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The Mutator tool (7) uses regular expressions to recognize mutations and was tested on mutations related to Fabry disease.
The modified pGPfs plasmid had eight processing site mutations and was designated as pGPfs-one cut (pGPfs-1C) (Figure 1B).
Median survival exceeded 28 months for 12 patients with EGFR mutations, and was 11 months for 38 patients with low BRCA1, 9 months for 40 patients with intermediate BRCA1, and 11 months for 33 patients with high BRCA1.
In contrast, 1-nitropyrene did not induce mutations and was not converted to 1-aminopyrene.
The sensitivity level varied for individual secondary mutations and was limited by sequencing artefacts on both systems.
Cleavage was severely impaired by G67P, G68P, Y69P and V70P mutations and was moderately impaired by I61P, L66P and K71P mutations.
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Mutations that confer a fitness advantage to the cell are known as driver mutations and are causally related to tumorigenesis.
All mutations were different missense mutations, and were shown to occur de novo.
The protein is thought to have appeared after a spontaneous genetic mutation and was found after a tissue sample was submitted for testing by the World Animal Health Organization (OIE).
The neutral theory considered that genetic variations were accumulation of neutral mutation, and were removed by genetic drift (Kimura, 1968).
Thirty-nine patients had H63D mutation and were all heterozygous.
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