Search alternatives:
de decrease » _ decrease (Expand Search), mean decrease (Expand Search), teer decrease (Expand Search)
we decrease » _ decrease (Expand Search), mean decrease (Expand Search), teer decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
2 de » 2 d (Expand Search), _ de (Expand Search), i de (Expand Search)
de decrease » _ decrease (Expand Search), mean decrease (Expand Search), teer decrease (Expand Search)
we decrease » _ decrease (Expand Search), mean decrease (Expand Search), teer decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
2 de » 2 d (Expand Search), _ de (Expand Search), i de (Expand Search)
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11601
Image1_miR-146a is a critical target associated with multiple biological pathways of skin aging.jpg
Published 2024“…Effects on markers of skin aging, including cell proliferation, production of Collagen-1 and inflammatory cytokines were assessed.</p><p>Results: We show that the expression of miR-146a decreases with age in dermal fibroblasts and inhibition of miR-146a in 19y and 62y old NHDFs induced significant changes in essential clock genes indicating an association with circadian rhythm control. …”
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11602
Image2_miR-146a is a critical target associated with multiple biological pathways of skin aging.jpg
Published 2024“…Effects on markers of skin aging, including cell proliferation, production of Collagen-1 and inflammatory cytokines were assessed.</p><p>Results: We show that the expression of miR-146a decreases with age in dermal fibroblasts and inhibition of miR-146a in 19y and 62y old NHDFs induced significant changes in essential clock genes indicating an association with circadian rhythm control. …”
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11603
DataSheet_1_Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient With Hemophagocytic Syndrome and Langerhans Cell Histiocytosis.docx
Published 2021“…In this study, we analyzed the molecular and functional impact of a novel monoallelic mutation found in a patient with two episodes of HLH. …”
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11604
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11605
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11606
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11607
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11608
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11609
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11610
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11611
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11612
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11613
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11614
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11615
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11616
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11617
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11618
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11619
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11620