Description
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- Title Page
- Copyright Page
- About the Authors
- Brief Contents
- Contents
- PART ONE GENES, CHROMOSOMES, AND HEREDITY
- 1 Introduction to Genetics
- 1.1 Genetics Has a Rich and Interesting History
- 1600–1850: The Dawn of Modern Biology
- Charles Darwin and Evolution
- 1.2 Genetics Progressed from Mendel to DNA in Less Than a Century
- Mendel’s Work on Transmission of Traits
- The Chromosome Theory of Inheritance: Uniting Mendel and Meiosis
- Genetic Variation
- The Search for the Chemical Nature of Genes: DNA or Protein?
- 1.3 Discovery of the Double Helix Launched the Era of Molecular Genetics
- The Structure of DNA and RNA
- Gene Expression: From DNA to Phenotype
- Proteins and Biological Function
- Linking Genotype to Phenotype: Sickle‐Cell Anemia
- 1.4 Development of Recombinant DNA Technology Began the Era of DNA Cloning
- 1.5 The Impact of Biotechnology Is Continually Expanding
- Plants, Animals, and the Food Supply
- Biotechnology in Genetics and Medicine
- 1.6 Genomics, Proteomics, and Bioinformatics Are New and Expanding Fields
- Modern Approaches to Understanding Gene Function
- 1.7 Genetic Studies Rely on the Use of Model Organisms
- The Modern Set of Genetic Model Organisms
- Model Organisms and Human Diseases
- 1.8 We Live in the Age of Genetics
- The Nobel Prize and Genetics
- Genetics, Ethics, and Society
- Summary Points
- Problems and Discussion Questions
- 2 Mitosis and Meiosis
- 2.1 Cell Structure Is Closely Tied to Genetic Function
- 2.2 Chromosomes Exist in Homologous Pairs in Diploid Organisms
- 2.3 Mitosis Partitions Chromosomes into Dividing Cells
- Interphase and the Cell Cycle
- Prophase
- Prometaphase and Metaphase
- Anaphase
- Telophase
- Cell‐Cycle Regulation and Checkpoints
- 2.4 Meiosis Creates Haploid Gametes and Spores and Enhances Genetic Variation in Species
- Meiosis: Prophase I
- Metaphase, Anaphase, and Telophase I
- The Second Meiotic Division
- 2.5 The Development of Gametes Varies in Spermatogenesis Compared to Oogenesis
- 2.6 Meiosis Is Critical to Sexual Reproduction in All Diploid Organisms
- 2.7 Electron Microscopy Has Revealed the Physical Structure of Mitotic and Meiotic Chromosomes
- EXPLORING GENOMICS PubMed: Exploring and Retrieving Biomedical Literature
- CASE STUDY Timing is everything
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 3 Mendelian Genetics
- 3.1 Mendel Used a Model Experimental Approach to Study Patterns of Inheritance
- 3.2 The Monohybrid Cross Reveals How One Trait Is Transmitted from Generation to Generation
- Mendel’s First Three Postulates
- Modern Genetic Terminology
- Punnett Squares
- The Testcross: One Character
- 3.3 Mendel’s Dihybrid Cross Generated a Unique Ratio
- Mendel’s Fourth Postulate: Independent Assortment
- The Testcross: Two Characters
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Identifying Mendel’s Gene for Regulating White Fl
- 3.4 The Trihybrid Cross Demonstrates That Mendel’s Principles Apply to Inheritance of Multiple Tra
- The Forked‐Line Method, or Branch Diagram
- 3.5 Mendel’s Work Was Rediscovered in the Early Twentieth Century
- Unit Factors, Genes, and Homologous Chromosomes
- Evolving Concept of the Gene
- 3.6 Independent Assortment Leads to Extensive Genetic Variation
- 3.7 Laws of Probability Help to Explain Genetic Events
- 3.8 Chi‐Square Analysis Evaluates the Influence of Chance on Genetic Data
- Chi‐Square Calculations and the Null Hypothesis
- Interpreting Probability Values
- 3.9 Pedigrees Reveal Patterns of Inheritance of Human Traits
- Pedigree Conventions
- Pedigree Analysis
- 3.10 Mutant Phenotypes Have Been Examined at the Molecular Level
- How Mendel’s Peas Become Wrinkled: A Molecular Explanation
- Tay—Sachs Disease: The Molecular Basis of a Recessive Disorder in Humans
- EXPLORING GENOMICS Online Mendelian Inheritance in Man
- CASE STUDY To test or not to test
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 4 Extensions of Mendelian Genetics
- 4.1 Alleles Alter Phenotypes in Different Ways
- 4.2 Geneticists Use a Variety of Symbols for Alleles
- 4.3 Neither Allele Is Dominant in Incomplete, or Partial, Dominance
- 4.4 In Codominance, the Influence of Both Alleles in a Heterozygote Is Clearly Evident
- 4.5 Multiple Alleles of a Gene May Exist in a Population
- The ABO Blood Groups
- The A and B Antigens
- The Bombay Phenotype
- The white Locus in Drosophila
- 4.6 Lethal Alleles Represent Essential Genes
- The Molecular Basis of Dominance, Recessiveness, and Lethality: The agouti Gene
- 4.7 Combinations of Two Gene Pairs with Two Modes of Inheritance Modify the 9:3:3:1 Ratio
- Evolving Concept of the Gene
- 4.8 Phenotypes Are Often Affected by More Than One Gene
- Epistasis
- Novel Phenotypes
- Other Modified Dihybrid Ratios
- 4.9 Complementation Analysis Can Determine if Two Mutations Causing a Similar Phenotype Are Alleles
- 4.10 Expression of a Single Gene May Have Multiple Effects
- 4.11 X‐Linkage Describes Genes on the X Chromosome
- X‐Linkage in Drosophila
- X‐Linkage in Humans
- 4.12 In Sex‐Limited and Sex‐Influenced Inheritance, an Individual’s Sex Influences the Phenoty
- 4.13 Genetic Background and the Environment May Alter Phenotypic Expression
- Penetrance and Expressivity
- Genetic Background: Position Effects
- Temperature Effects—An Introduction to Conditional Mutations
- Nutritional Effects
- Onset of Genetic Expression
- Genetic Anticipation
- GENETICS, ETHICS, AND SOCIETY Nature versus Nurture: Is the Debate Over?
