BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 35760371)

  • 1. Conformational Effects of a Cancer-Linked Mutation in Pri-miR-30c RNA.
    Jones AN; Walbrun A; Falleroni F; Rief M; Sattler M
    J Mol Biol; 2022 Sep; 434(18):167705. PubMed ID: 35760371
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structural basis for terminal loop recognition and stimulation of pri-miRNA-18a processing by hnRNP A1.
    Kooshapur H; Choudhury NR; Simon B; Mühlbauer M; Jussupow A; Fernandez N; Jones AN; Dallmann A; Gabel F; Camilloni C; Michlewski G; Caceres JF; Sattler M
    Nat Commun; 2018 Jun; 9(1):2479. PubMed ID: 29946118
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic variation and RNA structure regulate microRNA biogenesis.
    Fernandez N; Cordiner RA; Young RS; Hug N; Macias S; Cáceres JF
    Nat Commun; 2017 May; 8():15114. PubMed ID: 28466845
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Stimulation of pri-miR-18a Processing by hnRNP A1.
    Michlewski G; Guil S; Cáceres JF
    Adv Exp Med Biol; 2011; 700():28-35. PubMed ID: 21755470
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The multifunctional RNA-binding protein hnRNP A1 is required for processing of miR-18a.
    Guil S; Cáceres JF
    Nat Struct Mol Biol; 2007 Jul; 14(7):591-6. PubMed ID: 17558416
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Beyond secondary structure: primary-sequence determinants license pri-miRNA hairpins for processing.
    Auyeung VC; Ulitsky I; McGeary SE; Bartel DP
    Cell; 2013 Feb; 152(4):844-58. PubMed ID: 23415231
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bidirectional processing of pri-miRNAs with branched terminal loops by Arabidopsis Dicer-like1.
    Zhu H; Zhou Y; Castillo-González C; Lu A; Ge C; Zhao YT; Duan L; Li Z; Axtell MJ; Wang XJ; Zhang X
    Nat Struct Mol Biol; 2013 Sep; 20(9):1106-15. PubMed ID: 23934148
    [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. 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]  

  • 13. Role of pri-miRNA tertiary structure in miR-17~92 miRNA biogenesis.
    Chaulk SG; Thede GL; Kent OA; Xu Z; Gesner EM; Veldhoen RA; Khanna SK; Goping IS; MacMillan AM; Mendell JT; Young HS; Fahlman RP; Glover JN
    RNA Biol; 2011; 8(6):1105-14. PubMed ID: 21955497
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Posttranscriptional regulation of miRNAs harboring conserved terminal loops.
    Michlewski G; Guil S; Semple CA; Cáceres JF
    Mol Cell; 2008 Nov; 32(3):383-93. PubMed ID: 18995836
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stimulation of pri-miR-18a processing by hnRNP A1.
    Michlewski G; Guil S; Cáceres JF
    Adv Exp Med Biol; 2010; 700():28-35. PubMed ID: 21627027
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Subnuclear compartmentalization of transiently expressed polyadenylated pri-microRNAs: processing at transcription sites or accumulation in SC35 foci.
    Pawlicki JM; Steitz JA
    Cell Cycle; 2009 Feb; 8(3):345-56. PubMed ID: 19177009
    [TBL] [Abstract][Full Text] [Related]  

  • 17. RNA editing of the microRNA-151 precursor blocks cleavage by the Dicer-TRBP complex.
    Kawahara Y; Zinshteyn B; Chendrimada TP; Shiekhattar R; Nishikura K
    EMBO Rep; 2007 Aug; 8(8):763-9. PubMed ID: 17599088
    [TBL] [Abstract][Full Text] [Related]  

  • 18. N6-methyladenosine marks primary microRNAs for processing.
    Alarcón CR; Lee H; Goodarzi H; Halberg N; Tavazoie SF
    Nature; 2015 Mar; 519(7544):482-5. PubMed ID: 25799998
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA.
    Duan R; Pak C; Jin P
    Hum Mol Genet; 2007 May; 16(9):1124-31. PubMed ID: 17400653
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transcriptional, post-transcriptional and chromatin-associated regulation of pri-miRNAs, pre-miRNAs and moRNAs.
    Nepal C; Coolen M; Hadzhiev Y; Cussigh D; Mydel P; Steen VM; Carninci P; Andersen JB; Bally-Cuif L; Müller F; Lenhard B
    Nucleic Acids Res; 2016 Apr; 44(7):3070-81. PubMed ID: 26673698
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.