Genetic linkage

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    Gilford Progeria Syndrome

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    Introduction Hutchinson Gilford Progeria Syndrome (HGPS) is a fatal disease that is characterized by the appearance of rapid aging in children. HGPS is rare, affecting roughly 1 in 8 million live births. HGPS can be identified by early symptoms that include slow development, limited growth, alopecia, localized scleroderma, and a distinct facial structure which includes a small face, shallow jaw, and pinched nose. As the disease progresses, new symptoms arise, such as hearing and vision loss…

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    Antagonistic Pleiotropy

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    proposed by Williams in 1957, whereby Williams suggest a specific type of genetic inter-trait linkage, pleiotropy, as an evolutionary explanation for senescence (Williams 2001). Pleiotropy, or inter-trait linkage exists in a way to make it difficult for the evolution process to remove an individually adverse trait, such as aging, without simultaneously removing one or more beneficial traits. To explain further, inter-trait linkage is the phenomenon where one gene controls more than one…

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    Monozygotic Twins

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    Being a twin is a unique experience that can have a variety of effects on the lives of the twin pair. However, being a twin does come with challenges, especially in personality differentiation and identity formation for each child. There are many topics relating to the development of personality and sociality within the realms of Psychological Development. The purpose of this essay is to discern that relationship and whether or not evidence may be found to prove that twins have different of…

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    IMMUNE SYSYEM Assignment: 17TH SEPT 2015 GENETIC COUNSELLING, ETHICAL ISSUES IN MANAGEMENT OF HEMOGLOBINOPATHIES Objectives 1. Describe risk assessment in genetic counseling One of the most important aspects of genetic counseling is the provision of a risk factor. Estimation of the recurrence risk requires consideration of: i) The diagnosis and its mode of inheritance ii) Analysis of the family pedigree iii) The results of tests, which can include linkage studies using DNA markers. The…

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    Cas9 Essay

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    to each other, divided by dissimilar, short sequences of virus DNA. The Cas9 part is a linked nuclease that is aided by a guide RNA, used to cut DNA. The CRISPR/Cas9 system is an immune response in bacteria that works when a virus, releases its genetic code into the bacteria. The virus DNA is stored in the bacteria DNA, so that it can specifically attack that virus, where it to invade again. When the virus attacks the bacteria again, its DNA is detected through an RNA base pairing method. It…

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    Human Genome Project Essay

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    7. Identify one finding from the Human Genome Project and discuss how it might impact our understanding of human behavior. One finding from the Human Genome Project includes the identification of “approximately 200 disease-related genes” (Ginsberg, Nackerud & Larrison, 2004, p. 118). This finding impacts our understanding of human behavior as it gives a better biological understanding of these diseases and it helps social workers to be better advocates for those who have these diseases. Our…

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    scientific medicine and technology by American poet, fiction writer, and journalist Susan Scutti article The Government Owns Your DNA. What Are They Doing With It? Scutti’s Newsweek article is one of many articles published on genetic testing for newborns in the United States. Genetic testing for neonates dates back to the 1960s when President Kennedy signed…

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    Gene editing is the alteration of genes in germ cells which become either sperm or eggs and are inheritable to future generations. Genetic editing has been used in agriculture to enhance crops, it is now being explored in humans too. This technology could potentially eradicate genetic diseases and prevent future generations from passing it on. Gene editing is done through the CRISPR-Cas9 system, where the embryo is edited to the desired outcome. It identifies and attacks the viral DNA and then…

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    Causes Of Genetics

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    Danzi Engoron BI356 Genetics Currently, there are more than 600 genetic disorders known, all caused by defective genes. Genetic disorders result from the accumulation of the harmful substance in the body or from an inability of the body to produce or utilize essential substances that influence development and function. Most of the time genetic disorders are passed down through family, however, sometimes they can also be due to gene mutation caused by a combination of both genetic changes and…

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    In 2010, UC Berkeley offered a new fall orientation program for freshmen students. It consisted on testing student’s gene to find out how they metabolized lactose, alcohol, and folates. This program led to a huge argument about the ethics behind genetic testing conducted in a non-medical setting. Although UC Berkeley wanted to run this program, California Department of Public Health raised a question about having a doctor 's order that kind of test (Devore). Some people say that this program is…

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