- CASE STUDY Should the child be deaf?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 5 Sex Determination and Sex Chromosomes
- 5.1 X and Y Chromosomes Were First Linked to Sex Determination Early in the Twentieth Century
- 5.2 The Y Chromosome Determines Maleness in Humans
- Klinefelter and Turner Syndromes
- 47,XXX Syndrome
- 47,XYY Condition
- Sexual Differentiation in Humans
- The Y Chromosome and Male Development
- 5.3 The Ratio of Males to Females in Humans Is Not 1.0
- 5.4 Dosage Compensation Prevents Excessive Expression of X‐Linked Genes in Humans and Other Mammal
- Barr Bodies
- The Lyon Hypothesis
- The Mechanism of Inactivation
- 5.5 The Ratio of X Chromosomes to Sets of Autosomes Can Determine Sex
- D. melanogaster
- Caenorhabditis elegans
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Drosophila Sxl Gene Induces Female Development
- 5.6 Temperature Variation Controls Sex Determination in Many Reptiles
- GENETICS, ETHICS, AND SOCIETY A Question of Gender: Sex Selection in Humans
- CASE STUDY IS it a boy or a girl?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 6 Chromosomal Mutations: Variation in Number and Arrangement
- 6.1 Variation in Chromosome Number: Terminology and Origin
- 6.2 Monosomy and Trisomy Result in a Variety of Phenotypic Effects
- Monosomy
- Trisomy
- Down Syndrome: Trisomy 21
- The Down Syndrome Critical Region (DSCR)
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Mouse Models of Down Syndrome
- The Origin of the Extra Chromosome 21 in Down Syndrome
- Human Aneuploidy
- 6.3 Polyploidy, in Which More Than Two Haploid Sets of Chromosomes Are Present, Is Prevalent in Plan
- Autopolyploidy
- Allopolyploidy
- Endopolyploidy
- 6.4 Variation Occurs in the Composition and Arrangement of Chromosomes
- 6.5 A Deletion Is a Missing Region of a Chromosome
- Cri du Chat Syndrome in Humans
- 6.6 A Duplication Is a Repeated Segment of a Chromosome
- Gene Redundancy and Amplification—Ribosomal RNA Genes
- The Bar Mutation in Drosophila
- The Role of Gene Duplication in Evolution
- Duplications at the Molecular Level: Copy Number Variations (CNVs)
- 6.7 Inversions Rearrange the Linear Gene Sequence
- Consequences of Inversions during Gamete Formation
- Evolutionary Advantages of Inversions
- 6.8 Translocations Alter the Location of Chromosomal Segments in the Genome
- Translocations in Humans: Familial Down Syndrome
- 6.9 Fragile Sites in Human Chromosomes Are Susceptible to Breakage
- Fragile‐X Syndrome
- The Link between Fragile Sites and Cancer
- GENETICS, ETHICS, AND SOCIETY Down Syndrome and Prenatal Testing—The New Eugenics?
- CASE STUDY Fish tales
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 7 Chromosome Mapping in Eukaryotes
- 7.1 Genes Linked on the Same Chromosome Segregate Together
- The Linkage Ratio
- 7.2 Crossing Over Serves as the Basis for Determining the Distance between Genes in Chromosome Mappi
- Morgan and Crossing Over
- Sturtevant and Mapping
- Single Crossovers
- 7.3 Determining the Gene Sequence during Mapping Requires the Analysis of Multiple Crossovers
- Multiple Exchanges
- Three‐Point Mapping in Drosophila
- Determining the Gene Sequence
- An Autosomal Mapping Problem in Maize
- 7.4 As the Distance between Two Genes Increases, Mapping Estimates Become More Inaccurate
- Interference and the Coefficient of Coincidence
- 7.5 Drosophila Genes Have Been Extensively Mapped
- Evolving Concept of the Gene
- 7.6 Lod Score Analysis and Somatic Cell Hybridization Were Historically Important in Creating Human
- 7.7 Chromosome Mapping Is Currently Performed Using DNA Markers and Annotated Computer Databases
- 7.8 Crossing Over Involves a Physical Exchange between Chromatids
- 7.9 Exchanges Also Occur between Sister Chromatids during Mitosis
- EXPLORING GENOMICS Human Chromosome Maps on the Internet
- CASE STUDY Links to autism
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 8 Genetic Analysis and Mapping in Bacteria and Bacteriophages
- 8.1 Bacteria Mutate Spontaneously and Grow at an Exponential Rate
- 8.2 Genetic Recombination Occurs in Bacteria
- Conjugation in Bacteria: The Discovery of F+ and F– Strains
- Hfr Bacteria and Chromosome Mapping
- Recombination in F+ × F– Matings: A Reexamination
- The F State and Merozygotes
- 8.3 The F Factor Is an Example of a Plasmid
- 8.4 Transformation Is a Second Process Leading to Genetic Recombination in Bacteria
- The Transformation Process
- Transformation and Linked Genes
- 8.5 Bacteriophages Are Bacterial Viruses
- Phage T4: Structure and Life Cycle
- The Plaque Assay
- Lysogeny
- 8.6 Transduction Is Virus‐Mediated Bacterial DNA Transfer
- The Lederberg–Zinder Experiment
- Transduction and Mapping
- 8.7 Bacteriophages Undergo Intergenic Recombination
- Bacteriophage Mutations
- Mapping in Bacteriophages
- 8.8 Intragenic Recombination Occurs in Phage T4
- The rII Locus of Phage T4
- Complementation by rII Mutations
- Recombinational Analysis
- Deletion Testing of the rII Locus
- The rII Gene Map
- Evolving Concept of the Gene
- GENETICS, ETHICS, AND SOCIETY Multidrug‐Resistant Bacteria: Fighting with Phage
- CASE STUDY To treat or not to treat
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 9 Extranuclear Inheritance
- 9.1 Organelle Heredity Involves DNA in ‐Chloroplasts and Mitochondria
- Chloroplasts: Variegation in Four O’Clock Plants
- Chloroplast Mutations in Chlamydomonas
- Mitochondrial Mutations: Early Studies in Neurospora and Yeast
- 9.2 Knowledge of Mitochondrial and Chloroplast DNA Helps Explain Organelle Heredity
- Organelle DNA and the Endosymbiotic Theory
- Molecular Organization and Gene Products of ‐Chloroplast DNA
- Molecular Organization and Gene Products of ‐Mitochondrial DNA
- 9.3 Mutations in Mitochondrial DNA Cause Human Disorders
- Mitochondria, Human Health, and Aging
- Future Prevention of the Transmission of mtDNA‐Based Disorders
