Searching journal content for articles similar to Hammell et al. 9 (5): 417.

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  1. ...to explore the possibility that lncRNAencoded peptides might constitute part of the TP53 network. For this purpose, we combined CRISPR-Cas9 technology with the DNA-damage responsive system to investigate the expression of TP53-regulated lncRNAs, following by ribosome profiles and mass spectrometry (MS...
  2. ...the control of a GAL1 promoter and induced their expression in yeast tup1 knockout strain. By Western blot, we showed that the protein level of the RNA form (V459) of Tup1 is higher than that of the DNA form (A459), Table 1. Examples of RDDs in genes that play a role in ribosome biogenesis RDD levels (%) Gene...
  3. ...of putative programmed -1 ribosomal frameshift signals in large DNA databases. Genome Res. 9 : 417 -427. ↵ Harrison, P., Kumar, A., Lan, N., Echols, N., Snyder, M., and Gerstein, M. 2002 . A small reservoir of disabled ORFs in the yeast and its implications for the dynamics of proteome evolution. J. Mol. Biol...
  4. .... Identification of putative noncoding RNAs among the RIKEN mouse full-length cDNA collection. Genome Res. 13 : 1301 -1306. ↵ Okazaki, Y.M., Furuno, T., Kasukawa, J., Adachi, H., Bono, S., Kondo, I., Nikaido, N., Osato, R., Saito, H., Suzuki, I. et al. 2002 . Analysis of the mouse transcriptome based on functional...
  5. ...genomic DNA (NCBI Nicotiana tabacum gss) databases and extrapolated the number of hits retrieved to estimate -wide copy numbers as described in Supplemental Table S1.2. An extended data set of N. tabacum MiS1 , MiS5 , and MiS17 sequences is provided in Supplemental Data S1.2. Several MiS families from...
  6. ...DNA using the FASTA program ( Pearson et al. 1997 ), expanded on either side by the length of the matching sequence (in nucleotides). From these alignments, we picked any matching sequences that had more than one disablement (either a frameshift or a premature stop codon) as a potential pseudogene...
  7. ...(i.e., detection of multiple restriction fragments of several YACs) or gave no signal at all. Therefore, all clones containing repetitive elements were excluded from further analyses. A second source of non-specific hybridization were cDNA clones containing ribosomal DNA that were detected by YAC 986...
  8. ...of metaphase chromosome bands. Cell 53 : 391 – 400 . Kunkel, T. 1986 . Frameshift mutagenesis by eucaryotic DNA polymerases in vitro. J. Biol. Chem. 261 : 13581 – 13587 . La Mantia, G., Pengue, G. Maglione, D. Pannuti, A. Pascucci, A. and Lania. L. 1989 . Identification of new human repetitive sequences...
  9. ..., multiple studies across many taxa showed that some novel genes arise de novo, that is, from previously noncoding DNA. To characterize the underlying mutations that allowed de novo gene emergence and their order of occurrence, homologous regions must be detected within noncoding sequences in closely related...
  10. ...raw signal to DNA reference, UNCALLED has a lighter computational footprint than DTW (Kovaka et al. 2021). Still, it requires abundant computational resources. The newly designed Readfish toolkit eliminates the need for complex signal mapping algorithms and exploits existing ONT tools to provide...
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