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    exam 1

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    original DNA molecule)‚ each is a chromatid before they have been replicated and as soon as they separate‚ it becomes a chromosomes) Homologous pair – A pair of chromosomes of the same length‚ centromere position‚ and staining pattern that possess genes for the same characters at corresponding loci. One homologous chromosome is inherited from the organism’s father‚ the other from the mother. Also called homologs‚ or a homologous pair.   3. Write out a general life cycle with arrows linking these

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    relationships‚ in the heterozygote both alleles will be completely expressed. For example‚ in human ABO blood types‚ two of the three alleles (the A allele‚ properly designated as IA‚ and the B allele‚ properly designated as IB) are co-dominant. This gene controls the deposition of antigenic markers on cells. A person with blood type A (homozygous for IA or heterozygous for IA and the recessive i (for O type)) has one kind of antigen marker‚ while a person with blood type B (homozygous for IB or heterozygous

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    Genetic testing uses laboratory methods to look at your genes‚ which are the DNA instructions you inherit from your mother and your father. Genetic tests may be used to identify increased risks of health problems‚ to choose treatments‚ or to assess responses to treatments. There are many different types of genetic tests. Genetic tests can help to: • Diagnose disease • Identify gene changes that are responsible for an already diagnosed disease • Determine the severity of a disease • Guide doctors

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    Alcoholism and Gnes

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    The article Alcoholism and Genes was mainly concerning the issue between a person’s genes and how it can affect if they develop alcoholism in their later years. This occurs with the development of the ALDH1‚ which seems to be more present in the Asian race rather than the European community due to their blood. The ALDH1 gene breaks down acetaldehyde (breakdown product of alcohol) and when there is a different variation in a person’s genes‚ the enzyme works slower. In Asians‚ when they have alcohol

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    connected by hydrogen bonds between complementary nitrogenous bases. Segments of DNA carrying genetic information are called genes‚ which mostly code for a specific type of protein. This lab will focus on the gene pGLO. Thus transformation becomes specifically expressed as the intake and influence of new genetic material in the form of DNA. It involves a foreign gene being inserted into a cell‚ and causing changes in the organism’s traits. The trait changes are often caused by the new genetic

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    Angelman Syndrome.

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    example‚ some syndromes are the result of a trisomy in one of the chromosomes‚ which means that there is an extra copy of the chromosome in the cell nuclei. Another situation is when one of the parents’ genes is not present. Angelman syndrome (AS) is a disability that is caused by a missing gene. AS is a neuro-genetic disorder‚ this causes the child to have some development issues. Those who live with AS are affected in so many ways and some scientists say that there are different methods to treat

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    Human Genetic Engineering

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    a chromosome. Genes are formed in pairs are located in these chromosomes. During reproduction the gene pairs are split apart and randomly passed on to the offspring. During the replication of the gene pairs chance events such as mutations‚ can change their structure and prompt evolution. Through human interference we can compose our own evolution by using genetic engineering. By using this genetic engineering‚ scientist have the means to isolate‚ cut and split different genes from different

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    Genetic Disorder Essay

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    Genes are codes for certain function that are found in DNA. The combination of genes is what makes each individual unique. MCADD is a genetic disorder‚ caused by a mutation or damage to the gene‚ ACADM‚ that codes for the enzyme‚ medium chain acyl CoA dehydrogenase. This results in the enzyme being absent or existing in minimal quantities. An enzyme increases the rate of a chemical reaction. Our body needs many enzymes in order to make the materials needed for our bodies to function and be healthy

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    2011 Background Genetic Disorders occur when there is a change or mutation in the information contained in the genes. When cells get older or they have been exposed to something harmful disorders can occur. Genetic disorders can be caused by a mutation in one gene called monogenic disorder‚ by mutations in multiple genes called multifactorial inheritance disorder‚ by a combination of gene mutations and environmental factors‚ or by damage to chromosomes when there is changes in the number or structure

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    Exam 1 Study Guide

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    4 forces of evolution – natural selection‚ mutation‚ gene flow‚ genetic drift Lendius – father of taxonomy 3 different effects of selection: Stabalizing – ex. Birth weight Disruptive – Striped guppies (b/c their parents were diff. colors) are not able to camouflage Directional – peacock’s tail‚ female peacock will choose to mate with male with best/most colorful tail. But a tail too extravagent could harm against predators Evolutionary Developmental - A large amount of genetic material

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