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  2. Meiosis - Wikipedia

    en.wikipedia.org/wiki/Meiosis

    The normal separation of chromosomes in meiosis I or sister chromatids in meiosis II is termed disjunction. When the segregation is not normal, it is called nondisjunction. This results in the production of gametes which have either too many or too few of a particular chromosome, and is a common mechanism for trisomy or monosomy.

  3. Chromosome segregation - Wikipedia

    en.wikipedia.org/wiki/Chromosome_segregation

    Chromosome segregation is the process in eukaryotes by which two sister chromatids formed as a consequence of DNA replication, or paired homologous chromosomes, separate from each other and migrate to opposite poles of the nucleus. This segregation process occurs during both mitosis and meiosis. Chromosome segregation also occurs in prokaryotes ...

  4. Synapsis - Wikipedia

    en.wikipedia.org/wiki/Synapsis

    Synapsis or Syzygy is the pairing of two chromosomes that occurs during meiosis. It allows matching-up of homologous pairs prior to their segregation, and possible chromosomal crossover between them. Synapsis takes place during prophase I of meiosis. When homologous chromosomes synapse, their ends are first attached to the nuclear envelope.

  5. List of organisms by chromosome count - Wikipedia

    en.wikipedia.org/wiki/List_of_organisms_by...

    The list of organisms by chromosome count describes ploidy or numbers of chromosomes in the cells of various plants, animals, protists, and other living organisms.This number, along with the visual appearance of the chromosome, is known as the karyotype, [1] [2] [3] and can be found by looking at the chromosomes through a microscope.

  6. Nondisjunction - Wikipedia

    en.wikipedia.org/wiki/Nondisjunction

    Note that chromosome 21 is present in 3 copies, while all other chromosomes show the normal diploid state with 2 copies. Most cases of trisomy of chromosome 21 are caused by a nondisjunction event during meiosis I (see text). Down syndrome, a trisomy of chromosome 21, is the most common anomaly of chromosome number in humans. [2]

  7. Homologous chromosome - Wikipedia

    en.wikipedia.org/wiki/Homologous_chromosome

    Meiosis is a round of two cell divisions that results in four haploid daughter cells that each contain half the number of chromosomes as the parent cell. [10] It reduces the chromosome number in a germ cell by half by first separating the homologous chromosomes in meiosis I and then the sister chromatids in meiosis II.

  8. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    McClintock used the prophase and metaphase stages of mitosis to describe the morphology of corn's chromosomes, and later showed the first ever cytological demonstration of crossing over in meiosis. Working with student Harriet Creighton, McClintock also made significant contributions to the early understanding of codependency of linked genes.

  9. Genetic recombination - Wikipedia

    en.wikipedia.org/wiki/Genetic_recombination

    In meiosis, non-sister homologous chromosomes pair with each other so that recombination characteristically occurs between non-sister homologues. In both meiotic and mitotic cells, recombination between homologous chromosomes is a common mechanism used in DNA repair.