265 related articles for article (PubMed ID: 33665726)
1. A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome.
Wang J; Yang X; Sun X; Ma L; Yin Y; He G; Zhang Y; Zhou J; Cai L; Liu J; Ma X
J Assist Reprod Genet; 2021 Jun; 38(6):1459-1468. PubMed ID: 33665726
[TBL] [Abstract][Full Text] [Related]
2. Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida.
Luo G; Zhu L; Liu Z; Yang X; Xi Q; Li Z; Duan J; Jin L; Zhang X
J Assist Reprod Genet; 2020 Nov; 37(11):2853-2860. PubMed ID: 32829425
[TBL] [Abstract][Full Text] [Related]
3. A novel homozygous nonsense ZP1 variant causes human female infertility associated with empty follicle syndrome (EFS).
Xu Q; Zhu X; Maqsood M; Li W; Tong X; Kong S; Wang F; Liu X; Wei Z; Zhang Z; Zhu F; Cao Y; Bao J
Mol Genet Genomic Med; 2020 Jul; 8(7):e1269. PubMed ID: 32329253
[TBL] [Abstract][Full Text] [Related]
4. Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome.
Liu M; Shen Y; Zhang X; Wang X; Li D; Wang Y
J Assist Reprod Genet; 2020 Sep; 37(9):2151-2157. PubMed ID: 32556881
[TBL] [Abstract][Full Text] [Related]
5. The critical role of ZP genes in female infertility characterized by empty follicle syndrome and oocyte degeneration.
Yang P; Chen T; Liu Y; Hou Z; Wu K; Cao Y; Zhang J; Wang Z; Zhao H
Fertil Steril; 2021 May; 115(5):1259-1269. PubMed ID: 33272616
[TBL] [Abstract][Full Text] [Related]
6. Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation.
Zhou Z; Ni C; Wu L; Chen B; Xu Y; Zhang Z; Mu J; Li B; Yan Z; Fu J; Wang W; Zhao L; Dong J; Sun X; Kuang Y; Sang Q; Wang L
Hum Genet; 2019 Apr; 138(4):327-337. PubMed ID: 30810869
[TBL] [Abstract][Full Text] [Related]
7. Novel variants in ZP1, ZP2 and ZP3 associated with empty follicle syndrome and abnormal zona pellucida.
Sun L; Tong K; Liu W; Tian Y; Liu D; Huang G; Li J
Reprod Biomed Online; 2023 May; 46(5):847-855. PubMed ID: 36931917
[TBL] [Abstract][Full Text] [Related]
8. A Novel Homozygous Nonsense Mutation in ZP1 Causes Female Infertility due to Empty Follicle Syndrome.
Zou T; Xi Q; Liu Z; Li Z; Hou M; Zhu L; Jin L; Zhang X
Reprod Sci; 2022 Dec; 29(12):3516-3520. PubMed ID: 35773450
[TBL] [Abstract][Full Text] [Related]
9. A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.
Chen T; Bian Y; Liu X; Zhao S; Wu K; Yan L; Li M; Yang Z; Liu H; Zhao H; Chen ZJ
Am J Hum Genet; 2017 Sep; 101(3):459-465. PubMed ID: 28886344
[TBL] [Abstract][Full Text] [Related]
10. Novel mutation in the ZP1 gene and clinical implications.
Yuan P; Li R; Li D; Zheng L; Ou S; Zhao H; Zhang Q; Wang W
J Assist Reprod Genet; 2019 Apr; 36(4):741-747. PubMed ID: 30778819
[TBL] [Abstract][Full Text] [Related]
11. A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.
Zhang D; Zhu L; Liu Z; Ren X; Yang X; Li D; Luo Y; Peng X; Zhou X; Jia W; Hou M; Li Z; Jin L; Zhang X
J Assist Reprod Genet; 2021 Jan; 38(1):251-259. PubMed ID: 33140178
[TBL] [Abstract][Full Text] [Related]
12. Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters.
Sun L; Fang X; Chen Z; Zhang H; Zhang Z; Zhou P; Xue T; Peng X; Zhu Q; Yin M; Liu C; Deng Y; Hu H; Li N
Hum Mutat; 2019 Nov; 40(11):2001-2006. PubMed ID: 31292994
[TBL] [Abstract][Full Text] [Related]
13. ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report.
Dai C; Chen Y; Hu L; Du J; Gong F; Dai J; Zhang S; Wang M; Chen J; Guo J; Zheng W; Lu C; Wu Y; Lu G; Lin G
Hum Reprod; 2019 Nov; 34(11):2201-2207. PubMed ID: 31734689
[TBL] [Abstract][Full Text] [Related]
14. Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human.
Cao Q; Zhao C; Zhang X; Zhang H; Lu Q; Wang C; Hu Y; Ling X; Zhang J; Huo R
J Cell Mol Med; 2020 Aug; 24(15):8557-8566. PubMed ID: 32573113
[TBL] [Abstract][Full Text] [Related]
15. Novel mutations in ZP1: Expanding the mutational spectrum associated with empty follicle syndrome in infertile women.
Wu L; Li M; Yin M; Ou Y; Yan Z; Kuang Y; Yan Z; Li B
Clin Genet; 2021 Apr; 99(4):583-587. PubMed ID: 33423275
[TBL] [Abstract][Full Text] [Related]
16. A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility.
Sun Y; Zeng Y; Chen H; Zhou Z; Fu J; Sang Q; Wang L; Sun X; Chen B; Xu C
J Assist Reprod Genet; 2021 May; 38(5):1239-1245. PubMed ID: 33604805
[TBL] [Abstract][Full Text] [Related]
17. A ZP1 gene mutation in a patient with empty follicle syndrome: A case report and literature review.
Pujalte M; Camo M; Celton N; Attencourt C; Lefranc E; Jedraszak G; Scheffler F
Eur J Obstet Gynecol Reprod Biol; 2023 Jan; 280():193-197. PubMed ID: 36529558
[TBL] [Abstract][Full Text] [Related]
18. Mutant Zp1 impedes incorporation of ZP3 and ZP4 in the zona pellucida, resulting in zona absence and female infertility in rats†.
Lv C; Huang HL; Yi DJ; Peng TL; Tan HJ; Quan RP; Deng HW; Xiao HM
Biol Reprod; 2021 Jun; 104(6):1262-1270. PubMed ID: 33624742
[TBL] [Abstract][Full Text] [Related]
19. Identification of zona pellucida defects revealed a novel loss-of-function mutation in
Zeng J; Sun Y; Zhang J; Wu X; Wang Y; Quan R; Song W; Guo D; Wang S; Chen J; Xiao H; Huang HL
Front Endocrinol (Lausanne); 2023; 14():1169378. PubMed ID: 37293489
[TBL] [Abstract][Full Text] [Related]
20. [Loss of zona pellucida in oocytes due to compound heterozygous variants of ZP1 gene].
Zhang Z; Shangguan T; Li Y; He W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):789-791. PubMed ID: 32619266
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