- 9.4 In Maternal Effect, the Maternal Genotype Has a Strong Influence during Early Development
- Lymnaea Coiling
- Embryonic Development in Drosophila
- GENETICS, ETHICS, AND SOCIETY Mitochondrial Replacement and Three‐Parent Babies
- CASE STUDY Is it all in the genes?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- PART TWO DNA: STRUCTURE, REPLICATION, AND ORGANIZATION
- 10 DNA Structure and Analysis
- 10.1 The Genetic Material Must Exhibit Four Characteristics
- 10.2 Until 1944, Observations Favored Protein as the Genetic Material
- 10.3 Evidence Favoring DNA as the Genetic Material Was First Obtained during the Study of Bacteria a
- Transformation: Early Studies
- Transformation: The Avery, MacLeod, and McCarty Experiment
- The Hershey–Chase Experiment
- Transfection Experiments
- 10.4 Indirect and Direct Evidence Supports the Concept That DNA Is the Genetic Material in Eukaryote
- Indirect Evidence: Distribution of DNA
- Indirect Evidence: Mutagenesis
- Direct Evidence: Recombinant DNA Studies
- 10.5 RNA Serves as the Genetic Material in Some Viruses
- 10.6 Knowledge of Nucleic Acid Chemistry Is Essential to the Understanding of DNA Structure
- Nucleotides: Building Blocks of Nucleic Acids
- Nucleoside Diphosphates and Triphosphates
- Polynucleotides
- 10.7 The Structure of DNA Holds the Key to Understanding Its Function
- Base‐Composition Studies
- X‐Ray Diffraction Analysis
- The Watson–Crick Model
- Evolving Concept of the Gene
- 10.8 Alternative Forms of DNA Exist
- 10.9 The Structure of RNA Is Chemically Similar to DNA, but Single Stranded
- 10.10 Many Analytical Techniques Have Been Useful during the Investigation of DNA and RNA
- Electrophoresis
- EXPLORING GENOMICS Introduction to Bioinformatics: BLAST
- CASE STUDY Credit where credit is due
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 11 DNA Replication and Recombination
- 11.1 DNA Is Reproduced by Semiconservative Replication
- The Meselson–Stahl Experiment
- Semiconservative Replication in Eukaryotes
- Origins, Forks, and Units of Replication
- 11.2 DNA Synthesis in Bacteria Involves Five ‐Polymerases, as Well as Other Enzymes
- DNA Polymerase I
- DNA Polymerase II, III, IV, and V
- The DNA Pol III Holoenzyme
- 11.3 Many Complex Issues Must Be Resolved during DNA Replication
- Unwinding the DNA Helix
- Initiation of DNA Synthesis Using an RNA Primer
- Continuous and Discontinuous DNA Synthesis
- Concurrent Synthesis Occurs on the Leading and Lagging Strands
- Proofreading and Error Correction Occurs during DNA Replication
- 11.4 A Coherent Model Summarizes DNA Replication
- 11.5 Replication Is Controlled by a Variety of Genes
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Lethal Knockouts
- 11.6 Eukaryotic DNA Replication Is Similar to Replication in Bacteria, but Is More Complex
- Initiation at Multiple Replication Origins
- Multiple Eukaryotic DNA Polymerases
- Replication through Chromatin
- 11.7 Telomeres Solve Stability and Replication Problems at Eukaryotic Chromosome Ends
- Telomere Structure and Chromosome Stability
- Telomeres and Chromosome End Replication
- Telomeres in Disease, Aging, and Cancer
- 11.8 Recombination Is Essential for Genetic Exchange and DNA Repair
- Models of Homologous Recombination
- GENETICS, ETHICS, AND SOCIETY Telomeres: The Key to a Long Life?
- CASE STUDY At loose ends
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 12 DNA Organization in Chromosomes
- 12.1 Viral and Bacterial Chromosomes are Relatively Simple DNA Molecules
- 12.2 Supercoiling Facilitates Compaction of the DNA of Viral and Bacterial Chromosomes
- 12.3 Specialized Chromosomes Reveal Variations in the Organization of DNA
- Polytene Chromosomes
- Lampbrush Chromosomes
- 12.4 DNA Is Organized into Chromatin in Eukaryotes
- Chromatin Structure and Nucleosomes
- Chromatin Remodeling
- Heterochromatin
- 12.5 Chromosome Banding Differentiates Regions along the Mitotic Chromosome
- 12.6 Eukaryotic Genomes Demonstrate Complex Sequence Organization Characterized by Repetitive DNA
- Satellite DNA
- Centromeric DNA Sequences
- Middle Repetitive Sequences: VNTRs and STRs
- Repetitive Transposed Sequences: SINEs and LINEs
- Middle Repetitive Multiple‐Copy Genes
- 12.7 The Vast Majority of a Eukaryotic Genome Does Not Encode Functional Genes
- EXPLORING GENOMICS Database of Genomic Variants: Structural Variations in the Human Genome
- CASE STUDY Helping or hurting?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- PART THREE GENE EXPRESSION AND ITS REGULATION
- 13 The Genetic Code and Transcription
- 13.1 The Genetic Code Uses Ribonucleotide Bases as “Letters”
- 13.2 Early Studies Established the Basic Operational Patterns of the Code
- The Triplet Nature of the Code
- 13.3 Studies by Nirenberg, Matthaei, and Others Led to Deciphering of the Code
- Synthesizing Polypeptides in a Cell‐Free System
- Homopolymer Codes
- The Use of Mixed Heteropolymers
- The Triplet Binding Assay
- Repeating Copolymers
- 13.4 The Coding Dictionary Reveals Several Interesting Patterns among the 64 Codons
- Degeneracy and the Wobble Hypothesis
- The Ordered Nature of the Code
- Punctuating the Code: Initiation and Termination Codons
- 13.5 The Genetic Code Has Been Confirmed in Studies of Phage MS2
- 13.6 The Genetic Code Is Nearly Universal
- 13.7 Different Initiation Points Create Overlapping Genes
- 13.8 Transcription Synthesizes RNA on a DNA Template
- 13.9 RNA Polymerase Directs RNA Synthesis
- Promoters, Template Binding, and the Subunit
- Initiation, Elongation, and Termination of RNA Synthesis in Bacteria
- 13.10 Transcription in Eukaryotes Differs from Bacterial Transcription in Several Ways
- Initiation of Transcription in Eukaryotes
- Recent Discoveries Concerning Eukaryotic RNA Polymerase Function
- Processing Eukaryotic RNA: Caps and Tails
- 13.11 The Coding Regions of Eukaryotic Genes Are Interrupted by Intervening Sequences Called Introns
- Why Do Introns Exist?
