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home made matlab software  (MathWorks Inc)


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    MathWorks Inc home made matlab software
    Home Made Matlab Software, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 326 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/home-made+software/MATLAB+Compiler/pm26225640__nl5b01243_si_001-14-1-2
    Average 96 stars, based on 326 article reviews
    home made matlab software - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Refractive Index:

    Article Title: CFTR-deficient pigs display alterations of bone microarchitecture and composition at birth.
    Article Snippet: This was done with a home- ade software using the Matlab environment (The MathWorks, nc., Natick, Massachusetts).

    Article Title: Visible‐Light Photo‐Iniferter Polymerization of Molecularly Imprinted Polymers for Direct Integration with Nanotransducers
    Article Snippet: FFT of the reflectance spectra of PSiO 2 interferometers was performed to calculate the EOT values, namely, 2 nL, where n = effective refractive index and L = thickness of the PSi layer, using a home‐made software (MatLab, MathWorks, USA).

    Article Title: Sleep deprivation and Modafinil affect cortical sources of resting state electroencephalographic rhythms in healthy young adults.
    Article Snippet: The power density of the rsEEG rhythms (frequency resolution: 0.5 Hz) was computed with standard digital FFT-based power spectrum analysis (Hanning windowing function, Welch technique, no phase shift) using a home-made software getted under Matlab 6.5 (Mathworks Inc., Natick, MA).

    Article Title: Electrical Double Layer-Induced Ion Surface Accumulation for Ultrasensitive Refractive Index Sensing with Nanostructured Porous Silicon Interferometers.
    Article Snippet: Herein, we provide the first experimental evidence on the use of electrical double layer (EDL)induced accumulation of charged ions (using both Na + and K + ions in water as model) onto a negatively-charged nanostructured surface (e.g. thermally growth SiO2) – Ion Surface Accumulation, ISA – as a means of improving performance of nanostructured porous silicon (PSi) interferometers for optical refractometric applications.. Nanostructured PSi interferometers are very promising optical platforms for refractive index sensing due to PSi huge specific surface (hundreds of m 2 per gram) and low preparation cost (less than 0.01$ per 8’’silicon wafer), though they have shown poor resolution (R) and detection limit (DL) (in the order of 10 -4 – 10 -5 RIU) compared to other plasmonic and photonic platforms (R and DL in the order of 10 -7 – 10 -8 RIU).. This can be ascribed to both low sensitivity and high noise floor of PSi interferometers when bulk refractive index variation of the solution infiltrating the nanopores either approaches or is below 10 -4 RIU.

    Article Title: Protection against summer solar lentigo over-pigmentation with a SPF30 daily cream.
    Article Snippet: Solar lentigines (also called senile lentigines, “age spots,” “liver spots”) are macular hyperpigmented lesions, induced by chronic sun exposure and progressing with age.1 Solar lentigine spots are usually light brown with a diameter ranging from less than 1 mm to a few centimetres and are predominantly observed on the dorsa of the hands, the forearms and the face.. They affect more than 90% of white persons after the age of 50 years.2 Lentigine spots are usually considered unsightly and various depigmentation methods have been developed, including ablative therapies (cryotherapy, laser, pulsed light, chemical peels) and topical depigmenting agents.2 The lentigines have been widely investigated histologically, the main characteristics being epidermal hyperplasia, a budding of the rete ridges, and hyperpigmentation.3,4 Noninvasive imaging techniques have been shown to be very useful in analyzing the structures of pigmented lesions and in assessing the treatments’ efficacy.. Color measurements are usually performed with chromameters5 or with color calibrated camera.6 In vivo reflectance confocal microscopy (RCM) enables noninvasive imaging of indepth skin structure.

    Article Title: Entropy modulation of electroencephalographic signals in physiological aging.
    Article Snippet: Aging is a multifactorial physiological process characterized by the accumulation of degenerative processes impacting on different brain functions, including the cognitive one.. A tool largely employed in the investigation of brain networks is the electroencephalogram (EEG).. Given the cerebral complexity and dynamism, many nonlinear approaches have been applied to explore age-related brain electrical activity modulation detected by the EEG: one of them is the entropy, which measures the disorder of a system.

