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We also performed whole-exome sequencing, but no other pathogenic mutations were revealed.
Potential point mutations were revealed by dHPLC analyses.
Pathogenic mutations were revealed in 35 (36.5%) of the 96 analyzed families.
Additionally, 1454 and 724 nonsynonymous point mutations were revealed in IR-treated 3FB4-1 and MEF, respectively.
Contracted expression or loss-of-function mutations were revealed to contribute to the formation of excessive petals in various double flowers [ 1, 24- 26].
Similarly, no activating mutations were revealed in codon 12 of the KRAS2 gene (Supplementary Figure 2) in both tumour and normal stroma cells.
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The ability of avian influenza A viruses to carry OC-resistant mutations was revealed in this sequence screening.
A substantial overlapping between the KRAS and PIK3CA mutations was revealed.
This feature makes potential screens faster and more efficient as recessive mutations are revealed in these lines without the need for further crossing.
A clearly enhanced prognostic value of plasma mutations compared with tumour mutations was revealed when analysing the relationships between OR and DFS and the plasma KRAS mutation status (Table 2 and Figure 1).
The lineage of multiple tumors and liver tissues and the process of carcinogenesis will be identified when the somatic mutations are revealed by the entire genomic sequencing of multiple HCC.
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