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notes
notes

... Genes for many sex-linked traits, unrelated to gender, are found on the X chromosome Follow Mendelian Laws of Inheritance May be either dominant or recessive ...
9 Genetic diversity and adaptation Checklist AQA Biology
9 Genetic diversity and adaptation Checklist AQA Biology

... Can you explain that not all base substitutions cause a change in the sequence of encoded amino acids, due to the degenerate nature of the genetic code? ...
AQA Biology Genetic diversity and adaptation Specification
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Chapter 10: Genes and Chromosomes
Chapter 10: Genes and Chromosomes

... move along the genes on the chromosomes, producing mRNA in the process • Before the RNA polymerase can get to the desired genes, it must first attach to the promoter region near the genes • One the RNA polymerase attaches to the promoter, it can move along the chromosome, past the operator region, t ...
Biology 12
Biology 12

... 2. modifications of nucleosomal histones. (acetylation). These act to turn on or turn off genes. Many of these are activated by the environment. Some examples of diseases that are epigenetic include many of the cancers, heart disease and diabetes. Some examples of factors that can trigger epigenetic ...
mendel`s legacy
mendel`s legacy

... 3. If orange flower color in a plant is controlled by an allele F and red flower color is controlled by an allele f, which flower color is dominant? If true-breeding orange-flowered plants are crossed with true-breeding red-flowered plants, what will be the flower color(s) of the F1 plants? 4. Criti ...
Meiosis - Amok Science
Meiosis - Amok Science

... ----Gamete: Sex cell. Haploid. Egg & sperm. Nondisjunction: Mutation caused when a replicated chromosome pair fails to separate during cell division, causing changes in chromosome #. One gamete gets an extra chromosome, one gets one less! (Example: Down's Syndrome, Trisomy X) Mendel's Law of Segreg ...
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Are your Earlobes attached or detached?

...  The above steps are exactly the same as mitosis. ...
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KS4 Chromosomes, Genes and DNA

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Epigenetics concerns changes in gene expression states that are
Epigenetics concerns changes in gene expression states that are

... Epigenetics concerns changes in gene expression states that are stable over rounds of cell division, but do not involve changes in the underlying DNA sequence of the organism. In female mammals, one of the two X chromosomes is transcriptionally silenced during early development to compensate for the ...
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Williams` Sprawl

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chromosomes - Life Science Academy
chromosomes - Life Science Academy

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Keystone Review Question

...  Which of the following statements is true? A. Mitosis results in the formation of two haploid gametes which can then combine to form a diploid daughter cell. B. During the process of meiosis, haploid cells are formed. After fertilization, the diploid number of chromosomes is restored. C. The proc ...
Document
Document

... ○ Female has two X chromosomes ○ Male has one X and one Y chromosome ...
Chapter Three: Heredity and Environment
Chapter Three: Heredity and Environment

... Genes are made up of DNA: the complex protein code of genetic information DNA directs the form and function of each body cell as it develops Each molecule of DNA is called a chromosome Chromosomes contain instructions to make all the proteins a living being needs Each person has 23 sets of chromosom ...
Particulate Inheritance Patterns Blended Inheritance Particulate
Particulate Inheritance Patterns Blended Inheritance Particulate

... Definitions •  Monohybrid - a heterozygote resulting from the cross of two pure parental strains. •  Selfing- a cross in which individuals are allowed to self-fertilize (plants) or two phenotypically identical individuals from the same generation are allowed to mate. ...
CHROMOSOMES AND DISEASE
CHROMOSOMES AND DISEASE

... A chromosomal abnormality can be a numerical deviation from the diploid number (46, XX or 46, XY) or a structural rearrangement such as an inversion, translocation or deletion. The abnormalities may involve one or more than one autosome, sex chromosomes or both. Most chromosomal aberrations are prod ...
First question is how to create chromosomes, what type of encoding
First question is how to create chromosomes, what type of encoding

... Question- 2: How to select parents for crossover?  The main idea is to select the better parents (in hope that the better parents will produce better offspring).  Making new population only by new offspring can cause loss of the best chromosome from the last population.  Elitism is often used. T ...
Paper 1
Paper 1

... 14 chromosomes. A new fertile hybrid species called Emmer, which had 28 chromosomes, was produced. Emmer had many more seeds which were also larger than the wild wheat and the seeds were attached to the husk in such a way that it could easily be dispersed by wind. There was a second 'genetic acciden ...
Chromosomal Aberrations
Chromosomal Aberrations

... Tyler is a newborn baby suspected of having Down syndrome. Chromosome analysis reveals that he has three copies of chromosome 21, but the long arm of one chromosome 21 is translocated onto the long arm of one chromosome 14 at the centromere. Because chromosomes 14 and 21 are acrocentric chromosomes ...
File
File

... Part A Indicate whether the sentence or statement is true or false 1. Mendel restricted his observations to specific contrasting characteristics of pea plants 2. The phenotype is the appearance of the organism 3. The genotype is determined by the phenotype 4. A diploid organism is homozygous if it c ...
DRAGON GENETICS LAB
DRAGON GENETICS LAB

... under the appropriate MOM or DAD column. (ie. If the mother dragon had “F” on one side of the red autosome and “f” on the other, that parent would write “Ff” in the first box of the MOM column.) For each color autosome and then for the sex chromosomes, each parent will randomly drop his or her stick ...
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Ploidy



Ploidy is the number of sets of chromosomes in a cell. Usually a gamete (sperm or egg, which fuse into a single cell during the fertilization phase of sexual reproduction) carries a full set of chromosomes that includes a single copy of each chromosome, as aneuploidy generally leads to severe genetic disease in the offspring. The gametic or haploid number (n) is the number of chromosomes in a gamete. Two gametes form a diploid zygote with twice this number (2n, the zygotic or diploid number) i.e. two copies of autosomal chromosomes. For humans, a diploid species, n = 23. A typical human somatic cell contains 46 chromosomes: 2 complete haploid sets, which make up 23 homologous chromosome pairs.Because chromosome number is generally reduced only by the specialized process of meiosis, the somatic cells of the body inherit and maintain the chromosome number of the zygote. However, in many situations somatic cells double their copy number by means of endoreduplication as an aspect of cellular differentiation. For example, the hearts of two-year-old children contain 85% diploid and 15% tetraploid nuclei, but by 12 years of age the proportions become approximately equal, and adults examined contained 27% diploid, 71% tetraploid and 2% octaploid nuclei.Cells are described according to the number of sets present (the ploidy level): monoploid (1 set), diploid (2 sets), triploid (3 sets), tetraploid (4 sets), pentaploid (5 sets), hexaploid (6 sets), heptaploid or septaploid (7 sets), etc. The generic term polyploid is frequently used to describe cells with three or more sets of chromosomes (triploid or higher ploidy).
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