- Splicing Mechanisms: Self‐Splicing RNAs
- Splicing Mechanisms: The Spliceosome
- Evolving Concept of the Gene
- 13.12 RNA Editing May Modify the Final Transcript
- 13.13 Transcription Has Been Visualized by Electron Microscopy
- CASE STUDY Treatment dilemmas
- Summary Points
- GENETICS, ETHICS, AND SOCIETY Treating Duchenne Muscular Dystrophy with Exon‐Skipping Drugs
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 14 Translation and Proteins
- 14.1 Translation of mRNA Depends on Ribosomes and Transfer RNAs
- Ribosomal Structure
- tRNA Structure
- Charging tRNA
- 14.2 Translation of mRNA Can Be Divided into Three Steps
- Initiation
- Elongation
- Termination
- Polyribosomes
- 14.3 High‐Resolution Studies Have Revealed Many Details about the Functional Bacterial Ribosome
- 14.4 Translation Is More Complex in Eukaryotes
- 14.5 The Initial Insight That Proteins Are Important in Heredity Was Provided by the Study of Inborn
- Phenylketonuria
- 14.6 Studies of Neurospora Led to the One‐Gene:One‐Enzyme Hypothesis
- Analysis of Neurospora Mutants by Beadle and Tatum
- Genes and Enzymes: Analysis of Biochemical Pathways
- 14.7 Studies of Human Hemoglobin Established That One Gene Encodes One Polypeptide
- Sickle‐Cell Anemia
- Evolving Concept of the Gene
- 14.8 Variation in Protein Structure Provides the Basis of Biological Diversity
- 14.9 Posttranslational Modification Alters the Final Protein Product
- Protein Folding and Misfolding
- 14.10 Proteins Perform Many Diverse Roles
- 14.11 Proteins Often Include More Than One ‐Functional Domain
- Exon Shuffling
- Exploring Genomics Translation Tools and Swiss‐Prot for Studying ‐Protein Sequences
- CASE STUDY Crippled ribosomes
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 15 Gene Mutation, DNA Repair, and Transposition
- 15.1 Gene Mutations Are Classified in Various Ways
- Classification Based on Type of Molecular Change
- Classification Based on Effect on Function
- Classification Based on Location of Mutation
- 15.2 Mutations Occur Spontaneously and Randomly
- Spontaneous and Induced Mutations
- Spontaneous Germ‐Line Mutation Rates in Humans
- Spontaneous Somatic Mutation Rates in Humans
- The Fluctuation Test: Are Mutations Random or Adaptive?
- 15.3 Spontaneous Mutations Arise from ‐Replication Errors and Base Modifications
- DNA Replication Errors and Slippage
- Tautomeric Shifts
- Depurination and Deamination
- Oxidative Damage
- Transposable Elements
- 15.4 Induced Mutations Arise from DNA Damage Caused by Chemicals and Radiation
- Base Analogs
- Alkylating, Intercalating, and Adduct‐Forming Agents
- Ultraviolet Light
- Ionizing Radiation
- 15.5 Single‐Gene Mutations Cause a Wide Range of Human Diseases
- Single‐Gene Mutations and β‐Thalassemia
- Mutations Caused by Expandable DNA Repeats
- 15.6 Organisms Use DNA Repair Systems to Counteract Mutations
- Proofreading and Mismatch Repair
- Postreplication Repair and the SOS Repair System
- Photoreactivation Repair: Reversal of UV Damage
- Base and Nucleotide Excision Repair
- Nucleotide Excision Repair and Xeroderma ‐Pigmentosum in Humans
- Double‐Strand Break Repair in Eukaryotes
- 15.7 The Ames Test Is Used to Assess the Mutagenicity of Compounds
- 15.8 Transposable Elements Move within the Genome and May Create Mutations
- DNA Transposons
- DNA Transposons—the Ac–Ds System in Maize
- Retrotransposons
- Retrotransposons—the Copia –White‐Apricot ‐System in Drosophila
- Transposable Elements in Humans
- Transposable Elements, Mutations, and Evolution
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Transposon‐Mediated Mutations Reveal Genes Involv
- EXPLORING GENOMICS Sequence Alignment to Identify a Mutation
- CASE STUDY An Unexpected Diagnosis
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 16 Regulation of Gene Expression in Bacteria
- 16.1 Bacteria Regulate Gene Expression in Response to Environmental Conditions
- 16.2 Lactose Metabolism in E. coli Is Regulated by an Inducible System
- Structural Genes
- The Discovery of Regulatory Mutations
- The Operon Model: Negative Control
- Genetic Proof of the Operon Model
- Isolation of the Repressor
- 16.3 The Catabolite‐Activating Protein (CAP) Exerts Positive Control over the lac Operon
- 16.4 Crystal Structure Analysis of Repressor ‐Complexes Has Confirmed the Operon Model
- 16.5 The Tryptophan (trp) Operon in E. coli Is a Repressible Gene System
- Evidence for the trp Operon
- Evolving Concept of the Gene
- 16.6 RNA Plays Diverse Roles in Regulating Gene Expression in Bacteria
- Attenuation
- Riboswitches
- Small Noncoding RNAs Play Regulatory Roles in Bacteria
- CASE STUDY MRSA in the National Football League (NFL)
- Summary Points
