eLS

eLS

Online ISBN: 9780470015902

DOI: 10.1002/047001590X

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  1. Biochemistry
  2. Bioethics & Philosophy
  3. Cell Biology
  4. Developmental Biology
  5. Ecology
  6. Evolution & Diversity of Life
  7. Genetics & Disease
    1. Bioinformatics and Genetic Disease
    2. Cancer Genetics
    3. Chromosomal Disorders
    4. Epigenetics and Disease
    5. Forensic Genetics
    6. Gene and Genome Structure and Organisation
      1. Activating and Inactivating Mutations in the GNAS1 Gene
      2. Aging: Genetics
      3. Alternative Promoter Usage
      4. Alternative Promoters: Duchenne Muscular Dystrophy (DMD) Gene
      5. Alternative Splicing and Human Disease
      6. Alternative Splicing: Role of Pseudoexons in Human Genetic Disease
      7. Anticipation
      8. Apolipoprotein Gene Structure and Function
      9. Apoptosis: Regulatory Genes and Disease
      10. Application of Chromosome Conformation Capture (3C) to the Study of Human Genetic Disease
      11. Blocks of Limited Haplotype Diversity
      12. Caenorhabditis elegans Genome Project
      13. Cancer
      14. Cancer Cytogenetics
      15. Cancer Genome Sequencing
      16. Causes and Consequences of Structural Genomic Alterations in the Human Genome
      17. Characterising Structural Variation by Means of Next-Generation Sequencing
      18. Chimera-directed Gene Repair
      19. Chromosomal Genetic Disease: Structural Aberrations
      20. Chromosomal Instability (CIN) in Cancer
      21. Chromosome 2
      22. Chromosome 3
      23. Chromosome 4
      24. Chromosome 5
      25. Chromosome 6
      26. Chromosome 7
      27. Chromosome 9
      28. Chromosome 1
      29. Chromosome 10
      30. Chromosome 11
      31. Chromosome 12
      32. Chromosome 13
      33. Chromosome 14
      34. Chromosome 15
      35. Chromosome 16
      36. Chromosome 17
      37. Chromosome 18
      38. Chromosome 19
      39. Chromosome 20
      40. Chromosome 22
      41. Chromosome 22: Sequencing
      42. Chromosome 8
      43. Chromosome Function: Sex Differences
      44. Chromosome Instability (CIN), Aneuploidy and Cancer
      45. You have free access to this content
        Chromosome Structure
      46. Chromosome X
      47. You have free access to this content
        Chromosome X: General Features
      48. Chromosome Y
      49. Chromosome-specific Repeats (Low-copy Repeats)
      50. Chromosomes 21 and 22: Comparisons
      51. Chromosomes 21 and 22: Gene Density
      52. Chromosomes: Noncoding DNA (Including Satellite DNA)
      53. Clinical and Phenotypic Relevance of cis-Acting Regulatory Polymorphisms
      54. Clustered Mutations in Human Cancer
      55. Clustering of Highly Expressed Genes in the Human Genome
      56. Compensatory Evolution in Disease-Associated Genes
      57. Complex Multifactorial Genetic Diseases
      58. Cre–lox-Inducible Gene Targeting
      59. Cytochrome P450 (CYP) Gene Superfamily
      60. Development and Role of the Human Reference Sequence in Personal Genomics
      61. Digital Image Analysis
      62. DNA Chip Revolution
      63. You have free access to this content
        DNA Chips and Microarrays
      64. DNA Looping and Transcription Regulation
      65. DNA Methylation and Mutation
      66. DNA Sequencing
      67. Dominant Traits and Diseases
      68. Enhancers
      69. Environmental Carcinogens and Mutagens
      70. Eukaryotic Chromosomes
      71. Exonic Splicing Enhancers
      72. Facioscapulohumeral Muscular Dystrophy
      73. Flow-sorted Chromosomes
      74. Fragile Sites and Human Disease
      75. The Fragile X Syndrome
      76. Fusion Proteins and Diseases
      77. Gene Conversion
      78. Gene Distribution in Human Chromosomes
      79. Gene Duplication and Redundancy
      80. Gene Families
      81. Gene Mapping and Positional Cloning
      82. Gene Mapping: Comparative
      83. You have free access to this content
