originpro v. 2019b software Search Results


99
Sartorius AG incucyte s3 software
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Incucyte S3 Software, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/originpro+v%2E+2019b+software/pmc08146944-194-8-11?v=Sartorius+AG
Average 99 stars, based on 1 article reviews
incucyte s3 software - by Bioz Stars, 2026-06
99/100 stars
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90
OriginLab corp originpro 2019b software
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Originpro 2019b Software, supplied by OriginLab corp, 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/product/originpro+v%2E+2019b+software/pm38126895-465-17-20?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
originpro 2019b software - by Bioz Stars, 2026-06
90/100 stars
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99
Oxford Instruments algorithms originpro originlab corporation version 2019b imagej nih 1 53
Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the <t>Incucyte</t> <t>S3</t> live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).
Algorithms Originpro Originlab Corporation Version 2019b Imagej Nih 1 53, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/originpro+v%2E+2019b+software/pm33251491-281-248-257?v=Oxford+Instruments
Average 99 stars, based on 1 article reviews
algorithms originpro originlab corporation version 2019b imagej nih 1 53 - by Bioz Stars, 2026-06
99/100 stars
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90
OriginLab corp heatmaps originpro 2019 b software
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Heatmaps Originpro 2019 B Software, supplied by OriginLab corp, 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/product/originpro+v%2E+2019b+software/pmc07290368-78-17-22?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
heatmaps originpro 2019 b software - by Bioz Stars, 2026-06
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OriginLab corp dedicated software v. 2019b
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Dedicated Software V. 2019b, supplied by OriginLab corp, 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/product/originpro+v%2E+2019b+software/pm34719062-46-19-21?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
dedicated software v. 2019b - by Bioz Stars, 2026-06
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90
OriginLab corp originpro
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Originpro, supplied by OriginLab corp, 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/product/originpro+v%2E+2019b+software/pm40235337-151-31-36?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
originpro - by Bioz Stars, 2026-06
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90
GraphPad Software Inc graphpad prism 7
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Graphpad Prism 7, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
graphpad prism 7 - by Bioz Stars, 2026-06
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GraphPad Software Inc graphpad prism 8.4.3
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Graphpad Prism 8.4.3, supplied by GraphPad Software 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/product/originpro+v%2E+2019b+software/pm35153673-240-10-9?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
graphpad prism 8.4.3 - by Bioz Stars, 2026-06
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OriginLab corp origin software
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Origin Software, supplied by OriginLab corp, 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/product/originpro+v%2E+2019b+software/pm34666134-60-9-13?v=OriginLab+corp
Average 90 stars, based on 1 article reviews
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92
Addgene inc mscv 19a 20 19b
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Mscv 19a 20 19b, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mscv 19a 20 19b - by Bioz Stars, 2026-06
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2019b  (BASF)
90
BASF 2019b
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
2019b, supplied by BASF, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Playposit Inc playposit 2019b
<t>Heatmaps</t> showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.
Playposit 2019b, supplied by Playposit 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/product/originpro+v%2E+2019b+software/10__1080_slash_87567555__2020__1864615-16-30-29?v=Playposit+Inc
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Image Search Results


Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the Incucyte S3 live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).

Journal: Vaccines

Article Title: A Nanoscaffolded Spike-RBD Vaccine Provides Protection against SARS-CoV-2 with Minimal Anti-Scaffold Response

