142 related articles for article (PubMed ID: 37804378)
1. Compound heterozygous mutations in TBPL2 were identified in an infertile woman with impaired ovarian folliculogenesis.
Du T; Li M; Chen L; Shao Y; Wang Y; Wang H; Ma J; Yao B
J Assist Reprod Genet; 2023 Dec; 40(12):2945-2950. PubMed ID: 37804378
[TBL] [Abstract][Full Text] [Related]
2. A homozygous missense mutation in TBPL2 is associated with oocyte maturation arrest and degeneration.
Wang Y; Xiang M; Yu Z; Hao Y; Xu Q; Kong S; Wang F; Shi X; Song G; Cao Y; Huang L; Zhu F
Clin Genet; 2021 Sep; 100(3):324-328. PubMed ID: 33966269
[TBL] [Abstract][Full Text] [Related]
3. A homozygous variant in TBPL2 was identified in women with oocyte maturation defects and infertility.
Yang P; Chen T; Wu K; Hou Z; Zou Y; Li M; Zhang X; Xu J; Zhao H
Hum Reprod; 2021 Jun; 36(7):2011-2019. PubMed ID: 33893736
[TBL] [Abstract][Full Text] [Related]
4. A recurrent mutation in TBPL2 causes diminished ovarian reserve and female infertility.
He WB; Zhang YX; Tan C; Meng LL; Liu G; Li Y; Gong F; Wu BL; Lu GX; Lin G; Du J; Tan YQ
J Genet Genomics; 2020 Dec; 47(12):785-788. PubMed ID: 33541821
[No Abstract] [Full Text] [Related]
5. 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]
6. Genomics, evolution, and expression of TBPL2, a member of the TBP family.
Di Pietro C; Ragusa M; Duro L; Guglielmino MR; Barbagallo D; Carnemolla A; Laganà A; Buffa P; Angelica R; Rinaldi A; Calafato MS; Milicia I; Caserta C; Giugno R; Pulvirenti A; Giunta V; Rapisarda A; Di Pietro V; Grillo A; Messina A; Ferro A; Grzeschik KH; Purrello M
DNA Cell Biol; 2007 Jun; 26(6):369-85. PubMed ID: 17570761
[TBL] [Abstract][Full Text] [Related]
7. Novel homozygous mutations in PATL2 lead to female infertility with oocyte maturation arrest.
Liu Z; Zhu L; Wang J; Luo G; Xi Q; Zhou X; Li Z; Yang X; Duan J; Jin L; Zhang X
J Assist Reprod Genet; 2020 Apr; 37(4):841-847. PubMed ID: 32048119
[TBL] [Abstract][Full Text] [Related]
8. Successful Live Birth Following Natural Cycle Oocyte Retrieval in a Woman with Primary Infertility and Atypical Primary Ovarian Insufficiency with a
Liu M; Huang S; Zhao X; Wu F; Zhu D; Zhai X; Wang A
Genet Test Mol Biomarkers; 2021 Oct; 25(10):668-673. PubMed ID: 34672773
[No Abstract] [Full Text] [Related]
9. Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations.
Lu Q; Zhang X; Cao Q; Wang C; Ding J; Zhao C; Zhang J; Ling X; Meng Q; Huo R; Li H
Reprod Sci; 2021 Dec; 28(12):3448-3457. PubMed ID: 34494234
[TBL] [Abstract][Full Text] [Related]
10. Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development.
Chen B; Li B; Li D; Yan Z; Mao X; Xu Y; Mu J; Li Q; Jin L; He L; Kuang Y; Sang Q; Wang L
Hum Reprod; 2017 Feb; 32(2):457-464. PubMed ID: 27989988
[TBL] [Abstract][Full Text] [Related]
11. Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiency.
França MM; Nishi MY; Funari MFA; Lerario AM; Baracat EC; Hayashida SAY; Maciel GAR; Jorge AAL; Mendonca BB
Eur J Med Genet; 2019 Mar; 62(3):186-189. PubMed ID: 30006057
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A novel TLE6 mutation, c.541+1G>A, identified using whole-exome sequencing in a Chinese family with female infertility.
Mao B; Jia X; Liu H; Xu X; Zhao X; Yuan Y; Li H; Ma X; Zhang L
Mol Genet Genomic Med; 2021 Aug; 9(8):e1743. PubMed ID: 34264011
[TBL] [Abstract][Full Text] [Related]
14. Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
Jia W; Xi Q; Zhu L; Luo Y; Li Z; Hou M; Zhang D; Yang X; Hu J; Jin L; Zhang X
J Assist Reprod Genet; 2022 May; 39(5):1205-1215. PubMed ID: 35366744
[TBL] [Abstract][Full Text] [Related]
15. Bi-allelic mutations in MOS cause female infertility characterized by preimplantation embryonic arrest.
Zeng Y; Shi J; Xu S; Shi R; Wu T; Li H; Xue X; Zhu Y; Chen B; Sang Q; Wang L
Hum Reprod; 2022 Mar; 37(3):612-620. PubMed ID: 34997960
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Successful in vitro maturation of oocytes in a woman with gonadotropin-resistant ovary syndrome associated with a novel combination of FSH receptor gene variants: a case report.
Flageole C; Toufaily C; Bernard DJ; Ates S; Blais V; Chénier S; Benkhalifa M; Miron P
J Assist Reprod Genet; 2019 Mar; 36(3):425-432. PubMed ID: 30610662
[TBL] [Abstract][Full Text] [Related]
18. [Oocyte maturation arrest due to compound heterozygous variants of the PATL2 gene in a case].
Lei Q; Li J; Zhou X; Zhang W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jul; 39(7):759-762. PubMed ID: 35810437
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family.
Ma Y; Xie N; Xie D; Sun L; Li S; Li P; Li Y; Li J; Dong Z; Xie X
Fertil Steril; 2019 May; 111(5):909-917.e1. PubMed ID: 30878252
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
