450 related articles for article (PubMed ID: 34392356)
1. 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]
2. A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination.
Li Y; Wu Y; Zhou J; Zhang H; Zhang Y; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Apr; 36(5):1436-1445. PubMed ID: 33713115
[TBL] [Abstract][Full Text] [Related]
3. A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.
Gershoni M; Hauser R; Barda S; Lehavi O; Arama E; Pietrokovski S; Kleiman SE
Hum Reprod; 2019 Apr; 34(4):666-671. PubMed ID: 30838384
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.
Zhu X; Hu K; Cheng H; Wu H; Li K; Gao Y; Lv M; Xu C; Geng H; Shen Q; Cao Y; He X; Tang D; Guo R
Clin Genet; 2024 Jan; 105(1):99-105. PubMed ID: 37715646
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
Caburet S; Todeschini AL; Petrillo C; Martini E; Farran ND; Legois B; Livera G; Younis JS; Shalev S; Veitia RA
EBioMedicine; 2019 Apr; 42():524-531. PubMed ID: 31000419
[TBL] [Abstract][Full Text] [Related]
10. shani mutation in mouse affects splicing of Spata22 and leads to impaired meiotic recombination.
Petrillo C; Barroca V; Ribeiro J; Lailler N; Livera G; Keeney S; Martini E; Jain D
Chromosoma; 2020 Jun; 129(2):161-179. PubMed ID: 32388826
[TBL] [Abstract][Full Text] [Related]
11. Biallelic mutations in RNA-binding protein ADAD2 cause spermiogenic failure and non-obstructive azoospermia in humans.
Shi B; Shah W; Liu L; Gong C; Zhou J; Abbas T; Ma H; Zhang H; Yang M; Zhang Y; Ullah N; Mahammad Z; Khan M; Murtaza G; Ali A; Khan R; Sha J; Yuan Y; Shi Q
Hum Reprod Open; 2023; 2023(3):hoad022. PubMed ID: 37325547
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Spermatogenesis associated 22 is required for DNA repair and synapsis of homologous chromosomes in mouse germ cells.
Hays E; Majchrzak N; Daniel V; Ferguson Z; Brown S; Hathorne K; La Salle S
Andrology; 2017 Mar; 5(2):299-312. PubMed ID: 28297563
[TBL] [Abstract][Full Text] [Related]
14. Homozygous missense variant in MEIOSIN causes premature ovarian insufficiency.
Zhang Q; Zhang W; Wu X; Ke H; Qin Y; Zhao S; Guo T
Hum Reprod; 2023 Nov; 38(Supplement_2):ii47-ii56. PubMed ID: 37982418
[TBL] [Abstract][Full Text] [Related]
15. Rare missense variant in MSH4 associated with primary gonadal failure in both 46, XX and 46, XY individuals.
Akbari A; Padidar K; Salehi N; Mashayekhi M; Almadani N; Sadighi Gilani MA; Bashambou A; McElreavey K; Totonchi M
Hum Reprod; 2021 Mar; 36(4):1134-1145. PubMed ID: 33448284
[TBL] [Abstract][Full Text] [Related]
16. Meiosis-specific proteins MEIOB and SPATA22 cooperatively associate with the single-stranded DNA-binding replication protein A complex and DNA double-strand breaks.
Xu Y; Greenberg RA; Schonbrunn E; Wang PJ
Biol Reprod; 2017 May; 96(5):1096-1104. PubMed ID: 28453612
[TBL] [Abstract][Full Text] [Related]
17. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S; Jiao Y; Khan R; Jiang X; Javed AR; Ali A; Zhang H; Zhou J; Naeem M; Murtaza G; Li Y; Yang G; Zaman Q; Zubair M; Guan H; Zhang X; Ma H; Jiang H; Ali H; Dil S; Shah W; Ahmad N; Zhang Y; Shi Q
Am J Hum Genet; 2021 Feb; 108(2):324-336. PubMed ID: 33508233
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes.
Ghieh F; Barbotin AL; Swierkowski-Blanchard N; Leroy C; Fortemps J; Gerault C; Hue C; Mambu Mambueni H; Jaillard S; Albert M; Bailly M; Izard V; Molina-Gomes D; Marcelli F; Prasivoravong J; Serazin V; Dieudonne MN; Delcroix M; Garchon HJ; Louboutin A; Mandon-Pepin B; Ferlicot S; Vialard F
Hum Reprod; 2022 May; 37(6):1334-1350. PubMed ID: 35413094
[TBL] [Abstract][Full Text] [Related]
19. Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure.
Dong J; Zhang H; Mao X; Zhu J; Li D; Fu J; Hu J; Wu L; Chen B; Sun Y; Mu J; Zhang Z; Sun X; Zhao L; Wang W; Wang W; Zhou Z; Zeng Y; Du J; Li Q; He L; Jin L; Kuang Y; Wang L; Sang Q
Hum Reprod; 2021 Jul; 36(8):2371-2381. PubMed ID: 34037756
[TBL] [Abstract][Full Text] [Related]
20. Bi-allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest.
Yao C; Hou D; Ji Z; Pang D; Li P; Tian R; Zhang Y; Ou N; Bai H; Zhi E; Huang Y; Qin Y; Zhao J; Wang C; Zhou Z; Guo T; Li Z
Clin Genet; 2022 May; 101(5-6):507-516. PubMed ID: 35285020
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
