127 related articles for article (PubMed ID: 35240466)
1. Induced pluripotent stem cell line from a mouse model of human azoospermia with a frameshift mutation Tex11_1260Ins(TT).
Tran KTD; Sheng Y; Doungkamchan C; Castro CA; Orwig KE
Stem Cell Res; 2022 Apr; 60():102728. PubMed ID: 35240466
[TBL] [Abstract][Full Text] [Related]
2. A new
Yu XC; Li MJ; Cai FF; Yang SJ; Liu HB; Zhang HB
Asian J Androl; 2021; 23(5):510-515. PubMed ID: 33762476
[TBL] [Abstract][Full Text] [Related]
3. TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.
Yang F; Silber S; Leu NA; Oates RD; Marszalek JD; Skaletsky H; Brown LG; Rozen S; Page DC; Wang PJ
EMBO Mol Med; 2015 Sep; 7(9):1198-210. PubMed ID: 26136358
[TBL] [Abstract][Full Text] [Related]
4. Novel mutations of
Song J; Sha Y; Liu X; Zeng X; Zhao X
Front Endocrinol (Lausanne); 2023; 14():1159723. PubMed ID: 37124723
[TBL] [Abstract][Full Text] [Related]
5. X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
Yatsenko AN; Georgiadis AP; Röpke A; Berman AJ; Jaffe T; Olszewska M; Westernströer B; Sanfilippo J; Kurpisz M; Rajkovic A; Yatsenko SA; Kliesch S; Schlatt S; Tüttelmann F
N Engl J Med; 2015 May; 372(22):2097-107. PubMed ID: 25970010
[TBL] [Abstract][Full Text] [Related]
6. A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.
Sha Y; Zheng L; Ji Z; Mei L; Ding L; Lin S; Wang X; Yang X; Li P
BMC Med Genet; 2018 Apr; 19(1):63. PubMed ID: 29661171
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Expression analysis of genes encoding
Boroujeni PB; Sabbaghian M; Totonchi M; Sodeifi N; Sarkardeh H; Samadian A; Sadighi-Gilani MA; Gourabi H
JBRA Assist Reprod; 2018 Sep; 22(3):185-192. PubMed ID: 29932616
[TBL] [Abstract][Full Text] [Related]
9. A pathogenic DMC1 frameshift mutation causes nonobstructive azoospermia but not primary ovarian insufficiency in humans.
Cao D; Shi F; Guo C; Liu Y; Lin Z; Zhang J; Li RHW; Yao Y; Liu K; Ng EHY; Yeung WSB; Wang T
Mol Hum Reprod; 2021 Sep; 27(9):. PubMed ID: 34515795
[TBL] [Abstract][Full Text] [Related]
10. Rescue of male infertility through correcting a genetic mutation causing meiotic arrest in spermatogonial stem cells.
Wang YH; Yan M; Zhang X; Liu XY; Ding YF; Lai CP; Tong MH; Li JS
Asian J Androl; 2021; 23(6):590-599. PubMed ID: 33533741
[TBL] [Abstract][Full Text] [Related]
11. Novel Hemizygous Mutations of
Ji Z; Yao C; Yang C; Huang C; Zhao L; Han X; Zhu Z; Zhi E; Liu N; Zhou Z; Li Z
Front Genet; 2021; 12():741355. PubMed ID: 34621296
[TBL] [Abstract][Full Text] [Related]
12. Genetic mutations contributing to non-obstructive azoospermia.
Peña VN; Kohn TP; Herati AS
Best Pract Res Clin Endocrinol Metab; 2020 Dec; 34(6):101479. PubMed ID: 33390350
[TBL] [Abstract][Full Text] [Related]
13. Mutation in TDRD9 causes non-obstructive azoospermia in infertile men.
Arafat M; Har-Vardi I; Harlev A; Levitas E; Zeadna A; Abofoul-Azab M; Dyomin V; Sheffield VC; Lunenfeld E; Huleihel M; Parvari R
J Med Genet; 2017 Sep; 54(9):633-639. PubMed ID: 28536242
[TBL] [Abstract][Full Text] [Related]
14. Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.
Colombo R; Pontoglio A; Bini M
Gynecol Obstet Invest; 2017; 82(3):283-286. PubMed ID: 28355598
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. In Vitro Modeling of Human Germ Cell Development Using Pluripotent Stem Cells.
Zhao Y; Ye S; Liang D; Wang P; Fu J; Ma Q; Kong R; Shi L; Gong X; Chen W; Ding W; Yang W; Zhu Z; Chen H; Sun X; Zhu J; Li Z; Wang Y
Stem Cell Reports; 2018 Feb; 10(2):509-523. PubMed ID: 29398481
[TBL] [Abstract][Full Text] [Related]
17. Generation of an iPSC line (HRMSDUi001-A) from an azoospermic patient with 45,XY,der(13;14)(q10;q10) karyotype.
Guo L; Zhao Z; Zhao S; Kong F; Yuan M
Stem Cell Res; 2021 Aug; 55():102453. PubMed ID: 34284274
[TBL] [Abstract][Full Text] [Related]
18. Association of CATSPER1, SPATA16 and TEX11 genes polymorphism with idiopathic azoospermia and oligospermia risk in Iranian population.
Behvarz M; Rahmani SA; Siasi Torbati E; Danaei Mehrabad S; Bikhof Torbati M
BMC Med Genomics; 2022 Mar; 15(1):47. PubMed ID: 35248021
[TBL] [Abstract][Full Text] [Related]
19. Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
Kasak L; Punab M; Nagirnaja L; Grigorova M; Minajeva A; Lopes AM; Punab AM; Aston KI; Carvalho F; Laasik E; Smith LB; ; Conrad DF; Laan M
Am J Hum Genet; 2018 Aug; 103(2):200-212. PubMed ID: 30075111
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]