272 related articles for article (PubMed ID: 34718620)
1. Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia.
Hou D; Yao C; Xu B; Luo W; Ke H; Li Z; Qin Y; Guo T
J Clin Endocrinol Metab; 2022 Feb; 107(3):724-734. PubMed ID: 34718620
[TBL] [Abstract][Full Text] [Related]
2. 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]
3.
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]
4. 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]
5. The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.
Pashaei M; Rahimi Bidgoli MM; Zare-Abdollahi D; Najmabadi H; Haji-Seyed-Javadi R; Fatehi F; Alavi A
J Assist Reprod Genet; 2020 Feb; 37(2):451-458. PubMed ID: 31916078
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia.
Ali H; Unar A; Zubair M; Dil S; Ullah F; Khan I; Hussain A; Shi Q
Mol Genet Genomics; 2022 May; 297(3):719-730. PubMed ID: 35305148
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Consanguineous Chinese Familial Study Reveals that a Gross Deletion that Includes the SYCE1 Gene Region Is Associated with Premature Ovarian Insufficiency.
Zhe J; Ye D; Chen X; Liu Y; Zhou X; Li Y; Zhang J; Chen S
Reprod Sci; 2020 Feb; 27(2):461-467. PubMed ID: 31925770
[TBL] [Abstract][Full Text] [Related]
10. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
[TBL] [Abstract][Full Text] [Related]
11. Novel exon mutation in SYCE1 gene is associated with non-obstructive azoospermia.
Feng K; Ge H; Chen H; Cui C; Zhang S; Zhang C; Meng L; Guo H; Zhang L
J Cell Mol Med; 2022 Feb; 26(4):1245-1252. PubMed ID: 35023261
[TBL] [Abstract][Full Text] [Related]
12. A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia.
Hashemi Sheikhshabani S; Ghafouri-Fard S; Hosseini E; Omrani MD
Mol Biol Rep; 2024 Jan; 51(1):68. PubMed ID: 38175272
[TBL] [Abstract][Full Text] [Related]
13. Familial primary ovarian insufficiency associated with an SYCE1 point mutation: defective meiosis elucidated in humanized mice.
Hernández-López D; Geisinger A; Trovero MF; Santiñaque FF; Brauer M; Folle GA; Benavente R; Rodríguez-Casuriaga R
Mol Hum Reprod; 2020 Jul; 26(7):485-497. PubMed ID: 32402064
[TBL] [Abstract][Full Text] [Related]
14. Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency.
de Vries L; Behar DM; Smirin-Yosef P; Lagovsky I; Tzur S; Basel-Vanagaite L
J Clin Endocrinol Metab; 2014 Oct; 99(10):E2129-32. PubMed ID: 25062452
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family.
Akbari A; Zoha Tabatabaei S; Salehi N; Padidar K; Almadani N; Ali Sadighi Gilani M; Mashayekhi M; Motevaseli E; Totonchi M
Gene; 2022 May; 821():146281. PubMed ID: 35176428
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
