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  2. Polyploidy - Wikipedia

    en.wikipedia.org/wiki/Polyploidy

    Polyploidy is a condition in which the cells of an organism have more than two paired sets of chromosomes. Most species whose cells have nuclei ( eukaryotes ) are diploid , meaning they have two complete sets of chromosomes, one from each of two parents; each set contains the same number of chromosomes, and the chromosomes are joined in pairs ...

  3. Triploid syndrome - Wikipedia

    en.wikipedia.org/wiki/Triploid_syndrome

    Triploid syndrome, also called triploidy, is a chromosomal disorder in which a fetus has three copies of every chromosome instead of the normal two. If this occurs in only some cells, it is called mosaic triploidy and is less severe. Most embryos with triploidy miscarry early in development.

  4. Diploid-triploid mosaicism - Wikipedia

    en.wikipedia.org/wiki/Diploid-triploid_mosaicism

    Diploid-triploid mosaicism is a human chromosome disorder. Individuals with diploid-triploid syndrome have some cells with three copies of each chromosome for a total of 69 chromosomes (called triploid cells) and some cells with the usual 2 copies of each chromosome for a total of 46 chromosomes (called diploid cells).

  5. Ploidy - Wikipedia

    en.wikipedia.org/wiki/Ploidy

    Triploid organisms, for instance, are usually sterile. Because of this, triploidy is commonly exploited in agriculture to produce seedless fruit such as bananas and watermelons. If the fertilization of human gametes results in three sets of chromosomes, the condition is called triploid syndrome. [citation needed]

  6. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    Aneuploidy is the condition in which the chromosome number in the cells is not the typical number for the species. This would give rise to a chromosome abnormality such as an extra chromosome or one or more chromosomes lost. Abnormalities in chromosome number usually cause a defect in development.

  7. Molar pregnancy - Wikipedia

    en.wikipedia.org/wiki/Molar_pregnancy

    Most partial moles are triploid (three chromosome sets). The nucleus contains one maternal set of genes and two paternal sets. The mechanism is usually the reduplication of the paternal haploid set from a single sperm, but may also be the consequence of dispermic (two sperm) fertilization of the egg. [10]

  8. Endosperm - Wikipedia

    en.wikipedia.org/wiki/Endosperm

    An endosperm is formed after the two sperm nuclei inside a pollen grain reach the interior of a female gametophyte or megagametophyte, also called the embryonic sac.One sperm nucleus fertilizes the egg cell, forming a zygote, while the other sperm nucleus usually fuses with the binucleate central cell, forming a primary endosperm cell (its nucleus is often called the triple fusion nucleus).

  9. Diploidization - Wikipedia

    en.wikipedia.org/wiki/Diploidization

    Normally, homologous chromosomes pair up in bivalents during meiosis and separate into different daughter cells. However, when multiple copies of similar chromosomes are present in the nucleus, homeologous chromosomes can also pair with homologous chromosomes resulting in the formation of trivalents or multivalents. [3]