3d scans Search Results


90
Carl Zeiss 3d scanning
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Scanning, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d scanning/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
3d scanning - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
ARTEC CO LTD three-dimensional (3d) torso surface scans eva
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
Three Dimensional (3d) Torso Surface Scans Eva, supplied by ARTEC CO LTD, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/three-dimensional (3d) torso surface scans eva/product/ARTEC CO LTD
Average 90 stars, based on 1 article reviews
three-dimensional (3d) torso surface scans eva - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Amira Pharmaceuticals confocal image stacks
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
Confocal Image Stacks, supplied by Amira Pharmaceuticals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/confocal image stacks/product/Amira Pharmaceuticals
Average 90 stars, based on 1 article reviews
confocal image stacks - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Geomagic Inc 3d-laser scans of bones
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Laser Scans Of Bones, supplied by Geomagic Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d-laser scans of bones/product/Geomagic Inc
Average 90 stars, based on 1 article reviews
3d-laser scans of bones - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Polytec Inc 3d laser vibrometer system
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Laser Vibrometer System, supplied by Polytec Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d laser vibrometer system/product/Polytec Inc
Average 90 stars, based on 1 article reviews
3d laser vibrometer system - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Philips Healthcare 3d spiral computerized tomography ct scans 64 channel
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Spiral Computerized Tomography Ct Scans 64 Channel, supplied by Philips Healthcare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d spiral computerized tomography ct scans 64 channel/product/Philips Healthcare
Average 90 stars, based on 1 article reviews
3d spiral computerized tomography ct scans 64 channel - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Rapidform Inc three-dimensional laser scans
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
Three Dimensional Laser Scans, supplied by Rapidform Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/three-dimensional laser scans/product/Rapidform Inc
Average 90 stars, based on 1 article reviews
three-dimensional laser scans - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Siemens AG 3d spgr anatomical scan
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Spgr Anatomical Scan, supplied by Siemens AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d spgr anatomical scan/product/Siemens AG
Average 90 stars, based on 1 article reviews
3d spgr anatomical scan - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Hirschmann 3d-reconstructed ct scans
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Reconstructed Ct Scans, supplied by Hirschmann, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d-reconstructed ct scans/product/Hirschmann
Average 90 stars, based on 1 article reviews
3d-reconstructed ct scans - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
SOL Instruments GmbH 3d-scanning confocal raman/photoluminescence microscope-spectrometer confotec mr 520
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Scanning Confocal Raman/Photoluminescence Microscope Spectrometer Confotec Mr 520, supplied by SOL Instruments GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d-scanning confocal raman/photoluminescence microscope-spectrometer confotec mr 520/product/SOL Instruments GmbH
Average 90 stars, based on 1 article reviews
3d-scanning confocal raman/photoluminescence microscope-spectrometer confotec mr 520 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Chondrometrics GmbH 3d spoiled gradient recalled echo (spgr) scans for quantitative, manual, quality-controlled cartilage segmentation (qmri)
A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in <t>3D</t> and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 <t>in</t> <t>monolayer</t> of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).
3d Spoiled Gradient Recalled Echo (Spgr) Scans For Quantitative, Manual, Quality Controlled Cartilage Segmentation (Qmri), supplied by Chondrometrics GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d spoiled gradient recalled echo (spgr) scans for quantitative, manual, quality-controlled cartilage segmentation (qmri)/product/Chondrometrics GmbH
Average 90 stars, based on 1 article reviews
3d spoiled gradient recalled echo (spgr) scans for quantitative, manual, quality-controlled cartilage segmentation (qmri) - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Canon inc 3d landmark scan
Traditional and <t>3D</t> <t>Landmark</t> scout images and scan start/end positions for a chest CT of a 54-year old female. (a) Traditional AP and lateral scout images and start and end scan positions. Lines A and D, and corresponding axial images represent the actual start and end positions of the CT scan planned using traditional scout images where the radiographer estimates the organ locations. Lines B and C and corresponding axial images represent the proper start and end positions for the chest CT to start above the lung apex and go through both adrenal glands. (b) Axial ultra-low dose CT images generated by 3D Landmark scouting and corresponding coronal and lateral projections from the same patient. E and F represent the appropriate start and end positions of the CT planned using the axial 3D Landmark images resulting in a decreased scan length of 34 mm compared to prior imaging (panel a) planned using traditional scout imaging (325 vs 291 mm, respectively). Correspondingly, the radiation dose of the chest CT scan planned by 3D landmark was reduced by 12 % compared to her prior scan planned with traditional scout imaging (249.8 mGy·cm vs 283.7 mGy·cm), representing a 0.47 mSv effective dose savings. Scout image radiation dose itself was reduced by 48 % utilizing 3D Landmark (16.67 vs. 8.67 mGy·cm).
3d Landmark Scan, supplied by Canon inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d landmark scan/product/Canon inc
Average 90 stars, based on 1 article reviews
3d landmark scan - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

