When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Gene duplication - Wikipedia

    en.wikipedia.org/wiki/Gene_duplication

    Gene duplications can arise as products of several types of errors in DNA replication and repair machinery as well as through fortuitous capture by selfish genetic elements. Common sources of gene duplications include ectopic recombination, retrotransposition event, aneuploidy, polyploidy, and replication slippage. [1]

  3. Gene redundancy - Wikipedia

    en.wikipedia.org/wiki/Gene_redundancy

    The mode of duplication by which redundancy occurs has been found to impact the classifications in breast cancer disposition genes. [19] Gross duplications complicate clinical interpretation because it is difficult to discern if they occur in tandem. Recent methods, like DNA breakpoint assay, have been used to determine tandem status. [19]

  4. Evolution by gene duplication - Wikipedia

    en.wikipedia.org/wiki/Evolution_by_gene_duplication

    Evolution by gene duplication is an event by which a gene or part of a gene can have two identical copies that can not be distinguished from each other. This phenomenon is understood to be an important source of novelty in evolution, providing for an expanded repertoire of molecular activities.

  5. Repeated sequence (DNA) - Wikipedia

    en.wikipedia.org/wiki/Repeated_sequence_(DNA)

    Repeated sequences (also known as repetitive elements, repeating units or repeats) are short or long patterns that occur in multiple copies throughout the genome.In many organisms, a significant fraction of the genomic DNA is repetitive, with over two-thirds of the sequence consisting of repetitive elements in humans. [1]

  6. Chromosomal rearrangement - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_rearrangement

    It shows 22 homologous autosomal chromosome pairs, both the female (XX) and male (XY) versions of the two sex chromosomes, as well as the mitochondrial genome (at bottom left). In genetics , a chromosomal rearrangement is a mutation that is a type of chromosome abnormality involving a change in the structure of the native chromosome . [ 1 ]

  7. Structural variation in the human genome - Wikipedia

    en.wikipedia.org/wiki/Structural_variation_in...

    Structural variation is an important type of human genetic variation that contributes to phenotypic diversity. [2] There are microscopic and submicroscopic structural variants which include deletions, duplications, and large copy number variants as well as insertions, inversions, and translocations. [1]

  8. Why do we have useless body parts? - AOL

    www.aol.com/news/2014-08-14-why-do-we-have...

    Humans have many vestigial body parts that may have been useful for our ancestors but are obsolete for us. Useless. Have you ever wondered about why you grow wisdom teeth, only to have them ...

  9. Unequal crossing over - Wikipedia

    en.wikipedia.org/wiki/Unequal_crossing_over

    Gene duplications are the main reason for the increase of genome size, and as unequal crossing over is the main mechanism for gene duplication, unequal crossing over contributes to genome size evolution is the most common regional duplication event that increases the size of the genome.