doi: 10.3390/vaccines9050431

Figure Lengend Snippet: Augmented antibody titer, viral neutralization, and lymph node retention of RBD-bann protein vaccine. RBD variants were isolated from the supernatants of mammalian cells via affinity chromatography and analyzed for purity and specificity via SDS-PAGE ( a ) and the binding of recombinant proteins at a serial dilution, or buffer alone (0), to immobilized human ACE2 receptor was measured in an ELISA assay ( b ). Dissociation of RBD and RBD-bann from immobilized hACE2 was measured by SPR ( c ). Mice were immunized with RBD and RBD-bann proteins purified from mammalian cell supernatant with/without squalene-mediated adjuvant. End point titer (EPT) for total IgG against RBD ( d – e ) and against spike protein ( f – g ). Graphs represent the mean EPTs of groups of mice ( n = 6 per group). Each dot represents an individual animal. * p < 0.05; ** p < 0.01. All p values are from the Mann–Whitney test compared to RBD group + AddaVax. Neutralization titer in mice sera was determined using a pseudovirus system. Sera of mice immunized with isolated proteins were diluted 50-fold, and Spike-pseudotyped virus infection of ACE2 and TMPRSS2-transfected HEK293 cells was followed by luminescence. Mean and SEM biological replicates are shown ( b ). * p < 0.05, *** p < 0.001, **** p < 0.0001. All p values are from one-way ANOVA followed by Tukey’s multiple comparisons test compared to the buffer group ( h ). A serum virus neutralization assay was performed by infecting Vero E6 cells with SARS-CoV-2-GFP reporter virus (MOI 1) with prior incubation of inoculum with dilutions of mouse sera (1:50) immunized with indicated isolated proteins. As control cells were left uninfected (mock), GFP signal was measured 36-h post-infection using the Incucyte S3 live-cell imaging system. Each point represents the mean of two technical replicates, and the mean +/− SD from six mice per group is indicated. Indicated p -values apply for comparison between individual conditions and the dilution-matched buffer condition and were calculated using a one-sided Student’s t -test between RBD + Addaax and RBD-bann + Addavax. * p < 0.05 ( i ). Trafficking of labeled isolated proteins into the popliteal lymph nodes (PLN). AF-647 labeled RBD proteins were injected into the foot pad (RBD left, RBD-bann right). The fluorescence signal of AF-647 was determined in the popliteal lymph node, depicting the presence of labeled RBD. Each dot represents the measurement of the region of interest (ROI) of an individual animal PLN. * p < 0.05 derived from two-tailed paired t -test ( j ).

Article Snippet: The normalized GFP intensity was computed using the IncuCyte S3 software (Essen Bioscience; version 2019B Rev2, Sartorius, Göttingen, Germany) as integrated GFP intensity per well divided by the total area of the cells per well.

Techniques: Neutralization, Isolation, Affinity Chromatography, SDS Page, Binding Assay, Recombinant, Serial Dilution, Enzyme-linked Immunosorbent Assay, Purification, Adjuvant, MANN-WHITNEY, Virus, Infection, Transfection, Incubation, Control, Live Cell Imaging, Comparison, Labeling, Injection, Fluorescence, Derivative Assay, Two Tailed Test

Heatmaps showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in macular retinal nerve fiber layer (mRNFL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −20.70 and −1.35 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in ganglion cell layer (GCL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −6.85 and −1.35 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in ganglion cell layer (GCL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −6.85 and −1.35 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in inner plexiform layer (IPL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −3.36 and −1.22 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in inner plexiform layer (IPL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between −3.36 and −1.22 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in inner nuclear layer (INL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.33 and 2.52 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in inner nuclear layer (INL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.33 and 2.52 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in outer plexiform and outer nuclear segmentation (OPLONL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between the groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. The range of significant OHT-POAG differences in superpixels is between 2.68 and 5.66 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in outer plexiform and outer nuclear segmentation (OPLONL). Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between the groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. The range of significant OHT-POAG differences in superpixels is between 2.68 and 5.66 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in photoreceptor layer. Left map: this heatmap represents simple differences in the mean thickness between the OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents the statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.08 and 2.63 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in photoreceptor layer. Left map: this heatmap represents simple differences in the mean thickness between the OHT group and early POAG group in each superpixel, giving an idea of the trend. Right map: the heatmap represents the statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 1.08 and 2.63 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques:

Heatmaps showing differences in the retinal pigment epithelium layer. Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 0.51 and 0.75 microns.

Journal: Journal of Clinical Medicine

Article Title: Glaucomatous Maculopathy: Thickness Differences on Inner and Outer Macular Layers between Ocular Hypertension and Early Primary Open-Angle Glaucoma Using 8 × 8 Posterior Pole Algorithm of SD-OCT

doi: 10.3390/jcm9051503

Figure Lengend Snippet: Heatmaps showing differences in the retinal pigment epithelium layer. Left map: this heatmap represents simple differences of mean thickness between OHT group and early POAG group in each superpixel giving an idea of the trend. Right map: the heatmap represents statistically significant differences ( p < 0.05) of the mean thickness between groups in each superpixel. No significant difference ( p ≥ 0.05) is represented in black. Range of significant OHT-POAG differences in superpixels between 0.51 and 0.75 microns.

Article Snippet: The differences of mean thickness in each superpixel between OHT and early POAG groups were represented using heatmaps (OriginPro 2019 b software, Origin Lab, Northampton, USA).

Techniques: