Link: https://en.wikipedia.org/wiki/Frameshift_mutation
Description: WEBA frameshift mutation (also called a framing error or a reading frame shift) is a genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a DNA sequence that is not divisible by three.
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Link: https://biologydictionary.net/frameshift-mutation/
Description: WEBApr 28, 2017 · Frameshift mutations are among the most deleterious changes to the coding sequence of a protein. They are extremely likely to lead to large-scale changes to polypeptide length and chemical composition, resulting in a non-functional protein that often disrupts the biochemical processes of a cell.
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Link: https://www.genome.gov/genetics-glossary/Frameshift-Mutation
Description: WEBApr 9, 2024 · Definition. A frameshift mutation in a gene refers to the insertion or deletion of nucleotide bases in numbers that are not multiples of three. This is important because a cell reads a gene’s code in groups of three bases when making a protein.
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Link: https://www.technologynetworks.com/genomics/articles/missense-nonsense-and-frameshift-mutations-a-genetic-guide-329274
Description: WEBJan 13, 2020 · A visual depiction of a deletion mutation. What is a frameshift mutation? A frameshift mutation occurs when the aforementioned "addition" or "deletion" mutations result in a change to the gene's reading frame, which includes groups of three bases that encode for an amino acid.
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Link: https://www.nature.com/scitable/definition/frameshift-mutation-frame-shift-mutation-frameshift-203/
Description: WEBA frameshift mutation is a genetic mutation caused by a deletion or insertion in a DNA sequence that shifts the way the sequence is read. A DNA sequence is a chain of many smaller molecules...
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Link: https://www.biologyonline.com/dictionary/frameshift-mutation
Description: WEBJun 16, 2022 · Biology definition: A frameshift mutation is a type of gene mutation in which the addition or deletion of one or more nucleotides causes a shift in the reading frame of the codons in the mRNA, which may lead to the alteration in the amino acid sequence at protein translation. Variant: frame shift mutation.
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Link: https://www.sciencedirect.com/topics/neuroscience/frameshift-mutation
Description: WEBFrameshift mutations are produced by molecules that can insert (intercalate) between the normal bases to create mistakes during DNA synthesis. These are usually flat molecules, such as the acridine dyes, that have a hydrophobic nature (remember that hydrophobic base stacking is a contributing force in the structure of the helix).
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Link: https://www.jove.com/science-education/11483/point-mutations-and-frameshift-mutations
Description: WEBFrameshift mutations occur when one or more nucleotides are inserted into or deleted from a protein-coding DNA sequence, affecting all of the codons downstream of the location of the mutation. Chromosomal Alterations Are Large-Scale Mutations. The most drastic type of mutation, chromosomal alteration, changes the physical structure of a …
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Link: https://www.sciencedirect.com/topics/immunology-and-microbiology/frameshift-mutation
Description: WEBFrameshift mutations are deletions or additions of 1, 2, or 4 nucleotides that change the ribosome reading frame and cause premature termination of translation at a new nonsense or chain termination codon (TAA, TAG, and TGA).
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Link: https://link.springer.com/referenceworkentry/10.1007/978-1-4020-6754-9_6217
Description: WEBJan 1, 2016 · Frameshift mutations are caused frequently by acridine dyes and cross-linking mutagens. The discovery of frameshift mutagens contributed to the recognition that the genetic code relies on nucleotide triplets. Frame shift mutation can be represented by the following folly:
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