microscopy data Search Results


96
Gatan Inc orientation imaging microscopy oim software
Orientation Imaging Microscopy Oim Software, supplied by Gatan Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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orientation imaging microscopy oim software - by Bioz Stars, 2026-08
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Viollier AG microscopy data
Microscopy Data, supplied by Viollier AG, 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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GraphPad Software Inc microscopy data sets
Microscopy Data Sets, 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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GraphPad Software Inc 3d x-ray microscopy data analysis
Intracochlear neo-ossification relative to platinum and PDMS bearing surfaces. <t>3D</t> X-ray <t>microscopy</t> images of a single chronically implanted mouse cochlea (A,B,C) with the CI imaged in-situ were volumetrically segmented to compare the amount of neo-ossification in 3 separate areas: the area immediately adjacent to platinum electrode surfaces “Electrode” (red), the area adjacent to PDMS surfaces toward the backside of the electrode contact surface “Anti-electrode” (green), and the intracochlear portions basal to the E1 electrode “Non-electrode” (blue). Dashed lines in (A) denote the manual separation of the “Electrode” (red) and “Anti-electrode” (green) areas in which neo-ossification was volumetrically quantified and in (B,C) indicate the basal and apical limits confining the “Electrode” and “Anti-electrode” areas, with the “Non-electrode” area being basal to this area, stopping at the round window. “E1”, “E2” and “E3” denotes electrode contacts 1,2 and 3, respectively; “M” denotes modiolus; “RW” denotes the round window outlined by a red hashed circle in (B,C). The gray and dark yellow shading in (B) represent the open scala tympani space and areas of soft tissue fibrosis without neo-ossification, respectively. Mean quantification of volume of neo-ossification across n = 6 subjects with individual data points noted as dots and error bars representing 1 standard deviation is shown in (D). The greatest volume of neo-ossification was seen in the “Electrode” area immediately adjacent to the Platinum electrodes, followed by the “Anti-electrode” and “Non-electrode” areas, however these differences were not significant (p > 0.05).
3d X Ray Microscopy Data Analysis, 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
3d x-ray microscopy data analysis - by Bioz Stars, 2026-08
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NT MDT America Inc scanning probe microscopy data analysis software nova
Intracochlear neo-ossification relative to platinum and PDMS bearing surfaces. <t>3D</t> X-ray <t>microscopy</t> images of a single chronically implanted mouse cochlea (A,B,C) with the CI imaged in-situ were volumetrically segmented to compare the amount of neo-ossification in 3 separate areas: the area immediately adjacent to platinum electrode surfaces “Electrode” (red), the area adjacent to PDMS surfaces toward the backside of the electrode contact surface “Anti-electrode” (green), and the intracochlear portions basal to the E1 electrode “Non-electrode” (blue). Dashed lines in (A) denote the manual separation of the “Electrode” (red) and “Anti-electrode” (green) areas in which neo-ossification was volumetrically quantified and in (B,C) indicate the basal and apical limits confining the “Electrode” and “Anti-electrode” areas, with the “Non-electrode” area being basal to this area, stopping at the round window. “E1”, “E2” and “E3” denotes electrode contacts 1,2 and 3, respectively; “M” denotes modiolus; “RW” denotes the round window outlined by a red hashed circle in (B,C). The gray and dark yellow shading in (B) represent the open scala tympani space and areas of soft tissue fibrosis without neo-ossification, respectively. Mean quantification of volume of neo-ossification across n = 6 subjects with individual data points noted as dots and error bars representing 1 standard deviation is shown in (D). The greatest volume of neo-ossification was seen in the “Electrode” area immediately adjacent to the Platinum electrodes, followed by the “Anti-electrode” and “Non-electrode” areas, however these differences were not significant (p > 0.05).
Scanning Probe Microscopy Data Analysis Software Nova, supplied by NT MDT America 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
scanning probe microscopy data analysis software nova - by Bioz Stars, 2026-08
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MetaMorph Inc microscopy data
Intracochlear neo-ossification relative to platinum and PDMS bearing surfaces. <t>3D</t> X-ray <t>microscopy</t> images of a single chronically implanted mouse cochlea (A,B,C) with the CI imaged in-situ were volumetrically segmented to compare the amount of neo-ossification in 3 separate areas: the area immediately adjacent to platinum electrode surfaces “Electrode” (red), the area adjacent to PDMS surfaces toward the backside of the electrode contact surface “Anti-electrode” (green), and the intracochlear portions basal to the E1 electrode “Non-electrode” (blue). Dashed lines in (A) denote the manual separation of the “Electrode” (red) and “Anti-electrode” (green) areas in which neo-ossification was volumetrically quantified and in (B,C) indicate the basal and apical limits confining the “Electrode” and “Anti-electrode” areas, with the “Non-electrode” area being basal to this area, stopping at the round window. “E1”, “E2” and “E3” denotes electrode contacts 1,2 and 3, respectively; “M” denotes modiolus; “RW” denotes the round window outlined by a red hashed circle in (B,C). The gray and dark yellow shading in (B) represent the open scala tympani space and areas of soft tissue fibrosis without neo-ossification, respectively. Mean quantification of volume of neo-ossification across n = 6 subjects with individual data points noted as dots and error bars representing 1 standard deviation is shown in (D). The greatest volume of neo-ossification was seen in the “Electrode” area immediately adjacent to the Platinum electrodes, followed by the “Anti-electrode” and “Non-electrode” areas, however these differences were not significant (p > 0.05).