    Article Title: Visible-Light Photo-Iniferter Polymerization of Molecularly Imprinted Polymers for Direct Integration with Nanotransducers.
    Article Snippet: FFT of the reflectance spectra of PSiO2 interferometers was performed to calculate the EOT values, namely, 2 nL, where n = effective refractive index and L = thickness of the PSi layer, using a home-made software (MatLab, MathWorks, USA).

    Software:

    Article Title: CFTR-deficient pigs display alterations of bone microarchitecture and composition at birth.
    Article Snippet: This was done with a home- ade software using the Matlab environment (The MathWorks, nc., Natick, Massachusetts).

    Article Title: Visible‐Light Photo‐Iniferter Polymerization of Molecularly Imprinted Polymers for Direct Integration with Nanotransducers
    Article Snippet: FFT of the reflectance spectra of PSiO 2 interferometers was performed to calculate the EOT values, namely, 2 nL, where n = effective refractive index and L = thickness of the PSi layer, using a home‐made software (MatLab, MathWorks, USA).

    Article Title: Sleep deprivation and Modafinil affect cortical sources of resting state electroencephalographic rhythms in healthy young adults.
    Article Snippet: The power density of the rsEEG rhythms (frequency resolution: 0.5 Hz) was computed with standard digital FFT-based power spectrum analysis (Hanning windowing function, Welch technique, no phase shift) using a home-made software getted under Matlab 6.5 (Mathworks Inc., Natick, MA).

    Article Title: Electrical Double Layer-Induced Ion Surface Accumulation for Ultrasensitive Refractive Index Sensing with Nanostructured Porous Silicon Interferometers.
    Article Snippet: Herein, we provide the first experimental evidence on the use of electrical double layer (EDL)induced accumulation of charged ions (using both Na + and K + ions in water as model) onto a negatively-charged nanostructured surface (e.g. thermally growth SiO2) – Ion Surface Accumulation, ISA – as a means of improving performance of nanostructured porous silicon (PSi) interferometers for optical refractometric applications.. Nanostructured PSi interferometers are very promising optical platforms for refractive index sensing due to PSi huge specific surface (hundreds of m 2 per gram) and low preparation cost (less than 0.01$ per 8’’silicon wafer), though they have shown poor resolution (R) and detection limit (DL) (in the order of 10 -4 – 10 -5 RIU) compared to other plasmonic and photonic platforms (R and DL in the order of 10 -7 – 10 -8 RIU).. This can be ascribed to both low sensitivity and high noise floor of PSi interferometers when bulk refractive index variation of the solution infiltrating the nanopores either approaches or is below 10 -4 RIU.

    Article Title: Protection against summer solar lentigo over-pigmentation with a SPF30 daily cream.
    Article Snippet: Solar lentigines (also called senile lentigines, “age spots,” “liver spots”) are macular hyperpigmented lesions, induced by chronic sun exposure and progressing with age.1 Solar lentigine spots are usually light brown with a diameter ranging from less than 1 mm to a few centimetres and are predominantly observed on the dorsa of the hands, the forearms and the face.. They affect more than 90% of white persons after the age of 50 years.2 Lentigine spots are usually considered unsightly and various depigmentation methods have been developed, including ablative therapies (cryotherapy, laser, pulsed light, chemical peels) and topical depigmenting agents.2 The lentigines have been widely investigated histologically, the main characteristics being epidermal hyperplasia, a budding of the rete ridges, and hyperpigmentation.3,4 Noninvasive imaging techniques have been shown to be very useful in analyzing the structures of pigmented lesions and in assessing the treatments’ efficacy.. Color measurements are usually performed with chromameters5 or with color calibrated camera.6 In vivo reflectance confocal microscopy (RCM) enables noninvasive imaging of indepth skin structure.

