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
  8. Immunology
  9. Microbiology
  10. Molecular Biology
    1. Chromosomes and Chromatin Modifications
    2. Computational Molecular Biology
    3. DNA Damage and Repair
      1. Ageing
      2. Ageing Genes: Gerontogenes
      3. Aging: Genetics
      4. Assessing Genetic Variants of Uncertain Significance: The Example of Lynch Syndrome
      5. Bacterial DNA Polymerase I
      6. Bacterial Primosome
      7. Bacterial Replication Fork: Synthesis of Lagging Strand
      8. Base Excision Repair, AP Endonucleases and DNA Glycosylases
      9. Base Flipping
      10. Biallelic Germline Mutations of Mismatch-Repair Genes and Paediatric Malignancies
      11. Brain Cancers
      12. Breast Cancer
      13. Cancer
      14. Cancer Cytogenetics
      15. Cancer: Chromosomal Abnormalities
      16. Cell Death in C. elegans
      17. Checkpoints in the Cell Cycle
      18. Chemical, Biological, Radiological and Nuclear Weapons: Genotoxicity
      19. Chimera-directed Gene Repair
      20. Chromosomal Genetic Disease: Structural Aberrations
      21. Chromosome Instability (CIN), Aneuploidy and Cancer
      22. Chromosome Rearrangements
      23. Chromothripsis and Human Genetic Disease
      24. Colon Cancer
      25. Conditional Lethal Mutations as Experimental Tools
      26. Contig Assembly
      27. CpG Dinucleotides and Human Disorders
      28. Cytogenetic and Physical Chromosomal Maps: Integration
      29. DNA Chemical Instability
      30. DNA Damage
      31. DNA Damage Response: From Tumourigenesis to Therapy
      32. DNA Double-Strand Breaks and Their Consequences in Bacterial Genomes
      33. DNA Interstrand Crosslink Repair
      34. DNA Ligases
      35. DNA Looping and Transcription Regulation
      36. DNA Methylation and Mutation
      37. DNA Mismatch Repair: Eukaryotic
      38. DNA Polymerase Fidelity Mechanisms
      39. DNA Polymerases: Eukaryotic
      40. You have free access to this content
        DNA Recombination
      41. DNA Repair
      42. You have free access to this content
        DNA Repair
      43. DNA Repair by Reversal of Damage
      44. DNA Repair Disorders
      45. DNA Repair: Disorders
      46. DNA Repair: Evolution
      47. DNA Strand Break Repair and Human Genetic Disease
      48. DNA: Mechanical Breakage
      49. Environmental Carcinogens and Mutagens
      50. Environmental Mutagenesis
      51. Escherichia coli and the Development of Bacterial Genetics
      52. Eukaryotic DNA Polymerases
      53. Eukaryotic Recombination: Initiation by Double-strand Breaks
      54. Eukaryotic Replication Protein A
      55. Evolution of Common Fragile Sites
      56. Exonucleases
      57. Fragile Sites
      58. Fragile Sites and Human Disease
      59. The Fragile X Syndrome
      60. Free Radicals and Other Reactive Species in Disease
      61. Fusion Proteins and Diseases
      62. Gastric Cancer
      63. Gene Conversion
      64. Gene Duplication and Redundancy
      65. Gene Targeting by Homologous Recombination
      66. Genetic Variation: Human
      67. Genetics and Genomics of Malignant Rhabdoid Tumours
      68. Genomic and Chromosomal Instability
      69. Hereditary Nonpolyposis Colorectal Cancer
      70. Histidine Triad (HIT) Superfamily
      71. Histones: Gene Organisation and Post-translational Modification
      72. Human Chromosome Evolution
      73. Human Chromosomes
      74. Human Mismatch Repair: Defects and Predisposition to Cancer
      75. Immunoglobulin Genes
      76. In Vitro Mutagenesis
      77. Integrase Class Site-specific Recombinases
      78. Leukaemias and Lymphomas
      79. Ligation: Theory and Practice
      80. Long Interspersed Nuclear Elements (LINEs)
      81. Long-range PCR
      82. Loss of Heterozygosity
      83. Mechanisms of Chromosome Translocations in Cancer
      84. Meganucleases and Their Biomedical Applications
      85. Melanoma
      86. Microdeletion Syndromes
