يعرض 1 - 10 نتائج من 44 نتيجة بحث عن '"Patil, Rajkumar V."', وقت الاستعلام: 0.92s تنقيح النتائج
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    دورية أكاديمية

    المؤلفون: Patil, Rajkumar V.Aff1, IDs41870020005309_cor1, Mahalle, Parikshit N., Shinde, Gitanjali R.

    المصدر: International Journal of Information Technology: An Official Journal of Bharati Vidyapeeth's Institute of Computer Applications and Management. 14(3):1355-1365

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    كتاب إلكتروني

    المساهمون: Kacprzyk, Janusz, Series EditorAff1, Mahalle, Parikshit N., editorAff2, Shinde, Gitanjali R., editorAff3, Dey, Nilanjan, editorAff4, Hassanien, Aboul Ella, editorAff5

    المصدر: Security Issues and Privacy Threats in Smart Ubiquitous Computing. 341:195-211

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    دورية أكاديمية
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    كتاب إلكتروني

    المؤلفون: Han, ZhiqiangAff3, Patil, Rajkumar V.Aff3, Aff4

    المساهمون: Hohmann, Stefan, editorAff1, Nielsen, Søren, editorAff2

    المصدر: Molecular Biology and Physiology of Water and Solute Transport. :107-113

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    دورية أكاديمية

    المصدر: Proceedings of the National Academy of Sciences of the United States of America, 1987 Jan . 84(2), 393-397.

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    المصدر: Molecular Vision

    الوصف: Purpose The purpose of this study was to determine the effects of down-regulation of Aquaporin 1 (AQP1) and Aquaporin 5 (AQP5) on cell proliferation and migration in human corneal endothelial (HCEC) and human corneal epithelial (CEPI17) cell lines, respectively. Methods AQP1 and AQP5 were down regulated using siRNA following lipofectamine-mediated transfection in corneal endothelial and epithelial cells, respectively. Down-regulation was confirmed using RT–PCR, indirect immunofluorescence, and immunoblot analysis. Total internal reflection fluorescence (TIRF) microscopy was used to detect cell surface aquaporin expression. Cell proliferation was determined by SRB (sulfrodamine B) assay. Cell migration was determined by in vitro wound healing and migration assay. Results In HCEC cells, AQP1 was localized to the cytosol as well as cell membrane and its down-regulation resulted in decreased cell proliferation and migration with a significant decrease in phosphorylated ERK (pERK). In CEPI17 cells AQP5 protein expression was also localized to cytosol as well as cell membrane. AQP5 down-regulation resulted in an increase in proliferation and cell migration with no significant difference in pERK. Conclusions AQP1 plays a role in HCEC proliferation and migration via the ERK signaling pathway and therefore may have significant implications in corneal endothelial dysfunction whereas; AQP5 may play an indirect role in human corneal epithelial cell proliferation and migration.

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    دورية أكاديمية
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    دورية أكاديمية