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snoRNA analyses. (A) Northern blot analyses. Aliquots of 10 µg total cellular RNA were separated in each lane and hybridized with the labeled oligonucleotide probes described in Materials and Methods. Lane M, molecular weight markers (pBR322 digested with HaeIII and 5′-end-labeled with [γ-32P]ATP). (B) Reverse transcription analyses were carried out with the 5′-end-labeled primers described in Materials and Methods.