    Article Title: Entropy modulation of electroencephalographic signals in physiological aging.
    Article Snippet: Aging is a multifactorial physiological process characterized by the accumulation of degenerative processes impacting on different brain functions, including the cognitive one.. A tool largely employed in the investigation of brain networks is the electroencephalogram (EEG).. Given the cerebral complexity and dynamism, many nonlinear approaches have been applied to explore age-related brain electrical activity modulation detected by the EEG: one of them is the entropy, which measures the disorder of a system.

    Article Title: Visible-Light Photo-Iniferter Polymerization of Molecularly Imprinted Polymers for Direct Integration with Nanotransducers.
    Article Snippet: FFT of the reflectance spectra of PSiO2 interferometers was performed to calculate the EOT values, namely, 2 nL, where n = effective refractive index and L = thickness of the PSi layer, using a home-made software (MatLab, MathWorks, USA).

    Spectroscopy:

    Article Title: CFTR-deficient pigs display alterations of bone microarchitecture and composition at birth.
    Article Snippet: This was done with a home- ade software using the Matlab environment (The MathWorks, nc., Natick, Massachusetts).

    Article Title: Visible‐Light Photo‐Iniferter Polymerization of Molecularly Imprinted Polymers for Direct Integration with Nanotransducers
    Article Snippet: FFT of the reflectance spectra of PSiO 2 interferometers was performed to calculate the EOT values, namely, 2 nL, where n = effective refractive index and L = thickness of the PSi layer, using a home‐made software (MatLab, MathWorks, USA).

    Article Title: Sleep deprivation and Modafinil affect cortical sources of resting state electroencephalographic rhythms in healthy young adults.
    Article Snippet: The power density of the rsEEG rhythms (frequency resolution: 0.5 Hz) was computed with standard digital FFT-based power spectrum analysis (Hanning windowing function, Welch technique, no phase shift) using a home-made software getted under Matlab 6.5 (Mathworks Inc., Natick, MA).

    Article Title: Electrical Double Layer-Induced Ion Surface Accumulation for Ultrasensitive Refractive Index Sensing with Nanostructured Porous Silicon Interferometers.
    Article Snippet: Herein, we provide the first experimental evidence on the use of electrical double layer (EDL)induced accumulation of charged ions (using both Na + and K + ions in water as model) onto a negatively-charged nanostructured surface (e.g. thermally growth SiO2) – Ion Surface Accumulation, ISA – as a means of improving performance of nanostructured porous silicon (PSi) interferometers for optical refractometric applications.. Nanostructured PSi interferometers are very promising optical platforms for refractive index sensing due to PSi huge specific surface (hundreds of m 2 per gram) and low preparation cost (less than 0.01$ per 8’’silicon wafer), though they have shown poor resolution (R) and detection limit (DL) (in the order of 10 -4 – 10 -5 RIU) compared to other plasmonic and photonic platforms (R and DL in the order of 10 -7 – 10 -8 RIU).. This can be ascribed to both low sensitivity and high noise floor of PSi interferometers when bulk refractive index variation of the solution infiltrating the nanopores either approaches or is below 10 -4 RIU.

    Article Title: Protection against summer solar lentigo over-pigmentation with a SPF30 daily cream.
    Article Snippet: Solar lentigines (also called senile lentigines, “age spots,” “liver spots”) are macular hyperpigmented lesions, induced by chronic sun exposure and progressing with age.1 Solar lentigine spots are usually light brown with a diameter ranging from less than 1 mm to a few centimetres and are predominantly observed on the dorsa of the hands, the forearms and the face.. They affect more than 90% of white persons after the age of 50 years.2 Lentigine spots are usually considered unsightly and various depigmentation methods have been developed, including ablative therapies (cryotherapy, laser, pulsed light, chemical peels) and topical depigmenting agents.2 The lentigines have been widely investigated histologically, the main characteristics being epidermal hyperplasia, a budding of the rete ridges, and hyperpigmentation.3,4 Noninvasive imaging techniques have been shown to be very useful in analyzing the structures of pigmented lesions and in assessing the treatments’ efficacy.. Color measurements are usually performed with chromameters5 or with color calibrated camera.6 In vivo reflectance confocal microscopy (RCM) enables noninvasive imaging of indepth skin structure.

