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|a 9781592592487 (e-ISBN)
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|a 1592592481 (e-ISBN)
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|a 0585244014 (netLibrary e-ISBN)
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|a (OCoLC)45729923
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|a (OCoLC)45729923
|z (OCoLC)80551729
|z (OCoLC)232302212
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|b eng
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|a dlr
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|a HCDD
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|a E-Book RC647.C55
|b H458 1999
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|a WH 322
|b H4885 1999
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| 072 |
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|a MED
|x 038000
|2 bisacsh
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| 084 |
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|a 44.86
|2 bcl
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| 245 |
0 |
0 |
|a Hemostasis and thrombosis protocols
|h [electronic resource] /
|c edited by David J. Perry and K. John Pasi.
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| 260 |
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|a Totowa, N.J. :
|b Humana Press,
|c c1999.
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| 300 |
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|a 1 online resource (xiii, 368 p.) :
|b ill.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a Methods in molecular medicine ;
|v 31
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| 490 |
1 |
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|a Ebsco e-book purchased
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| 504 |
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|a Includes bibliographical references and index.
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| 505 |
0 |
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|a pt. 1. Introduction -- Hemostasis: components and processes / K. John Pasi -- pt. 2. Basic techniques -- Isolation of DNA and RNA / David J. Perry -- Amplification of DNA and RNA by PCR / David J. Perry -- Direct sequencing of PCR products / David J. Perry -- Solid-phase sequencing of biotinylated PCR products with streptavidin-coated magnetic beads / David J. Perry -- Automated DNA sequencing / Helen L. Devereux -- Detection of DNA by silver staining / David J. Perry -- Promoter studies in hemostasis / Peter R. Winship -- pt. 3. Methods of mutational analysis -- Detection of mutations and polymorphisms in clotting factors by denaturing gradient gel electrophoresis / Rainer Schwaab -- Screening for mutations in DNA by single-stranded conformation polymorphism (SSCP) analysis / David J. Perry -- Screening for DNA heteroduplexes in the factor VII gene using ethylene glycol gel electrophoresis of solvent-treated 32P-labeled PCR products / Peter M. Baker -- Detection of mutations causing hemophilia A using in vitro coupled transcription and translation system / Chike Ononye -- Screening for mutations in the human antithrombin gene by Hydrolink D-5000 and MDE gel electrophoresis / David J. Perry -- pt. 4. Methods for analyzing inherited/acquired disorders of hemostasis -- Detection of mutations in hemophilia A patients by chemical cleavage of mismatch method / Naushin H. Waseem -- Inversion mutation analysis in hemophilia A by restriction enzyme analysis and southern blotting / Chike Ononye -- Hemophilia B mutational analysis / Peter M. Green -- Screening for candidate mutations causing von Willebrand's Disease (vWD) / P. Vincent Jenkins -- Use of intron 40 VNTR I in vWD gene tracking / Mohammed S. Enayat -- Mutlimeric analysis of von Willebrand Factor (vWF) / Mohammed S. Enayat -- Identification of mutations in the human factor VII gene / Peter M. Baker -- Molecular analysis in factor XI deficiency / Karen M. Johnson -- Mutational analysis in antithrombin deficiency / David J. Perry -- Ectopic transcript analysis in human antithrombin deficiency / David J. Perry -- Mutational analysis of the human protein C gene / Roger Luddington -- Analysis of the protein S gene in protein S deficiency / Núria Sala -- Screening for the G to A transition at position 20210 in the 3'-untranslated region (UTR) of the prothrombin gene / Karen P. Brown -- Screening for the factor V leiden mutation / Karen P. Brown -- Multiplex PCR for detection of the prothrombin 3' UTR (C20210A) polymorphism and the factor V leiden mutation / Gillian Mellars -- Isoelectric focusing and immunodetection of plasma antithrombin / Martina Daly -- Characterization of heparin binding variants of antithrombin by crossed immunoelectrophoresis in the presence of heparin / Martina Daly -- The determination of amino acid sequence abnormalities in proteins by HPLC peptide analysis / David Williamson -- pt. 5. Platelet and megakaryocyte analysis -- Molecular biological identification and characterization of inherited platelet receptor disorders / Ramesh B. Basani -- In vitro expansion of megakaryocytes from peripheral blood hematopoietic progenitors / Michael A. Thornton -- Molecular biology studies with primary megakaryocytes / Yaping Shou.
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| 588 |
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|a Description based on print version record.
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| 506 |
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|a Access restricted by licensing agreement.
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| 530 |
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|a Also available in print.
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| 538 |
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|a System requirements: World Wide Web browser, internet connectivity, Adobe Acrobat reader.
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| 538 |
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|a Mode of access: World Wide Web.
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| 506 |
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|3 Use copy
|f Restrictions unspecified
|2 star
|5 MiAaHDL
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| 533 |
|
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|a Electronic reproduction.
|b [S.l.] :
|c HathiTrust Digital Library,
|d 2010.
|5 MiAaHDL
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| 538 |
|
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|a Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002.
|u http://purl.oclc.org/DLF/benchrepro0212
|5 MiAaHDL
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| 583 |
1 |
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|a digitized
|c 2010
|h HathiTrust Digital Library
|l committed to preserve
|2 pda
|5 MiAaHDL
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| 590 |
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|a Loaded electronically.
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| 590 |
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|a Electronic access restricted to members of the Holy Cross Community.
|
| 590 |
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|a This was purchased from Ebsco with a single user license.
|
| 650 |
|
0 |
|a Blood coagulation disorders
|x Molecular aspects
|v Laboratory manuals.
|
| 650 |
|
0 |
|a Blood
|x Coagulation
|v Laboratory manuals.
|
| 650 |
|
0 |
|a Thrombosis
|v Laboratory manuals.
|
| 690 |
|
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|a Electronic resources (E-books)
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| 700 |
1 |
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|a Perry, David
|q (David J.)
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| 700 |
1 |
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|a Pasi, K. John.
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| 830 |
|
0 |
|a Methods in molecular medicine ;
|v 31.
|x 1543-1894
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| 830 |
|
0 |
|a Ebsco e-book purchased.
|
| 856 |
4 |
0 |
|u https://holycross.idm.oclc.org/login?auth=cas&url=https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=28042
|3 Click to view e-book
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