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  • Open Access

    ARTICLE

    Enhanced Diagnostic Precision: Deep Learning for Tumors Lesion Classification in Dermatology

    Rafid Sagban1,2,*, Haydar Abdulameer Marhoon3,4, Saadaldeen Rashid Ahmed5,6,*

    Intelligent Automation & Soft Computing, Vol.39, No.6, pp. 1035-1051, 2024, DOI:10.32604/iasc.2024.058416 - 30 December 2024

    Abstract Skin cancer is a highly frequent kind of cancer. Early identification of a phenomenon significantly improves outcomes and mitigates the risk of fatalities. Melanoma, basal, and squamous cell carcinomas are well-recognized cutaneous malignancies. Malignant We can differentiate Melanoma from non-pigmented carcinomas like basal and squamous cell carcinoma. The research on developing automated skin cancer detection systems has primarily focused on pigmented malignant type melanoma. The limited availability of datasets with a wide range of lesion categories has hindered in-depth exploration of non-pigmented malignant skin lesions. The present study investigates the feasibility of automated methods for… More >

  • Open Access

    ARTICLE

    Basal cell carcinoma stem cells exhibit osteogenic and chondrogenic differentiation potential

    MAJA MILOSEVIC1,2, MILOS LAZAREVIC1,2, BOSKO TOLJIC1, MILAN PETROVIC2, MIROSLAV VUKADINOVIC2, ZORAN JEZDIC2, BOBAN ANICIC2, DRAGO JELOVAC2, SVETLANA JOVANOVIC3, JELENA MILASIN1,*

    BIOCELL, Vol.45, No.6, pp. 1543-1550, 2021, DOI:10.32604/biocell.2021.015060 - 01 September 2021

    Abstract Specific cell subpopulations identified as cancer stem cells (CSCs) can be found in basal cell carcinoma (BCC). Generally, CSCs have a marked trans-differentiation potential that could potentially be used in differentiation therapies. However, there are no studies regarding BCC CSCs multipotency. The aim of the study was to analyze the characteristic of CSCs of BCC with emphasis on their differentiation potential upon specific induction. Specific staining and cell morphology were used for differentiation confirmation, along with the expression analysis of osteogenic (ALP, BSP, Runx2, OCN, BMP2), chondrogenic (COL1 and COL2A1), adipogenic (PPAR-γ) and neurogenic (Nestin More >

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