BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 33893736)

  • 1. 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]  

  • 2. FBXO43 variants in patients with female infertility characterized by early embryonic arrest.
    Wang W; Wang W; Xu Y; Shi J; Fu J; Chen B; Mu J; Zhang Z; Zhao L; Lin J; Du J; Li Q; He L; Jin L; Sun X; Wang L; Sang Q
    Hum Reprod; 2021 Jul; 36(8):2392-2402. PubMed ID: 34052850
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biallelic variants in MOS cause large polar body in oocyte and human female infertility.
    Zhang YL; Zheng W; Ren P; Jin J; Hu Z; Liu Q; Fan HY; Gong F; Lu GX; Lin G; Zhang S; Tong X
    Hum Reprod; 2022 Jul; 37(8):1932-1944. PubMed ID: 35670744
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Novel mutations in PATL2 cause female infertility with oocyte germinal vesicle arrest.
    Huang L; Tong X; Wang F; Luo L; Jin R; Fu Y; Zhou G; Li D; Song G; Liu Y; Zhu F
    Hum Reprod; 2018 Jun; 33(6):1183-1190. PubMed ID: 29697801
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Novel mutations in PLCZ1 cause male infertility due to fertilization failure or poor fertilization.
    Yan Z; Fan Y; Wang F; Yan Z; Li M; Ouyang J; Wu L; Yin M; Zhao J; Kuang Y; Li B; Lyu Q
    Hum Reprod; 2020 Feb; 35(2):472-481. PubMed ID: 32048714
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility.
    Liu R; Yan Z; Fan Y; Qu R; Chen B; Li B; Wu L; Wu H; Mu J; Zhao L; Wang W; Dong J; Zeng Y; Li Q; Wang L; Sang Q; Zhang Z; Kuang Y
    Hum Reprod; 2022 Jun; 37(7):1394-1405. PubMed ID: 35551387
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.
    Wang W; Su L; Meng L; He J; Tan C; Yi D; Cheng D; Zhang H; Lu G; Du J; Lin G; Zhang Q; Tu C; Tan YQ
    Hum Reprod; 2023 Jul; 38(7):1399-1411. PubMed ID: 37192818
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole exome sequencing in unexplained recurrent miscarriage families identified novel pathogenic genetic causes of euploid miscarriage.
    Wang X; Shi W; Zhao S; Gong D; Li S; Hu C; Chen ZJ; Li Y; Yan J
    Hum Reprod; 2023 May; 38(5):1003-1018. PubMed ID: 36864708
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure.
    Dong J; Zhang H; Mao X; Zhu J; Li D; Fu J; Hu J; Wu L; Chen B; Sun Y; Mu J; Zhang Z; Sun X; Zhao L; Wang W; Wang W; Zhou Z; Zeng Y; Du J; Li Q; He L; Jin L; Kuang Y; Wang L; Sang Q
    Hum Reprod; 2021 Jul; 36(8):2371-2381. PubMed ID: 34037756
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel homozygous mutation of phospholipase C zeta leading to defective human oocyte activation and fertilization failure.
    Yuan P; Yang C; Ren Y; Yan J; Nie Y; Yan L; Qiao J
    Hum Reprod; 2020 Apr; 35(4):977-985. PubMed ID: 32142120
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel bi-allelic variants in ACTL7A are associated with male infertility and total fertilization failure.
    Wang J; Zhang J; Sun X; Lin Y; Cai L; Cui Y; Liu J; Liu M; Yang X
    Hum Reprod; 2021 Nov; 36(12):3161-3169. PubMed ID: 34727571
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transcriptome analysis of rhesus monkey failed-to-mature oocytes: deficiencies in transcriptional regulation and cytoplasmic maturation of the oocyte mRNA population.
    Ruebel ML; Schall PZ; Midic U; Vincent KA; Goheen B; VandeVoort CA; Latham KE
    Mol Hum Reprod; 2018 Oct; 24(10):478-494. PubMed ID: 30085220
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CDC26 is a key factor in human oocyte aging.
    Li L; Xia Y; Yang Y; Zhang W; Yan H; Yin P; Li K; Chen Y; Lu L; Tong G
    Hum Reprod; 2021 Nov; 36(12):3095-3107. PubMed ID: 34590680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Single-cell RNA sequencing identifies molecular targets associated with poor in vitro maturation performance of oocytes collected from ovarian stimulation.
    Lee AWT; Ng JKW; Liao J; Luk AC; Suen AHC; Chan TTH; Cheung MY; Chu HT; Tang NLS; Zhao MP; Lian Q; Chan WY; Chan DYL; Leung TY; Chow KL; Wang W; Wang LH; Chen NCH; Yang WJ; Huang JY; Li TC; Lee TL
    Hum Reprod; 2021 Jun; 36(7):1907-1921. PubMed ID: 34052851
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Endothelin-1 promotes human germinal vesicle-stage oocyte maturation by downregulating connexin-26 expression in cumulus cells.
    Cui L; Shen J; Fang L; Mao X; Wang H; Ye Y
    Mol Hum Reprod; 2018 Jan; 24(1):27-36. PubMed ID: 29126233
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
    Wu Y; Li Y; Murtaza G; Zhou J; Jiao Y; Gong C; Hu C; Han Q; Zhang H; Zhang Y; Shi B; Ma H; Jiang X; Shi Q
    Hum Reprod; 2021 Sep; 36(10):2793-2804. PubMed ID: 34392356
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.