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M Petitou

Showing results (41-50 of 112) with videos related to

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Biochimica Et Biophysica Acta|August 11, 1988
Studies on the structural requirements of heparin for the catalysis of thrombin inhibition by heparin cofactor IIP Sié, M Petitou, J C Lormeau, et al.
The Biochemical Journal|June 1, 1988
Inhibition of leucocyte elastase by heparin and its derivativesF Redini, J M Tixier, M Petitou, et al.
The Journal of Biological Chemistry|April 21, 1995
Mechanism of acceleration of antithrombin-proteinase reactions by low affinity heparin. Role of the antithrombin binding pentasaccharide in heparin rate enhancementV J Streusand, I Björk, P G Gettins, et al.
British Journal of Haematology|December 1, 1986
Respective role of antithrombin III and heparin cofactor II in the in vitro anticoagulant effect of heparin and of various sulphated polysaccharidesP Sie, F Ofosu, F Fernandez, et al.
Biochemical and Biophysical Research Communications|October 31, 1983
Structure-activity relationship in heparin: a synthetic pentasaccharide with high affinity for antithrombin III and eliciting high anti-factor Xa activityJ Choay, M Petitou, J C Lormeau, et al.
Bioorganic & Medicinal Chemistry|October 26, 1999
Oligosaccharides corresponding to the regular sequence of heparin: chemical synthesis and interaction with FGF-2C Tabeur, J M Mallet, F Bono, et al.
Developmental Biology|October 1, 1994
Defined glycosaminoglycan motifs have opposite effects on neuronal polarity in vitroF Lafont, A Prochiantz, C Valenza, et al.
Bioorganic & Medicinal Chemistry|October 24, 1998
Synthesis of a 3-deoxy-L-iduronic acid containing heparin pentasaccharide to probe the conformation of the antithrombin III binding sequenceP S Lei, P Duchaussoy, P Sizun, et al.
Nature Structural Biology|September 1, 1995
Rational design of synthetic heparin analogues with tailor-made coagulation factor inhibitory activityP D Grootenhuis, P Westerduin, D Meuleman, et al.
Carbohydrate Research|February 23, 1996
L-iduronic acid derivatives as glycosyl donorsC Tabeur, F Machetto, J M Mallet, et al.
Pageof 12

Showing results (41-50 of 112) with videos related to

Sort By:
Pageof 12
Biochimica Et Biophysica Acta|August 11, 1988
Studies on the structural requirements of heparin for the catalysis of thrombin inhibition by heparin cofactor IIP Sié, M Petitou, J C Lormeau, et al.
The Biochemical Journal|June 1, 1988
Inhibition of leucocyte elastase by heparin and its derivativesF Redini, J M Tixier, M Petitou, et al.
The Journal of Biological Chemistry|April 21, 1995
Mechanism of acceleration of antithrombin-proteinase reactions by low affinity heparin. Role of the antithrombin binding pentasaccharide in heparin rate enhancementV J Streusand, I Björk, P G Gettins, et al.
British Journal of Haematology|December 1, 1986
Respective role of antithrombin III and heparin cofactor II in the in vitro anticoagulant effect of heparin and of various sulphated polysaccharidesP Sie, F Ofosu, F Fernandez, et al.
Biochemical and Biophysical Research Communications|October 31, 1983
Structure-activity relationship in heparin: a synthetic pentasaccharide with high affinity for antithrombin III and eliciting high anti-factor Xa activityJ Choay, M Petitou, J C Lormeau, et al.
Bioorganic & Medicinal Chemistry|October 26, 1999
Oligosaccharides corresponding to the regular sequence of heparin: chemical synthesis and interaction with FGF-2C Tabeur, J M Mallet, F Bono, et al.
Developmental Biology|October 1, 1994
Defined glycosaminoglycan motifs have opposite effects on neuronal polarity in vitroF Lafont, A Prochiantz, C Valenza, et al.
Bioorganic & Medicinal Chemistry|October 24, 1998
Synthesis of a 3-deoxy-L-iduronic acid containing heparin pentasaccharide to probe the conformation of the antithrombin III binding sequenceP S Lei, P Duchaussoy, P Sizun, et al.
Nature Structural Biology|September 1, 1995
Rational design of synthetic heparin analogues with tailor-made coagulation factor inhibitory activityP D Grootenhuis, P Westerduin, D Meuleman, et al.
Carbohydrate Research|February 23, 1996
L-iduronic acid derivatives as glycosyl donorsC Tabeur, F Machetto, J M Mallet, et al.
Pageof 12