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  2. Genetic recombination - Wikipedia

    en.wikipedia.org/wiki/Genetic_recombination

    Contents. Genetic recombination. A model of meiotic recombination, initiated by a double-strand break or gap, followed by pairing with an homologous chromosome and strand invasion to initiate the recombinational repair process. Repair of the gap can lead to crossover (CO) or non-crossover (NCO) of the flanking regions.

  3. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    A double crossing over. Chromosomal crossover, or crossing over, is the exchange of genetic material during sexual reproduction between two homologous chromosomes ' non-sister chromatids that results in recombinant chromosomes. It is one of the final phases of genetic recombination, which occurs in the pachytene stage of prophase I of meiosis ...

  4. Nondisjunction - Wikipedia

    en.wikipedia.org/wiki/Nondisjunction

    In general, nondisjunction can occur in any form of cell division that involves ordered distribution of chromosomal material. Higher animals have three distinct forms of such cell divisions: Meiosis I and meiosis II are specialized forms of cell division occurring during generation of gametes (eggs and sperm) for sexual reproduction, mitosis is the form of cell division used by all other cells ...

  5. Homologous recombination - Wikipedia

    en.wikipedia.org/wiki/Homologous_recombination

    During meiosis, homologous recombination can produce new combinations of genes as shown here between similar but not identical copies of human chromosome 1. Homologous recombination is a type of genetic recombination in which genetic information is exchanged between two similar or identical molecules of double-stranded or single-stranded ...

  6. Meiosis - Wikipedia

    en.wikipedia.org/wiki/Meiosis

    meiosis. produces four genetically unique cells, each with half the number of chromosomes as in the parent. mitosis. produces two genetically identical cells, each with the same number of chromosomes as in the parent. Meiosis begins with a diploid cell, which contains two copies of each chromosome, termed homologs.

  7. Dicentric chromosome - Wikipedia

    en.wikipedia.org/wiki/Dicentric_chromosome

    Dicentric chromosome. A dicentric chromosome is an abnormal chromosome with two centromeres. It is formed through the fusion of two chromosome segments, each with a centromere, resulting in the loss of acentric fragments (lacking a centromere) and the formation of dicentric fragments. [1] The formation of dicentric chromosomes has been ...

  8. Genetic linkage - Wikipedia

    en.wikipedia.org/wiki/Genetic_linkage

    Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more linked than markers that are far apart.

  9. Boveri–Sutton chromosome theory - Wikipedia

    en.wikipedia.org/wiki/Boveri–Sutton_chromosome...

    The Boveri–Sutton chromosome theory (also known as the chromosome theory of inheritance or the Sutton–Boveri theory) is a fundamental unifying theory of genetics which identifies chromosomes as the carriers of genetic material. [ 1 ][ 2 ][ 3 ] It correctly explains the mechanism underlying the laws of Mendelian inheritance by identifying ...