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Additional info for (NAS Colloquium) Molecular Kinesis in Cellular Function and Plasticity
These, and other activated functions, can provide gene products needed to construct new cell structures such as neuronal processes or dendritic spines (13–15). Therefore, if functional linkage is defined as the mobilization of a variety of gene products needed to remodel cell structure or behavior, it is expected that mRNA subsets clustered in mRNP complexes would encode proteins with seemingly diverse properties. How Many Different RNA-Binding Proteins Exist in Model Organisms? The complexity of mRNPs and their potential roles in posttranscriptional regulation can be approximated by considering the number of RNA-binding proteins available for interactions with RNA.
1998) Proc. Natl. Acad. Sci. USA 95, 2313–2318. 40. , Podsypanina, K. R. (1996) Proc. Natl. Acad. Sci. USA 93, 13250–13255. 41. Schuman, E. (1999) Neuron 23, 645–648. 42. , Oleynikov, Y. H. (1999) FASEB J. 13, 447–454. 43. T. D. (1994) J. Neurosci. 14, 1943–1952. 44. , Stella, G. R. (1989) Science 244, 339–343. 45. , Patel, D. D. (1998) J. Cell Sci. 111, 3145–3156. 46. -X. M. (1999) J. Exp. Med. 189, 1101–1110. 47. R. I. (2000) Cell 100, S1-S55. 48. A. D. (1997) Curr. Top. Cell. Regul. 35, 1–19.
W. (1992) Genes Dev. 6, 1927–1939. 33. , Hood, L. R. (1999) Proc. Natl. Acad. Sci. USA 96, 10632–10636. 34. , Raught, B. & Sonenberg, N. (1999) Annu. Rev. Biochem. 68, 913–963. 35. -L. G. (2000) Micro. Mol. Biol. Rev. 64, 239–280. 36. J. M. (1993) J. Neurosci. Res. 35, 585–602. 37. L. F. (1998) Neuron 21, 741–751. 38. Steward, O. A. (1992) Trends Neurosci. 15, 180–186. 39. , Hemby, S. & Eberwine, J. (1998) Proc. Natl. Acad. Sci. USA 95, 2313–2318. 40. , Podsypanina, K. R. (1996) Proc. Natl. Acad.
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