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Sickle Cell Part_Natural Selection
Sickle Cell Part_Natural Selection

... As discussed, Sickle Cell Disease is one of thousands of disorders caused by a single gene. Sickle-cell anemia is an autosomal, recessive human disease. It is caused by a flawed allele for a polypeptide in hemoglobin. As a result, this oxygen carrying protein in the red blood cell causes it to have ...
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... - Describe genes and relate them to protein synthesis leading to genetic traits - Explain the rules governing gene transmission to offspring and prediction of inherited traits - Understand gene mutation and relate it to inherited and non-inherited diseases such sickle cell anemia and cancer - Unders ...
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... After mRNA is transcribed, it moves to the ribosome and is read. As it is read, specific tRNA molecules with a specific amino acid attached, base pair match with the codons, to help create the strand of amino acids that become the protein. 37) What term is used to describe the making of RNA in the n ...
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... • Know the base pairing rules (A=T & G=C). • If given one DNA strand, provide the complementary strand. • What kind of bonds hold the two strands of DNA together. • What is DNA polymerase? • What is semiconservative replication? • Understand the flow of genetic information from DNA to RNA to protein ...
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DNA - VanityWolveriine
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Chapter 8

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Point mutation



A point mutation, or single base modification, is a type of mutation that causes a single nucleotide base change, insertion, or deletion of the genetic material, DNA or RNA. The term frameshift mutation indicates the addition or deletion of a base pair. A point mutant is an individual that is affected by a point mutation.Repeat induced point mutations are recurring point mutations, discussed below.
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