Small Scale Preparation and Clinical Use of Factor IX-Prothrombin Complex

Vox Sanguinis ◽  
1973 ◽  
Vol 25 (5) ◽  
pp. 426-441 ◽  
Author(s):  
T. W. Barrowcliffe ◽  
Penelope Stableforth ◽  
Katharine M. Dormandy
Vox Sanguinis ◽  
1973 ◽  
Vol 25 (5) ◽  
pp. 426-441 ◽  
Author(s):  
T.W. Barrowcliffe ◽  
P. Stableforth ◽  
Katharine M. Dormandy

1975 ◽  
Vol 33 (03) ◽  
pp. 403-404
Author(s):  
Rosemary Biggs
Keyword(s):  

1980 ◽  
Vol 44 (02) ◽  
pp. 081-086 ◽  
Author(s):  
C V Prowse ◽  
A E Williams

SummaryThe thrombogenic effects of selected factor IX concentrates were evaluated in two rabbit models; the Wessler stasis model and a novel non-stasis model. Concentrates active in either the NAPTT or TGt50 in vitro tests of potential thrombogenicity, or both, caused thrombus formation in the Wessler technique and activation of the coagulation system in the non-stasis model. A concentrate with low activity in both in vitro tests did not have thrombogenic effects in vivo, at the chosen dose. Results in the non-stasis model suggested that the thrombogenic effects of factor IX concentrates may occur by at least two mechanisms. A concentrate prepared from platelet-rich plasma and a pyrogenic concentrate were also tested and found to have no thrombogenic effect in vivo.These studies justify the use of the NAPTT and TGt50 in vitro tests for the screening of factor IX concentrates prior to clinical use.


1989 ◽  
Vol 10 (4) ◽  
pp. 279-286 ◽  
Author(s):  
Peter Feldman ◽  
Lowell Winkelman ◽  
Helen Evans ◽  
Martin Pinnell ◽  
Fiona Murdoch ◽  
...  

Vox Sanguinis ◽  
1969 ◽  
Vol 16 (5) ◽  
pp. 398-411 ◽  
Author(s):  
C. Haanen ◽  
R. L. McShine ◽  
A. Kunst
Keyword(s):  

1972 ◽  
Vol 126 (4) ◽  
pp. 781-790 ◽  
Author(s):  
N. W. Penn ◽  
R. Suwalski ◽  
C. O'Riley ◽  
K. Bojanowski ◽  
R. Yura

A method is given for small-scale preparation of DNA from 1.0–1.5g of adult rat tissues. The product from brain or liver is characterized by base ratios and phosphorus content which accord with reported values for rat tissue. It is reasonably free of RNA, protein and glycogen. It contains 5-hydroxymethylcytosine at a content of about 15% of the total cytosine bases present. 5-Hydroxymethylcytosine is also demonstrable in mouse and frog brain DNA and in the crude cytidylic acid fractions obtained from RNA hydrolysates of rat brain and liver. 5-Hydroxymethylcytosine is identified by paper chromatography, u.v. spectra in acid and alkaline solutions and by its conversion into 5-hydroxymethyluracil.


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