Microscopy Data, supplied by MetaMorph 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/microscopy+data/pmc07411022__42003_2020_1136_MOESM6_ESM-9-8-18?v=MetaMorph+Inc
Average 90 stars, based on 1 article reviews
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90
GraphPad Software Inc interference reflection microscopy (irm) data
Intracochlear neo-ossification relative to platinum and PDMS bearing surfaces. <t>3D</t> X-ray <t>microscopy</t> images of a single chronically implanted mouse cochlea (A,B,C) with the CI imaged in-situ were volumetrically segmented to compare the amount of neo-ossification in 3 separate areas: the area immediately adjacent to platinum electrode surfaces “Electrode” (red), the area adjacent to PDMS surfaces toward the backside of the electrode contact surface “Anti-electrode” (green), and the intracochlear portions basal to the E1 electrode “Non-electrode” (blue). Dashed lines in (A) denote the manual separation of the “Electrode” (red) and “Anti-electrode” (green) areas in which neo-ossification was volumetrically quantified and in (B,C) indicate the basal and apical limits confining the “Electrode” and “Anti-electrode” areas, with the “Non-electrode” area being basal to this area, stopping at the round window. “E1”, “E2” and “E3” denotes electrode contacts 1,2 and 3, respectively; “M” denotes modiolus; “RW” denotes the round window outlined by a red hashed circle in (B,C). The gray and dark yellow shading in (B) represent the open scala tympani space and areas of soft tissue fibrosis without neo-ossification, respectively. Mean quantification of volume of neo-ossification across n = 6 subjects with individual data points noted as dots and error bars representing 1 standard deviation is shown in (D). The greatest volume of neo-ossification was seen in the “Electrode” area immediately adjacent to the Platinum electrodes, followed by the “Anti-electrode” and “Non-electrode” areas, however these differences were not significant (p > 0.05).
Interference Reflection Microscopy (Irm) Data, 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/microscopy+data/pm20357244-80-9-15?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
interference reflection microscopy (irm) data - by Bioz Stars, 2026-08
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Eight laboratories smear microscopy (qc) data
Flow chart showing series of participants’ recruitment and the outcome of different tuberculosis testing methods used. +: Positive, - : Negative, AFB: Acid Fast Bacilli, PTB: Pulmonary tuberculosis, ZN Lab: Ziehl Nelsen health facility laboratories-, LED-FM Lab: Light emitting diode-fluorescence <t>microscopy</t> using health facility laboratories, NTM: Non-tuberculous Mycobacteria, cont.: contaminated
Smear Microscopy (Qc) Data, supplied by Eight laboratories, 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
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GraphPad Software Inc fluorescence microscopy data analysis
Flow chart showing series of participants’ recruitment and the outcome of different tuberculosis testing methods used. +: Positive, - : Negative, AFB: Acid Fast Bacilli, PTB: Pulmonary tuberculosis, ZN Lab: Ziehl Nelsen health facility laboratories-, LED-FM Lab: Light emitting diode-fluorescence <t>microscopy</t> using health facility laboratories, NTM: Non-tuberculous Mycobacteria, cont.: contaminated
Fluorescence Microscopy Data Analysis, 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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UES Inc optical microscopy image data
Flow chart showing series of participants’ recruitment and the outcome of different tuberculosis testing methods used. +: Positive, - : Negative, AFB: Acid Fast Bacilli, PTB: Pulmonary tuberculosis, ZN Lab: Ziehl Nelsen health facility laboratories-, LED-FM Lab: Light emitting diode-fluorescence <t>microscopy</t> using health facility laboratories, NTM: Non-tuberculous Mycobacteria, cont.: contaminated
Optical Microscopy Image Data, supplied by UES 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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TPLSM laboratories microscopy data
Flow chart showing series of participants’ recruitment and the outcome of different tuberculosis testing methods used. +: Positive, - : Negative, AFB: Acid Fast Bacilli, PTB: Pulmonary tuberculosis, ZN Lab: Ziehl Nelsen health facility laboratories-, LED-FM Lab: Light emitting diode-fluorescence <t>microscopy</t> using health facility laboratories, NTM: Non-tuberculous Mycobacteria, cont.: contaminated
Microscopy Data, supplied by TPLSM laboratories, 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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Natural Immunogenics Corp electron microscopy data
Flow chart showing series of participants’ recruitment and the outcome of different tuberculosis testing methods used. +: Positive, - : Negative, AFB: Acid Fast Bacilli, PTB: Pulmonary tuberculosis, ZN Lab: Ziehl Nelsen health facility laboratories-, LED-FM Lab: Light emitting diode-fluorescence <t>microscopy</t> using health facility laboratories, NTM: Non-tuberculous Mycobacteria, cont.: contaminated
Electron Microscopy Data, supplied by Natural Immunogenics Corp, 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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Image Search Results