Image Search Results


A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in 3D and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 in monolayer of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).

Journal: Nature Communications

Article Title: Scar matrix drives Piezo1 mediated stromal inflammation leading to placenta accreta spectrum

doi: 10.1038/s41467-024-52351-0

Figure Lengend Snippet: A Heatmap showing significant differential ligand encoding genes expressed in dESFs on Scar and Physio matrices. B Representative IL-8 immunofluorescence images of dESFs treated with protein transport inhibitor GolgiStop for 6 h on Physio and Scar matrices, quantification shown in right panel; n = 49 and 53 cells for Physio and Scar, respectively. p = 5 × 10 −11 . C , D ELISA based analysis of IL-8 and G-CSF concentration in supernatant of dESFs on Physio and Scar in 3D and 2D; n = 3 samples. p = 0.0007 in ( C ) and p = 0.04 and 2 × 10 −5 in ( D ). E ELISA based measurement of IL-8 concentration in supernatant of dESFs treated overnight with DMSO, or 100 ng/ml TNFα; n = 3 samples. p = 0.0097. F Experimental workflow to test migration of HTR8 in medium conditioned from dESFs with gene silenced for IL-8 and G-CSF encoding genes, CXCL8 and CSF3, respectively. G Migration trajectories (initial location (x, y = 0,0)) of HTR8 conditioned with medium from dESFs silenced for CXCL8 and CSF3 genes, without or with addition of recombinant human (rh) IL-8 and G-CSF; Quantification of averaged velocities over 24 h shown in ( H ); p = 1×10 −8 , 8×10 −7 , 8×10 −9 , and 6 × 10 −5 ; n listed below each condition. I 3D chemotaxis of primary EVTs in collagen gel towards IL-8 and G-CSF gradient; Shown is a representative image of EVTs in collagen gel (left); Trajectories of individually tracked EVTs from their initial location (0,0) (middle and right); Cell trajectory with mean displacement towards cytokine end are labeled red, and counted ( n ); p value showing Rayleigh test of cell trajectories: p < 0.05 is considered chemotaxis. J ANSIA-based stromal invasion analysis of HTR8 in monolayer of dESFs silenced for CXCL8 and CSF3 genes; Control refers to scrambled sgRNA. p = 0.003 and 0.005. Data in figures B–E, H and J are showing as mean ± s.d.; statistical significance is determined by unpaired two-tailed t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001). Source data are provided as a Source Data file. Figure 3F created with BioRender.com released under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International license ( https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en ).

Article Snippet: After 4 days of decidualization, HTR8 spheroids prepared as aforementioned were suspended in 1 mg/ml collagen solution and plated on the 3D decidualization ESFs and incubated at 37 °C for 1 h to allow spheroid settle down and gel formation. dESF monolayer and HTR8 nuclear locations were recorded by Zeiss Apotome 3D scanning.

