Showing 961 - 980 results of 3,088 for search '(( significant decrease decrease ) OR ( significant cause decrease ))~', query time: 0.35s Refine Results
  1. 961

    Nanoparticle tracking analysis. by Halime Tozak Yıldız (21238185)

    Published 2025
    “…</p><p>Results</p><p>Cisplatin exposure caused significant testicular damage, characterized by reduced germinal epithelium and degeneration of seminiferous tubules (p < 0.001). …”
  2. 962

    Sperm count and motility. by Halime Tozak Yıldız (21238185)

    Published 2025
    “…</p><p>Results</p><p>Cisplatin exposure caused significant testicular damage, characterized by reduced germinal epithelium and degeneration of seminiferous tubules (p < 0.001). …”
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  11. 971

    Eligibility criteria. by Keean Nanji (16516622)

    Published 2024
    “…Data will be collected and synthesized for seven pre-specified outcomes at 6 weeks and 3 months following surgery: i) change in central retinal thickness measured by optical coherence tomography (OCT), ii) best-recorded visual acuity iii) the rate of CME measured by OCT, and fluorescein angiography (FA) iv) the rate of patients experiencing clinically significant macular edema defined as the presence of CME and pre-specified thresholds for decreased visual acuity, v) patient quality of life, vi) intraocular pressure and vii) the number of patients experiencing one or more pre-specified adverse events. …”
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    Mass spectrometric analyses for crystallins. by Akosua K. Boateng (21672931)

    Published 2025
    “…<div><p>CRYβA1-ΔG91 (βA3ΔG91) is a mutational hotspot in CRYβA1, which causes autosomal dominant congenital nuclear cataract in humans and mice. …”
  14. 974

    RNA-seq data showing top 15 downregulated genes. by Akosua K. Boateng (21672931)

    Published 2025
    “…<div><p>CRYβA1-ΔG91 (βA3ΔG91) is a mutational hotspot in CRYβA1, which causes autosomal dominant congenital nuclear cataract in humans and mice. …”
  15. 975

    RNA-seq data showing top 15 upregulated genes. by Akosua K. Boateng (21672931)

    Published 2025
    “…<div><p>CRYβA1-ΔG91 (βA3ΔG91) is a mutational hotspot in CRYβA1, which causes autosomal dominant congenital nuclear cataract in humans and mice. …”
  16. 976

    Overview of selected datasets. by Tejaswini Baral (14320736)

    Published 2025
    “…</p><p>Results</p><p>Our analysis revealed statistically significant alpha diversity differences in West Africa with decreased microbial diversity in pulmonary tuberculosis patients after two months of antitubercular therapy. …”
  17. 977

    Flowchart of analysis. by Fanqiang Meng (4786071)

    Published 2025
    “…</p><p>Results</p><p>A total of 168,693 primary KA patients were included during the study period. The migration rate decreased from 17.6% in 2013 to 7.6% in 2018 (<i><i>P</i></i> < 0.001). …”
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