Showing 141 - 160 results of 95,642 for search '(( significant ((cause case) OR (base case)) ) OR ( significant ((we decrease) OR (a decrease)) ))', query time: 1.52s Refine Results
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    Drug-induced decrease of cell anisotropy reduces pattern fidelity. by Camille Curantz (7456499)

    Published 2022
    “…<b>(B)</b> Quantifications of primordia spacing variability on phalloïdin-stained control flat skins (explant; triangles) and LatA-treated cultured explants (+LatA; squares) of Japanese quail embryos showed that LatA treatment caused a significant decrease in pattern fidelity at condensation stage (explants, <i>n</i> = 9; +LatA, <i>n</i> = 9; unpaired 2-tailed <i>t</i> test; <i>p</i> = 0.0233) and differentiation stage (explants, <i>n</i> = 8; +LatA, <i>n</i> = 9; <i>p</i> = 0.002). …”
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    Full list of proteins significantly enriched by BioID2 labelling. by Jan Pyrih (229124)

    Published 2020
    “…Lower case letters a, b, and c represent each replicate. …”
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    Illustration of an example case. by Dominik F. Vollherbst (5492690)

    Published 2020
    “…<p>This case demonstrates a 28-year-old female patient who suffered from pain and dysphagia, caused by a VM of the right-sided floor of mouth with involvement of the tongue. …”
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    Table1_CLEC16A variants conferred a decreased risk to allergic rhinitis in the Chinese population.DOCX by Yongliang Niu (14245295)

    Published 2022
    “…</p><p>Conclusion:CLEC16A variants conferred a decreased risk to AR in the Chinese population.…”
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    Table1_CLEC16A variants conferred a decreased risk to allergic rhinitis in the Chinese population.DOCX by Yongliang Niu (14245295)

    Published 2022
    “…</p><p>Conclusion:CLEC16A variants conferred a decreased risk to AR in the Chinese population.…”
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    Data Sheet 1_Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.pdf by Nourhen Agrebi (14151222)

    Published 2025
    “…</p>Methods<p>We present immunological and genetic analysis of a Tunisian patient with two homozygous variants of uncertain significance (VUSs) in the IKBKB and AICDA genes, suspected of causing hyper-IgM and immune deficiency. …”
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    S1 Data - by Miki Doi (15347878)

    Published 2024
    Subjects: