BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 31000419)

  • 1. A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
    Caburet S; Todeschini AL; Petrillo C; Martini E; Farran ND; Legois B; Livera G; Younis JS; Shalev S; Veitia RA
    EBioMedicine; 2019 Apr; 42():524-531. PubMed ID: 31000419
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Meiosis-specific proteins MEIOB and SPATA22 cooperatively associate with the single-stranded DNA-binding replication protein A complex and DNA double-strand breaks.
    Xu Y; Greenberg RA; Schonbrunn E; Wang PJ
    Biol Reprod; 2017 May; 96(5):1096-1104. PubMed ID: 28453612
    [TBL] [Abstract][Full Text] [Related]  

  • 4. shani mutation in mouse affects splicing of Spata22 and leads to impaired meiotic recombination.
    Petrillo C; Barroca V; Ribeiro J; Lailler N; Livera G; Keeney S; Martini E; Jain D
    Chromosoma; 2020 Jun; 129(2):161-179. PubMed ID: 32388826
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.
    Zhu X; Hu K; Cheng H; Wu H; Li K; Gao Y; Lv M; Xu C; Geng H; Shen Q; Cao Y; He X; Tang D; Guo R
    Clin Genet; 2024 Jan; 105(1):99-105. PubMed ID: 37715646
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The meiosis-specific MEIOB-SPATA22 complex cooperates with RPA to form a compacted mixed MEIOB/SPATA22/RPA/ssDNA complex.
    Ribeiro J; Dupaigne P; Petrillo C; Ducrot C; Duquenne C; Veaute X; Saintomé C; Busso D; Guerois R; Martini E; Livera G
    DNA Repair (Amst); 2021 Jun; 102():103097. PubMed ID: 33812231
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A cell-based high-content screen identifies isocotoin as a small molecule inhibitor of the meiosis-specific MEIOB-SPATA22 complex†.
    Xu Y; Liu R; Leu NA; Zhang L; Ibragmova I; Schultz DC; Wang PJ
    Biol Reprod; 2020 Aug; 103(2):333-342. PubMed ID: 32463099
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Nuclear localization of human MEIOB requires its NLS in the OB domain and interaction with SPATA22.
    Xu Y; Chen Z; Wu P; Qu W; Shi H; Cheng M; Xu Y; Jin T; Liu C; Li Y; Luo M
    Acta Biochim Biophys Sin (Shanghai); 2022 Nov; 55(1):154-161. PubMed ID: 36331299
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.
    Wang B; Li L; Zhu Y; Zhang W; Wang X; Chen B; Li T; Pan H; Wang J; Kee K; Cao Y
    Hum Reprod; 2017 Oct; 32(10):2138-2146. PubMed ID: 28938739
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MEIOB targets single-strand DNA and is necessary for meiotic recombination.
    Souquet B; Abby E; Hervé R; Finsterbusch F; Tourpin S; Le Bouffant R; Duquenne C; Messiaen S; Martini E; Bernardino-Sgherri J; Toth A; Habert R; Livera G
    PLoS Genet; 2013; 9(9):e1003784. PubMed ID: 24068956
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation.
    Heddar A; Beckers D; Fouquet B; Roland D; Misrahi M
    J Clin Endocrinol Metab; 2020 Jun; 105(6):. PubMed ID: 32242235
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare missense variant in MSH4 associated with primary gonadal failure in both 46, XX and 46, XY individuals.
    Akbari A; Padidar K; Salehi N; Mashayekhi M; Almadani N; Sadighi Gilani MA; Bashambou A; McElreavey K; Totonchi M
    Hum Reprod; 2021 Mar; 36(4):1134-1145. PubMed ID: 33448284
    [TBL] [Abstract][Full Text] [Related]  

  • 15. STAG3 truncating variant as the cause of primary ovarian insufficiency.
    Le Quesne Stabej P; Williams HJ; James C; Tekman M; Stanescu HC; Kleta R; Ocaka L; Lescai F; Storr HL; Bitner-Glindzicz M; Bacchelli C; Conway GS;
    Eur J Hum Genet; 2016 Jan; 24(1):135-8. PubMed ID: 26059840
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency.
    Chen B; Li L; Wang J; Li T; Pan H; Liu B; Zhou Y; Cao Y; Wang B
    J Ovarian Res; 2018 Jun; 11(1):48. PubMed ID: 29914564
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency.
    Fauchereau F; Shalev S; Chervinsky E; Beck-Fruchter R; Legois B; Fellous M; Caburet S; Veitia RA
    Clin Genet; 2016 May; 89(5):603-7. PubMed ID: 26771056
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    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]  

  • 20. MEIOB exhibits single-stranded DNA-binding and exonuclease activities and is essential for meiotic recombination.
    Luo M; Yang F; Leu NA; Landaiche J; Handel MA; Benavente R; La Salle S; Wang PJ
    Nat Commun; 2013; 4():2788. PubMed ID: 24240703
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.