BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

358 related articles for article (PubMed ID: 30554947)

  • 21. 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]  

  • 22. Engineering double-stranded RNA binding activity into the Drosha double-stranded RNA binding domain results in a loss of microRNA processing function.
    Kranick JC; Chadalavada DM; Sahu D; Showalter SA
    PLoS One; 2017; 12(8):e0182445. PubMed ID: 28792523
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cloning, expression, and characterization of the zebrafish Dicer and Drosha enzymes.
    Li P; Tian Q; Hu M; Li W; Zhang X; Zeng Y
    Biochem Biophys Res Commun; 2019 Jun; 514(1):200-204. PubMed ID: 31029426
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Post-transcriptional control of DGCR8 expression by the Microprocessor.
    Triboulet R; Chang HM; Lapierre RJ; Gregory RI
    RNA; 2009 Jun; 15(6):1005-11. PubMed ID: 19383765
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dissection of the Caenorhabditis elegans Microprocessor.
    Nguyen TL; Nguyen TD; Ngo MK; Nguyen TA
    Nucleic Acids Res; 2023 Feb; 51(4):1512-1527. PubMed ID: 36598924
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Primary microRNA processing assay reconstituted using recombinant Drosha and DGCR8.
    Barr I; Guo F
    Methods Mol Biol; 2014; 1095():73-86. PubMed ID: 24166303
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Deformability in the cleavage site of primary microRNA is not sensed by the double-stranded RNA binding domains in the microprocessor component DGCR8.
    Quarles KA; Chadalavada D; Showalter SA
    Proteins; 2015 Jun; 83(6):1165-79. PubMed ID: 25851436
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Structure of Human DROSHA.
    Kwon SC; Nguyen TA; Choi YG; Jo MH; Hohng S; Kim VN; Woo JS
    Cell; 2016 Jan; 164(1-2):81-90. PubMed ID: 26748718
    [TBL] [Abstract][Full Text] [Related]  

  • 31. DGCR8 recognizes primary transcripts of microRNAs through highly cooperative binding and formation of higher-order structures.
    Faller M; Toso D; Matsunaga M; Atanasov I; Senturia R; Chen Y; Zhou ZH; Guo F
    RNA; 2010 Aug; 16(8):1570-83. PubMed ID: 20558544
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Orientation of Human Microprocessor on Primary MicroRNAs.
    Nguyen HM; Nguyen TD; Nguyen TL; Nguyen TA
    Biochemistry; 2019 Jan; 58(4):189-198. PubMed ID: 30481000
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The DGCR8 RNA-binding heme domain recognizes primary microRNAs by clamping the hairpin.
    Quick-Cleveland J; Jacob JP; Weitz SH; Shoffner G; Senturia R; Guo F
    Cell Rep; 2014 Jun; 7(6):1994-2005. PubMed ID: 24910438
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pri-miRNA cleavage assays for the Microprocessor complex.
    Le TN; Le CT; Nguyen TA
    Methods Enzymol; 2023; 692():217-230. PubMed ID: 37925180
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The insertion in the double-stranded RNA binding domain of human Drosha is important for its function.
    Zhang X; Li P; Lin J; Huang H; Yin B; Zeng Y
    Biochim Biophys Acta Gene Regul Mech; 2017 Dec; 1860(12):1179-1188. PubMed ID: 29109067
    [TBL] [Abstract][Full Text] [Related]  

  • 37. MicroRNA biogenesis: isolation and characterization of the microprocessor complex.
    Gregory RI; Chendrimada TP; Shiekhattar R
    Methods Mol Biol; 2006; 342():33-47. PubMed ID: 16957365
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Select amino acids in DGCR8 are essential for the UGU-pri-miRNA interaction and processing.
    Dang TL; Le CT; Le MN; Nguyen TD; Nguyen TL; Bao S; Li S; Nguyen TA
    Commun Biol; 2020 Jul; 3(1):344. PubMed ID: 32620823
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Processing of primary microRNAs by the Microprocessor complex.
    Denli AM; Tops BB; Plasterk RH; Ketting RF; Hannon GJ
    Nature; 2004 Nov; 432(7014):231-5. PubMed ID: 15531879
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Processing of microRNA primary transcripts requires heme in mammalian cells.
    Weitz SH; Gong M; Barr I; Weiss S; Guo F
    Proc Natl Acad Sci U S A; 2014 Feb; 111(5):1861-6. PubMed ID: 24449907
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.