- GENETICS, ETHICS, AND SOCIETY Quorum Sensing: Social Networking and Gene Regulation in Bacteria
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 17 Transcriptional Regulation in Eukaryotes
- 17.1 Organization of the Eukaryotic Cell Facilitates Gene Regulation at Several Levels
- 17.2 Eukaryotic Gene Expression Is Influenced by Chromatin Modifications
- Chromosome Territories and Transcription Factories
- Open and Closed Chromatin
- Histone Modifications and Chromatin Remodeling
- DNA Methylation
- 17.3 Eukaryotic Transcription Initiation Requires Specific Cis‐Acting Sites
- Promoters and Promoter Elements
- Enhancers, Insulators, and Silencers
- 17.4 Eukaryotic Transcription Initiation Is Regulated by Transcription Factors That Bind to Cis‐Ac
- The Human Metallothionein 2A Gene: Multiple Cis‐Acting Elements and Transcription Factors
- Functional Domains of Eukaryotic Transcription Factors
- 17.5 Activators and Repressors Interact with General Transcription Factors and Affect Chromatin Stru
- Formation of the RNA Polymerase II Transcription Initiation Complex
- Mechanisms of Transcription Activation and Repression
- 17.6 Gene Regulation in a Model Organism: Transcription of the GAL Genes of Yeast
- 17.7 ENCODE Data Are Transforming Our Concepts of Eukaryotic Gene Regulation
- Enhancer and Promoter Elements
- Transcripts and Noncoding RNA
- Many Disease‐Associated Genome Variations Affect Regulatory Regions
- Evolving Concept of a Gene
- Exploring Genomics Tissue‐Specific Gene Expression
- CASE STUDY Risk assessment
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 18 Posttranscriptional Regulation in Eukaryotes
- 18.1 Regulation of Alternative Splicing Determines Which RNA Spliceforms of a Gene Are Translated
- Types of Alternative Splicing
- Alternative Splicing and the Proteome
- Regulation of Alternative Splicing
- Sex Determination in Drosophila: A Model for Regulation of Alternative Splicing
- Alternative Splicing and Human Diseases
- 18.2 Gene Expression Is Regulated by mRNA Stability and Degradation
- Mechanisms of mRNA Decay
- Regulation of mRNA Stability and Degradation
- mRNA Surveillance and Nonsense‐Mediated Decay
- 18.3 Noncoding RNAs Play Diverse Roles in ‐Posttranscriptional Regulation
- The Discovery of RNA Interference and microRNAs
- Mechanisms of RNA Interference
- RNA Interference in Research, Biotechnology, and Medicine
- Long Noncoding RNAs and Posttranscriptional Regulation
- Circular RNAs
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION MicroRNAs Regulate Ovulation in Female Mice
- 18.4 mRNA Localization and Translation Initiation Are Highly Regulated
- Cytoplasmic Polyadenylation
- mRNA Localization and Localized Translational Control
- 18.5 Posttranslational Modifications Regulate ‐Protein Activity
- Regulation of Proteins by Phosphorylation
- Ubiquitin‐Mediated Protein Degradation
- GENETICS, ETHICS, AND SOCIETY Is DNA Enough?
- CASE STUDY A mysterious muscular dystrophy
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 19 Epigenetic Regulation of Gene Expression
- 19.1 Molecular Alterations to the Genome Create an Epigenome
- DNA Methylation and the Methylome
- Histone Modification and Chromatin Remodeling
- Short and Long Noncoding RNAs
- 19.2 Epigenetics and Monoallelic Gene Expression
- Parent‐of‐Origin Monoallelic Expression: Imprinting
- Random Monoallelic Expression: Inactivation of the X Chromosome
- Random Monoallelic Expression of Autosomal Genes
- Assisted Reproductive Technologies (ART) and Imprinting Defects
- 19.3 Epigenetics and Cancer
- DNA Methylation and Cancer
- Chromatin Remodeling and Histone Modification in Cancer
- Epigenetic Cancer Therapy
- 19.4 Epigenetic Traits Are Heritable
- Environmental Induction of Epigenetic Change
- Stress‐Induced Behavior Is Heritable
- 19.5 Epigenome Projects and Databases
- CASE STUDY Food for Thought
- Summary Points
- EXPLORING GENOMICS The International Human Epigenome Consortium (IHEC)
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- PART FOUR GENETIC TECHNOLOGY AND GENOMICS
- 20 Recombinant DNA Technology
- 20.1 Recombinant DNA Technology Began with Two Key Tools: Restriction Enzymes and ‐Cloning Vectors
- Restriction Enzymes Cut DNA at Specific ‐Recognition Sequences
- DNA Vectors Accept and Replicate DNA Molecules to Be Cloned
- Bacterial Plasmid Vectors
- Other Types of Cloning Vectors
- Host Cells for Cloning Vectors
- 20.2 DNA Libraries Are Collections of Cloned Sequences
- Genomic Libraries
- Complementary DNA (cDNA) Libraries
- Specific Genes Can Be Recovered from a Library by Screening
- 20.3 The Polymerase Chain Reaction Is a Powerful Technique for Copying DNA
- PCR Limitations
- PCR Applications
