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Mark scheme - biologypost
Mark scheme - biologypost

... Difficulty of finding one gene among all the genes in the nucleus / large amounts of mRNA coding for insulin will be present in insulin producing cells / idea that mRNA will be ‘edited’ ...
Facts About Genetics and Neuromuscular Diseases
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Linköping University Post Print β-tubulin mutations in ovarian cancer using
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10.6AC The Pattern - Texarkana Independent School District

... What is the major difference between a DNA nucleotide and an RNA nucleotide? Deoxyribose sugar is in DNA and ribose sugar is in RNA. May also include uracil substitutes for thymine in RNA. Why is mRNA single-stranded? So it can leave the nucleus. Double-stranded DNA cannot fit through the nuclear me ...
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... _______________ of genes that code for thousands of __________________. 28. Another type of molecule that helps make proteins is called ____________. 29. RNA stands for ___________________________. One difference between DNA and RNA is that RNA has the base __________________ or U instead of thymine ...
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DNA: The Molecule of Heredity

... 4. Genes in the DNA are the body’s directions for making proteins • Proteins make us: – look the way we do – function the way we do – develop and grow the way we do – behave the way we do – think the way we do ...
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...  Females are carriers and have a 50% chance of transmitting the disease in ...
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... mutations within the same gene did not complement each other. He then could map the distance between two mutations within the same gene. The map distances defined each gene as a linear, divisible unit. In this regard, the gene is divisible due to crossing over. E10. Explain why deletion mapping was ...
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... which to utilize, a species is confined to what is available; even if it is weak or unfavorable. Variation, on the most basic level, will only come into existence with a change in the DNA nucleotide sequence, what we refer to as a mutation. Some mutations are favorable, but most are harmful. C. Vari ...
BioSc 231 Exam 2 2008
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... supplement were analyzed with 4 compounds that are precursors in the synthesis of compound E. Each mutant was grown on a minimal medium supplemented with each of the indicated compounds. + indicates growth that is supported by the indicated precursor. Using the diagram below, show the order of the i ...
Codominance
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Codominance
Codominance

... Development of pigment patterns in mice is an example of epistasis. The gray color pattern in horses is another example of epistasis. In this case, the gray gene is dominant, so if a horse inherits the gray gene, it will be gray regardless of genes present at the primary color locus. ...
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Mutation



In biology, a mutation is a permanent change of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements. Mutations result from damage to DNA which is not repaired or to RNA genomes (typically caused by radiation or chemical mutagens), errors in the process of replication, or from the insertion or deletion of segments of DNA by mobile genetic elements. Mutations may or may not produce discernible changes in the observable characteristics (phenotype) of an organism. Mutations play a part in both normal and abnormal biological processes including: evolution, cancer, and the development of the immune system, including junctional diversity.Mutation can result in several different types of change in sequences. Mutations in genes can either have no effect, alter the product of a gene, or prevent the gene from functioning properly or completely. Mutations can also occur in nongenic regions. One study on genetic variations between different species of Drosophila suggests that, if a mutation changes a protein produced by a gene, the result is likely to be harmful, with an estimated 70 percent of amino acid polymorphisms that have damaging effects, and the remainder being either neutral or weakly beneficial. Due to the damaging effects that mutations can have on genes, organisms have mechanisms such as DNA repair to prevent or correct mutations by reverting the mutated sequence back to its original state.
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