Nicolas‚ Vida Marie C. February 24‚ 2014 IA12116 Prof. Brenda Lansang GENETIC DISORDERS 22q11.2 Deletion Syndrome 22q11.2 deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2. 22q11.2 deletion syndrome has many possible signs and symptoms that can affect almost any part of the body. The features of this syndrome vary widely‚ even among affected members
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TimeLine of Genetics 1750 B.C.E. The Sumerians brew beer. 500 B.C.E. The Chinese use moldy soybean curds as an antibiotic to treat boils. C.E. 100 Powdered chrysanthemum is used in China as an insecticide. 1590 The microscope is invented by Zacharias Janssen. 1663 Cells are first described by Robert Hooke. 1675 Antonie van Leeuwenhoek discovers bacteria. 1797 Edward Jenner inoculates a child with a viral vaccine to protect him from smallpox. 1830 Proteins are
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This journal article review is to discuss hemorrhagic ovarian cysts (HOC) and how sonography can be used to determine and diagnose these findings. Using sonography can help identify the type of cysts present to get the correct diagnosis. While reading this article it had been mentioned that this type of condition can be diagnosed incorrectly. Sonography can help identify the different appearances that go along with hemorrhagic ovarian cysts. Endovaginal sonography is the best for finding and diagnosing
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GENETIC ENGINEERING GENETIC ENGINEERING GENERAL STEPS What is Genetic Engineering? Genetic Engineering = inserting a foreign gene of interest into a host to transcribe and translate a particular protein. Ex. Inserting the human insulin gene into bacteria to mass produce it. General Steps Obtain the gene of interest (ex. insulin gene) Insert the gene into the host (ex. bacteria) Allow the host to multiply and express the foreign gene get your desired protein! Get lots of cells that can
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Associate Program Material Genetics Worksheet Review the images below and answer the follow-up questions. Questions: 1. According to the pedigree‚ is cystic fibrosis inherited as a dominant or as a recessive trait? Explain how you made your conclusion using evidence from the pedigree and the principles of genetics. Cystic fibrosis is a recessive trait. If you have one CF gene and one non-CF gene‚ you will be a carrier but not
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becoming keener to the field of engineering. Genetic engineering that is. When one thinks of “genetic engineering‚” the first thought is probably a perfect child‚ or paradoxically some inconceivable creature‚ forged under the microscope in a scientific laboratory. Though both of these are genetic engineering‚ many people do not consider other things‚ such as genetic engineering of agriculture and medicine‚ both of which are extremely useful. Through the genetic altering of plants and crops‚ scientists
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Genetic disorders are a topic in biology that can not be avoided. The fact is that genetic disorders can happen in humans‚ plants or animal. No one and nothing is safe from a genetic disorder. A genetic disorder can appear in the first years off life‚ or can appear much later in life when least expected. A basic principal of biology states that the behavior of chromosomes during the meiosis process can account for genetic inheritance patterns. There are many reasons for genetic disorders. To start
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from your father.” (Nordqvist‚ 2008) Genes are essential to the function of the human body. They determine how the body functions and how it responds to various stimuli. The latter are internal and external factors. Internal factors include genetic coding and base pairing‚ and external factors are ones based on the environment. Genes account for the differences in the biological differences when comparing humans. This is what makes each and every one of us unique. However‚ this variance in traits
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used for this syndrome (Cardiac Abnormality/abnormal facies‚ T cell deficit due to thymic hypoplasia‚ Cleft palate‚ Hypocalcemia ) (2) a variation in the phenotype and deletion can be in both maternal or paternal origin (1) Figure 1: shows the genetic map of chromosomal region 22q11.2‚ 85% individuals have a large 3-Mb deletion (40 genes) (3). Clinical features (1) Cardiac malformations (aortic arch anomalies) Dysmorphic facial features (low set ears ‚ upward and downward slanting eyes
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Chapter 10 Foundations of Genetics Lecture Notes 1 Foundations of Genetics Mendel and the Garden pea The father of modern Genetics is Gregor Mendel. Gregor Mendel (1822-1884) was an Austrian monk who lived in a monastery where the experiments with the garden pea were performed. Mendel’s work with the garden pea was the fundamental study which unveiled the laws that govern genetics and heredity. Mendel was the first to use the scientific method in a very systematic and analysed his results
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