    Article Title: Entropy modulation of electroencephalographic signals in physiological aging.
    Article Snippet: Aging is a multifactorial physiological process characterized by the accumulation of degenerative processes impacting on different brain functions, including the cognitive one.. A tool largely employed in the investigation of brain networks is the electroencephalogram (EEG).. Given the cerebral complexity and dynamism, many nonlinear approaches have been applied to explore age-related brain electrical activity modulation detected by the EEG: one of them is the entropy, which measures the disorder of a system.

    Article Title: Visible-Light Photo-Iniferter Polymerization of Molecularly Imprinted Polymers for Direct Integration with Nanotransducers.
    Article Snippet: FFT of the reflectance spectra of PSiO2 interferometers was performed to calculate the EOT values, namely, 2 nL, where n = effective refractive index and L = thickness of the PSi layer, using a home-made software (MatLab, MathWorks, USA).



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    Arraystar inc home‐made mirna target prediction software
    circ‐TNRC6B serves as a miR‐452‐5p sponge in ESCC cells. (A) <t>CircRNA‐miRNA</t> binding circle diagram showing potential miRNA targets of circ‐TNRC6B predicted by Arraystar's home‐made miRNA target prediction software based on TargetScan and miRanda. (B) Venn diagram showing the intersection of potential miRNA targets of circ‐TNRC6B based on Arraystar's home‐made miRNA target prediction software, ENCORI, and circBank databases. (C) The complementary sequences of circ‐TNRC6B and miR‐452‐5p were predicted by Arraystar's home‐made miRNA target prediction software. (D) The MFE secondary structure of circ‐TNRC6B predicted by RNAfold web server and the part where the secondary structure of circ‐TNRC6B is relevant for the binding of miR‐452‐5p. (E) FISH assay indicated circ‐TNRC6B and miR‐452‐5p were co‐localized in the cytoplasm of KYSE150 cells ( n = 3). Scale bar: 20 μm. (F) RIP analysis in KYSE150 cells co‐transfected with Myc‐AGO2 vector and miR‐452‐5p mimics. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (G) RIP analysis in KYSE150 cells co‐transfected with Myc‐AGO2 vector and NC ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). Data are represented as mean ± SD. (H) Dual‐luciferase reporter gene analysis detected the luciferase activity of circ‐TNRC6B when co‐transfected with luc‐empty vector or wild‐type luc‐circ‐TNRC6B vector and NC or miR‐452‐5p mimics in KYSE150 cells. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (I) Dual‐luciferase reporter gene analysis detected the luciferase activity of circ‐TNRC6B when co‐transfected with mutant luc‐circ‐TNRC6B vector and NC or miR‐452‐5p mimics in KYSE150 cells. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (J) TE1 cells were transfected with pLC5 empty vector or circ‐TNRC6B vector; then, the relative expression of circ‐TNRC6B and miR‐452‐5p were detected by qRT‐PCR assay. Data are represented as mean ± SD ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). (K) KYSE150 cells were transfected with si‐NC or si‐circ‐TNRC6B; then, the relative expression of circ‐TNRC6B and miR‐452‐5p was detected by qRT‐PCR assay. Data are represented as mean ± SD ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). * P < 0.05, ** P < 0.01.
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    circ‐TNRC6B serves as a miR‐452‐5p sponge in ESCC cells. (A) CircRNA‐miRNA binding circle diagram showing potential miRNA targets of circ‐TNRC6B predicted by Arraystar's home‐made miRNA target prediction software based on TargetScan and miRanda. (B) Venn diagram showing the intersection of potential miRNA targets of circ‐TNRC6B based on Arraystar's home‐made miRNA target prediction software, ENCORI, and circBank databases. (C) The complementary sequences of circ‐TNRC6B and miR‐452‐5p were predicted by Arraystar's home‐made miRNA target prediction software. (D) The MFE secondary structure of circ‐TNRC6B predicted by RNAfold web server and the part where the secondary structure of circ‐TNRC6B is relevant for the binding of miR‐452‐5p. (E) FISH assay indicated circ‐TNRC6B and miR‐452‐5p were co‐localized in the cytoplasm of KYSE150 cells ( n = 3). Scale bar: 20 μm. (F) RIP analysis in KYSE150 cells co‐transfected with Myc‐AGO2 vector and miR‐452‐5p mimics. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (G) RIP analysis in KYSE150 cells co‐transfected with Myc‐AGO2 vector and NC ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). Data are represented as mean ± SD. (H) Dual‐luciferase reporter gene analysis detected the luciferase activity of circ‐TNRC6B when co‐transfected with luc‐empty vector or wild‐type luc‐circ‐TNRC6B vector and NC or miR‐452‐5p mimics in KYSE150 cells. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (I) Dual‐luciferase reporter gene analysis detected the luciferase activity of circ‐TNRC6B when co‐transfected with mutant luc‐circ‐TNRC6B vector and NC or miR‐452‐5p mimics in KYSE150 cells. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (J) TE1 cells were transfected with pLC5 empty vector or circ‐TNRC6B vector; then, the relative expression of circ‐TNRC6B and miR‐452‐5p were detected by qRT‐PCR assay. Data are represented as mean ± SD ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). (K) KYSE150 cells were transfected with si‐NC or si‐circ‐TNRC6B; then, the relative expression of circ‐TNRC6B and miR‐452‐5p was detected by qRT‐PCR assay. Data are represented as mean ± SD ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). * P < 0.05, ** P < 0.01.

