Overview

insertion mutation


'insertion mutation' can also refer to...

insertion mutation

An analysis of substitution, deletion and insertion mutations in cancer genes

The Zebrafish Insertion Collection (ZInC): a web based, searchable collection of zebrafish mutations generated by DNA insertion

Inferences on the Role of Insertion in a Mutation Accumulation Experiment with Drosophila melanogaster Using RAPDs

BayGenomics: a resource of insertional mutations in mouse embryonic stem cells

Insertion of disease-causing mutations in BACs by homologous recombination in Escherichia coli

Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays

RAISE: a simple and novel method of generating random insertion and deletion mutations

Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic heterogeneity

History of Plastid DNA Insertions Reveals Weak Deletion and AT Mutation Biases in Angiosperm Mitochondrial Genomes

PBmice: an integrated database system of piggyBac (PB) insertional mutations and their characterizations in mice

Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria

A Novel Mechanism Generating Short Deletion/Insertions Following Slippage is Suggested by a Mutation in the Human α2-Globin Gene

An Insertion Mutation of the CHRNA4 Gene in a Family With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

A Translation Frameshift Mutation Induced by a Cytosine Insertion in the Polycystic Kidney Disease 2 Gene (PKD2)

On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria

Treacher Collins Syndrome may Result from Insertions, Deletions or Splicing Mutations, Which Introduce a Termination Codon into the Gene

Deletion/Insertion Mutation That Causes Biotinidase Deficiency May Result from the Formation of a Quasipalindromic Structure

 

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Quick Reference

Any mutation caused by insertion of an extranumerary nucleotide residue between two successive nucleotide residues in a DNA molecule.

Subjects: Chemistry.


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