        Gene Structure and Organization
      84. Gene Targeting by Homologous Recombination
      85. Genes: Types
      86. Genetic and Epigenetic Heterogeneity in Cancer
      87. Genetic and Physical Map Correlation
      88. Genetic Distance and Mapping Functions
      89. Genetic Mapping: Comparison of Direct and Indirect Approaches
      90. Genetic Maps: Direct Meiotic Analysis
      91. Genetic Maps: Integration
      92. Genetic Networks
      93. Genetic Susceptibility to Autoimmune Disorders
      94. Genetics and Epigenetics of Autoimmune Diseases
      95. Genome Databases
      96. Genome Inserts
      97. Genome Mapping
      98. Genome Organization of Vertebrates
      99. Genome Organization: Human
      100. Genome Sequence Analysis
      101. Genome Sequencing
      102. Genome Size
      103. Genomic Rearrangements: Mutational Mechanisms
      104. Genomics, Pharmacogenetics and Proteomics: An Integration
      105. Germline Copy Number Variation and Cancer Risk
      106. Germline Genomic Copy Number Variation Contribution to Cancer Predisposition
      107. Histone Acetylation and Disease
      108. Histones
      109. Housekeeping Genes
      110. Human Chromosome Evolution
      111. Human Chromosomes
      112. Human Gene Nomenclature
      113. Human Genetics: Principles
      114. Human Genome Variation Society
      115. Human Genome: Draft Sequence
      116. Human Intronless Genes and their Associated Diseases
      117. Human Variation Databases
      118. You have free access to this content
        Immunoglobulin Gene Construction: Human
      119. Imprinting (Mammals)
      120. Infertility: Genetic Disorders
      121. Integrins
      122. Intronless Genes
      123. Isochores
      124. Karyotype Analysis and Chromosome Banding
      125. Kilobase Pair (kbp)
      126. L Isochore Map: Gene-poor Isochores
      127. Long Interspersed Nuclear Elements (LINEs)
      128. Long Noncoding RNAs and Tumorigenesis
      129. Major Histocompatibility Complex (MHC) Genes
      130. Male Sex Determination: Genetics
      131. Mammalian Artificial Chromosomes (MACs)
      132. You have free access to this content
        Mechanisms of X-inactivation
      133. Megabase Pair (Mbp)
      134. Megasatellite DNA
      135. You have free access to this content
        Mendelian Genetic Disorders
      136. Microarrays: Use in Gene Identification
      137. Microdeletions and Microduplications: Mechanism
      138. Microsatellite Instability
      139. Microsatellites
      140. Minigenes
      141. Minisatellites
      142. Molecular Genetic Causes of Discordance in Monozygotic Twins
      143. Molecular Genetics of Polygenic Hypertension
      144. You have free access to this content
        The Molecular Genetics of Trisomy 18: Phenotype–Genotype Correlations
      145. You have free access to this content
        Monosomies
      146. Mutation Nomenclature
      147. Mutations and the Genetic Code
      148. Negative Regulatory Elements (NREs)
      149. Next-Generation Sequencing in Cancer: Tools for Fusion Gene Detection
      150. Nonsense Mutations Causing Inherited Diseases: Therapeutic Approaches
      151. Nucleic Acid Hybridization
      152. You have free access to this content
        Oncogenes
      153. Patenting of Genes: Discoveries or Inventions?
      154. Pathological Mutations in 5′ Untranslated Regions of Human Genes
      155. Pathological Variations in 3′-untranslated Regions of Human Genes
      156. Plant Storage Products (Carbohydrates, Oils and Proteins)
      157. Polymorphism of TNF Genes and Disease Susceptibility
      158. Polyploidy
      159. Primer Walking
      160. Promoter Haplotypes and Gene Expression
      161. Promoters
      162. Protein-Coding Segments: Evolution of Exon–Intron Gene Structure
      163. Pseudoautosomal Inheritance
      164. The Rat Genome as a Rodent Model in Evolutionary Studies
      165. Relevance of Copy Number Variation to Human Genetic Disease