Techniques: Immunofluorescence, Enzyme-linked Immunosorbent Assay, Concentration Assay, Migration, Recombinant, Chemotaxis Assay, Labeling, Control, Two Tailed Test

Traditional and 3D Landmark scout images and scan start/end positions for a chest CT of a 54-year old female. (a) Traditional AP and lateral scout images and start and end scan positions. Lines A and D, and corresponding axial images represent the actual start and end positions of the CT scan planned using traditional scout images where the radiographer estimates the organ locations. Lines B and C and corresponding axial images represent the proper start and end positions for the chest CT to start above the lung apex and go through both adrenal glands. (b) Axial ultra-low dose CT images generated by 3D Landmark scouting and corresponding coronal and lateral projections from the same patient. E and F represent the appropriate start and end positions of the CT planned using the axial 3D Landmark images resulting in a decreased scan length of 34 mm compared to prior imaging (panel a) planned using traditional scout imaging (325 vs 291 mm, respectively). Correspondingly, the radiation dose of the chest CT scan planned by 3D landmark was reduced by 12 % compared to her prior scan planned with traditional scout imaging (249.8 mGy·cm vs 283.7 mGy·cm), representing a 0.47 mSv effective dose savings. Scout image radiation dose itself was reduced by 48 % utilizing 3D Landmark (16.67 vs. 8.67 mGy·cm).

Journal: European Journal of Radiology Open

Article Title: Reduced dose helical CT scout imaging on next generation wide volume CT system decreases scan length and overall radiation exposure

doi: 10.1016/j.ejro.2024.100578

Figure Lengend Snippet: Traditional and 3D Landmark scout images and scan start/end positions for a chest CT of a 54-year old female. (a) Traditional AP and lateral scout images and start and end scan positions. Lines A and D, and corresponding axial images represent the actual start and end positions of the CT scan planned using traditional scout images where the radiographer estimates the organ locations. Lines B and C and corresponding axial images represent the proper start and end positions for the chest CT to start above the lung apex and go through both adrenal glands. (b) Axial ultra-low dose CT images generated by 3D Landmark scouting and corresponding coronal and lateral projections from the same patient. E and F represent the appropriate start and end positions of the CT planned using the axial 3D Landmark images resulting in a decreased scan length of 34 mm compared to prior imaging (panel a) planned using traditional scout imaging (325 vs 291 mm, respectively). Correspondingly, the radiation dose of the chest CT scan planned by 3D landmark was reduced by 12 % compared to her prior scan planned with traditional scout imaging (249.8 mGy·cm vs 283.7 mGy·cm), representing a 0.47 mSv effective dose savings. Scout image radiation dose itself was reduced by 48 % utilizing 3D Landmark (16.67 vs. 8.67 mGy·cm).

Article Snippet: 61 consecutive patients with prior CT examination of the same body region that underwent clinical CT planned using 3D Landmark Scan and ALD (Canon Medical Aquilion ONE Insight Edition; Otawara, Tochigi, Japan) at a single center over a 3-month period from 7/17/23–10/16/23 were included in this study.

Techniques: Computed Tomography, Generated, Imaging

Demographics of 61 patients undergoing a total of 104 CT examinations. Weight and BMI is presented for patients at time of prior CT examination planned with traditional scout imaging (“prior”) and at time of recent CT examination planned with  3D Landmark  and ALD (“new”).

Journal: European Journal of Radiology Open

Article Title: Reduced dose helical CT scout imaging on next generation wide volume CT system decreases scan length and overall radiation exposure

doi: 10.1016/j.ejro.2024.100578

Figure Lengend Snippet: Demographics of 61 patients undergoing a total of 104 CT examinations. Weight and BMI is presented for patients at time of prior CT examination planned with traditional scout imaging (“prior”) and at time of recent CT examination planned with 3D Landmark and ALD (“new”).

