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Genetic code key
Genetic code key

... transporter made up of 1480 amino acids and whose gene is located on the long arm of chromosome 7. In healthy humans, the protein is found in the plasma membranes of the cells that line the lungs, allowing the movement of Cl-. In people with cystic fibrosis, no functional CFTR is made. a. Do you exp ...
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7.1 DNA Structure

... • How are the two strands of nucleotides connected? • Two strands arrange themselves so that the Nbases are in the center • N-bases complementary bond with each other using hydrogen bonds ▫ Cytosine – Guanine (C-G) ▫ Adenine – Thymine (A-T) ...
Genetic disorders
Genetic disorders

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Alternative splicing
Alternative splicing

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Chapter 13 – RNA and Protein Synthesis Study Guide
Chapter 13 – RNA and Protein Synthesis Study Guide

... Point mutation is a form of gene mutation where only a specific amino acid is affected. When nitrogen bases are replaced by a different nitrogen base (substitution), a point mutation occurs. 6. What is a frameshift mutation? What causes it? Frameshift mutations are mutations that change the entire s ...
Did you ever get a message from a friend that was in code
Did you ever get a message from a friend that was in code

... c. One strand begins at the end and works towards the original unwinding DNA fork. This is continuous until the end of the DNA split. d. The other strand elongates away from the replication fork -Made in discontinuous small segments called Okazaki fragments -Enzymes attach this strand together so it ...
Genes and Natural Selection
Genes and Natural Selection

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No Slide Title

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10th Grade Genetics Content - Red Clay Secondary Science Wiki
10th Grade Genetics Content - Red Clay Secondary Science Wiki

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Genetic Engineering - University of Rhode Island

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Wanganui High School
Wanganui High School

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Chapter 9, part A
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Meiosis - Answers - Iowa State University

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lecture 01 - sources of variation - Cal State LA

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CHAPTER 10 - Protein Synthesis The DNA genotype is expressed
CHAPTER 10 - Protein Synthesis The DNA genotype is expressed

... – Polypeptides form proteins that cells and organisms use Describe the process of translation. Include the following: • mRNA termination • tRNA start codon • Ribosome P site • Amino acid A site • Initiation stop codon • Elongation Modification Mutations can change the meaning of genes • Mutations ar ...
B3Revision LVW
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Mid-Term Exam 3a - Buffalo State College Faculty and Staff Web

... _____ 25. Which of the following best describes why DNA replication is called semi-conservative? A. Replication of DNA in the nucleus is catalyzed by two different enzymes, RNA polymerase and DNA polymerase B. Only deoxynucleotides are used during DNA replication C. A equal mixture of deoxynucleotid ...
Sem2 Final SG 12 Part1
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3.4: Transcription and Translation

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Bio07_TR__U04_CH12.QXD

... replace another, only one amino acid is affected. If a nucleotide is added or taken away, it causes a frameshift mutation. All the groupings of three nucleotides, or codons, are changed. This can cause the gene to produce a completely different protein. In a chromosomal mutation, there is a change i ...
Biology 303 EXAM II 3/14/00 NAME
Biology 303 EXAM II 3/14/00 NAME

... Trisomy 21, or Down syndrome, usually occurs when there is a normal diploid chromosomal complement of 46 chromosomes plus one (extra) chromosome #21. Such individuals therefore have 47 chromosomes. While there is impaired fertility of both sexes, females are more likely to be fertile than males. Ass ...
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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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