    Journal: Molecular Oncology

    Article Title: Circular RNA circ‐TNRC6B inhibits the proliferation and invasion of esophageal squamous cell carcinoma cells by regulating the miR ‐452‐5p/ DAG1 axis

    doi: 10.1002/1878-0261.13432

    Figure Lengend Snippet: circ‐TNRC6B serves as a miR‐452‐5p sponge in ESCC cells. (A) CircRNA‐miRNA binding circle diagram showing potential miRNA targets of circ‐TNRC6B predicted by Arraystar's home‐made miRNA target prediction software based on TargetScan and miRanda. (B) Venn diagram showing the intersection of potential miRNA targets of circ‐TNRC6B based on Arraystar's home‐made miRNA target prediction software, ENCORI, and circBank databases. (C) The complementary sequences of circ‐TNRC6B and miR‐452‐5p were predicted by Arraystar's home‐made miRNA target prediction software. (D) The MFE secondary structure of circ‐TNRC6B predicted by RNAfold web server and the part where the secondary structure of circ‐TNRC6B is relevant for the binding of miR‐452‐5p. (E) FISH assay indicated circ‐TNRC6B and miR‐452‐5p were co‐localized in the cytoplasm of KYSE150 cells ( n = 3). Scale bar: 20 μm. (F) RIP analysis in KYSE150 cells co‐transfected with Myc‐AGO2 vector and miR‐452‐5p mimics. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (G) RIP analysis in KYSE150 cells co‐transfected with Myc‐AGO2 vector and NC ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). Data are represented as mean ± SD. (H) Dual‐luciferase reporter gene analysis detected the luciferase activity of circ‐TNRC6B when co‐transfected with luc‐empty vector or wild‐type luc‐circ‐TNRC6B vector and NC or miR‐452‐5p mimics in KYSE150 cells. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (I) Dual‐luciferase reporter gene analysis detected the luciferase activity of circ‐TNRC6B when co‐transfected with mutant luc‐circ‐TNRC6B vector and NC or miR‐452‐5p mimics in KYSE150 cells. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). (J) TE1 cells were transfected with pLC5 empty vector or circ‐TNRC6B vector; then, the relative expression of circ‐TNRC6B and miR‐452‐5p were detected by qRT‐PCR assay. Data are represented as mean ± SD ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). (K) KYSE150 cells were transfected with si‐NC or si‐circ‐TNRC6B; then, the relative expression of circ‐TNRC6B and miR‐452‐5p was detected by qRT‐PCR assay. Data are represented as mean ± SD ( n = 2, P ‐values were determined by Mann–Whitney U ‐test). * P < 0.05, ** P < 0.01.

