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 *

155 related articles for article (PubMed ID: 11453684)

  • 41. Major centers of motion in the large ribosomal RNAs.
    Paci M; Fox GE
    Nucleic Acids Res; 2015 May; 43(9):4640-9. PubMed ID: 25870411
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Improved statistical methods reveal direct interactions between 16S and 23S rRNA.
    Kelley ST; Akmaev VR; Stormo GD
    Nucleic Acids Res; 2000 Dec; 28(24):4938-43. PubMed ID: 11121485
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Topological classification of RNA structures.
    Bon M; Vernizzi G; Orland H; Zee A
    J Mol Biol; 2008 Jun; 379(4):900-11. PubMed ID: 18485361
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The conserved A-site finger of the 23S rRNA: just one of the intersubunit bridges or a part of the allosteric communication pathway?
    Sergiev PV; Kiparisov SV; Burakovsky DE; Lesnyak DV; Leonov AA; Bogdanov AA; Dontsova OA
    J Mol Biol; 2005 Oct; 353(1):116-23. PubMed ID: 16165153
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Double molecular mimicry in Escherichia coli: binding of ribosomal protein L20 to its two sites in mRNA is similar to its binding to 23S rRNA.
    Guillier M; Allemand F; Dardel F; Royer CA; Springer M; Chiaruttini C
    Mol Microbiol; 2005 Jun; 56(6):1441-56. PubMed ID: 15916597
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Structures and Energetics of Four Adjacent G·U Pairs That Stabilize an RNA Helix.
    Gu X; Mooers BH; Thomas LM; Malone J; Harris S; Schroeder SJ
    J Phys Chem B; 2015 Oct; 119(42):13252-61. PubMed ID: 26425937
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Interaction of the Bacillus stearothermophilus ribosomal protein S15 with 16 S rRNA: II. Specificity determinants of RNA-protein recognition.
    Batey RT; Williamson JR
    J Mol Biol; 1996 Aug; 261(4):550-67. PubMed ID: 8794876
    [TBL] [Abstract][Full Text] [Related]  

  • 48. RNAMotif, an RNA secondary structure definition and search algorithm.
    Macke TJ; Ecker DJ; Gutell RR; Gautheret D; Case DA; Sampath R
    Nucleic Acids Res; 2001 Nov; 29(22):4724-35. PubMed ID: 11713323
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mutational analysis of the conserved bases C1402 and A1500 in the center of the decoding domain of Escherichia coli 16 S rRNA reveals an important tertiary interaction.
    Vila-Sanjurjo A; Dahlberg AE
    J Mol Biol; 2001 May; 308(3):457-63. PubMed ID: 11327780
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A common motif organizes the structure of multi-helix loops in 16 S and 23 S ribosomal RNAs.
    Leontis NB; Westhof E
    J Mol Biol; 1998 Oct; 283(3):571-83. PubMed ID: 9784367
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Hinge-like motions in RNA kink-turns: the role of the second a-minor motif and nominally unpaired bases.
    Rázga F; Koca J; Sponer J; Leontis NB
    Biophys J; 2005 May; 88(5):3466-85. PubMed ID: 15722438
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Interaction of Escherichia coli DbpA with 23S rRNA in different functional states of the enzyme.
    Karginov FV; Uhlenbeck OC
    Nucleic Acids Res; 2004; 32(10):3028-32. PubMed ID: 15173385
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Effects of base change mutations within an Escherichia coli ribosomal RNA leader region on rRNA maturation and ribosome formation.
    Schäferkordt J; Wagner R
    Nucleic Acids Res; 2001 Aug; 29(16):3394-403. PubMed ID: 11504877
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Importance of transient structures during post-transcriptional refolding of the pre-23S rRNA and ribosomal large subunit assembly.
    Liiv A; Remme J
    J Mol Biol; 2004 Sep; 342(3):725-41. PubMed ID: 15342233
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Structure and function of the conserved 690 hairpin in Escherichia coli 16 S ribosomal RNA. II. NMR solution structure.
    Morosyuk SV; Cunningham PR; SantaLucia J
    J Mol Biol; 2001 Mar; 307(1):197-211. PubMed ID: 11243814
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Singly and bifurcated hydrogen-bonded base-pairs in tRNA anticodon hairpins and ribozymes.
    Auffinger P; Westhof E
    J Mol Biol; 1999 Sep; 292(3):467-83. PubMed ID: 10497015
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A functional relationship between helix 1 and the 900 tetraloop of 16S ribosomal RNA within the bacterial ribosome.
    Bélanger F; Théberge-Julien G; Cunningham PR; Brakier-Gingras L
    RNA; 2005 Jun; 11(6):906-13. PubMed ID: 15872184
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Correlation of RNA secondary structure statistics with thermodynamic stability and applications to folding.
    Wu JC; Gardner DP; Ozer S; Gutell RR; Ren P
    J Mol Biol; 2009 Aug; 391(4):769-83. PubMed ID: 19540243
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Photolabile oligoDNA probes of internal Escherichia coli ribosomal structure.
    Cooperman BS; Alexander RW; Muralikrishna P
    Nucleic Acids Symp Ser; 1995; (33):59-62. PubMed ID: 8643399
    [TBL] [Abstract][Full Text] [Related]  

  • 60. G-ribo: a new structural motif in ribosomal RNA.
    Steinberg SV; Boutorine YI
    RNA; 2007 Apr; 13(4):549-54. PubMed ID: 17283211
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.