      87. Microsatellite Instability
      88. Mismatch Repair Genes
      89. Mitochondria as a Key Determinant of Aging
      90. Mitochondrial DNA Repair in Mammals
      91. Mitosis: Chromosomal Rearrangements
      92. Mitosis: Chromosome Segregation and Stability
      93. Molecular Biology of Breast Cancer
      94. Molecular Genetics of Fanconi Anaemia
      95. Molecular Genetics of Oral Cancer
      96. Mouse N-ethyl-N-nitrosourea (ENU) Mutagenesis
      97. Mutagenesis
      98. Mutagenesis Mechanisms
      99. You have free access to this content
        Mutation
      100. Mutation Detection
      101. Mutation Rate of Non-CpG DNA
      102. Mutations and the Genetic Code
      103. Nick Translation
      104. Non-B DNA Structure and Mutations Causing Human Genetic Disease
      105. Nonsense Mutations and Suppression
      106. Nonsense Mutations Causing Inherited Diseases: Therapeutic Approaches
      107. Nucleases
      108. Nucleotide Excision Repair in Bacteria
      109. Nucleotide Excision Repair in Eukaryotes
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        Oncogenes
      111. Oxidative Stress
      112. Paramutation in Plants
      113. PCR-mediated Mutagenesis
      114. Plant Mutagenesis and Mutant Screening
      115. Polyploidy
      116. Position Effect Variegation in Human Genetic Disease
      117. Prostate Cancer
      118. Pseudoautosomal Inheritance
      119. RecA Protein
      120. RecBCD Helicase/Nuclease
      121. RecFOR Protein
      122. Recombinant DNA
      123. Recombinational DNA Repair in Bacteria: Postreplication
      124. Recombinational DNA Repair in Eukaryotes
      125. Relevance of Copy Number Variation to Human Genetic Disease
      126. Restriction Enzymes
      127. Restriction Enzymes
      128. Retrotransposons and Human Disease
      129. Ribonucleotide Reduction
      130. Role of Chromosomal Reorganisations in the Human–Chimpanzee Speciation
      131. Segmental Duplications and Genetic Disease
      132. Segmental Duplications: A Source of Diversity, Evolution and Disease
      133. Short Interspersed Elements (SINEs)
      134. Single Nucleotide Polymorphism (SNP)
      135. Single-base Mutation
      136. Single-stranded DNA-binding Proteins
      137. Site-directed Mutagenesis of Double-stranded Plasmids
      138. Site-directed Mutagenesis Using PCR
      139. Site-specific Recombination in Chromosome Function
      140. SOS Response
      141. Spontaneous Function Correction of Pathogenic Alleles in Inherited Diseases Resulting in Somatic Mosaicism
      142. Stress-induced Premature Senescence (SIPS)
      143. Telomere
      144. Telomere Dysfunction in Human Genetic Disease
      145. Telomeres
      146. Telomeres in Cell Function: Cancer and Ageing
      147. Telomeres: Protection and Maintenance
      148. Transcription-coupled DNA Repair
      149. The Transcription/DNA Repair Factor TFIIH
      150. Transposons as Natural and Experimental Mutagens
      151. Trinucleotide Repeat Expansions: Disorders
      152. Trinucleotide Repeat Expansions: Mechanisms and Disease Associations
      153. Uniparental Disomy in Cancer – A New Tool in Molecular Cancer
      154. Virus-Induced Human Oncogenesis
      155. Y-chromosome-linked Traits
    4. DNA Structure and function
    5. Evolution of Coding and Functional Modules
    6. General Molecular Biology
    7. Genetic Code
    8. Mechanisms of Cell Death, Senescence and Metabolism
    9. Nonchromosomal DNA
    10. Noncoding RNA
    11. Posttranscriptional Modification
    12. Posttranslational Modification
    13. Protein Degradation
    14. RNA Structure and Function
    15. Techniques and Tools in Molecular Biology
    16. Transcription of DNA
    17. Transcriptional Regulation
    18. Translation of RNA
    19. Translational Regulation
  11. Neuroscience
  12. Plant Science
  13. Science & Society
  14. Structural Biology
  15. Virology

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