    Article Snippet: The results were compared with the miRNAs predicted by home‐made miRNA target prediction software from Arraystar. miR‐452‐5p was selected as a candidate miRNA for further analysis (Fig. ).

    Techniques: Binding Assay, Software, Transfection, Plasmid Preparation, MANN-WHITNEY, Luciferase, Activity Assay, Mutagenesis, Expressing, Quantitative RT-PCR

    miR‐452‐5p promotes the proliferation, migration, and invasion abilities of ESCC cells. (A) The relative expression level of miR‐452‐5p in four ESCC cell lines was examined by qRT‐PCR ( n = 2). Data are represented as mean ± SD. (B, C) The proliferative and clonogenic ability of TE1 cells after exogenous miR‐452‐5p mimics transfection was detected by CCK‐8 ( n = 4, P ‐values were determined by two‐way ANOVA) and colony formation assay ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). NC: negative control of miRNA mimics. Data are represented as mean ± SD. (D, E) The migration ability of TE1 cells after exogenous miR‐452‐5p mimics transfection was detected by wound healing and transwell migration assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. (F) The invasion ability of TE1 cells after exogenous miR‐452‐5p mimics transfection was detected by transwell invasion assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. (G, H) The proliferative and clonogenic ability of KYSE170 cells after miR‐452‐5p inhibitor transfection was detected by CCK‐8 ( n = 4, P ‐values were determined by two‐way ANOVA) and colony formation assay ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Inhibitor NC: negative control of miRNA inhibitor. Data are represented as mean ± SD. (I, J) The migration ability of KYSE170 cells after miR‐452‐5p inhibitor transfection was detected by wound‐healing and transwell migration assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. (K) The invasion ability of KYSE170 cells after miR‐452‐5p inhibitor transfection was detected by transwell invasion assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: Molecular Oncology

    Article Title: Circular RNA circ‐TNRC6B inhibits the proliferation and invasion of esophageal squamous cell carcinoma cells by regulating the miR ‐452‐5p/ DAG1 axis

    doi: 10.1002/1878-0261.13432

    Figure Lengend Snippet: miR‐452‐5p promotes the proliferation, migration, and invasion abilities of ESCC cells. (A) The relative expression level of miR‐452‐5p in four ESCC cell lines was examined by qRT‐PCR ( n = 2). Data are represented as mean ± SD. (B, C) The proliferative and clonogenic ability of TE1 cells after exogenous miR‐452‐5p mimics transfection was detected by CCK‐8 ( n = 4, P ‐values were determined by two‐way ANOVA) and colony formation assay ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). NC: negative control of miRNA mimics. Data are represented as mean ± SD. (D, E) The migration ability of TE1 cells after exogenous miR‐452‐5p mimics transfection was detected by wound healing and transwell migration assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. (F) The invasion ability of TE1 cells after exogenous miR‐452‐5p mimics transfection was detected by transwell invasion assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. (G, H) The proliferative and clonogenic ability of KYSE170 cells after miR‐452‐5p inhibitor transfection was detected by CCK‐8 ( n = 4, P ‐values were determined by two‐way ANOVA) and colony formation assay ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Inhibitor NC: negative control of miRNA inhibitor. Data are represented as mean ± SD. (I, J) The migration ability of KYSE170 cells after miR‐452‐5p inhibitor transfection was detected by wound‐healing and transwell migration assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. (K) The invasion ability of KYSE170 cells after miR‐452‐5p inhibitor transfection was detected by transwell invasion assay. Data are represented as mean ± SD ( n = 3, P ‐values were determined by Mann–Whitney U ‐test). Scale bar: 100 μm. * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: The results were compared with the miRNAs predicted by home‐made miRNA target prediction software from Arraystar. miR‐452‐5p was selected as a candidate miRNA for further analysis (Fig. ).

    Techniques: Migration, Expressing, Quantitative RT-PCR, Transfection, CCK-8 Assay, Colony Assay, MANN-WHITNEY, Negative Control, Transwell Migration Assay, Transwell Invasion Assay