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  2. Frameshift mutation - Wikipedia

    en.wikipedia.org/wiki/Frameshift_mutation

    A frameshift mutation can drastically change the coding capacity (genetic information) of the message. [1] Small insertions or deletions (those less than 20 base pairs) make up 24% of mutations that manifest in currently recognized genetic disease. [10] Frameshift mutations are found to be more common in repeat regions of DNA.

  3. Slippery sequence - Wikipedia

    en.wikipedia.org/wiki/Slippery_sequence

    The frameshift occurs due to wobble pairing. The Gibbs free energy of secondary structures downstream give a hint at how often frameshift happens. [7] Tension on the mRNA molecule also plays a role. [8] A list of slippery sequences found in animal viruses is available from Huang et al. [9]

  4. Protein-truncating variants - Wikipedia

    en.wikipedia.org/wiki/Protein-truncating_variants

    Protein-truncating variants (PTVs) are genetic variants predicted to shorten the coding sequence of genes, [1] through ways like a stop-gain mutation. [2] [3] [4] [5 ...

  5. Crick, Brenner et al. experiment - Wikipedia

    en.wikipedia.org/wiki/Crick,_Brenner_et_al...

    The Crick, Brenner et al. experiment (1961) was a scientific experiment performed by Francis Crick, Sydney Brenner, Leslie Barnett and R.J. Watts-Tobin. It was a key experiment in the development of what is now known as molecular biology and led to a publication entitled "The General Nature of the Genetic Code for Proteins" and according to the historian of Science Horace Judson is "regarded ...

  6. Insertion (genetics) - Wikipedia

    en.wikipedia.org/wiki/Insertion_(genetics)

    In genetics, an insertion (also called an insertion mutation) is the addition of one or more nucleotide base pairs into a DNA sequence. This can often happen in microsatellite regions due to the DNA polymerase slipping. Insertions can be anywhere in size from one base pair incorrectly inserted into a DNA sequence to a section of one chromosome ...

  7. Mutation - Wikipedia

    en.wikipedia.org/wiki/Mutation

    Neomorphic mutations are a part of the gain-of-function mutations and are characterized by the control of new protein product synthesis. The newly synthesized gene normally contains a novel gene expression or molecular function. The result of the neomorphic mutation is the gene where the mutation occurs has a complete change in function. [56]

  8. Ribosomal frameshift - Wikipedia

    en.wikipedia.org/wiki/Ribosomal_frameshift

    In the case where a frameshift results in nonsense, the nonsense-mediated mRNA decay (NMD) pathway may destroy the mRNA transcript, so frameshifting would serve as a method of regulating the expression level of the associated gene. [6] If a novel or off-target protein is produced, it can trigger other unknown consequences. [4]

  9. Reading frame - Wikipedia

    en.wikipedia.org/wiki/Reading_frame

    An open reading frame (ORF) is a reading frame that has the potential to be transcribed into RNA and translated into protein. It requires a continuous sequence of DNA which may include a start codon, through a subsequent region which has a length that is a multiple of 3 nucleotides, to a stop codon in the same reading frame.