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largest decrease » largest decreases (Expand Search), larger decrease (Expand Search), marked decrease (Expand Search)
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21401
data_sheet_2_High-Frequency Repetitive Magnetic Stimulation Enhances the Expression of Brain-Derived Neurotrophic Factor Through Activation of Ca2+–Calmodulin-Dependent Protein Kin...
Published 2018“…Therefore, in this study, we examined the global gene expression patterns depending on different frequencies of repetitive magnetic stimulation (rMS) in both undifferentiated and differentiated Neuro-2a cells to generate a comprehensive view of the biological mechanisms. …”
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21402
DataSheet_1_Integration of mRNA and microRNA analysis reveals the molecular mechanisms underlying drought stress tolerance in maize (Zea mays L.).doc
Published 2022“…Furthermore, preliminary investigation of the biological function of miR408a in the maize root system was also conducted. …”
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21403
Mk2/3-dependent regulation of Khsrp and <i>Cdkn1a</i><sup><i>p21</i></sup>.
Published 2015“…<b>(C)</b> Despite a typical arrest in G<sub><b>2</b></sub> upon etoposide treatment, <b>(D)</b><i>Mk2</i><sup><b><i>-/-</i></b></sup><i>;Mk3</i><sup><b><i>-/-</i></b></sup> MEFs show a decreased G<sub><b>1</b></sub> population in comparison to wt cells. …”
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21404
Numerical data for Fig 4A, 4B, 4C, 4D and 4E.
Published 2023“…Together, these studies identify a promising therapeutic strategy for CRPC and suggest that these two major epigenetic regulators buffer prostate cancers from a lethal response to cellular stresses, thereby conferring a tractable therapeutic vulnerability.…”
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21405
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21406
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21407
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21408
Changes in optic nerve head blood flow following eye drop administration in a representative case.
Published 2023“…In the brinzolamide and brimonidine fixed combination (BBFC) group, a suppression of diurnal fluctuation-induced decreases in optic nerve head blood flow was observed 6 hours after administration compared to the baseline.…”
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21409
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21410
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21411
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21412
Numerical data for Fig 2A, 2B, 2C, 2D and 2G.
Published 2023“…Together, these studies identify a promising therapeutic strategy for CRPC and suggest that these two major epigenetic regulators buffer prostate cancers from a lethal response to cellular stresses, thereby conferring a tractable therapeutic vulnerability.…”
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21413
DataSheet1_EPM2A acts as a protective factor in prostate cancer, evidence from a real-world patient cohort.docx
Published 2022“…The results showed decreased expression of EPM2A in 95.65% of tumor tissues and was related to their prognosis, especially PCA (p = 0.008, HR = 0.57, 95% CI: 0.371–0.863). …”
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21414
The ORF7a protein of SARS-CoV-2 initiates autophagy and limits autophagosome-lysosome fusion via degradation of SNAP29 to promote virus replication
Published 2022“…In this study, we demonstrate that overexpression of the SARS-CoV-2 ORF7a protein activates LC3-II and leads to the accumulation of autophagosomes in multiple cell lines, while knockdown of the viral <i>ORF7a</i> gene via shRNAs targeting <i>ORF7a</i> sgRNA during SARS-CoV-2 infection decreased autophagy levels. …”
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21415
Ubiquitination of UVRAG by SMURF1 promotes autophagosome maturation and inhibits hepatocellular carcinoma growth
Published 2019“…Interestingly, ZRANB1 is phosphorylated at Thr35, and Ser209 residues by CSNK1A1, and this phosphorylation activates its deubiquitinating activity. …”
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21416
Image2_Ghrelin enhances tubular magnesium absorption in the kidney.TIF
Published 2024“…As GHSR initiates downstream signaling via protein kinase A (PKA), we found that the PKA inhibitor H89 abrogated TRPM6/7 stimulation by Ghrelin. …”
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21417
Image3_Ghrelin enhances tubular magnesium absorption in the kidney.TIFF
Published 2024“…As GHSR initiates downstream signaling via protein kinase A (PKA), we found that the PKA inhibitor H89 abrogated TRPM6/7 stimulation by Ghrelin. …”
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21418
Image1_Ghrelin enhances tubular magnesium absorption in the kidney.TIF
Published 2024“…As GHSR initiates downstream signaling via protein kinase A (PKA), we found that the PKA inhibitor H89 abrogated TRPM6/7 stimulation by Ghrelin. …”
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21419
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21420