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Aiforia Technologies deep-learning dedicated algorithm
Deep Learning Dedicated Algorithm, supplied by Aiforia Technologies, 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/deep-learning+dedicated+algorithm/deep+learning+dedicated+algorithm/pm39487447-102-5-11
Average 90 stars, based on 1 article reviews
deep-learning dedicated algorithm - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia®) that has been successfully validated and published by Penttinen et al. [61].

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia®), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia ® ), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia ® ), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE-003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File ).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia®), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File 7).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia ® ) that has been successfully validated and published by Penttinen et al. [ ].

Preserving:

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia®) that has been successfully validated and published by Penttinen et al. [61].

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia®), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia ® ), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia ® ), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE-003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File ).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia®), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File 7).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia ® ) that has been successfully validated and published by Penttinen et al. [ ].

Immunostaining:

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia®) that has been successfully validated and published by Penttinen et al. [61].

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia®), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia ® ), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia ® ), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE-003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File ).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia®), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File 7).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia ® ) that has been successfully validated and published by Penttinen et al. [ ].

Control:

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia®) that has been successfully validated and published by Penttinen et al. [61].

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia®), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: Supplementary Material 7: Number of TH-positive neurons measured, using a deep-learning dedicated algorithm (Aiforia ® ), in a selected area of the SNpc of vehicle-treated control (sham-operated) adult male mice and unilaterally AAV9-SynA53T-injected adult male mice treated with vehicle or VCE-00.2 (20 mg/kg) given orally.

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia ® ), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE-003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File ).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy.
Article Snippet: In a further analysis, using a stereological-like analysis based on a deep-learning dedicated algorithm (Aiforia®), we could confirm that the reduction in TH measured in the SNpc of mice injected with AAV9-SynA53T, as well as the recovery detected after the treatment with VCE003.2, reflected both a loss and a preservation in the number of TH-positive neurons, respectively (F(2,21) = 6.72, p < 0.01; see Supplementary File 7).

Article Title: Investigation in the cannabigerol derivative VCE-003.2 as a disease-modifying agent in a mouse model of experimental synucleinopathy
Article Snippet: The analysis of nigral dopaminergic neurons was carried out using first classic immunostaining, but the results were furtherly confirmed with a stereological-like procedure based on a deep-learning dedicated algorithm (Aiforia ® ) that has been successfully validated and published by Penttinen et al. [ ].



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