166 related articles for article (PubMed ID: 35011680)
1. Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes
Cazin C; Neirijnck Y; Loeuillet C; Wehrli L; Kühne F; Lordey I; Mustapha SFB; Bouker A; Zouari R; Thierry-Mieg N; Nef S; Arnoult C; Ray PF; Kherraf ZE
Cells; 2021 Dec; 11(1):. PubMed ID: 35011680
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Human X chromosome exome sequencing identifies
Lu C; Zhang Y; Qin Y; Xu Q; Zhou R; Cui Y; Zhu Y; Zhang X; Zhang J; Wei X; Wang M; Hang B; Mao JH; Snijders AM; Liu M; Hu Z; Shen H; Zhou Z; Guo X; Wu X; Wang X; Xia Y
J Med Genet; 2021 Jan; 58(1):56-65. PubMed ID: 32376790
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia.
Tang D; Lv M; Gao Y; Cheng H; Li K; Xu C; Geng H; Li G; Shen Q; Wang C; He X; Cao Y
Reprod Biol Endocrinol; 2021 Aug; 19(1):129. PubMed ID: 34429122
[TBL] [Abstract][Full Text] [Related]
9. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
Tang D; Li K; Geng H; Xu C; Lv M; Gao Y; Wang G; Yu H; Shao Z; Shen Q; Jiang H; Zhang X; He X; Cao Y
Reprod Biol Endocrinol; 2022 Apr; 20(1):63. PubMed ID: 35366911
[TBL] [Abstract][Full Text] [Related]
10. Point-of-care whole-exome sequencing of idiopathic male infertility.
Fakhro KA; Elbardisi H; Arafa M; Robay A; Rodriguez-Flores JL; Al-Shakaki A; Syed N; Mezey JG; Abi Khalil C; Malek JA; Al-Ansari A; Al Said S; Crystal RG
Genet Med; 2018 Nov; 20(11):1365-1373. PubMed ID: 29790874
[TBL] [Abstract][Full Text] [Related]
11. Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia.
Kherraf ZE; Cazin C; Bouker A; Fourati Ben Mustapha S; Hennebicq S; Septier A; Coutton C; Raymond L; Nouchy M; Thierry-Mieg N; Zouari R; Arnoult C; Ray PF
Am J Hum Genet; 2022 Mar; 109(3):508-517. PubMed ID: 35172124
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Wyrwoll MJ; Temel ŞG; Nagirnaja L; Oud MS; Lopes AM; van der Heijden GW; Heald JS; Rotte N; Wistuba J; Wöste M; Ledig S; Krenz H; Smits RM; Carvalho F; Gonçalves J; Fietz D; Türkgenç B; Ergören MC; Çetinkaya M; Başar M; Kahraman S; McEleny K; Xavier MJ; Turner H; Pilatz A; Röpke A; Dugas M; Kliesch S; Neuhaus N; ; Aston KI; Conrad DF; Veltman JA; Friedrich C; Tüttelmann F
Am J Hum Genet; 2020 Aug; 107(2):342-351. PubMed ID: 32673564
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Restore natural fertility of Kit
Li X; Sun T; Wang X; Tang J; Liu Y
Stem Cell Res Ther; 2019 Aug; 10(1):271. PubMed ID: 31445521
[TBL] [Abstract][Full Text] [Related]
16. Whole Exome Sequencing and In Silico Analysis of Human Sertoli in Patients with Non-Obstructive Azoospermia.
Azizi H; Hashemi Karoii D; Skutella T
Int J Mol Sci; 2022 Oct; 23(20):. PubMed ID: 36293429
[TBL] [Abstract][Full Text] [Related]
17. Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing.
Liu YJ; Zhuang XJ; An JT; Jiang H; Li R; Qiao J; Yan LY; Zhi X
Asian J Androl; 2023; 25(1):66-72. PubMed ID: 36259570
[TBL] [Abstract][Full Text] [Related]
18. CRISPR/Cas9 Promotes Functional Study of Testis Specific X-Linked Gene In Vivo.
Li M; Huang R; Jiang X; Chen Y; Zhang Z; Zhang X; Liang P; Zhan S; Cao S; Songyang Z; Huang J
PLoS One; 2015; 10(11):e0143148. PubMed ID: 26599493
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]