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anaphase
mitotic phase during which daughter chromosomes move toward the poles of the spindle
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apoptosis
programmed cell death involving a cascade of specific cellular events leading to death and destruction of the cell
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aster
short, radiating fibers about the centrioles at the poles of a spindle
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barr body
dark-staining body in the nuclei of female mammals that contains a condensed, inactive X chromosome.
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cell cycle
repeating sequence of cellular events that consists of interphase, mitosis, and cytokinesis
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centriole
cellular structure, existing in pairs, that possibly organizes the mitotic spindle for chromosomal movement during mitosis and meiosis
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centromere
constriction where sister chromatids of a chromosome are held together
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centrosome
central microtubule organizing center of cells. in animal cells, it contains two centrioles
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cleavage furrow
indentation that begins the process of cleavage, by which human cells undergo cytokinesis
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crossing over
exchange of segments between non sister chromatids of a tetrad during meiosis
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cytokinesis
division of the cytoplasm following mitosis and meiosis
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daughter cell
cell that arises from a parent cell by mitosis or meiosis
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deletion
change in chromosome structure in which the end of a chromosome breaks off or two simultaneous breaks lead to the loss of an internal segment; often causes abnormalities
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diploid (2n)
cell condition in which two of each type of chromosome are present in the nucleus
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duplication
change in chromosome structure in which a particular segment is present more than once in the same chromosome
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fertilization
union of a sperm nucleus and an egg nucleus, which creates a zygote
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gamete
haploid sex cell; the egg or a sperm, which join in fertilization to form a zygote
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halpoid (n)
the n number of chromosomes - half the diploid number; the number characteristic of gametes, which contain only one set of chromosomes
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homologous chromosome
member of a pair of chromosomes that are alike and come together in synapsis during prophase of the first meiotic division
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homologue
member of a homologous pair of chromosomes
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interkinesis
period between meiosis I and meiosis II, during which no DNA replication takes place.
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interphase
cell cycle stage during which growth and DNA synthesis occur when the nucleus is not actively dividing
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inversion
change in chromosome structure in which a segment of a chromosome is turned around 180 degrees; this reversed sequence of genes can lead to altered gene activity and abnormalties
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meiosis
type of a nuclear division that occurs as part of sexual reproduction in which the daughter cells receive the haploid number of chromosomes in varied combinations
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metaphase
mitotic phase during which chromosomes are aligned at the equator of the mitotic spindle
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mitosis
type of cell division in which daughter cells receive the exact chromosomal and genetic makeup of the parent cell; occurs during growth and repair
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mitotic spindle
microtubule structure that brings about chromosomal movement during nuclear division
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monosomy
one less chromosome than usual
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nondisjunction
failure of homologous chromosomes or daughter chromosomes to separate during meiosis I and meiosis II, respectively
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oogenesis
production of an egg in females by the process of meiosis and maturation
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parent cell
cell that divides so as to form daughter cells
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polar body
in oogenesis, a nonfunctional product; two to three meiotic products are of this type
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prophase
mitotic phase during which chromatin condenses so that chromosomes appear; chromosomes are scattered
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secondary oocyte
in oogenesis, the functional product of meiosis I; becomes the egg
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sister chromatids
one of two genetically identical chromosomal units that are the result of DNA replication and are attached to each other at the centromere
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spermatogenesis
production of sperm in males by the process of meiosis and maturation
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synapsis
pairing of homologous chromosomes during prophase I of meiosis I
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syndrome
group of symptoms that appear together and tend to indicate the presence of a particular disorder
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telophase
mitotic phase during which daughter chromosomes are located at each pole
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translocation
movement of a chromosomal segment from one chromosome to another non homologous, leading to abnormalities; down syndrome
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trisomy
one more chromosome than usual
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zygote
diploid cell formed by the union of sperm and egg; the product of fertilization
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