enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Chromosome segregation - Wikipedia

    en.wikipedia.org/wiki/Chromosome_segregation

    During the phase of meiosis labeled “interphase s” in the meiosis diagram there is a round of DNA replication, so that each of the chromosomes initially present is now composed of two copies called chromatids. These chromosomes (paired chromatids) then pair with the homologous chromosome (also paired chromatids) present in the same nucleus ...

  3. Meiosis - Wikipedia

    en.wikipedia.org/wiki/Meiosis

    Mechanically, the process is similar to mitosis, though its genetic results are fundamentally different. The result is the production of four haploid cells (n chromosomes; 23 in humans) from the two haploid cells (with n chromosomes, each consisting of two sister chromatids) [clarification needed] produced in meiosis I. The four main steps of ...

  4. Chromosome 3 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_3

    Chromosome 3 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 3 spans more than 198 million base pairs (the building material of DNA ) and represents about 6.5 percent of the total DNA in cells .

  5. Non-random segregation of chromosomes - Wikipedia

    en.wikipedia.org/wiki/Non-random_segregation_of...

    Non-random segregation of chromosomes is a deviation from the usual distribution of chromosomes during meiosis, that is, during segregation of the genome among gametes.While usually according to the 2nd Mendelian rule (“Law of Segregation of genes“) homologous chromosomes are randomly distributed among daughter nuclei, there are various modes deviating from this in numerous organisms that ...

  6. Homologous chromosome - Wikipedia

    en.wikipedia.org/wiki/Homologous_chromosome

    So, humans have two sets of 23 chromosomes in each cell that contains a nucleus. One set of 23 chromosomes (n) is from the mother (22 autosomes, 1 sex chromosome (X only)) and one set of 23 chromosomes (n) is from the father (22 autosomes, 1 sex chromosome (X or Y)). Ultimately, this means that humans are diploid (2n) organisms. [2]

  7. Origin and function of meiosis - Wikipedia

    en.wikipedia.org/wiki/Origin_and_function_of_meiosis

    The two chromosomes which pair are referred to as non-sister chromosomes, since they did not arise simply from the replication of a parental chromosome. Recombination between non-sister chromosomes at meiosis is known to be a recombinational repair process that can repair double-strand breaks and other types of double-strand damage. [2]

  8. Synapsis - Wikipedia

    en.wikipedia.org/wiki/Synapsis

    [3] This is not to be confused with mitosis. Mitosis also has prophase, but does not ordinarily do pairing of two homologous chromosomes. [4] In contrast to the mitosis cycle, during meiosis, the number of chromosomes is reduced by half to create haploid gametes; this reduction is called Haploidization; after fertilization, diploidy is restored.

  9. Chiasma (genetics) - Wikipedia

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

    [3] [4] When each tetrad , which is composed of two pairs of sister chromatids , begins to split, the only points of contact are at the chiasmata. The chiasmata become visible during the diplotene stage of prophase I of meiosis , but the actual "crossing-overs" of genetic material are thought to occur during the previous pachytene stage.