research advances and clinical challenges;Matzuk;Nat. Med.,2008

4. Structural complexity in the KCTD family of Cullin3-dependent E3 ubiquitin ligases;Pinkas;Biochem. J.,2017

5. In-depth mutational analysis of the promyelocytic leukemia zinc finger BTB/POZ domain reveals motifs and residues required for biological and transcriptional functions;Melnick;Mol. Cell Biol.,2000

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1. Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non‐obstructive azoospermia in an Iranian family;Clinical Genetics;2024-07-02

2. Insight into the complexity of male infertility: a multi-omics review;Systems Biology in Reproductive Medicine;2024-03-22

3. A Comprehensive Analysis of the Structural Recognition between KCTD Proteins and Cullin 3;International Journal of Molecular Sciences;2024-02-04