- 20.4 Molecular Techniques for Analyzing DNA and RNA
- Restriction Mapping
- Nucleic Acid Blotting
- In Situ Hybridization
- 20.5 DNA Sequencing Is the Ultimate Way to Characterize DNA at the Molecular Level
- Sequencing Technologies Have Progressed Rapidly
- Next‐Generation Sequencing Technology
- Third‐Generation Sequencing Technology
- DNA Sequencing and Genomics
- 20.6 Creating Knockout and Transgenic Organisms for Studying Gene Function
- Gene Targeting and Knockout Animal Models
- Making a Transgenic Animal: The Basics
- Gene Editing with CRISPR‐Cas
- EXPLORING GENOMICS Manipulating Recombinant DNA: Restriction ‐Mapping and Designing PCR Primers
- CASE STUDY Ethical issues and genetic technology
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 21 Genomic Analysis
- 21.1 Genomic Analysis Before Modern Sequencing Methods Involved Classical Genetics Approaches and Cl
- 21.2 Whole‐Genome Sequencing Is Widely Used for Sequencing and Assembling Entire Genomes
- High‐Throughput Sequencing and Its Impact on Genomics
- The Clone‐by‐Clone Approach
- Draft Sequences and Reference Genomes
- 21.3 DNA Sequence Analysis Relies on Bioinformatics Applications and Genome Databases
- Annotation to Identify Gene Sequences
- Hallmark Characteristics of a Gene Sequence Can Be Recognized during Annotation
- 21.4 Functional Genomics Establishes Gene Function and Identifies Regulatory Elements in a Genome
- Predicting Gene and Protein Functions by Sequence Analysis
- Predicting Function from Structural Analysis of Protein Domains and Motifs
- Investigators Are Using Genomics Techniques Such as Chromatin Immunoprecipitation to Investigate Asp
- 21.5 The Human Genome Project Revealed Many Important Aspects of Genome Organization in Humans
- Origins of the Project
- Major Features of the Human Genome
- Individual Variations in the Human Genome
- Accessing the Human Genome Project on the Internet
- 21.6 The “Omics” Revolution Has Created a New Era of Biological Research
- After the HGP, What’s Next?
- Personal Genome Projects
- Somatic Genome Mosaicism and the Emerging Pangenome
- Whole‐Exome Sequencing
- Encyclopedia of DNA Elements (ENCODE) Project
- Nutrigenomics Considers Genetics and Diet
- No Genome Left Behind and the Genome 10K Plan
- Stone‐Age Genomics
- 21.7 Comparative Genomics Analyzes and Compares Genomes from Different Organisms
- Bacterial and Eukaryotic Genomes Display Common Structural and Functional Features and Important Dif
- Comparative Genomics Provides Novel Information about the Genomes of Model Organisms and the Human G
- The Sea Urchin Genome
- The Dog Genome
- The Chimpanzee Genome
- The Rhesus Monkey Genome
- The Neanderthal Genome and Modern Humans
- 21.8 Metagenomics Applies Genomics Techniques to Environmental Samples
- The Human Microbiome Project
- 21.9 Transcriptome Analysis Reveals Profiles of Expressed Genes in Cells and Tissues
- DNA Microarray Analysis
- RNA Sequencing Technology Allows for In Situ Analysis of Gene Expression
- 21.10 Proteomics Identifies and Analyzes the Protein Composition of Cells
- Reconciling the Number of Genes and the Number of Proteins Expressed by a Cell or Tissue
- Mass Spectrometry for Protein Identification
- EXPLORING GENOMICS Contigs, Shotgun Sequencing, and Comparative Genomics
- CASE STUDY Your microbiome may be a risk factor for disease
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 22 Applications of Genetic Engineering and Biotechnology
- 22.1 Genetically Engineered Organisms Synthesize a Variety of Valuable Biopharmaceutical Products
- Recombinant Protein Production in Bacteria
- Transgenic Animal Hosts and Biopharmaceutical Products
- Recombinant DNA Approaches for Vaccine Production
- Vaccine Proteins Can Be Produced by Plants
- DNA‐Based Vaccines
- 22.2 Genetic Engineering of Plants Has Revolutionized Agriculture
- 22.3 Genetically Modified Animals Serve Important Roles in Biotechnology
- Examples of Transgenic Animals
- 22.4 Genetic Testing, Including Genomic Analysis, Is Transforming Medical Diagnosis
- Genetic Testing for Prognostic or Diagnostic Purposes
- Prenatal Genetic Testing
- Genetic Testing Using Allele‐Specific Oligonucleotides
- Genetic Testing Using Microarrays
- Applications of Gene‐Expression Microarrays and Next–Generation Sequencing for Pathogen Identifi
- Screening the Genome for Genes or Mutations You Want
- 22.5 Genetic Analysis of Individual Genomes
- 22.6 Genetic Analysis from Single Cells
- 22.7 Genome‐Wide Association Studies Identify Genome Variations That Contribute to Disease
- 22.8 Synthetic Genomes and the Emergence of Synthetic Biology
- The Minimal Genome: How Many Essential Genes Are Required by a Living Cell?
