Description
Humana Press Molecular Pathology Protocols 1st Editon 2010 Softbound by Anthony A. Killeen
The era of molecular pathology has arrived. From its promising beg- nings in research laboratories, the field has grown, and continues to grow, to become a vital part of the care of an ever-increasing number of patients. Because of its recent emergence from the research taboratory, many molecuIar pathology protocols we still to be found in the primary litcramre, and have not appeared in a text. MO~PCU~Q~ Padhoiogy Protocob contains la- ratory protocoIs that have been developed by many of the authors for use in clinical molecular pathology laboratories and describe in detail Row to perform these assays. This book is therefore intended for clinical laboratory use by medical technologists and pathologists. It will dso be of interest to research workers who are performing these assays. In its broadest meaning, pathology is the study of disease, and therefore it follows that any disease for which the molecular basis is understood would be suitable as a topic for inclusion in this work. When seiecting protocols, it was necessary to place limits on the number of chapters that could be feasibly presented in a single work. Those protoculs that were selected are performed more frequently, or have achieved recognition as having important diagnostic utility in contemporary practice. A decision was made to exclude inherited genetic diseases with certain exceptions, such as those diseases that are associated with thrombotic states and are part of the traditional dumain of pathology. DNA Extraction from Paraffin-Embedded Tissues.- DNA Extraction from Fresh or Frozen Tissues.- RNA Extraction from Fresh or Frozen Tissues.- Single-Strand Conformation Polymorphism Analysis of Mutations in Exons 4-8 of the TP53 Gene.- Cleavase® Fragment Length Polymorphism Analysis for Genotyping and Mutation Detection.- Detection of Telomerase by In Situ Hybridization and by the Polymerase Chain Reaction-Based Telomerase Activity Assay.- Detection of Microsatellite Instability.- Polymerase Chain Reaction Clonality Assays Based on X-Linked Genes.- Fluorescent In Situ Hybridization.- HER-2/neu Oncogene Amplification Determined by Fluorescence In Situ Hybridization.- A Nested Reverse Transcription-Polymerase Chain Reaction Assay to Detect BCR/abl.- Detection of t(15;17)(q24;q21), inv(16)/t(16;16)(p13;q22), and t(8;21)(q22;q22) Anomalies in Acute Myeloid Leukemias.- Detection of t(14; 18)(q32;q21)-Associated BCL-2/JH Gene Fusion in Non-Hodgkin Lymphoma.- Detection of Breast Cancer Cells Using Immunomagnetic Beads and Reverse Transcriptase Polymerase Chain Reaction.- Molecular Detection of Circulating Prostate Cancer Cells.- Methods to Detect Clonal Gene Rearrangements in Lymphomas and Leukemias.- Monitoring of Bone Marrow Transplant Engraftment.- Direct Molecular Diagnosis of Multiple Endocrine Neoplasia Type 1.- Molecular Detection of Multiple Endocrine Neoplasia Type 2.- Assay for Detecting the I1307K Susceptibility Allele within the Adenomatous Polyposis ColiGene.- Detection of Human Papillomaviruses by Polymerase Chain Reaction and In Situ Hybridization.- Molecular Methods for Detecting Epstein-Barr Virus (Part I).- Molecular Methods for Detecting Epstein-Barr Virus (Part II).- Molecular Methods for Detecting Epstein-Barr Virus (Part III).- Molecular Detection of Kaposi’s Sarcoma-Associated Herpesvirus/ Human Herpesvirus-8.- Diagnostic Applications of Quantitative Polymerase Chain Reaction for Cytomegalovirus.- A Colorimetric Microtiter Plate Polymerase Chain Reaction System That Detects Herpes Simplex Virus in Cerebrospinal Fluid and Discriminates Genotypes 1 and 2.- Detection and Typing of Hepatitis C Virus.- Detection and Speciation of Mycobacteria in Formalin-Fixed, Paraffin-Embedded Tissue Sections.- Ultrasensitive Quantitation of Human Immunodeficiency Virus Type 1 RNA in Plasma by the AMPLICOR and COBAS AMPLICOR HIV-1 MONITOR™ Tests.- Molecular Diagnosis of Hereditary Thrombotic Disorders.- Prenatal Genotyping of the RhD Locus to Identify Fetuses at Risk for Hemolytic Disease of the Newborn.- Molecular Diagnosis of Hereditary Hemochromatosis.- Genotyping of Apolipoprotein E.- Genotyping for Functionally Important Human CYP2D6*4 (B) Mutation Using TaqMan Probes.