      166. Relevance of Pseudogenes to Human Genetic Disease
      167. Repetitive Elements and Human Disorders
      168. Repetitive Elements: Bioinformatic Identification, Classification and Analysis
      169. Restriction Mapping of Cloned DNA
      170. Retrotransposons and Human Disease
      171. Retroviral Repeat Sequences
      172. Retroviruses in Human Gene Therapy
      173. RNA Therapy for Polyglutamine Neurodegenerative Diseases
      174. The Role of Insulators in Genome Organization and Gene Expression
      175. Segmental Duplications and Genetic Disease
      176. Segmental Duplications: A Source of Diversity, Evolution and Disease
      177. Sequence Accuracy and Verification
      178. Sequence Assembly
      179. You have free access to this content
        Sequencing the Human Genome: Novel Insights into its Structure and Function
      180. Sex Chromosome Abnormalities
      181. Short DNA Sequence Repeats
      182. Short Interspersed Elements (SINEs)
      183. Shotgunning the Human Genome: A Personal View
      184. Simple Repeats
      185. Single Nucleotide Polymorphism (SNP)
      186. Single Nucleotide Polymorphisms (SNPs): Identification and Scoring
      187. Site-specific Recombination: Uses in Biotechnology
      188. Skin Pigmentation: Genetics
      189. Somatic Genome Variations
      190. Somatic Hypermutation in Antibody Evolution
      191. Splice Sites
      192. Splicing Modulation as Therapy for Human Genetic Disease
      193. SRY, Sex Determination and Gonadal Differentiation
      194. Structural Diversity of the Human Genome and Disease Susceptibility
      195. Structural Proteins: Genes for Collagen
      196. Synonymous Mutations as a Cause of Human Genetic Disease
      197. Technological Advances in the Detection of Novel Fusion Genes
      198. Telomeres in Cell Function: Cancer and Ageing
      199. Telomeres: Protection and Maintenance
      200. Telomeric and Subtelomeric Repeat Sequences
      201. The Gene Content of Mammalian and Avian Sex Chromosomes
      202. Tissue-specific Locus Control: Structure and Function
      203. Titin Gene (TTN)
      204. Transcription Factors
      205. Translocation Breakpoints in Cancer
      206. Transposons
      207. Transposons as Natural and Experimental Mutagens
      208. Trinucleotide Repeat Expansions: Disorders
      209. Trinucleotide Repeat Expansions: Mechanisms and Disease Associations
      210. You have free access to this content
        Trisomy
      211. You have free access to this content
        Turner Syndrome
      212. Upstream Open Reading Frames and Human Genetic Disease
      213. 3′ UTR Mutations and Human Disorders
      214. Whole Animal Cloning
      215. X and Y Chromosomes: Homologous Regions
      216. X-Chromosome Inactivation
      217. X-chromosome Inactivation
      218. Y Chromosome
      219. Y-chromosome-linked Traits
      220. Yeast (YAC) and Human (HAC) Artificial Chromosome Clones
    7. Gene Expression Profiling of Genetic Disease
    8. Gene Mapping by Disease Association
    9. Gene Therapy
    10. General Genetics and Disease
    11. Genetic Counseling
    12. Genetic Models
    13. Genetics of Intelligence and Cognition
    14. Genomic Disorders
    15. Inter-Individual Variation and Polymorphism
    16. Linkage Analysis
    17. Mitochondrial Diseases
    18. Model Organisms and Human Disease
    19. Molecular Genetics of Common and Complex Disease
    20. Mutational Mechanisms of Genetic Disease
    21. Pharmacogenetics and Pharmacogenomics
    22. Proteomic Studies of Genetic Disease
    23. Quantitative Genetics
    24. Specific Genetic Disorders
    25. Statistical Methodology in Genetics
    26. Techniques and Tools in Clinical Genetics
  8. Immunology
  9. Microbiology
  10. Molecular Biology
  11. Neuroscience
  12. Plant Science
  13. Science & Society
  14. Structural Biology
  15. Virology

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