Showing 15,121 - 15,140 results of 74,781 for search '(( 50 ((a decrease) OR (nn decrease)) ) OR ( 5 ((we decrease) OR (mean decrease)) ))', query time: 1.33s Refine Results
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    DNMT1 reduces cisplatin sensitivity partially through downregulating FOXO3a in ovarian cancer cells by Chong Guo (5819105)

    Published 2025
    “…Knocking down of DNMT1 could decrease the IC<sub>50</sub> of cisplatin. Treatment with cisplatin may reduce FOXO3a expression in OC cells. …”
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    Hopping into a hot seat: Role of DNA structural features on IS<i>5</i>-mediated gene activation and inactivation under stress - Fig 7 by M. Zafri Humayun (4217524)

    Published 2017
    “…The G(x) values are decreased for the <i>ORF-3</i> mutation (blue), meaning that the duplex is further destabilized relative to the wild type sequence. …”
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    Exploring the relationship between collaterals and vessel density in retinal vein occlusions using optical coherence tomography angiography by Hee Eun Lee (538675)

    Published 2019
    “…Located exclusively in the SCP, true superficial collaterals were all arteriovenous (A-V), while diving collaterals were all veno-venular (V-V). …”
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    Validation of hTERT mRNA as a direct target of miR-512-5p in CNE cells. by Jun Li (6494)

    Published 2015
    “…(B) MiR-512-5p resulted in a significant decrease in luciferase expression in hTERT-3’UTR transfected cells compared with the scramble, while MiR-512-5p caused no statistical change in luciferase expression in mut-hTERT-3’UTR compared with the scramble(C) miR-512-5p mimic led to down-regulation of hTERT and TRF2 in CNE cells. …”
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    Data_Sheet_1_The Virulence of Escherichia coli O157:H7 Isolates in Mice Depends on Shiga Toxin Type 2a (Stx2a)-Induction and High Levels of Stx2a in Stool.docx by Jocelyn R. Hauser (8493432)

    Published 2020
    “…<p>In this study we compared nine Shiga toxin (Stx)-producing Escherichia coli O157:H7 patient isolates for Stx levels, stx-phage insertion site(s), and pathogenicity in a streptomycin (Str)-treated mouse model. …”
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    Molecular insights in the pathogenesis of classical Ehlers-Danlos syndrome from transcriptome-wide expression profiling of patients’ skin fibroblasts by Nicola Chiarelli (756982)

    Published 2019
    “…<div><p>Classical Ehlers-Danlos syndrome (cEDS) is a dominant inherited connective tissue disorder mainly caused by mutations in the <i>COL5A1</i> and <i>COL5A2</i> genes encoding type V collagen (COLLV), which is a fibrillar COLL widely distributed in a variety of connective tissues. cEDS patients suffer from skin hyperextensibility, abnormal wound healing/atrophic scars, and joint hypermobility. …”
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