Intracochlear neo-ossification relative to platinum and PDMS bearing surfaces. 3D X-ray microscopy images of a single chronically implanted mouse cochlea (A,B,C) with the CI imaged in-situ were volumetrically segmented to compare the amount of neo-ossification in 3 separate areas: the area immediately adjacent to platinum electrode surfaces “Electrode” (red), the area adjacent to PDMS surfaces toward the backside of the electrode contact surface “Anti-electrode” (green), and the intracochlear portions basal to the E1 electrode “Non-electrode” (blue). Dashed lines in (A) denote the manual separation of the “Electrode” (red) and “Anti-electrode” (green) areas in which neo-ossification was volumetrically quantified and in (B,C) indicate the basal and apical limits confining the “Electrode” and “Anti-electrode” areas, with the “Non-electrode” area being basal to this area, stopping at the round window. “E1”, “E2” and “E3” denotes electrode contacts 1,2 and 3, respectively; “M” denotes modiolus; “RW” denotes the round window outlined by a red hashed circle in (B,C). The gray and dark yellow shading in (B) represent the open scala tympani space and areas of soft tissue fibrosis without neo-ossification, respectively. Mean quantification of volume of neo-ossification across n = 6 subjects with individual data points noted as dots and error bars representing 1 standard deviation is shown in (D). The greatest volume of neo-ossification was seen in the “Electrode” area immediately adjacent to the Platinum electrodes, followed by the “Anti-electrode” and “Non-electrode” areas, however these differences were not significant (p > 0.05).

