The methods of the invention provide a means for rapid analysis of gene function in a variety of systems. The invention allows screening of large libraries of nucleotide sequences for involvement in physiological pathways of interest. The methods of the invention also provide an efficient means of identifying and isolating nucleotide sequences that modulate a physiological pathway of interest from a population of nucleotide sequences.

 
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< Fluorescent nucleotide analogs and uses therefor

> Reducing cellular dysfunction caused by mitochondrial gene mutations

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