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insertion mutation
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mutación por inserción
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Insert a “T” between bases 10 and 11, representing a base insertion mutation.
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In some cases an insertion mutation can involve the insertion of more than a single nucleotide.
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As mistakes happen during replication and insertion, mutations can occur — the basis of material for change and evolution.
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To create P element insertion mutations, they cross two strains of flies.
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Finally, there are insertion mutations.
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An insertional mutation is a mechanism that a transposable element might cause.
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In doing so, they create insertion mutations.
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"A novel complex deletion-insertion mutation mediated by Alu repetitive elements leads to lipoprotein lipase deficiency".
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Changes made by the project restricted chromosome damage and genetic instability that had interfered with the identification of the newly inserted mutations, or transposons.
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These effects of the insertional event, e.g. the insertional mutation itself or a genomic rearrangement will influence the overall outcome of the genetic modification.
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For example, given only a pairwise alignment with a gap region, it is impossible to determine whether one sequence bears an insertion mutation or the other carries a deletion.
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To clarify the disputed functions of CoQ and evaluate possible therapies for CoQ deficiency, COQMITMEL generated a knock-in mouse model with an inserted mutation in Coq9, a CoQ biosynthetic gene.
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For a given gapped MSA, several rooted phylogenetic trees can be constructed that vary in their interpretations of which changes are "mutations" versus ancestral characters, and which events are insertion mutations or deletion mutations.
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Mutations of F8 include deletions, insertions, inversions, and point mutations.
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A thermophilic bacterium, its protein capsule or coat is stable at over 700 ̊C so inserting multiple mutations does not usually affect its structure.
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These researchers induced insertion and deletion mutations in the rII locus of phage T4 (see Chapter 6).
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The most common mechanism of transposon generated mutations is insertional mutagenesis.
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These large insertions usually create null mutations if they transpose into a gene’s ORF.
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The mutation is an insertion of a Cytosine at position 3020.
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Mutations include substitutions, insertions, deletions, inversions, and translocations.
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Snps, mutations, deletions, and insertions
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BRCA2 mutations are usually insertions or deletions of a small number of DNA base pairs in the gene.
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What he was looking for was the area of mutation where he’d inserted the foreign genes.
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Reagents and/or diagnostic kits for the detection of genetic markers including: SNPs, mutations, deletions, and insertions
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Allozymes may result from point mutations or from insertion-deletion (indel) events that affect the coding sequence of the gene.
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