Hemostasis and Thrombosis Protocols
posted in Library, Molecular Medicine |
Leading experimentalists describe in detail their proven, cutting-edge methods for research on hemostasis and thrombosis, as well as their diagnostics. The techniques range from widely used basic assays to methods that are specialized for mutational analysis and specific disorders. Readily reproducible, these powerful methods can be used to screen for such inherited disorders as hemophilia A and B, von Willebrand’s Disease, factor XI and antithrombin deficiency, protein S deficiency, factor V Leiden mutation, and other problems. Hemostasis and Thrombosis Protocols reflects the many major advances that have occurred in our understanding of the molecular genetics of normal hemostasis and its variants. It enables experienced and novice investigators readily to master the complexities of research on molecular hemostasis and thrombosis, as well as work toward the development of new molecular diagnostics. Ed. Perry, David J.; Pasi, K. John
Table of Contents Hemostasis: Components and Processes (pp. 3-22) Pasi, K. John Isolation of DNA and RNA (pp. 25-30) Perry, David J. Amplification of DNA and RNA by PCR (pp. 31-38) Perry, David J. Direct Sequencing of PCR Products (pp. 39-48) Perry, David J. Solid-Phase Sequencing of Biotinylated PCR Products with Streptavidin-Coated Magnetic Beads (pp. 49-54) Perry, David J. Automated DNA Sequencing (pp. 55-62) Devereux, Helen L. Detection of DNA by Silver Staining (pp. 63-64) Perry, David J.; Peyvandi, Flora Promoter Studies in Hemostasis (pp. 65-82) Winship, Peter R.; Spray, Jonathan R. K. Detection of Mutations and Polymorphisms in Clotting Factors by Denaturing Gradient Gel Electrophoresis (pp. 85-104) Schwaab, Rainer; Schmidt, Winfried Screening for Mutations in DNA by Single-Stranded Conformation Polymorphism (SSCP) Analysis (pp. 105-110) Perry, David J. Screening for DNA Heteroduplexes in the Factor VII Gene Using Ethylene Glycol Gel Electrophoresis of Solvent-Treated 32P-Labeled PCR Products (pp. 111-116) Baker, Peter Detection of Mutations Causing Hemophilia A Using an In Vitro Coupled Transcription and Translation System (pp. 117-124) Ononye, Chike; Jenkins, P. Vincent Screening for Mutations in the Human Antithrombin Gene by Hydrolink D-5000??? and MDE??? Gel Electrophoresis (pp. 125-130) Perry, David J. Detection of Mutations in Hemophilia A Patients by Chemical Cleavage of Mismatch Method (pp. 133-150) Waseem, Naushin H.; Bagnall, Richard; Green, Peter M.; Giannelli, Francesco Inversion Mutation Analysis in Hemophilia A by Restriction Enzyme Analysis and Southern Blotting (pp. 151-158) Ononye, Chike; Jenkins, P. Vincent Hemophilia B Mutational Analysis (pp. 159-168) Green, Peter M. Screening for Candidate Mutations Causing von Willebrand???s Disease (vWD) (pp. 169-178) Jenkins, P. Vincent Use of Intron 40 VNTR I in vWD Gene Tracking (pp. 179-186) Enayat, Mohammed S.; Surdhar, Gurcharan K. Multimeric Analysis of von Willebrand Factor (pp. 187-200) Enayat, Mohammed S. Identification of Mutations in the Human Factor VII Gene (pp. 201-210) Baker, Peter M. Molecular Analysis in Factor XI Deficiency (pp. 211-222) Johnson, Karen M.; McVey, John H. Mutational Analysis in Antithrombin Deficiency (pp. 223-230) Perry, David J. Ectopic Transcript Analysis in Human Antithrombin Deficiency (pp. 231-238) Perry, David J. Mutational Analysis of the Human Protein C Gene (pp. 239-248) Luddington, Roger Analysis of the Protein S Gene in Protein S Deficiency (pp. 249-268) Sala, Nuria; Espinosa-Parrilla, Yolanda Screening for the G to A Transition at Position 20210 in the 3???-Untranslated Region (UTR) of the Prothrombin Gene (pp. 269-274) Brown, Karen P. Screening for the Factor V Leiden Mutation (pp. 275-286) Brown, Karen P. Multiplex PCR for Detection of the Prothrombin 3???-UTR (G20210A) Polymorphism and the Factor V Leiden Mutation (pp. 287-290) Mellars, Gillian; Jenkins, P. Vincent; Perry, David J. Isoelectric Focusing and Immunodetection of Plasma Antithrombin (pp. 291-296) Daly, Martina Characterization of Heparin Binding Variants of Antithrombin by Crossed Immunoelectrophoresis in the Presence of Heparin (pp. 297-302) Daly, Martina The Determination of Amino Acid Sequence Abnormalities in Proteins by HPLC Peptide Analysis (pp. 303-310) Williamson, David Molecular Biological Identification and Characterization of Inherited Platelet Receptor Disorders (pp. 313-336) Basani, Ramesh B.; Richberg, Mark; Poncz, Mortimer In Vitro Expansion of Megakaryocytes from Peripheral Blood Hematopoietic Progenitors (pp. 337-346) Thornton, Michael A.; Poncz, Mortimer Molecular Biology Studies with Primary Megakaryocytes (pp. 347-354) Shou, Yaping; Poncz, Mortimer