eLS

eLS

Online ISBN: 9780470015902

DOI: 10.1002/047001590X

Browse by Topic

  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
    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
      1. Absolute Pitch: Genetics
      2. Addiction and Genes: Animal Models
      3. Adoption Strategies
      4. Alcoholism and Drug Addictions
      5. Allele Spectrum of Human Genetic Disease
      6. Allelic and Locus Heterogeneity
      7. Alternative Processing: Neuronal Nitric Oxide Synthase
      8. Analysis of Gene–Gene Interactions Underlying Human Disease
      9. Anticipation
      10. Assessing Genetic Variants of Uncertain Significance: The Example of Breast Cancer
      11. Assessing Genetic Variants of Uncertain Significance: The Example of Lynch Syndrome
      12. Balancing Selection in Human Evolution
      13. Balancing Selection in the Human Genome
      14. Behaviour Genetics – Human
      15. Behavioural Genetics in the Postgenomics Era
      16. Bioethics: ELSI
      17. You have free access to this content
        Bioinformatics
      18. Blood Group Genetics
      19. Blood Groups: Molecular Genetic Basis
      20. Causes and Consequences of Structural Genomic Alterations in the Human Genome
      21. Characterising Structural Variation by Means of Next-Generation Sequencing
      22. Chromosome 2
      23. Chromosome 3
      24. Chromosome 4
      25. Chromosome 5
      26. Chromosome 6
      27. Chromosome 7
      28. Chromosome 9
      29. Chromosome 1
      30. Chromosome 10
      31. Chromosome 11
      32. Chromosome 12
      33. Chromosome 13
      34. Chromosome 14
      35. Chromosome 15
      36. Chromosome 16
      37. Chromosome 17
      38. Chromosome 18
      39. Chromosome 19
      40. Chromosome 20
      41. Chromosome 22
      42. Chromosome 8
      43. Clinical and Phenotypic Relevance of cis-Acting Regulatory Polymorphisms
      44. Comparative Genomic Hybridization in the Study of Human Disease
      45. CpG Dinucleotides and Human Disorders
      46. Cytochrome P450 (CYP) Gene Superfamily
      47. Development and Role of the Human Reference Sequence in Personal Genomics
      48. Direct-to-Consumer Genetic Testing
      49. Disability, Human Rights and Contemporary Genetics
      50. Disease Associations: Human Leukocyte Antigen (HLA) and Apolipoprotein E (APOE) Gene
      51. Dopamine D4 Receptor (DRD4) Box Score
      52. Drug-Metabolising Enzymes: Genetic Polymorphisms
      53. Dysmorphic Syndromes
      54. Electroencephalogram (EEG) and Evoked Potentials
      55. Ethnicity and Disease
      56. Evolution of Genetic Resistance/Susceptibility to Malaria Infection
      57. Evolution of Skin Pigmentation Differences in Humans
      58. An Evolutionary Genetic Framework for Heritable Disorders
      59. Family-based Association Test (FBAT)
      60. Forensic Genetics
      61. Genetic Determinants of Human Life-Span
      62. Genetic Disease in the Ashkenazim: Role of a Founder Effect
      63. Genetic Factors Involved in Human Susceptibility to Infection by Schistosomiasis
      64. Genetic Isolates and Behavioral Gene Searches
      65. Genetic Risk
      66. Genetic Screening and Testing
      67. Genetic Susceptibility to Autoimmune Disorders
      68. Genetic Variation: Human
      69. You have free access to this content
        Genetic Variation: Polymorphisms and Mutations
      70. Genetic, Epigenetic and Environmental Influences on Human Tooth Size, Shape and Number
      71. Genetics and Genomics of Human Longevity
      72. Genetics and the Origin of the Finns
      73. Genetics of Adaptation to High Altitude
      74. Genetics of Adult Antisocial Behaviour
      75. Genetics of Age at Menarche
      76. Genetics of Athletic Performance
      77. Genetics of Birth Weight
      78. Genetics of Disordered Gambling
      79. The Genetics of Human Aggressive Behaviour
      80. Genetics of Human Social Behaviour
      81. Genetics of Nicotine Addiction
      82. Genetics of Preterm Birth
      83. Genetics of Susceptibility to Leprosy
      84. Genetics of Susceptibility to Mycobacterial Disease
      85. Genetics of Taste Perception
      86. Genome Organization: Human
      87. Genome-wide Association Studies of Cancers
      88. Genotype–Phenotype Relationships