Article Snippet: 61 consecutive patients with prior CT examination of the same body region that underwent clinical CT planned using 3D Landmark Scan and ALD (Canon Medical Aquilion ONE Insight Edition; Otawara, Tochigi, Japan) at a single center over a 3-month period from 7/17/23–10/16/23 were included in this study.

Techniques: Imaging, Standard Deviation

Scan lengths and radiation doses for 104 CT examinations planned using traditional scout imaging (“prior”) and planned using  3D Landmark  and ALD (“new”). Radiation doses presented as dose length product (DLP), effective dose (in milisieverts), and CT dose index (CTDI). Total DLP and CTDI reflect the sum of the scout imaging dose and acquisition dose. Scan lengths, DLP and corresponding effective doses of diagnostic acquisitions are further broken into subgroup by body region. Effective radiation dose in millisieverts (mSv) was calculated from the DLP using a k factor of 0.014 for chest, 0.015 for abdomen, and 0.0145 for chest/abdomen/pelvis <xref ref-type= [13] . Data represented as median and interquartile range. n = 50 for chest CT scan length, n = 16 for abdomen scan length, n = 38 for chest/abdomen/pelvis scan length, and n = 104 for scout scan length. n = 49 for chest radiation doses, n = 15 for abdomen radiation doses, n = 36 for chest/abdomen/pelvis radiation doses, and n = 100 for scout radiation doses." width="100%" height="100%">

Journal: European Journal of Radiology Open

Article Title: Reduced dose helical CT scout imaging on next generation wide volume CT system decreases scan length and overall radiation exposure

doi: 10.1016/j.ejro.2024.100578

Figure Lengend Snippet: Scan lengths and radiation doses for 104 CT examinations planned using traditional scout imaging (“prior”) and planned using 3D Landmark and ALD (“new”). Radiation doses presented as dose length product (DLP), effective dose (in milisieverts), and CT dose index (CTDI). Total DLP and CTDI reflect the sum of the scout imaging dose and acquisition dose. Scan lengths, DLP and corresponding effective doses of diagnostic acquisitions are further broken into subgroup by body region. Effective radiation dose in millisieverts (mSv) was calculated from the DLP using a k factor of 0.014 for chest, 0.015 for abdomen, and 0.0145 for chest/abdomen/pelvis [13] . Data represented as median and interquartile range. n = 50 for chest CT scan length, n = 16 for abdomen scan length, n = 38 for chest/abdomen/pelvis scan length, and n = 104 for scout scan length. n = 49 for chest radiation doses, n = 15 for abdomen radiation doses, n = 36 for chest/abdomen/pelvis radiation doses, and n = 100 for scout radiation doses.

Article Snippet: 61 consecutive patients with prior CT examination of the same body region that underwent clinical CT planned using 3D Landmark Scan and ALD (Canon Medical Aquilion ONE Insight Edition; Otawara, Tochigi, Japan) at a single center over a 3-month period from 7/17/23–10/16/23 were included in this study.

Techniques: Imaging, Diagnostic Assay, Computed Tomography

Dose-length product (DLP) (mGy·cm) for (a) chest, (b) abdomen, and (c) chest/abdomen/pelvis CT exams planned using 3D Landmark Scan and Anatomic Landmark Detection and performed on next generation CT (“new DLP”) versus those planned using traditional scout methods (“prior DLP”). (a) Median DLP for chest CT was reduced by 11.9 %, from 182.1 (IQR 146.1–283.7) to 160.4 (IQR 133.8–223.6) mGy·cm, p = 0.007, n = 49. (b). Median DLP for abdomen CT was reduced by 47.3 % from 236.8 (IQR 178.1–284.60) to 124.9 (96.8–166.8) mGy·cm, p = 0.004, n = 15. (c) Median DLP for chest/abdomen/pelvis CT was reduced by 28.6 %, from 531.6 (IQR 465.4–689.2) to 379.7 (IQR 319.0–531.8) mGy·cm, respectively, p = 0.001, n = 36.

