These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 37236670)

  • 41. 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]  

  • 42. 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]  

  • 43. Genome-wide identification of targets of the drosha-pasha/DGCR8 complex.
    Kadener S; Rodriguez J; Abruzzi KC; Khodor YL; Sugino K; Marr MT; Nelson S; Rosbash M
    RNA; 2009 Apr; 15(4):537-45. PubMed ID: 19223442
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. Efficient processing of primary microRNA hairpins by Drosha requires flanking nonstructured RNA sequences.
    Zeng Y; Cullen BR
    J Biol Chem; 2005 Jul; 280(30):27595-603. PubMed ID: 15932881
    [TBL] [Abstract][Full Text] [Related]  

  • 46. In vitro and in vivo assays for the activity of Drosha complex.
    Lee Y; Kim VN
    Methods Enzymol; 2007; 427():89-106. PubMed ID: 17720480
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. 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]  

  • 49. Smad proteins bind a conserved RNA sequence to promote microRNA maturation by Drosha.
    Davis BN; Hilyard AC; Nguyen PH; Lagna G; Hata A
    Mol Cell; 2010 Aug; 39(3):373-84. PubMed ID: 20705240
    [TBL] [Abstract][Full Text] [Related]  

  • 50. DICER-LIKE1a autoregulation based on intronic microRNA processing is required for stress adaptation in Physcomitrium patens.
    Arif MA; Top O; Csicsely E; Lichtenstern M; Beheshti H; Adjabi K; Frank W
    Plant J; 2022 Jan; 109(1):227-240. PubMed ID: 34743365
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Reliable prediction of Drosha processing sites improves microRNA gene prediction.
    Helvik SA; Snøve O; Saetrom P
    Bioinformatics; 2007 Jan; 23(2):142-9. PubMed ID: 17105718
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The Drosha-DGCR8 complex in primary microRNA processing.
    Han J; Lee Y; Yeom KH; Kim YK; Jin H; Kim VN
    Genes Dev; 2004 Dec; 18(24):3016-27. PubMed ID: 15574589
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Coupled RNA processing and transcription of intergenic primary microRNAs.
    Ballarino M; Pagano F; Girardi E; Morlando M; Cacchiarelli D; Marchioni M; Proudfoot NJ; Bozzoni I
    Mol Cell Biol; 2009 Oct; 29(20):5632-8. PubMed ID: 19667074
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. Biogenesis of mammalian microRNAs by a non-canonical processing pathway.
    Havens MA; Reich AA; Duelli DM; Hastings ML
    Nucleic Acids Res; 2012 May; 40(10):4626-40. PubMed ID: 22270084
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Microprocessor-dependent processing of splice site overlapping microRNA exons does not result in changes in alternative splicing.
    Pianigiani G; Licastro D; Fortugno P; Castiglia D; Petrovic I; Pagani F
    RNA; 2018 Sep; 24(9):1158-1171. PubMed ID: 29895677
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex.
    Han J; Lee Y; Yeom KH; Nam JW; Heo I; Rhee JK; Sohn SY; Cho Y; Zhang BT; Kim VN
    Cell; 2006 Jun; 125(5):887-901. PubMed ID: 16751099
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Parameters of clustered suboptimal miRNA biogenesis.
    Shang R; Lai EC
    Proc Natl Acad Sci U S A; 2023 Oct; 120(41):e2306727120. PubMed ID: 37788316
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Dicer cleaves 5'-extended microRNA precursors originating from RNA polymerase II transcription start sites.
    Sheng P; Fields C; Aadland K; Wei T; Kolaczkowski O; Gu T; Kolaczkowski B; Xie M
    Nucleic Acids Res; 2018 Jun; 46(11):5737-5752. PubMed ID: 29746670
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.