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Hemostasis and Thrombosis Protocols (Methods in Molecular Medicine)
 
 
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Hemostasis and Thrombosis Protocols (Methods in Molecular Medicine) [Hardcover]

David J. Perry (Editor), K. John Pasi (Editor)

Price: $114.50 & this item ships for FREE with Super Saver Shipping. Details
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Book Description

August 4, 1999 0896034194 978-0896034198 1
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.

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Editorial Reviews

Review

"...The book by Perry and Pasi confirms ...that with good recipes and kits the DNA analysis of disorders of thrombosis and hemostasis is indeed feasible for many diagnostic laboratories. The book describes in great detail a variety of laboratory protocols aimed primarily at analyzing inherited disorders of the hemostatic system. These protocols vary from simple procedures to detect factor V Leiden and prothrombin 20210 to elaborate techniques for finding mutations in disorders like hemophilia A or protein S deficiency. In addition ...this book is a useful book for those attempting to introduce or maintain DNA analysis in their laboratory...laboratory technicians may find many useful suggestions to improve their work."-Haemostasis

"Each cheater is presented in a recipe format so that the methods can e reproduced. All chapters subdivided into sections for easy reading: introduction, material, methods, and notes. ...The chapters on mutation detection in clotting factor deficiencies will be useful to hemostasis laboratories that are interested in carrier detection, prenatal diagnosis, or research. The chapters on von Willbrand factor multimer analysis, factor V Leiden mutation, an prothrombin G20210A mutation will be useful to hemostasis laboratories that want to set up these important diagnostic tests...This manual does well at meeting its goal of providing a broad overview of techniques used in the analysis of hemostatic disorders and providing strategies for future problem solving. It will be a great utility to hemostasis laboratories that wish to advance their research or diagnostic capabilities."-Modern Pathology

"very valuable for the laboratory staff in charge of gene analysis of known genetic defects in known diseases of hemostasis and thrombosis." - Bloodline

From the Back Cover

In Hemostasis and Thrombosis Protocols, 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 Willebrands Disease, Factor XI and antithrombin deficiency, protein'S deficiency, factor V Leiden mutation, and other problems. The protocols reflect the many major advances that have occurred in our understanding of the molecular genetics of normal hemostasis and it variants, as well as of the coagulation cascade itself. Suitable for both diagnostic and research laboratories, Hemostasis and Thrombosis Protocols enables experienced and novice investigators alike readily to master the complexities of research on molecular hemostasis and thrombosis, as well as work toward the development of productive new molecular diagnostics.

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Inside This Book (learn more)
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
schedule gel, nuclear lysis buffer, antithrombin gene, cold cell lysis buffer, silanizing solution, rapid thermal ramp, sucrose loading buffer, magnetic separation unit, polyadenylation signal region, sequencing master mix, multimer bands, wedge gel, enzyme dilution buffer, benchtop microfuge, multimeric analysis, sequencing plates, mussel glycogen, normal control plasma, mismatch method, barbitone buffer, termination mix, melting domain, formamide loading dye, plasma prothrombin levels, amplification primer
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Humana Press Inc, Molecular Medicine, Perkin Elmer, Nucleic Acids Res, Inherited Platelet Receptor Disorder, Glass Milk, Life Technologies, Promoter Studies, Human Genetics, Pharmacia Biotech, Ploos Van Amstel, Materials All, New England Biolabs, Amplification of the Factor, Boehringer Mannheim, Cold Spring Harbor, Interpretation of Results, Isolation of Genomic, Methods Enzymol, Functional Analysis of the Mutation, Inner Segment, Practical Approach, Human Mol, Inversion Mutation Analysis, Isolation of Mononuclear Cells
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