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Eukaryo c cell Fundamentals The Cell Cycle Cellular Division
Eukaryo c cell Fundamentals The Cell Cycle Cellular Division

... Review of haploid, diploid, mitosis and meiosis  ...
Section 3 Exam
Section 3 Exam

... 22. Sexual reproduction and meiosis do not generate much significant genetic variability through: A. The random alignment of homologous pairs of DNA ‘packages’ during meiosis B. Crossing over (also called homologous recombination) during meiosis C. The fact that fertilization is a random phenomenon ...
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... passed along, the “how’is not known clearly Aristotle – passed through the blood (“bloodline”) Early naturalists – believed in “hybrids”–where species result from breeding between other species Georges Buffon (1700s) – head and limbs from (male), rest of body from (female) 1800s – common belief was ...
The Process of Meiosis
The Process of Meiosis

... together half the genetic information from the parents into one new cell that is now genetically different from both its parents. •This increases genetic diversity, as half of the genetic content from each of the parents brings about unique offspring, which possesses a unique genome presenting uniqu ...
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An Aside: X Inactivation in Female Mammals

... If a color blind man has children with a “wild-type” woman, what are the chances that a daughter of theirs will be colorblind? What are the chances that their son will be ...
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7.1 Chromosomes and Phenotype

... • Mendel’s rules of inheritance apply to autosomal genetic disorders. – A heterozygote for a recessive disorder is a carrier. – Disorders caused by dominant alleles are uncommon. ...
CHAPTER 14 VOCAB
CHAPTER 14 VOCAB

... hemo- blood (hemophilia: a human genetic disease caused by a sex-linked recessive allele, characterized by excessive bleeding following injury) mono- one (monosomic: a chromosomal condition in which a particular cell has only one copy of a chromosome, instead of the normal two; the cell is said to b ...
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File - Mrs. Riggs Online

... • all normal humans have 23 pairs of chromosomes; each pair responsible for certain functions, but pair #23 determines gender and has distinct appearance in each sex • females: XX • males: XY • --> male contributes one of two chromosomes which determines gender of offspring depending on whether that ...
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Prentice Hall Biology

... neurofibromatosis. Also contains long stretches of repetitive DNA that are unstable sites where rearrangements can occur (breakage). ...
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Station Lab Part 2

... Haploid & Diploid Background Information All animal cells have a fixed number of chromosomes in their body cells which exist in homologous pairs (2n). Each pair of chromosomes consists of one chromosome from the mother and the second from the father. During the process of meiosis, the sex cells divi ...
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Cells, DNA and Genetics

... You would wind up with two identical molecules of DNA that you started with. One strand will be old and one new (I indicated old strands by bolding). ...
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Topic 4.1: Chromosomes, genes, alleles, and mutations

...  If DNA replication works correctly, this should ...
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CHROMOSOMAL BASIS OF INHERITANCE

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meiosis - Cloudfront.net

... STAINING PATTERN • AUTOSOME - A CHROMOSOME THAT IS NOT A SEX CHROMOSOME (22 PAIRS IN HUMANS) • SEX CHROMOSOMES = IT IS THE 23RD CHROMOSOME PAIR IN HUMANS • FEMALES (XX) • MALES (XY) ...
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Cell cycle
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... 1. Chromatin: the relaxed, uncoiled state of the chromosome 2. Chromatid: one of two identical “sister” parts of a duplicated chromosome 3. Chromosome: threadlike structures within the nucleus containing genetic information that is passed on from generation to generation 4. Centromere: chromosome re ...
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Chromosome structure & Gene Expression

... fully condensed then stained with Giemsa stain. This staining forms G bands which are interchangeable dark and light bands along the chromosome. These bands are identical and characteristic for each pair of homologous chromosomes but differ between different chromosomes. At low resolution, human chr ...
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... into compact chromosomes. • Nuclear envelope disappears. • Synapsis occurs. – Homologous pairs of chromosomes closely align allowing exchange of chromosome segments ...
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... The female sex cell is called the (1)__________________ and always carries the (2)_____ sex chromosome. The male sex cell is called the (3)____________________ and could carry the (4)_____ or (5)_____ sex chromosome, and therefore, determines the sex of the baby. There are 46 chromosomes in normal b ...
10-11_the_story_of_conception
10-11_the_story_of_conception

... The female sex cell is called the (1)__________________ and always carries the (2)_____ sex chromosome. The male sex cell is called the (3)____________________ and could carry the (4)_____ or (5)_____ sex chromosome, and therefore, determines the sex of the baby. There are 46 chromosomes in normal b ...
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Meiosis

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< 1 ... 458 459 460 461 462 463 464 465 466 ... 538 >

Chromosome



A chromosome (chromo- + -some) is a packaged and organized structure containing most of the DNA of a living organism. It is not usually found on its own, but rather is complexed with many structural proteins called histones as well as associated transcription (copying of genetic sequences) factors and several other macromolecules. Two ""sister"" chromatids (half a chromosome) join together at a protein junction called a centromere. Chromosomes are normally visible under a light microscope only when the cell is undergoing mitosis. Even then, the full chromosome containing both joined sister chromatids becomes visible only during a sequence of mitosis known as metaphase (when chromosomes align together, attached to the mitotic spindle and prepare to divide). This DNA and its associated proteins and macromolecules is collectively known as chromatin, which is further packaged along with its associated molecules into a discrete structure called a nucleosome. Chromatin is present in most cells, with a few exceptions - erythrocytes for example. Occurring only in the nucleus of eukaryotic cells, chromatin composes the vast majority of all DNA, except for a small amount inherited maternally which is found in mitochondria. In prokaryotic cells, chromatin occurs free-floating in cytoplasm, as these cells lack organelles and a defined nucleus. The main information-carrying macromolecule is a single piece of coiled double-stranded DNA, containing many genes, regulatory elements and other noncoding DNA. The DNA-bound macromolecules are proteins, which serve to package the DNA and control its functions. Chromosomes vary widely between different organisms. Some species such as certain bacteria also contain plasmids or other extrachromosomal DNA. These are circular structures in the cytoplasm which contain cellular DNA and play a role in horizontal gene transfer.Compaction of the duplicated chromosomes during cell division (mitosis or meiosis) results either in a four-arm structure (pictured to the right) if the centromere is located in the middle of the chromosome or a two-arm structure if the centromere is located near one of the ends. Chromosomal recombination during meiosis and subsequent sexual reproduction plays a vital role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe and die, or it may unexpectedly evade apoptosis leading to the progression of cancer.In prokaryotes (see nucleoids) and viruses, the DNA is often densely packed and organized. In the case of archaea by homologs to eukaryotic histones, in the case of bacteria by histone-like proteins. Small circular genomes called plasmids are often found in bacteria and also in mitochondria and chloroplasts, reflecting their bacterial origins.
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