Showing 100,861 - 100,880 results of 106,197 for search '(( 3 points decrease ) OR ( 5 ((step decrease) OR (((mean decrease) OR (a decrease)))) ))', query time: 1.24s Refine Results
  1. 100861

    Table_3_Gut–Liver Immune Response and Gut Microbiota Profiling Reveal the Pathogenic Mechanisms of Vibrio harveyi in Pearl Gentian Grouper (Epinephelus lanceolatus♂ × E. fuscogutta... by Yiqin Deng (3186063)

    Published 2020
    “…Although no V. harveyi was detected in the gut, the infection simultaneously induced a gut-liver immune response. …”
  2. 100862

    Table_2_Gut–Liver Immune Response and Gut Microbiota Profiling Reveal the Pathogenic Mechanisms of Vibrio harveyi in Pearl Gentian Grouper (Epinephelus lanceolatus♂ × E. fuscogutta... by Yiqin Deng (3186063)

    Published 2020
    “…Although no V. harveyi was detected in the gut, the infection simultaneously induced a gut-liver immune response. …”
  3. 100863

    Differentially expressed proteins between chemosensitive and chemoresistant ovarian cancer ascites identified by MALDI-TOF/TOF MS. by He Huang (50693)

    Published 2013
    “…a<p>Spot no. assigned by DeCyder 2-D Differential Analysis Software V6.0. corresponding to the DIGE image in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0051256#pone-0051256-g001" target="_blank">Figure 1</a>.…”
  4. 100864
  5. 100865

    Eighteen types of embryonic-born adPNs. by Hung-Hsiang Yu (117523)

    Published 2010
    “…<p>Embryonic-derived twin-spot clones labeled with <i>GAL4-GH146</i> (AV) or <i>acj6-GAL4</i> (X–Z). Top two panels: composite confocal images of the AL showing single adPNs (magenta) and the paired NB clones (green); middle panels: single focal sections of the AL covering the glomerular targets of single adPNs; bottom two panels: axon projections of single adPNs (magenta) and the accompanying NB clones (green). 22 types of GH146-labeled NB clones can be distinguished and are shown in the order of decreasing complexity from (A) to (V). 15 of them pair with distinct adPNs while seven of them exist alone (no magenta labeling). …”
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  11. 100871

    Table_1_Multiple Myeloma-Derived Extracellular Vesicles Impair Normal Hematopoiesis by Acting on Hematopoietic Stem and Progenitor Cells.DOCX by Ilaria Laurenzana (1528111)

    Published 2021
    “…Our data showed that: (i) MM cells released a heterogeneous population of EVs; (ii) MM-EVs caused a dose-dependent reduction of HSPCs viability; (iii) MM-EVs caused a redistribution of the HSPC pool characterized by a significant increase in the frequency of stem and early precursors accompanied by a reduction of late precursor cells, such as common myeloid progenitors (CMPs), megakaryocyte erythroid progenitors (MEPs), B and NK progenitors, and a slight increase of granulocyte macrophage progenitors (GMPs); (iv) MM-EVs caused an increase of stem and early precursors in S phase with a decreased number of cells in G<sub>0</sub>/G<sub>1</sub> phase in a dose-dependent manner; (v) MM-EVs reduced the HSPC colony formation; and (vi) MM-EVs caused an increased expression level of C-X-C motif chemokine receptor type 4 (CXCR4) and activation of miRNAs. …”
  12. 100872

    Data_Sheet_1_Brain-machine interface based on transfer-learning for detecting the appearance of obstacles during exoskeleton-assisted walking.PDF by Vicente Quiles (14786527)

    Published 2023
    “…</p>Material and methods<p>First, the interface was tested on a treadmill with five subjects, in which the user stopped when an obstacle appeared (simulated by a laser). …”
  13. 100873

    Table_2_Multiple Myeloma-Derived Extracellular Vesicles Impair Normal Hematopoiesis by Acting on Hematopoietic Stem and Progenitor Cells.xlsx by Ilaria Laurenzana (1528111)

    Published 2021
    “…Our data showed that: (i) MM cells released a heterogeneous population of EVs; (ii) MM-EVs caused a dose-dependent reduction of HSPCs viability; (iii) MM-EVs caused a redistribution of the HSPC pool characterized by a significant increase in the frequency of stem and early precursors accompanied by a reduction of late precursor cells, such as common myeloid progenitors (CMPs), megakaryocyte erythroid progenitors (MEPs), B and NK progenitors, and a slight increase of granulocyte macrophage progenitors (GMPs); (iv) MM-EVs caused an increase of stem and early precursors in S phase with a decreased number of cells in G<sub>0</sub>/G<sub>1</sub> phase in a dose-dependent manner; (v) MM-EVs reduced the HSPC colony formation; and (vi) MM-EVs caused an increased expression level of C-X-C motif chemokine receptor type 4 (CXCR4) and activation of miRNAs. …”
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