      89. Genotype–Phenotype Relationships: Fatal Familial Insomnia and Creutzfeldt–Jakob Disease
      90. Germline Copy Number Variation and Cancer Risk
      91. Germline Genomic Copy Number Variation Contribution to Cancer Predisposition
      92. HapMap Project
      93. Heritability
      94. Heritability Wars
      95. Human Genetics: Online Resources
      96. Human Genome Diversity Project (HGDP)
      97. Human Genome Diversity Studies: Impact on Indigenous Communities
      98. Human Genome Project: Importance in Clinical Genetics
      99. Human Immunodeficiency Virus (HIV) Infection: Genetics
      100. Human Leukocyte Antigen (HLA) System and Human Disorders
      101. Human Variation Databases
      102. You have free access to this content
        Immunoglobulin Gene Construction: Human
      103. Impact of Missense Variants on Protein–Protein Interactions
      104. Imprinting (Mammals)
      105. Infectious Diseases: Predisposition
      106. Intelligence and Cognition
      107. Interpreting Disease Relevance of Amino Acid Substitutions
      108. Is There a Role for Genetic Testing in Sports?
      109. Language and Genes
      110. Longevity: Genetics
      111. Major Histocompatibility Complex (MHC)
      112. Major Histocompatibility Complex (MHC) Genes
      113. Major Histocompatibility Complex: Human
      114. Malarial Resistance and Susceptibility, Genetics of
      115. Markov Chain Monte Carlo Methods
      116. Metabolism: Hereditary Errors
      117. Microarrays and Single Nucleotide Polymorphism (SNP) Genotyping
      118. Microdeletion Syndromes
      119. MicroRNA Polymorphisms
      120. Microsatellite Instability
      121. Microsatellites
      122. Mitochondrial DNA Polymorphisms
      123. Molecular Basis of Complex Traits
      124. Molecular Genetic Causes of Discordance in Monozygotic Twins
      125. Molecular Genetics of Anxiety
      126. Molecular Genetics of Hyperuricaemia and Gout
      127. Molecular Genetics of Hypophosphatasia
      128. Molecular Genetics of Type 1 Diabetes
      129. Molecular Genetics of Variability in Human Pain
      130. Molecular Mechanisms Underlying Pathogenic Missense Mutations
      131. Multidrug Resistance in Cancer: Genetics of ABC Transporters
      132. Mutations in Human Genetic Disease
      133. Mutations: Penetrance
      134. Next-generation Sequencing in Clinical Molecular Diagnostics
      135. Personal Identity: Genetics and Determinism
      136. Pharmacogenetics and Pharmacogenomics
      137. Pharmacogenetics of Pain
      138. Polymorphism of TNF Genes and Disease Susceptibility
      139. Polymorphisms: Origins and Maintenance
      140. Population Genetics: Historical Aspects
      141. Population History and Linkage Disequilibrium
      142. Quantitative Genetics
      143. ‘Race’: What Biology Can Tell Us about a Social Construct
      144. Recent Insights into the Genetics of Plasma Triglycerides and Possible Causal Mechanisms in Cardiovascular Disease
      145. Restriction Fragment Length Polymorphism (RFLP)
      146. Rhesus Haemolytic Disease of the Newborn
      147. Selection and Common Monogenic Disease
      148. Selective Constraints and Human Disease Genes: Evolutionary and Bioinformatics Approaches
      149. Sexual Orientation
      150. Sexual Orientation: Genetics
      151. Single Nucleotide Polymorphism (SNP)
      152. Single Nucleotide Polymorphisms (SNPs): Identification and Scoring
      153. Single Nucleotide Polymorphisms in Human Disease and Evolution: Phylogenies and Genealogies
      154. Somatic Hypermutation in Antibody Evolution
      155. Spectrum of Point Mutations in the Human Genome and Major Subpopulations
      156. Structural Diversity of the Human Genome and Disease Susceptibility
      157. Susceptibility to Human Infectious Diseases, Genetics of
      158. Susceptibility to Malaria, Genetics of
      159. Synonymous Mutations as a Cause of Human Genetic Disease
      160. Thalassaemias
      161. Twin Methodology
      162. Twin Studies
      163. Twin Studies: Software and Algorithms
      164. Unravelling the Mystery of Sudden Cardiac Death Through Genetic Approaches
      165. Use of Personalized Genomic Information
      166. Variable Drug Response: Genetic Evaluation
      167. Variation: Measures
