Kenneth Mann - Grand Isle VT, US Stephen Everse - Shelburne VT, US Matthew Hockin - Salt Lake City UT, US Kenneth Jones - Montpeller VT, US
International Classification:
G06F 19/00 G01N 33/48 G01N 33/50
US Classification:
702019000
Abstract:
A computer program product for predicting the speed and efficacy of a blood-clotting agent is disclosed. The product comprises a computer usable medium having computer readable program code means embodied in the medium for causing an application program to execute on a computer with a database for storing data therein. The computer readable program code means comprises a first computer readable program code means for causing the computer to enter data into the database from a user interface, a second computer readable program code means for causing the computer to enter chemical equations into the database according to a user's input, a third computer readable program code means for causing the computer to compile differential equations corresponding to the chemical equations, a fourth computer readable program code means for causing the computer to solve the differential equations, and a fifth computer readable program code means for causing the computer to display the results of the solution to the differential equations.
Predicting Hemostatic Risk; Dependence On Plasma Composition
Kenneth G. Mann - Grand Isle VT, US Kathleen B. Ziedins - Waterbury Center VT, US Thomas Orfeo - Westford VT, US Matthew F. Hockin - Salt Lake City UT, US Stephen J. Everse - South Burlington VT, US
Assignee:
The University of Vermont and State Agriculture College - Burlington VT
International Classification:
C12Q 1/56 G01N 33/48
US Classification:
435 13, 702 19
Abstract:
Featured are methods for assessing hemostatic risk including the risk for ACS. Such methods include acquiring blood/plasma composition based on a biological sample obtained from a subject, determining parameters associated with blood clotting, simulating in silico blood clotting using the determined parameters and comparing the results of such simulation to a reference and to determine the hemostatic risk from said comparing. In further embodiments, such methods further include selecting a treatment regime or protocol based on the results of such comparing. In yet further embodiments, such methods further include assessing the efficacy of medicants, drugs and the like of a given treatment protocol such as by simulating in silico the application of such medicants, drugs and the like.
Crystal Structure Of Factor Vai And Method For Identifying Blood Factor Va Modulators
Stephen Everse - Shelburne VT, US Ty Adams - Cambridge, GB Matthew Hockin - Salt Lake City UT, US Kenneth Mann - Grand Isle VT, US
International Classification:
C07K 14/745 G01N 33/48 A61K 38/48
US Classification:
530384000, 702019000
Abstract:
The present invention shows the crystal structure of protein C inactivated factor Va (A-A-C-C) that depicts a novel domain arrangement. The newly disclosed orientation has implications for binding to membranes essential for function. A high-affinity calcium binding site and a copper binding site have been identified, neither of which show a direct involvement in chain association. This structure represents the largest physiologically relevant fragment of factor Va solved to date and provides a new scaffold for generation of models of coagulation factors.
- Salt Lake City UT, US - Marcy-L'Etoile, FR Stefanie Marxreiter - Salt Lake City UT, US Eric Lo - Salt Lake City UT, US Laurent Eugène Paul Drazek - Grenoble, FR Matthew F. Hockin - Salt Lake City UT, US Joshua Earle Jackson - Cottonwood Heights UT, US
International Classification:
C12Q 1/18 C12Q 1/6806 C12Q 1/6851
Abstract:
Methods, sample vessels, and instruments are provided for determining antibiotic resistance of a bacterium.