Encyclopedia of Medical Genomics and Proteomics, 2 Volume Set
eBook - PDF

Encyclopedia of Medical Genomics and Proteomics, 2 Volume Set

  1. 1,480 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Encyclopedia of Medical Genomics and Proteomics, 2 Volume Set

Book details
Table of contents
Citations

About This Book

The Encyclopedia of Medical Genomics and Proteomics offers trail-blazing studies and authoritative contributions from more than 400 specialists on molecular diagnostics, genomics, microbiology, genetics, pharmacogenetics, pathology, forensics, tissue and cell typing, and disease susceptibility. It features coverage of key methods and technologies such as predictive genetic and pharmacogenetic testing and tissue typing for transplantation. It compiles recommendations, research, spanning critical subjects such as DNA sequencing, point-of-care testing, quality management, oncology, cancer screening, and ethical issues related to genetics.

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Yes, you can access Encyclopedia of Medical Genomics and Proteomics, 2 Volume Set by Jürgen Fuchs,Maurizio Podda in PDF and/or ePUB format, as well as other popular books in Medicine & Pharmacology. We have over one million books available in our catalogue for you to explore.

Information

Publisher
CRC Press
Year
2004
ISBN
9780203997352
Edition
1
Topic
Medicine
Subtopic
Pharmacology