      168. Absolute Pitch: Genetics
      169. Addiction and Genes: Animal Models
      170. Adoption Strategies
      171. Alcoholism and Drug Addictions
      172. Allele Spectrum of Human Genetic Disease
      173. Allelic and Locus Heterogeneity
      174. Alternative Processing: Neuronal Nitric Oxide Synthase
      175. Analysis of Gene–Gene Interactions Underlying Human Disease
      176. Anticipation
      177. Assessing Genetic Variants of Uncertain Significance: The Example of Breast Cancer
      178. Assessing Genetic Variants of Uncertain Significance: The Example of Lynch Syndrome
      179. Balancing Selection in Human Evolution
      180. Balancing Selection in the Human Genome
      181. Behaviour Genetics – Human
      182. Behavioural Genetics in the Postgenomics Era
      183. Bioethics: ELSI
      184. You have free access to this content
        Bioinformatics
      185. Blood Group Genetics
      186. Blood Groups: Molecular Genetic Basis
      187. Causes and Consequences of Structural Genomic Alterations in the Human Genome
      188. Characterising Structural Variation by Means of Next-Generation Sequencing
      189. Chromosome 2
      190. Chromosome 3
      191. Chromosome 4
      192. Chromosome 5
      193. Chromosome 6
      194. Chromosome 7
      195. Chromosome 9
      196. Chromosome 1
      197. Chromosome 10
      198. Chromosome 11
      199. Chromosome 12
      200. Chromosome 13
      201. Chromosome 14
      202. Chromosome 15
      203. Chromosome 16
      204. Chromosome 17
      205. Chromosome 18
      206. Chromosome 19
      207. Chromosome 20
      208. Chromosome 22
      209. Chromosome 8
      210. Clinical and Phenotypic Relevance of cis-Acting Regulatory Polymorphisms
      211. Comparative Genomic Hybridization in the Study of Human Disease
      212. CpG Dinucleotides and Human Disorders
      213. Cytochrome P450 (CYP) Gene Superfamily
      214. Development and Role of the Human Reference Sequence in Personal Genomics
      215. Direct-to-Consumer Genetic Testing
      216. Disability, Human Rights and Contemporary Genetics
      217. Disease Associations: Human Leukocyte Antigen (HLA) and Apolipoprotein E (APOE) Gene
      218. Dopamine D4 Receptor (DRD4) Box Score
      219. Drug-Metabolising Enzymes: Genetic Polymorphisms
      220. Dysmorphic Syndromes
      221. Electroencephalogram (EEG) and Evoked Potentials
      222. Ethnicity and Disease
      223. Evolution of Genetic Resistance/Susceptibility to Malaria Infection
      224. Evolution of Skin Pigmentation Differences in Humans
      225. An Evolutionary Genetic Framework for Heritable Disorders
      226. Family-based Association Test (FBAT)
      227. Forensic Genetics
      228. Genetic Determinants of Human Life-Span
      229. Genetic Disease in the Ashkenazim: Role of a Founder Effect
      230. Genetic Factors Involved in Human Susceptibility to Infection by Schistosomiasis
      231. Genetic Isolates and Behavioral Gene Searches
      232. Genetic Risk
      233. Genetic Screening and Testing
      234. Genetic Susceptibility to Autoimmune Disorders
      235. Genetic Variation: Human
      236. You have free access to this content
        Genetic Variation: Polymorphisms and Mutations
      237. Genetic, Epigenetic and Environmental Influences on Human Tooth Size, Shape and Number
      238. Genetics and Genomics of Human Longevity
      239. Genetics and the Origin of the Finns
      240. Genetics of Adaptation to High Altitude
      241. Genetics of Adult Antisocial Behaviour
      242. Genetics of Age at Menarche
      243. Genetics of Athletic Performance
      244. Genetics of Birth Weight
      245. Genetics of Disordered Gambling
      246. The Genetics of Human Aggressive Behaviour
      247. Genetics of Human Social Behaviour
      248. Genetics of Nicotine Addiction
      249. Genetics of Preterm Birth
      250. Genetics of Susceptibility to Leprosy
      251. Genetics of Susceptibility to Mycobacterial Disease
      252. Genetics of Taste Perception
      253. Genome Organization: Human
      254. Genome-wide Association Studies of Cancers
      255. Genotype–Phenotype Relationships
      256. Genotype–Phenotype Relationships: Fatal Familial Insomnia and Creutzfeldt–Jakob Disease
