BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 30625327)

  • 1. Structural Differences between Pri-miRNA Paralogs Promote Alternative Drosha Cleavage and Expand Target Repertoires.
    Bofill-De Ros X; Kasprzak WK; Bhandari Y; Fan L; Cavanaugh Q; Jiang M; Dai L; Yang A; Shao TJ; Shapiro BA; Wang YX; Gu S
    Cell Rep; 2019 Jan; 26(2):447-459.e4. PubMed ID: 30625327
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Flexible pri-miRNA structures enable tunable production of 5' isomiRs.
    Bofill-De Ros X; Hong Z; Birkenfeld B; Alamo-Ortiz S; Yang A; Dai L; Gu S
    RNA Biol; 2022; 19(1):279-289. PubMed ID: 35188062
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A central role for the primary microRNA stem in guiding the position and efficiency of Drosha processing of a viral pri-miRNA.
    Burke JM; Kelenis DP; Kincaid RP; Sullivan CS
    RNA; 2014 Jul; 20(7):1068-77. PubMed ID: 24854622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome-wide Mapping of DROSHA Cleavage Sites on Primary MicroRNAs and Noncanonical Substrates.
    Kim B; Jeong K; Kim VN
    Mol Cell; 2017 Apr; 66(2):258-269.e5. PubMed ID: 28431232
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SRSF3 recruits DROSHA to the basal junction of primary microRNAs.
    Kim K; Nguyen TD; Li S; Nguyen TA
    RNA; 2018 Jul; 24(7):892-898. PubMed ID: 29615481
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Bulges control pri-miRNA processing in a position and strand-dependent manner.
    Li S; Le TN; Nguyen TD; Trinh TA; Nguyen TA
    RNA Biol; 2021 Nov; 18(11):1716-1726. PubMed ID: 33382955
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of a peptoid ligand with the apical loop of pri-miR-21 inhibits cleavage by Drosha.
    Diaz JP; Chirayil R; Chirayil S; Tom M; Head KJ; Luebke KJ
    RNA; 2014 Apr; 20(4):528-39. PubMed ID: 24497550
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lower and upper stem-single-stranded RNA junctions together determine the Drosha cleavage site.
    Ma H; Wu Y; Choi JG; Wu H
    Proc Natl Acad Sci U S A; 2013 Dec; 110(51):20687-92. PubMed ID: 24297910
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Human disease-associated single nucleotide polymorphism changes the orientation of DROSHA on pri-mir-146a.
    Le CT; Nguyen TL; Nguyen TD; Nguyen TA
    RNA; 2020 Dec; 26(12):1777-1786. PubMed ID: 32994184
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structural Basis for pri-miRNA Recognition by Drosha.
    Jin W; Wang J; Liu CP; Wang HW; Xu RM
    Mol Cell; 2020 May; 78(3):423-433.e5. PubMed ID: 32220645
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A quantitative map of human primary microRNA processing sites.
    Kim K; Baek SC; Lee YY; Bastiaanssen C; Kim J; Kim H; Kim VN
    Mol Cell; 2021 Aug; 81(16):3422-3439.e11. PubMed ID: 34320405
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The core microprocessor component DiGeorge syndrome critical region 8 (DGCR8) is a nonspecific RNA-binding protein.
    Roth BM; Ishimaru D; Hennig M
    J Biol Chem; 2013 Sep; 288(37):26785-99. PubMed ID: 23893406
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytoplasmic Drosha activity generated by alternative splicing.
    Dai L; Chen K; Youngren B; Kulina J; Yang A; Guo Z; Li J; Yu P; Gu S
    Nucleic Acids Res; 2016 Dec; 44(21):10454-10466. PubMed ID: 27471035
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular Basis for the Single-Nucleotide Precision of Primary microRNA Processing.
    Kwon SC; Baek SC; Choi YG; Yang J; Lee YS; Woo JS; Kim VN
    Mol Cell; 2019 Feb; 73(3):505-518.e5. PubMed ID: 30554947
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-canonical RNA substrates of Drosha lack many of the conserved features found in primary microRNA stem-loops.
    Gu K; Mok L; Wakefield MJ; Chong MMW
    Sci Rep; 2024 Mar; 14(1):6713. PubMed ID: 38509178
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Noncanonical processing by animal Microprocessor.
    Nguyen TL; Nguyen TD; Ngo MK; Le TN; Nguyen TA
    Mol Cell; 2023 Jun; 83(11):1810-1826.e8. PubMed ID: 37267903
    [TBL] [Abstract][Full Text] [Related]  

  • 17. siRNA release from pri-miRNA scaffolds is controlled by the sequence and structure of RNA.
    Galka-Marciniak P; Olejniczak M; Starega-Roslan J; Szczesniak MW; Makalowska I; Krzyzosiak WJ
    Biochim Biophys Acta; 2016 Apr; 1859(4):639-49. PubMed ID: 26921501
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The kinase ABL phosphorylates the microprocessor subunit DGCR8 to stimulate primary microRNA processing in response to DNA damage.
    Tu CC; Zhong Y; Nguyen L; Tsai A; Sridevi P; Tarn WY; Wang JY
    Sci Signal; 2015 Jun; 8(383):ra64. PubMed ID: 26126715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The internal loops in the lower stem of primary microRNA transcripts facilitate single cleavage of human Microprocessor.
    Nguyen TL; Nguyen TD; Bao S; Li S; Nguyen TA
    Nucleic Acids Res; 2020 Mar; 48(5):2579-2593. PubMed ID: 31956890
    [TBL] [Abstract][Full Text] [Related]  

  • 20. HP1BP3, a Chromatin Retention Factor for Co-transcriptional MicroRNA Processing.
    Liu H; Liang C; Kollipara RK; Matsui M; Ke X; Jeong BC; Wang Z; Yoo KS; Yadav GP; Kinch LN; Grishin NV; Nam Y; Corey DR; Kittler R; Liu Q
    Mol Cell; 2016 Aug; 63(3):420-32. PubMed ID: 27425409
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.