- Design and Transplantation of a Synthetic Genome Defines the Minimal Bacterial Genome
- The Essential Genes of Human Cells and the Quest to Create a Synthetic Human Genome
- Synthetic Biology for Bioengineering Applications
- 22.9 Genetic Engineering, Genomics, and Biotechnology Raise Ethical, Social, and Legal Questions
- Genetic Testing and Ethical Dilemmas
- Direct‐to‐Consumer Genetic Testing and Regulating the Genetic Test Providers
- DNA and Gene Patents
- Whole‐Genome Sequence Analysis Presents Many Questions of Ethics
- Privacy and Anonymity in the Era of Genomic Big Data
- GENETICS, ETHICS, AND SOCIETY Privacy and Anonymity in the Era of Genomic Big Data
- Preconception Testing, Destiny Predictions, and Baby‐Predicting Patents
- Patents and Synthetic Biology
- CASE STUDY “Driving” to Extinction
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- PART FIVE GENETIC ANALYSIS OF ORGANISMS AND POPULATIONS
- 23 Developmental Genetics
- 23.1 Differentiated States Develop from Coordinated Programs of Gene Expression
- Genetic and Epigenetic Regulation of Development
- 23.2 Evolutionary Conservation of Developmental Mechanisms Can Be Studied Using Model Organisms
- Analysis of Developmental Mechanisms
- 23.3 Genetic Analysis of Embryonic Development in Drosophila Reveals How the Body Axis of Animals Is
- Overview of Drosophila Development
- Genetic Analysis of Embryogenesis
- 23.4 Segment Formation and Body Plans in Drosophila and Mammals
- Gap Genes
- Pair‐Rule Genes
- Segment Polarity Genes
- Segmentation Genes in Mice and Humans
- 23.5 Homeotic Selector Genes Specify Body Parts of the Adult
- Hox Genes in Drosophila
- Hox Genes and Human Genetic Disorders
- 23.6 Plants Have Evolved Developmental Regulatory Systems That Parallel Those of Animals
- Homeotic Genes in Arabidopsis
- Divergence in Homeotic Genes
- 23.7 C. elegans Serves as a Model for Cell–Cell Interactions in Development
- Signaling Pathways in Development
- The Notch Signaling Pathway
- Overview of C. elegans Development
- Genetic Analysis of Vulva Formation
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Downregulating a Single Gene Reveals Secrets to Hea
- 23.8 Binary Switch Genes and Regulatory Networks Program Genomic Expression
- The Control of Eye Formation
- GENETICS, ETHICS, AND SOCIETY Stem Cell Wars
- CASE STUDY One foot or another
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 24 Cancer Genetics
- 24.1 Cancer Is a Genetic Disease at the Level of Somatic Cells
- What Is Cancer?
- The Clonal Origin of Cancer Cells
- Driver Mutations and Passenger Mutations
- The Cancer Stem Cell Hypothesis
- Cancer as a Multistep Process, Requiring Multiple Mutations and Clonal Expansions
- 24.2 Cancer Cells Contain Genetic Defects Affecting Genomic Stability, DNA Repair, and Chromatin Mod
- Genomic Instability and Defective DNA Repair
- Chromatin Modifications and Cancer Epigenetics
- 24.3 Cancer Cells Contain Genetic Defects Affecting Cell‐Cycle Regulation
- The Cell Cycle and Signal Transduction
- Cell‐Cycle Control and Checkpoints
- Control of Apoptosis
- Cancer Therapies and Cancer Cell Biology
- 24.4 Proto‐oncogenes and Tumor‐Suppressor Genes Are Altered in Cancer Cells
- The ras Proto‐oncogenes
- The TP53 Tumor‐Suppressor Gene
- 24.5 Cancer Cells Metastasize and Invade Other Tissues
- 24.6 Predisposition to Some Cancers Can Be Inherited
- 24.7 Viruses Contribute to Cancer in Both Humans and Animals
- 24.8 Environmental Agents Contribute to Human Cancers
- Natural Environmental Agents
- Human‐Made Chemicals and Pollutants
- Tobacco Smoke and Cancer
- CASE STUDY Cancer‐killing bacteria
- Summary Points
- Exploring Genomics The Cancer Genome Anatomy Project (CGAP)
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 25 Quantitative Genetics and Multifactorial Traits
- 25.1 Not All Polygenic Traits Show Continuous Variation
- 25.2 Quantitative Traits Can Be Explained in ‐Mendelian Terms
- The Multiple‐Gene Hypothesis for Quantitative Inheritance
- Additive Alleles: The Basis of Continuous Variation
- Calculating the Number of Polygenes
- 25.3 The Study of Polygenic Traits Relies on Statistical Analysis
- The Mean
- Variance
- Standard Deviation
- Standard Error of the Mean
- Covariance and Correlation Coefficient
- Analysis of a Quantitative Character
- 25.4 Heritability Values Estimate the Genetic Contribution to Phenotypic Variability
- Broad‐Sense Heritability
- Narrow‐Sense Heritability
- Artificial Selection
- Limitations of Heritability Studies
- 25.5 Twin Studies Allow an Estimation of Heritability in Humans
- Large‐Scale Analysis of Twin Studies
- Twin Studies Have Several Limitations
- 25.6 Quantitative Trait Loci Are Useful in Studying Multifactorial Phenotypes
- Expression QTLs Regulate Gene Expression
- Expression QTLs and Genetic Disorders
- GENETICS, ETHICS, AND SOCIETY Rice, Genes, and the Second Green Revolution
- CASE STUDY A Chance Discovery
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 26 Population and Evolutionary Genetics
- 26.1 Genetic Variation Is Present in Most Populations and Species
- Detecting Genetic Variation
- Recombinant DNA Technology and Genetic Variation
- Genetic Variation in Genomes
- Explaining the High Level of Genetic Variation in Populations
- 26.2 The Hardy–Weinberg Law Describes Allele Frequencies and Genotype Frequencies in Population Ge
- Calculating Genotype Frequencies
- Calculating Allele Frequencies
- The Hardy–Weinberg Law and Its Assumptions
- 26.3 The Hardy–Weinberg Law Can Be Applied to Human Populations
- Testing for Hardy–Weinberg Equilibrium in a Population
- Calculating Frequencies for Multiple Alleles in Populations
- Calculating Allele Frequencies for X‐linked Traits
- Calculating Heterozygote Frequency
- 26.4 Natural Selection Is a Major Force Driving Allele Frequency Change
