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55 Cards in this Set
- Front
- Back
Cell Division
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When a cell undergoes reproduction.(2) the reproduction of a cell through duplication of the genome and division of the cytoplasm.
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Chromosomes
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The structures that contain most of the cells DNA.(2) A threadlike, gene-carrying structure found in the nucleus of a eukaryotic cell and most visible during mitosis and meiosis;also, the main gene-carrying structure of a prokaryotic cell. A chromosome consists of one wery long piece of chromatin, a combination of DNA and protien.
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Asexual Reproduction
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The creation of genetically identical offspring by a single parent.
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Sexual Reproduction
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Requires fertilization of an egg by a sperm.
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Chromatin
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Fibers composed of roughly equal amounts of DNA and protein molecules.
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Sister Chromatids
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One of the two identical parts of a duplicated chromosome in a eukaryotic cell.Prior to mitosis, sister chromatids remain attached to each another at the centromere.
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Centromere
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The region of a duplicated chromosome where two sister chromatids are joined.
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Cell Cycle
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An ordered sequence of events that extends from the time a cell is first formed from a dividing parent cell until it's own division into two cells.
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Interphase
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This is a time when a cell's metabolic activity is very high and the cell performs it's various functions within the organism.
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Miotic Phase
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The part of the cell cycle when the cell actually divides.
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Mitosis
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The nucleus and it's contents divide and are evenly distributed forming two daughter nuclei.
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Cytokinesis
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The cytoplasm is divided into two.
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Interphase
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The period of cell growth, when the cell synthesizes new molecules and organelles.
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Prophase
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Changes occur in both the nucleus and the cytoplasm
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Prometphase
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The nuclear envelope breaks into fragments and disappears
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Metaphase
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The miotic spindle is fully formed
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Anaphase
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When the two centromeres of each chromosome come apart.
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Telophase
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The cell elongation that started in the Anaphase continues
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Miotic Spindle
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A football shaped structure of microtubules that guides the separation of the two sets of daughter chromosomes.
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Centrosomes
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(1)Clouds of cytoplasmic material that in animal cells contain pairs of centrioles. (2) Material in the cytoplasm of a eukaryotic cell that gives rise to microtubules; important in mitosis and meiosis; also called the microtubule-organising center.
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Cell Cycle Control System
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A cyclically operation set of molecules in the cell that both triggers and coordinates key events in the cell cycle.
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Tumor
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An abnormally growing mass of body cells.
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Benign Tumor
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Abnormal cells that remain at the original site.
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Malignant Tumor
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An abnormal tissue mass that can spread into neighboring tissue and to other parts of the body.
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Metastasis
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The spread of cancer cells beyond their original site.
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Carcinomas
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Cancers that originate in the originate in the external or internal coverings of the body.
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Sarcomas
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Arise in tissues that support the body
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Leukemias and Lymphomas
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Cancers of blood-forming tissues, such as bone marrow, spleen, and lymph nodes.
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Somatic Cell
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A typical body cell that has 46 chromosomes.
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Homologous Chromosomes
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The two chromosomes that make up a matched pair in a diploid cell.
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Locus
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The particular site where a gene is found on a chromosome.
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Sex Chromosomes
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What determines an individuals sex.
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Autosomes
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The 22 remaining chromosomes foind in both males and females.
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Life Cycle
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The sequence of stages leading from the adults of one generation to the adults of the next.
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Diploid
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A cell containing two homologous sets of chromosomes.(2) In an organism that reproduces sexually, a cell containing two homologous sets of chromosomes, one set inherited from each parent; a 2n cell.
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Gametes
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Egg and sperm cells.
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Haploid
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A cell with a single chromosome set.(2) In the life cycle of an organism that reproduces sexually, a cell containing a single set of chromosomes; a n cell.
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Fertilization
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When a haploid cell from the father fuses with a haploid cell from the mother.
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Zygote
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A fertilized egg.
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Alleles
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The alternative versions of a gene
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Meiosis
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A type of cell division that produces haploid gametes in diploid organisms.
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Crossing over
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An exchange of corresponding segmentsbetween nonsister chromatids of homologous chromosomes,
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Chiasma
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The microscopially visible site where crossing over has occured between chromatids of homologous chromosomes during prophase I of meiosis.
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Tetrad
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A paired set of homologous chromosomes, each composed of two sister chromatids. Tetradsform during prophase I of meiosis,when crossing over may occur.
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Genetic recombination
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The production, by crossing over and/or independent assortment of chromosomes during meiosis, of offspring with allele combinations different from those in the parents. The term also may be used more specifically to mean the production by crossing over of eukaryotic or prokaryotic chromosomes with gene combinations different from those in the original chromosomes.
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Karotype
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A display of micrographs of the metaphase chrosomes of a cell, arranged by size and centromere position. Karotypes may be used to identify certain chromosomal abnormalities.
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Trisomy 21
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See Down syndrome
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Down Syndrome
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A human genetic disorder resulting from the presence of an extra chromosome 21; characterized by heart and respiratory defects and varying degrees of mental retardation.
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Nondisjunction
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An accident of meiosis or mitosis in which a pair of homologous chromosomes or a pair of sister chromatids fail to seperate at anaphase.
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Polypoid
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Am organism that has more than two complete sets of chromosomes as a result of an accident of cell division.
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Deletion
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The loss of one or more nucleotides from a gene by mutation; the loss of a fragment of a chromosome.
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Duplication
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Repetition of part of a chromosome resulting from fusion with a fragment from homologous chromosome; can result from an error in meiosis or from mutagenesis.
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Inversion
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A change in a chromosome resulting from reattachment of a chromosome fragment to the original chromosome, but in a reverse direction. Mutagens and errors during meiosis can cause inversions.
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Translocation
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(1) During protien synthesis,the movement of a tRNA molecule carrying a growing polypeptide chain from the A site to the P site on a ribosome.(The mRNA travels with it.) (2) A change in a chromosonoe resulting from a chromosomal fragment attaching to a nonhomologous chromosome; can occur as a result of an error in meiosis or from mutagenesis
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Mutagen
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A chemical or physical agent that interacts with DNA and causes a mutation.
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