Journal: Hearing research

Article Title: Cochlear implant material effects on inflammatory cell function and foreign body response

doi: 10.1016/j.heares.2022.108597

Figure Lengend Snippet: Intracochlear neo-ossification relative to platinum and PDMS bearing surfaces. 3D X-ray microscopy images of a single chronically implanted mouse cochlea (A,B,C) with the CI imaged in-situ were volumetrically segmented to compare the amount of neo-ossification in 3 separate areas: the area immediately adjacent to platinum electrode surfaces “Electrode” (red), the area adjacent to PDMS surfaces toward the backside of the electrode contact surface “Anti-electrode” (green), and the intracochlear portions basal to the E1 electrode “Non-electrode” (blue). Dashed lines in (A) denote the manual separation of the “Electrode” (red) and “Anti-electrode” (green) areas in which neo-ossification was volumetrically quantified and in (B,C) indicate the basal and apical limits confining the “Electrode” and “Anti-electrode” areas, with the “Non-electrode” area being basal to this area, stopping at the round window. “E1”, “E2” and “E3” denotes electrode contacts 1,2 and 3, respectively; “M” denotes modiolus; “RW” denotes the round window outlined by a red hashed circle in (B,C). The gray and dark yellow shading in (B) represent the open scala tympani space and areas of soft tissue fibrosis without neo-ossification, respectively. Mean quantification of volume of neo-ossification across n = 6 subjects with individual data points noted as dots and error bars representing 1 standard deviation is shown in (D). The greatest volume of neo-ossification was seen in the “Electrode” area immediately adjacent to the Platinum electrodes, followed by the “Anti-electrode” and “Non-electrode” areas, however these differences were not significant (p > 0.05).

Article Snippet: 3D X-ray microscopy data were analyzed in GraphPad Prism software (Graph-Pad Software, USA) via ordinary one-way ANOVA.

Techniques: Microscopy, In Situ, Standard Deviation

Flow chart showing series of participants’ recruitment and the outcome of different tuberculosis testing methods used. +: Positive, - : Negative, AFB: Acid Fast Bacilli, PTB: Pulmonary tuberculosis, ZN Lab: Ziehl Nelsen health facility laboratories-, LED-FM Lab: Light emitting diode-fluorescence microscopy using health facility laboratories, NTM: Non-tuberculous Mycobacteria, cont.: contaminated

Journal: BMC Infectious Diseases

Article Title: Diagnostic performance of smear microscopy and incremental yield of Xpert in detection of pulmonary tuberculosis in Rwanda

doi: 10.1186/s12879-016-2009-x

Figure Lengend Snippet: Flow chart showing series of participants’ recruitment and the outcome of different tuberculosis testing methods used. +: Positive, - : Negative, AFB: Acid Fast Bacilli, PTB: Pulmonary tuberculosis, ZN Lab: Ziehl Nelsen health facility laboratories-, LED-FM Lab: Light emitting diode-fluorescence microscopy using health facility laboratories, NTM: Non-tuberculous Mycobacteria, cont.: contaminated

Article Snippet: Based on quality control of smear microscopy (QC) data of 2012 and 2013 these eight laboratories performed equally well, though the QC for intermediate is performed by the NRL whereas QC for peripheral are subsequently done by ILs.

Techniques: Fluorescence, Microscopy

Yield of smear  microscopy  versus Xpert among culture confirmed tuberculosis patients ( n =96)

Journal: BMC Infectious Diseases

Article Title: Diagnostic performance of smear microscopy and incremental yield of Xpert in detection of pulmonary tuberculosis in Rwanda

doi: 10.1186/s12879-016-2009-x

Figure Lengend Snippet: Yield of smear microscopy versus Xpert among culture confirmed tuberculosis patients ( n =96)

Article Snippet: Based on quality control of smear microscopy (QC) data of 2012 and 2013 these eight laboratories performed equally well, though the QC for intermediate is performed by the NRL whereas QC for peripheral are subsequently done by ILs.

Techniques: Microscopy