Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

< Back to Article

Figure 1.

Variation of thrombin generation in familial PC deficiency.

Thrombin generation profiles were generated from each individual’s plasma composition (n = 364), containing fII, fV, fVII, fVIII, fIX, fX, AT, TFPI and PC and a 5 pM Tf initiator. The mean thrombin curve is shown in maroon with the standard deviation in salmon. A control curve, representing mean physiologic concentrations of each factor is illustrated in gold as a comparison.

More »

Figure 1 Expand

Table 1.

Plasma composition within familial PC deficiency.

More »

Table 1 Expand

Figure 2.

Investigating the range of thrombin generation within familial PC deficiency.

Individuals within the family were segregated by A) Protein C mutation, B) Prothombin G20210A polymorphism, and C) Thrombosis history. The groups with the mutation/history are shown in green (+SD) and without the mutation/history are shown in grey (–SD). A control curve, representing mean physiologic concentrations of each factor is illustrated in gold as a comparison.

More »

Figure 2 Expand

Table 2.

Thrombin generation parameters within groups and stratified by gender.

More »

Table 2 Expand

Table 3.

Plasma composition comparison within groups and stratified by gender.

More »

Table 3 Expand

Figure 3.

Thrombin generation by gender.

Individuals within the family were segregated by gender for A) Protein C mutation, B) Prothrombin mutation, and C) Thrombosis history. The groups with the mutation/history are shown in green (+SD) and without the mutation/history are shown in grey (–SD) A control curve, representing mean physiologic concentrations of each factor is illustrated in gold as a comparison.

More »

Figure 3 Expand

Figure 4.

Thrombin generation stratified by gender and additional risk.

Males to females with an additional category of risk were compared for either PC mutation (panels A and B), prothrombin G2010A polymorphism (panels C and D), or previous history of thrombosis (panels E and F). Female profiles are shown in pink (+SD). Male profiles are shown in blue (–SD).

More »

Figure 4 Expand