Additional file 2: Table S2. of HDP2: a ribosomal DNA (NTS-ETS) sequence as a target for species-specific molecular diagnosis of intestinal taeniasis in humans

References included in Additional file 1: Table S1. (PDF 18 kb

Additional file 1: Table S1. of HDP2: a ribosomal DNA (NTS-ETS) sequence as a target for species-specific molecular diagnosis of intestinal taeniasis in humans

DNA markers and molecular protocols used to identify the taeniid species involved in human taeniasis. (PDF 35 kb

Supplementary Figure 4.tiff

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p

Supplementary Figure 7.tiff

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p

Supplementary Figure 5.tiff

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p

Supplementary Figure 2.tiff

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p

Supplementary Figure 3.tiff

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p

Supplementary Tables.docx

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p

Supplementary Figure 1.tiff

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p

Supplementary Figure legends.docx

In a mouse arteriovenous fistula model, disturbed flow at the JAA correlates with early EC loss, early thrombus formation, and later NIH, with increased NIH at the JAA compared to the outflow vein during venous remodeling. This suggests the increased importance of using the JAA, rather than the outflow vein, to assess potential data for translational applications. </p