- Detecting Natural Selection in Populations
- Fitness and Selection
- There Are Several Types of Selection
- 26.5 Mutation Creates New Alleles in a Gene Pool
- 26.6 Migration and Gene Flow Can Alter Allele Frequencies
- 26.7 Genetic Drift Causes Random Changes in Allele Frequency in Small Populations
- Founder Effects in Human Populations
- 26.8 Nonrandom Mating Changes Genotype Frequency but Not Allele Frequency
- Inbreeding
- 26.9 Speciation Can Occur through Reproductive Isolation
- Changes Leading to Speciation
- The Rate of Macroevolution and Speciation
- 26.10 Phylogeny Can Be Used to Analyze Evolutionary History
- Constructing Phylogenetic Trees from DNA Sequences
- Reconstructing Vertebrate Evolution by Phylogenetic Analysis
- Molecular Clocks Measure the Rate of Evolutionary Change
- The Complex Origins of the Human Genome
- GENETICS ,ETHICS, AND SOCIETY Tracking Our Genetic Footprints out of Africa
- CASE STUDY A Tale of Two Olivias
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- Special Topics In Modern Genetics 1
- CRISPR‐Cas and Genome Editing
- CRISPR‐Cas Is an Adaptive Immune System in Prokaryotes
- Discovery of CRISPR
- The CRISPR‐Cas Mechanism for RNA‐Guided Destruction of Invading DNA
- Type II CRISPR‐Cas Systems
- CRISPR‐Cas has been Adapted as a Powerful Tool for Genome Editing
- CRISPR‐Cas9 In Vitro
- CRISPR‐Cas9 Genome Editing of Mammalian Cells
- CRISPR‐Cas Infidelity
- CRISPR‐Cas Technology Has Diverse Applications
- CRISPR‐Cas as a Tool for Basic Genetic Research
- Box 1 The CRISPR‐Cas9 Patent Battle
- CRISPR‐Cas in Biotechnology
- Clinical Use of CRISPR‐Cas to Treat or Cure Disease
- Box 2 Ethical Concerns of Human Genome Editing
- Special Topics In Modern Genetics 2
- DNA Forensics
- DNA Profiling Methods
- VNTR‐Based DNA Fingerprinting
- Box 1 The Pitchfork Case: The First Criminal Conviction Using DNA Profiling
- Autosomal STR DNA Profiling
- Y‐Chromosome STR Profiling
- Mitochondrial DNA Profiling
- Single‐Nucleotide Polymorphism Profiling
- DNA Phenotyping
- Box 2 Putting a Face to DNA: The Bouzigard Case
- Interpreting DNA Profiles
- The Uniqueness of DNA Profiles
- DNA Profile Databases
- Technical and Ethical Issues Surrounding DNA Profiling
- Box 3 The Kennedy Brewer Case: Two Bite‐Mark Errors and One Hit
- Box 4 A Case of Transference: The Lukis Anderson Story
- Special Topics In Modern Genetics 3
- Genomics and Precision Medicine
- Pharmacogenomics
- Optimizing Drug Responses
- Developing Targeted Drugs
- Box 1 Preemptive Pharmacogenomic Screening: The PGEN4Kids Program
- Precision Oncology
- Targeted Cancer Immunotherapies
- Box 2 Precision Cancer Diagnostics and Treatments: The Lukas Wartman Story
- Box 3 Cell Types in the Innate and Adaptive Immune Systems
- Box 4 Steps in Cytotoxic T‐cell Recognition, Activation, and Destruction of Cancer Cells
- Precision Medicine and Disease Diagnostics
- Technical, Social, and Ethical Challenges
- Box 5 Beyond Genomics: Personal Omics Profiling
- Special Topics In Modern Genetics 4
- Genetically Modified Foods
- What Are GM Foods?
- Herbicide‐Resistant GM Crops
- Box 1 The Tale of GM Salmon—Downstream Effects?
- Insect‐Resistant GM Crops
- GM Crops for Direct Consumption
- Methods Used to Create GM Plants
- Selectable Markers
- Roundup‐Ready® Soybeans
- Golden Rice 2
- Gene Editing and GM Foods
- GM Foods Controversies
- Box 2 The New CRISPR Mushroom
- Health and Safety
- Environmental Effects
- The Future of GM Foods
- Special Topics In Modern Genetics 5
- Gene Therapy
- What Genetic Conditions Are Candidates for Treatment by Gene Therapy?
- How Are Therapeutic Genes Delivered?
- Viral Vectors for Gene Therapy
- Box 1 ClinicalTrials.gov
- Nonviral Delivery Methods
- Stem Cells for Delivering Therapeutic Genes
- The First Successful Gene Therapy Trial
- Gene Therapy Setbacks
- Problems with Gene Therapy Vectors
- Recent Successful Trials by Conventional Gene Therapy Approaches
- Treating Retinal Blindness
- Successful Treatment of Hemophilia B
- HIV as a Vector Shows Promise in Recent Trials
- Box 2 Glybera: The First Commercial Gene Therapy to be Approved in the West Lasted Only 5 Years
- Gene Editing Approaches to Gene Therapy
- DNA‐Editing Nucleases
- CRISPR‐Cas Method Revolutionizes Gene Editing Applications and Renews Optimism in Gene Therapy
- RNA‐Based Therapeutics
- Future Challenges and Ethical Issues
- Ethical Concerns Surrounding Gene Therapy
- Box 3 Gene Doping for Athletic Performance?
- Special Topics In Modern Genetics 6
- Advances in Neurogenetics: The Study of Huntington Disease
- Box 1 George Huntington and His Namesake Disease
- The Search for the Huntington Gene
- Finding Linkage between Huntington Disease and an RFLP Marker
- Box 2 Nancy Wexler and the Venezuelan Pedigree
- Assigning the HD Gene to Chromosome 4
- The Identification and Cloning of the Huntington Gene
- Box 3 Genetic Testing for Huntington Disease
- The HTT Gene and Its Protein Product
- Molecular and Cellular Alterations in Huntington Disease
- Transcriptional Disruption
- Impaired Protein Folding and Degradation
- Synaptic Dysfunction
- Impaired Mitochondrial Function
- Transgenic Animal Models of Huntington Disease
- Using Transgenic Mice to Study Huntington Disease
- Transgenic Sheep as an Animal Model of Huntington Disease
- Cellular and Molecular Approaches to Therapy
- Stem Cells for Transplantation
- Identifying Potential Drugs for Therapy
- Gene Silencing to Reduce mHTT Levels
- Gene Editing in Huntington Disease
- The Relationship between HD and Other Neurodegenerative Disorders
- Box 4 Huntington Disease and Behavior
- Appendix A Selected Readings
- Appendix B Answernto Selected Problems
- Glossary
- Credits
- Index
- Evolving Concept of The Gene
- Back Cover
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