Journal: European Journal of Radiology Open

Article Title: Reduced dose helical CT scout imaging on next generation wide volume CT system decreases scan length and overall radiation exposure

doi: 10.1016/j.ejro.2024.100578

Figure Lengend Snippet: Dose-length product (DLP) (mGy·cm) for (a) chest, (b) abdomen, and (c) chest/abdomen/pelvis CT exams planned using 3D Landmark Scan and Anatomic Landmark Detection and performed on next generation CT (“new DLP”) versus those planned using traditional scout methods (“prior DLP”). (a) Median DLP for chest CT was reduced by 11.9 %, from 182.1 (IQR 146.1–283.7) to 160.4 (IQR 133.8–223.6) mGy·cm, p = 0.007, n = 49. (b). Median DLP for abdomen CT was reduced by 47.3 % from 236.8 (IQR 178.1–284.60) to 124.9 (96.8–166.8) mGy·cm, p = 0.004, n = 15. (c) Median DLP for chest/abdomen/pelvis CT was reduced by 28.6 %, from 531.6 (IQR 465.4–689.2) to 379.7 (IQR 319.0–531.8) mGy·cm, respectively, p = 0.001, n = 36.

Article Snippet: 61 consecutive patients with prior CT examination of the same body region that underwent clinical CT planned using 3D Landmark Scan and ALD (Canon Medical Aquilion ONE Insight Edition; Otawara, Tochigi, Japan) at a single center over a 3-month period from 7/17/23–10/16/23 were included in this study.

Techniques:

Scan length (mm) for (a) chest, (b), abdomen, and (c) chest/abdomen/pelvis CT exams planned using 3D Landmark Scan and Anatomic Landmark Detection versus those planned using traditional scout images. (a) Median scan length 317.3 (IQR 302.3–338)mm compared to 330 (IQR 325.8–360)mm, respectively (p < 0.001, n = 50). Median reduction of 12.7 mm represented by the black dashed line. (b) Median scan length 235.5 (IQR 209.5–246)mm compared to 250 (IQR 240.1–260)mm respectively(p = 0.003, n = 16). Median reduction of 14.5 mm represented by the black line. (c) Median scan length 635 (IQR 625–667.3)mm compared to 660 (IQR 641.3–687.3)mm respectively (p < 0.001, n = 38). Median reduction of 25.0 mm represented by the black line.

Journal: European Journal of Radiology Open

Article Title: Reduced dose helical CT scout imaging on next generation wide volume CT system decreases scan length and overall radiation exposure

doi: 10.1016/j.ejro.2024.100578

Figure Lengend Snippet: Scan length (mm) for (a) chest, (b), abdomen, and (c) chest/abdomen/pelvis CT exams planned using 3D Landmark Scan and Anatomic Landmark Detection versus those planned using traditional scout images. (a) Median scan length 317.3 (IQR 302.3–338)mm compared to 330 (IQR 325.8–360)mm, respectively (p < 0.001, n = 50). Median reduction of 12.7 mm represented by the black dashed line. (b) Median scan length 235.5 (IQR 209.5–246)mm compared to 250 (IQR 240.1–260)mm respectively(p = 0.003, n = 16). Median reduction of 14.5 mm represented by the black line. (c) Median scan length 635 (IQR 625–667.3)mm compared to 660 (IQR 641.3–687.3)mm respectively (p < 0.001, n = 38). Median reduction of 25.0 mm represented by the black line.

Article Snippet: 61 consecutive patients with prior CT examination of the same body region that underwent clinical CT planned using 3D Landmark Scan and ALD (Canon Medical Aquilion ONE Insight Edition; Otawara, Tochigi, Japan) at a single center over a 3-month period from 7/17/23–10/16/23 were included in this study.

Techniques: