194 related articles for article (PubMed ID: 30827524)
1. Novel WEE2 gene variants identified in patients with fertilization failure and female infertility.
Zhao S; Chen T; Yu M; Bian Y; Cao Y; Ning Y; Su S; Zhang J; Zhao S
Fertil Steril; 2019 Mar; 111(3):519-526. PubMed ID: 30827524
[TBL] [Abstract][Full Text] [Related]
2. New biallelic mutations in WEE2: expanding the spectrum of mutations that cause fertilization failure or poor fertilization.
Dai J; Zheng W; Dai C; Guo J; Lu C; Gong F; Li Y; Zhou Q; Lu G; Lin G
Fertil Steril; 2019 Mar; 111(3):510-518. PubMed ID: 30827523
[TBL] [Abstract][Full Text] [Related]
3. Clinical exome sequencing identifies novel compound heterozygous mutations of the
Wang A; Huang S; Liu M; Wang B; Wu F; Zhu D; Zhao X
Gynecol Endocrinol; 2021 Dec; 37(12):1096-1101. PubMed ID: 33904356
[TBL] [Abstract][Full Text] [Related]
4. Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure.
Zhou X; Zhu L; Hou M; Wu Y; Li Z; Wang J; Liu Z; Zhang D; Jin L; Zhang X
J Assist Reprod Genet; 2019 Sep; 36(9):1957-1962. PubMed ID: 31428887
[TBL] [Abstract][Full Text] [Related]
5. Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.
Sang Q; Li B; Kuang Y; Wang X; Zhang Z; Chen B; Wu L; Lyu Q; Fu Y; Yan Z; Mao X; Xu Y; Mu J; Li Q; Jin L; He L; Wang L
Am J Hum Genet; 2018 Apr; 102(4):649-657. PubMed ID: 29606300
[TBL] [Abstract][Full Text] [Related]
6. Novel compound heterozygous mutation in WEE2 is associated with fertilization failure: case report of an infertile woman and literature review.
Tian Y; Wang G; Wang J; Mu X; Chen H; Song X; Bai X
BMC Womens Health; 2020 Nov; 20(1):246. PubMed ID: 33148236
[TBL] [Abstract][Full Text] [Related]
7. Homozygous missense mutation Arg207Cys in the WEE2 gene causes female infertility and fertilization failure.
Yang X; Shu L; Cai L; Sun X; Cui Y; Liu J
J Assist Reprod Genet; 2019 May; 36(5):965-971. PubMed ID: 30826994
[TBL] [Abstract][Full Text] [Related]
8. Novel WEE2 compound heterozygous mutations identified in patients with fertilization failure or poor fertilization.
Jin J; Tong X; Zhang YL; Yang W; Ma Y; Ren P; Zhou F; Zhang S
J Assist Reprod Genet; 2021 Nov; 38(11):2861-2869. PubMed ID: 34476630
[TBL] [Abstract][Full Text] [Related]
9. Novel mutations in WEE2: Expanding the spectrum of mutations responsible for human fertilization failure.
Zhang Z; Mu J; Zhao J; Zhou Z; Chen B; Wu L; Yan Z; Wang W; Zhao L; Dong J; Sun X; Kuang Y; Li B; Wang L; Sang Q
Clin Genet; 2019 Apr; 95(4):520-524. PubMed ID: 30628060
[TBL] [Abstract][Full Text] [Related]
10. Association between estrogen receptor 1 (ESR1) and leukemia inhibitory factor (LIF) polymorphisms can help in the prediction of recurrent implantation failure.
Vagnini LD; Renzi A; Petersen B; Canas MDCT; Petersen CG; Mauri AL; Mattila MC; Ricci J; Dieamant F; Oliveira JBA; Baruffi RLR; Franco JG
Fertil Steril; 2019 Mar; 111(3):527-534. PubMed ID: 30611552
[TBL] [Abstract][Full Text] [Related]
11. Novel WEE2 homozygous mutations c.1346C>T and c.949A>T identified in primary infertile women due to unexplained fertilization failure.
Guo H; Wu H; Yan Z; Yin M; Wu L; Li B
Clin Genet; 2023 Dec; 104(6):700-704. PubMed ID: 37772619
[TBL] [Abstract][Full Text] [Related]
12. Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations.
Lin J; Xu H; Chen B; Wang W; Wang L; Sun X; Sang Q
J Assist Reprod Genet; 2020 Feb; 37(2):437-442. PubMed ID: 31897846
[TBL] [Abstract][Full Text] [Related]
13. A new
Li M; Jia M; Zhao X; Shi R; Xue X
Gynecol Endocrinol; 2021 Mar; 37(3):283-284. PubMed ID: 33073652
[TBL] [Abstract][Full Text] [Related]
14. Novel mutations in the PLCZ1 gene associated with human low or failed fertilization.
Yuan P; Zheng L; Liang H; Lin Q; Ou S; Zhu Y; Lai L; Zhang Q; He Z; Wang W
Mol Genet Genomic Med; 2020 Oct; 8(10):e1470. PubMed ID: 32840018
[TBL] [Abstract][Full Text] [Related]
15. Total fertilization failure with in vitro fertilization-intracytoplasmic sperm injection related to WEE2 mutation highlights emerging importance of genetic causes of in vitro fertilization failure.
Weiner HS; Ulrich ND; Hipp L; Hammoud A; Xu M; Schon SB
F S Rep; 2022 Dec; 3(4):355-360. PubMed ID: 36568932
[TBL] [Abstract][Full Text] [Related]
16. Maternal common variant rs2305957 spanning PLK4 is associated with blastocyst formation and early recurrent miscarriage.
Zhang Q; Li G; Zhang L; Sun X; Zhang D; Lu J; Ma J; Yan J; Chen ZJ
Fertil Steril; 2017 Apr; 107(4):1034-1040.e5. PubMed ID: 28238495
[TBL] [Abstract][Full Text] [Related]
17. Oocyte-specific Wee1-like protein kinase 2 is dispensable for fertility in mice.
Nozawa K; Liao Z; Satouh Y; Geng T; Ikawa M; Monsivais D; Matzuk MM
PLoS One; 2023; 18(8):e0289083. PubMed ID: 37527245
[TBL] [Abstract][Full Text] [Related]
18. FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women.
Rull K; Grigorova M; Ehrenberg A; Vaas P; Sekavin A; Nõmmemees D; Adler M; Hanson E; Juhanson P; Laan M
Hum Reprod; 2018 May; 33(5):954-966. PubMed ID: 29617818
[TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of tubulin beta 8 class VIII in infertile females with oocyte or embryonic defects.
Yang P; Yin C; Li M; Ma S; Cao Y; Zhang C; Chen T; Zhao H
Clin Genet; 2021 Jan; 99(1):208-214. PubMed ID: 33009822
[TBL] [Abstract][Full Text] [Related]
20. Identification novel mutations and phenotypic spectrum expanding in PATL2 in infertile women with IVF/ICSI failure.
Ye Z; Li D; Niu X; Yang A; Pan Z; Yu R; Gu H; Shi R; Wu L; Xiang Y; Hao G; Kuang Y; Chen B; Wang L; Sang Q; Li L; Shi J; Li Q
J Assist Reprod Genet; 2024 May; 41(5):1233-1243. PubMed ID: 38536595
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