Table of contents

  1. Book Cover
  2. Half-Title
  3. Title
  4. Copyright
  5. Dedication
  6. Contributors
  7. Contents
  8. Preface
  9. Keratin Disorders
  10. Lamivudine resistance-associated gene mutations
  11. Laser capture microdissection
  12. Legionella spp.
  13. Ligase chain reaction(LCR) and ligase detection reaction (LDR)
  14. Lightup probes
  15. Liposomal nonviral delvery vehicles
  16. Listeria spp.: DMA probes and conventional PCR assays
  17. Listeria spp.: Other DMA-Based identification procedures and DMA-based typing methods
  18. Long-distance PCR
  19. Long QT syndrome
  20. Loop-mediated Isothermal amplification
  21. MALDI-MS coupled with capillary LC and CE
  22. MALDI-TOF mass spectrometry
  23. Marfan syndrome and related fibrillinopathies
  24. Mass spectrometric genotyping of single
  25. Mastocytosis—c-Kit mutations
  26. Medullary thyroid carcinoma (MTC) and multiple endocrine neoplasia (MEN 1, MEN 2)
  27. Medulloblastoma—MYC messenger RNA expression
  28. Melanoma biomakers—Molecular profiling and its clinical implications
  29. Melanoma, Familial
  30. Metabonomics and its role in disease diagnosis
  31. Microarrays—confocal scanning
  32. Microarrays—Detecting DMA copy-number changes
  33. Microarrays—Electronic microarrays
  34. Fabricating microarrays
  35. Microarrays—Standard operating procedures
  36. Microduplication syndromes—17p11.2 Duplications, proximal 15 Duplications, and cat eye syndrome
  37. Microplate array diagonal gel electrophoresis for SNP and microsatellite genotyping and for mutation scanning
  38. Microsatellite Instability
  39. Molecular beacons and other Hairpin probes
  40. Mucopolysaccharidosis types IMA and 11 1B
  41. Multiplex real-time PCR
  42. Murrary valley encephalitis virus
  43. Mycobacteria, atypical
  44. Mycobacterium leprae
  45. Mycoplasma spp. and ureaplasma spp.
  46. Myelodysplastic syndrome—Risk class analysis by microarray
  47. Myotonic dystrophy
  48. Nanotechnology-based lab-on-a-chip devices
  49. NEBcutter—A program to cleave DNA with restriction enzymes
  50. Neisseria meningitidis
  51. Nested PCR and multiplex nested PCR
  52. Neuroblastoma—Clinical implications of real-time PCR
  53. Neurofibromatosis type 1
  54. Neuronal ceroid lipofuscinoses
  55. Nipah virus
  56. NIST references materials for medical testing
  57. Nuclei acid sequence-based amplifications (NASBA) and transcription mediated amplification (TMA)
  58. Obligonucleotide design for PCR primers and microarrays probes
  59. Onchocerca volvulus
  60. Orthopoxviruses—Monkeypox, cowpox, vaccinia, Camel pox, Mousepox
  61. Osteogenesis imperfecta anna Gajko-Galicka
  62. p53 status of tumors: Diagnostic, prognostic, and Therapeutic exploitation
  63. Padlock probes
  64. Paraoxonase (PONI) gene polymorphisms
  65. Parkinsonism, autosomal dominant
  66. Parovirus B19
  67. Patent aspects in proteomics and genomics
  68. PCR and RT-PCR analysis in archival postmortem tissues
  69. PCR chemiluminescent immunoassay (PCR-CLEIA)
  70. Personalised medicine
  71. Peutz-Jeghers syndrome
  72. Plasmodium spp.—Detection by molecular techniques
  73. Plasmodium spp.-Detection of Drug Resistance by Molecular Techniques
  74. Platelet Antigen Genotyping
  75. PML/RARA and RARA FISH in follow-up of acute promyelocytic leukemia
  76. PNA-FISH—Applications for chromosomal analysis and other forms of genetic testing
  77. PNA-FISH-Applications for Rapid Diagnosis of Bloodstream Infections
  78. Pneumocystis jiroveci
  79. Point-of-Care Testing (POCT)-Nucleic Acid-Based Testing in a Point-of-Care Setting
  80. Polymer Nonviral Delivery Vehicles
  81. Polymerase Chain Reaction (PCR)
  82. Prader-Willi Syndrome
  83. Preimplantation Genetic Diagnosis-An Overview
  84. Preimplantation Genetic Diagnosis-Single-Cell DMA and FISH Analysis
  85. Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Blood
  86. Prenatal Diagnosis Using Fetal Cells and Cell-Free Fetal DMA in Maternal Blood
  87. Protein microarrays
  88. Protein trucation test (PTT)
  89. Pseudoxanthoma Elasticum
  90. Pulsed field gel electrophoresis (PFGE)
  91. Pyrosequencing
  92. Quality of In-house made high-Density microarrays
  93. Ramification amplification
  94. Real-time PCR
  95. Real-time PCR platforms
  96. Real-Time reverse transcription PCR
  97. Restriction Fragment Length Polymorphism (RFLP)-Application for Mycobacteria Typing '
  98. Retinobalstoma
  99. Retinoschisis, juvenile (X-Linked)
  100. Retroviral vectors
  101. Reversed line blot hybridization
  102. Rh Genotyping—Clinical aspects
  103. Ribotyping
  104. RNA strorage
  105. Rolling-circle amplification (RCA)
  106. Rota virus
  107. Salmonella spp.
  108. Serial analysis of gene expression (SAGE) technology
  109. Single cell gel electrophoresis assay (Comet Assay)
  110. Single Nucleotide Polymorphism (SNP) Genotyping Techniques-An Overview
  111. Single-tube two-Round real-time PCR
  112. SNP Genotyping using single molecule fluorescence
  113. Spinal muscular atrophy
  114. Staphylococcus aureus-Detection of MRSA
  115. Staphylococcus aureus-Toxin Detection
  116. Streptococcus pneumoniae
  117. Streptococcus, Group A
  118. Subtelomeric Rearrangements in Unexplained Mental Retardation
  119. TaqMan oligoprobes
  120. Temporal Temperature Gradient Gel Electrophoresis
  121. Tetracycline Resistance
  122. Thyroid Cancer-Detection of Tumor Cells by Molecular Methods
  123. Tissue Microarrays in Pathology
  124. Treponema pallidum, T.pertenue, T.endemicum, and T.carateum
  125. Trichinella spp.
  126. Trichomonas spp.
  127. Tropheryma whipplei
  128. Trypanosoma cruzi
  129. Tuberous Sclerosis
  130. Vibrio cholerae
  131. Vibrio vulnificus
  132. Viral Encephalitis-Japanese Encephalitis, Tick-Born Encephalitis, and St. Louis Encephalitis
  133. Viral Hemorrhagic Fevers-Arenaviridae, Filoviridae, Bunyaviridae, and Flaviviridae
  134. von Hippel-Lindau Disease
  135. von Willebrand Disease
  136. Wilson Disease
  137. Wolff-Parkinson-White Syndrome, Familial
  138. Wuchereria bancrofti
  139. Yersinia spp.
  140. Index