135 related articles for article (PubMed ID: 35674372)
1. Novel bi-allelic variants in KASH5 are associated with meiotic arrest and non-obstructive azoospermia.
Yang C; Lin X; Ji Z; Huang Y; Zhang L; Luo J; Chen H; Li P; Tian R; Zhi E; Hong Y; Zhou Z; Zhang F; Li Z; Yao C
Mol Hum Reprod; 2022 Jun; 28(7):. PubMed ID: 35674372
[TBL] [Abstract][Full Text] [Related]
2. A homozygous
Hou X; Zeb A; Dil S; Zhou J; Zhang H; Shi B; Muhammad Z; Khan I; Zaman Q; Shah WA; Jiang X; Wu L; Ma H; Shi Q
Front Endocrinol (Lausanne); 2023; 14():1128362. PubMed ID: 36864840
[TBL] [Abstract][Full Text] [Related]
3. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C
Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest.
van der Bijl N; Röpke A; Biswas U; Wöste M; Jessberger R; Kliesch S; Friedrich C; Tüttelmann F
Hum Reprod; 2019 Nov; 34(11):2112-2119. PubMed ID: 31682730
[TBL] [Abstract][Full Text] [Related]
5. Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia.
Li P; Ji Z; Zhi E; Zhang Y; Han S; Zhao L; Tian R; Chen H; Huang Y; Zhang J; Chen H; Zhao F; Zhou Z; Li Z; Yao C
Reprod Biol Endocrinol; 2022 Jan; 20(1):21. PubMed ID: 35090489
[TBL] [Abstract][Full Text] [Related]
6. Homozygous Variant in KASH5 Causes Premature Ovarian Insufficiency by Disordered Meiotic Homologous Pairing.
Zhang Q; Tao C; Gao S; Li S; Xu B; Ke H; Wang Y; Zhang F; Qin Y; Zhang L; Guo T
J Clin Endocrinol Metab; 2022 Aug; 107(9):2589-2597. PubMed ID: 35708642
[TBL] [Abstract][Full Text] [Related]
7. The missing LINC: a mammalian KASH-domain protein coupling meiotic chromosomes to the cytoskeleton.
Stewart CL; Burke B
Nucleus; 2014; 5(1):3-10. PubMed ID: 24637401
[TBL] [Abstract][Full Text] [Related]
8. Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.
Huang Y; Tian R; Xu J; Ji Z; Zhang Y; Zhao L; Yang C; Li P; Zhi E; Bai H; Han S; Luo J; Zhao J; Zhang J; Zhou Z; Li Z; Yao C
BMC Med Genomics; 2022 Jun; 15(1):137. PubMed ID: 35718780
[TBL] [Abstract][Full Text] [Related]
9. Bi-allelic
Yao C; Yang C; Zhao L; Li P; Tian R; Chen H; Guo Y; Huang Y; Zhi E; Zhai J; Sun H; Zhang J; Hong Y; Zhang L; Ji Z; Zhang F; Zhou Z; Li Z
J Med Genet; 2021 Oct; 58(10):679-686. PubMed ID: 32900840
[TBL] [Abstract][Full Text] [Related]
10. A Homozygous Loss-of-Function Mutation in
Gong C; Abbas T; Muhammad Z; Zhou J; Khan R; Ma H; Zhang H; Shi Q; Shi B
Int J Mol Sci; 2022 Jun; 23(12):. PubMed ID: 35742973
[TBL] [Abstract][Full Text] [Related]
11. Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.
Wu H; Zhang X; Hua R; Li Y; Cheng L; Li K; Liu Y; Gao Y; Shen Q; Wang G; Lv M; Xu Y; He X; Cao Y; Liu M
Hum Genet; 2022 Nov; 141(11):1795-1809. PubMed ID: 35587281
[TBL] [Abstract][Full Text] [Related]
12. Bi-allelic MEI1 variants cause meiosis arrest and non-obstructive azoospermia.
Zhang Y; Li N; Ji Z; Bai H; Ou N; Tian R; Li P; Zhi E; Huang Y; Zhao J; Han Y; Zhang J; Zhou Y; Li Z; Yao C
J Hum Genet; 2023 Jun; 68(6):383-392. PubMed ID: 36759719
[TBL] [Abstract][Full Text] [Related]
13. Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
Wu Y; Li Y; Murtaza G; Zhou J; Jiao Y; Gong C; Hu C; Han Q; Zhang H; Zhang Y; Shi B; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Sep; 36(10):2793-2804. PubMed ID: 34392356
[TBL] [Abstract][Full Text] [Related]
14. Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees.
Xie X; Murtaza G; Li Y; Zhou J; Ye J; Khan R; Jiang L; Khan I; Zubair M; Yin H; Jiang H; Liu W; Shi B; Hou X; Gong C; Fan S; Wang Y; Jiang X; Zhang Y; Zhang H; Ma H; Shi Q
Hum Reprod; 2022 Jun; 37(7):1664-1677. PubMed ID: 35526155
[TBL] [Abstract][Full Text] [Related]
15. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.
Wang W; Meng L; He J; Su L; Li Y; Tan C; Xu X; Nie H; Zhang H; Du J; Lu G; Luo M; Lin G; Tu C; Tan YQ
Mol Hum Reprod; 2022 May; 28(6):. PubMed ID: 35485979
[TBL] [Abstract][Full Text] [Related]
16. A homozygous frameshift variant in SYCP2 caused meiotic arrest and non-obstructive azoospermia.
Xu J; Sun Y; Zhang Y; Ou N; Bai H; Zhao J; Xu S; Luo J; Han S; Li P; Tian R; Zhi E; Huang Y; Zhang J; Liu G; Li Z; Yao C
Clin Genet; 2023 Nov; 104(5):577-581. PubMed ID: 37337432
[TBL] [Abstract][Full Text] [Related]
17. A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
Okutman O; Boivin M; Muller J; Charlet-Berguerand N; Viville S
Hum Reprod; 2023 Feb; 38(2):306-314. PubMed ID: 36524333
[TBL] [Abstract][Full Text] [Related]
18. Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.
Wyrwoll MJ; van Walree ES; Hamer G; Rotte N; Motazacker MM; Meijers-Heijboer H; Alders M; Meißner A; Kaminsky E; Wöste M; Krallmann C; Kliesch S; Hunt TJ; Clark AT; Silber S; Stallmeyer B; Friedrich C; van Pelt AMM; Mathijssen IB; Tüttelmann F
Hum Reprod; 2021 Dec; 37(1):178-189. PubMed ID: 34755185
[TBL] [Abstract][Full Text] [Related]
19.
He WB; Tu CF; Liu Q; Meng LL; Yuan SM; Luo AX; He FS; Shen J; Li W; Du J; Zhong CG; Lu GX; Lin G; Fan LQ; Tan YQ
J Med Genet; 2018 Mar; 55(3):198-204. PubMed ID: 29331980
[TBL] [Abstract][Full Text] [Related]
20. Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
Salas-Huetos A; Tüttelmann F; Wyrwoll MJ; Kliesch S; Lopes AM; Goncalves J; Boyden SE; Wöste M; Hotaling JM; ; Nagirnaja L; Conrad DF; Carrell DT; Aston KI
Hum Genet; 2021 Jan; 140(1):217-227. PubMed ID: 33211200
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]