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values increased » cases increased (Expand Search), also increased (Expand Search), rate increased (Expand Search)
large decrease » marked decrease (Expand Search), large increases (Expand Search), large degree (Expand Search)
c values » ct values (Expand Search), _ values (Expand Search), i values (Expand Search)
i large » _ large (Expand Search), via large (Expand Search), i larvae (Expand Search)
a large » _ large (Expand Search)
values increased » cases increased (Expand Search), also increased (Expand Search), rate increased (Expand Search)
large decrease » marked decrease (Expand Search), large increases (Expand Search), large degree (Expand Search)
c values » ct values (Expand Search), _ values (Expand Search), i values (Expand Search)
i large » _ large (Expand Search), via large (Expand Search), i larvae (Expand Search)
a large » _ large (Expand Search)
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Differential expression analysis of nuclear transcripts after siAPOBEC3A depletion reveals induction of TP53 targets and decreases in cell cycle and cell growth regulator transcrip...
Published 2024“…(B) siAPOBEC3A treatment increases <i>CDKN1A</i> nuclear transcript levels in MCF10A cells by RNA-seq. …”
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Ribosomal subunit pathways are decreased in <i>Resf1</i> knockdown cells.
Published 2024“…<p>(A) GO Pathway analysis snapshots of various ribosomal subunit pathways that are decreased in 6DT1 <i>Resf1</i> KD cells. …”
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Results from linear regression analysis for δ<sup>13</sup>C or δ<sup>15</sup>N and collection date.
Published 2025Subjects: -
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Distribution of stable isotope values for consumers faceted by coastscape and feeding habit.
Published 2025Subjects: -
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Supplementary Material for: High-sensitivity Troponin I Measurement in a Large Contemporary Cohort: Implications for Clinical Care
Published 2025“…Male sex, higher HDL-C, higher Hgb A1c, decreasing eGFR, and increasing systolic blood pressure were significant predictors of increased hsTnI. …”
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Supplementary Materials for Genotypic and phenotypic spectrum and pathogenesis of WNT1 variants in a large cohort of patients with OI / osteoporosis
Published 2022“…Due to its rarity, the clinical characteristics and pathogenic mechanism of <em>WNT1</em> mutations remain unclear. We aimed to explore the phenotypic and genotypic spectrum and treatment responses of a large cohort of patients with WNT1-related OI/OP and the molecular mechanisms of <em>WNT1 </em>variants. …”