      257. Germline Copy Number Variation and Cancer Risk
      258. Germline Genomic Copy Number Variation Contribution to Cancer Predisposition
      259. HapMap Project
      260. Heritability
      261. Heritability Wars
      262. Human Genetics: Online Resources
      263. Human Genome Diversity Project (HGDP)
      264. Human Genome Diversity Studies: Impact on Indigenous Communities
      265. Human Genome Project: Importance in Clinical Genetics
      266. Human Immunodeficiency Virus (HIV) Infection: Genetics
      267. Human Leukocyte Antigen (HLA) System and Human Disorders
      268. Human Variation Databases
      269. You have free access to this content
        Immunoglobulin Gene Construction: Human
      270. Impact of Missense Variants on Protein–Protein Interactions
      271. Imprinting (Mammals)
      272. Infectious Diseases: Predisposition
      273. Intelligence and Cognition
      274. Interpreting Disease Relevance of Amino Acid Substitutions
      275. Is There a Role for Genetic Testing in Sports?
      276. Language and Genes
      277. Longevity: Genetics
      278. Major Histocompatibility Complex (MHC)
      279. Major Histocompatibility Complex (MHC) Genes
      280. Major Histocompatibility Complex: Human
      281. Malarial Resistance and Susceptibility, Genetics of
      282. Markov Chain Monte Carlo Methods
      283. Metabolism: Hereditary Errors
      284. Microarrays and Single Nucleotide Polymorphism (SNP) Genotyping
      285. Microdeletion Syndromes
      286. MicroRNA Polymorphisms
      287. Microsatellite Instability
      288. Microsatellites
      289. Mitochondrial DNA Polymorphisms
      290. Molecular Basis of Complex Traits
      291. Molecular Genetic Causes of Discordance in Monozygotic Twins
      292. Molecular Genetics of Anxiety
      293. Molecular Genetics of Hyperuricaemia and Gout
      294. Molecular Genetics of Hypophosphatasia
      295. Molecular Genetics of Type 1 Diabetes
      296. Molecular Genetics of Variability in Human Pain
      297. Molecular Mechanisms Underlying Pathogenic Missense Mutations
      298. Multidrug Resistance in Cancer: Genetics of ABC Transporters
      299. Mutations in Human Genetic Disease
      300. Mutations: Penetrance
      301. Next-generation Sequencing in Clinical Molecular Diagnostics
      302. Personal Identity: Genetics and Determinism
      303. Pharmacogenetics and Pharmacogenomics
      304. Pharmacogenetics of Pain
      305. Polymorphism of TNF Genes and Disease Susceptibility
      306. Polymorphisms: Origins and Maintenance
      307. Population Genetics: Historical Aspects
      308. Population History and Linkage Disequilibrium
      309. Quantitative Genetics
      310. ‘Race’: What Biology Can Tell Us about a Social Construct
      311. Recent Insights into the Genetics of Plasma Triglycerides and Possible Causal Mechanisms in Cardiovascular Disease
      312. Restriction Fragment Length Polymorphism (RFLP)
      313. Rhesus Haemolytic Disease of the Newborn
      314. Selection and Common Monogenic Disease
      315. Selective Constraints and Human Disease Genes: Evolutionary and Bioinformatics Approaches
      316. Sexual Orientation
      317. Sexual Orientation: Genetics
      318. Single Nucleotide Polymorphism (SNP)
      319. Single Nucleotide Polymorphisms (SNPs): Identification and Scoring
      320. Single Nucleotide Polymorphisms in Human Disease and Evolution: Phylogenies and Genealogies
      321. Somatic Hypermutation in Antibody Evolution
      322. Spectrum of Point Mutations in the Human Genome and Major Subpopulations
      323. Structural Diversity of the Human Genome and Disease Susceptibility
      324. Susceptibility to Human Infectious Diseases, Genetics of
      325. Susceptibility to Malaria, Genetics of
      326. Synonymous Mutations as a Cause of Human Genetic Disease
      327. Thalassaemias
      328. Twin Methodology
      329. Twin Studies
      330. Twin Studies: Software and Algorithms
      331. Unravelling the Mystery of Sudden Cardiac Death Through Genetic Approaches
      332. Use of Personalized Genomic Information
      333. Variable Drug Response: Genetic Evaluation
      334. Variation: Measures
    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

SEARCH