special gui software matlab r2023b Search Results


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MathWorks Inc special gui software matlab r2023b
Imaging system speckle generation, speckle acquisition, power supply, and <t>GUI</t> <t>controlling</t> units and their hardware components.
Special Gui Software Matlab R2023b, supplied by MathWorks 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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MathWorks Inc custom-written gui in matlab r2023a
Imaging system speckle generation, speckle acquisition, power supply, and <t>GUI</t> <t>controlling</t> units and their hardware components.
Custom Written Gui In Matlab R2023a, supplied by MathWorks 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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Imaging system speckle generation, speckle acquisition, power supply, and <t>GUI</t> <t>controlling</t> units and their hardware components.
Matlab R2021b, supplied by MathWorks 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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Designed <t>GUI</t> application with <t>MATLAB</t>
Gui Application R2020b, supplied by MathWorks 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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MathWorks Inc gui
Designed <t>GUI</t> application with <t>MATLAB</t>
Gui, supplied by MathWorks 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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Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using <t>MATLAB.</t> (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.
R2021b, supplied by MathWorks 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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Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using <t>MATLAB.</t> (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.
R2020b, supplied by MathWorks 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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MathWorks Inc spectral processing gui script
Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using <t>MATLAB.</t> (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.
Spectral Processing Gui Script, supplied by MathWorks 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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MathWorks Inc graphical user interface matlab r2022b
Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using <t>MATLAB.</t> (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.
Graphical User Interface Matlab R2022b, supplied by MathWorks 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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Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using <t>MATLAB.</t> (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.
Matlab R2020b, supplied by MathWorks 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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MathWorks Inc graphical user interface (gui)
Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using <t>MATLAB.</t> (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.
Graphical User Interface (Gui), supplied by MathWorks 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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Image Search Results


Imaging system speckle generation, speckle acquisition, power supply, and GUI controlling units and their hardware components.

Journal: Journal of Imaging

Article Title: The Methodology of Adaptive Levels of Interval for Laser Speckle Imaging

doi: 10.3390/jimaging10110289

Figure Lengend Snippet: Imaging system speckle generation, speckle acquisition, power supply, and GUI controlling units and their hardware components.

Article Snippet: GUI controlling Unit: This unit executes a special GUI software (MATLAB R2023b) to control the process of dynamic laser speckle generation and acquisition.

Techniques: Imaging

Designed GUI application with MATLAB

Journal: Analog Integrated Circuits and Signal Processing

Article Title: Auricular vagus nerve stimulator for closed-loop biofeedback-based operation

doi: 10.1007/s10470-022-02037-8

Figure Lengend Snippet: Designed GUI application with MATLAB

Article Snippet: We designed a system which can be operated in two modes: (1) experimental setup with external biosignal acquisition and a PC running a MATLAB GUI application (R2020b, the MathWorks Inc., Natick, MA, USA), and (2) standalone setup with a microcontroller unit (MCU) as the main processor, with integrated or Bluetooth-connected biosensors for portable closed-loop wearable aVNS (Fig. ).

Techniques:

Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using MATLAB. (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.

Journal: bioRxiv

Article Title: Therapeutic suppression of Tubb4a rescues H-ABC leukodystrophy

doi: 10.1101/2024.08.27.609903

Figure Lengend Snippet: Treatment groups include WT PBS, WT ASO, Tubb4a D249N/KO PBS-treated, and Tubb4a D249N/KO ASO-treated. (A) Study design (B) Representative EM images of ASO-treated mice of the corpus callosum at P48. (C) Graphical presentation of g-ratio across different treatment groups. (D) Graphical presentation of % unmyelinated axons across different treatment groups. (E) Graphical presentation of the number of vacuoles (Vacuoles #). For EM data, n=3-4 animals are used, and at least 4-5 images per animal are used. For the g-ratio, at least 30-40 axons per image were used to measure the g-ratio. (F) Representative histochemical images of Eri-C (myelin) staining in the cerebellum at P48. (G) The mean of visual evoked potential peaks of all groups generated using MATLAB. (H) Representative immunofluorescent images of ASPA+ (red) DAPI+ (blue) cells in the corpus callosum at P48 (I) Graphical presentation of myelin quantification (Eri-C) analysis across treatment groups. (J) Graphical presentation of ASPA+ Olig2+ cells in the corpus callosum. (K and L) Graphical presentation of N1 and P2 latencies at P48. n=3-9 animals per treatment group. p-values are calculated using one-way or two-way ANOVA with Tukey corrections. *p<0.05, **p<0.001, ***p<0.0001. Connected Supplemental Figures are Supplemental Figures 24-31.

Article Snippet: Raw EVP data was imported into MATLAB R2021b (Mathworks Inc., Natick, MA) via read_Intan Gui (Intan Technologies, Los Angeles, CA).

Techniques: Staining, Generated