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April 1, 2005Genes & DevelopmentOpen Access

Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes

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Authors

JDJennifer C. DarnellUniversity of EdinburghCFClaire FraserRockefeller UniversityOMOlga MostovetskyUniversity of California, San Francisco

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Darnell et al. (2005) studied this question.

synapsesocial.com/papers/6a74ad2b8d2049c8dd03345ehttps://doi.org/10.1101/gad.1276805
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The role of a clinically important mutation in the fold and RNA-binding properties of KH motifs2003 · 20 citations
  2. 2A Decade of Molecular Studies of Fragile X Syndrome2002 · 484 citations
  3. 3Two ZBP1 KH domains facilitate β-actin mRNA localization, granule formation, and cytoskeletal attachment2002 · 279 citations
  4. 4A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P2001 · 367 citations