Showing 19,921 - 19,940 results of 81,797 for search '(( a d decrease ) OR ( 50 ((((mean decrease) OR (nn decrease))) OR (a decrease)) ))', query time: 1.43s Refine Results
  1. 19921

    Data_Sheet_2_D-galactose Intake Alleviates Atopic Dermatitis in Mice by Modulating Intestinal Microbiota.DOCX by Dong-Yeon Kim (770670)

    Published 2022
    “…Our results suggest the possible use of D-galactose as a prebiotic to alleviate AD by altering gut microbiota.…”
  2. 19922

    Data_Sheet_3_D-galactose Intake Alleviates Atopic Dermatitis in Mice by Modulating Intestinal Microbiota.DOCX by Dong-Yeon Kim (770670)

    Published 2022
    “…Our results suggest the possible use of D-galactose as a prebiotic to alleviate AD by altering gut microbiota.…”
  3. 19923

    Data_Sheet_6_D-galactose Intake Alleviates Atopic Dermatitis in Mice by Modulating Intestinal Microbiota.DOCX by Dong-Yeon Kim (770670)

    Published 2022
    “…Our results suggest the possible use of D-galactose as a prebiotic to alleviate AD by altering gut microbiota.…”
  4. 19924

    Data_Sheet_4_D-galactose Intake Alleviates Atopic Dermatitis in Mice by Modulating Intestinal Microbiota.DOCX by Dong-Yeon Kim (770670)

    Published 2022
    “…Our results suggest the possible use of D-galactose as a prebiotic to alleviate AD by altering gut microbiota.…”
  5. 19925

    Video_1_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.avi by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  6. 19926

    Image_3_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.tif by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  7. 19927

    Video_3_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.avi by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  8. 19928

    Image_2_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.tif by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  9. 19929

    Image_4_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.tif by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  10. 19930

    Video_2_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.avi by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  11. 19931

    Image_1_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.tif by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  12. 19932

    Image_5_Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation.tif by Yongchan Lee (8128929)

    Published 2021
    “…During bacterial or viral infection, macrophages release DNA decorated with nuclear and cytoplasmic proteins known as macrophage extracellular traps (METs). Gasdermin D (GSDMD) is a pore-forming protein that has been involved in extracellular trap formation in neutrophils. …”
  13. 19933

    Engineering 3D-Bioplotted scaffolds to induce aligned extracellular matrix deposition for musculoskeletal soft tissue replacement by Paul B. Warren (3604013)

    Published 2016
    “…<b><i>Materials and Methods</i></b>: 3D-Bioplotted polycaprolactone scaffolds with 100, 200, or 400 μm interstrand spacing were implanted subcutaneously in a rat model for 4, 8, or 12 weeks. …”
  14. 19934

    Lithocholic acid controls adaptive immune responses by inhibition of Th1 activation through the Vitamin D receptor by Thijs W. H. Pols (4019975)

    Published 2017
    “…We here aimed to identify a potential interaction between bile acids and CD4<sup>+</sup> Th cells, which are central in adaptive immune responses. …”
  15. 19935

    Data_Sheet_1_Modulation of Titin-Based Stiffness in Hypertrophic Cardiomyopathy via Protein Kinase D.pdf by Melissa Herwig (8710386)

    Published 2020
    “…Multiple conserved PKD-dependent phosphosites were identified within the Z-disk, A-band and M-band regions of titin by quantitative mass spectrometry, and many PKD-dependent phosphosites detected in the elastic titin I-band region were significantly decreased in cKO. …”
  16. 19936

    3D Nanoscale Structures of Hydrated Polyamide Desalination Membranes Revealed by Cryogenic Transmission Electron Microscopy Tomography by Chenhao Yao (1569328)

    Published 2025
    “…Additionally, while the surface area decreases upon hydration for both SW and BW membranes, indicating a smoothing of surface nodules and cavities, surface roughness remains unchanged, suggesting that current roughness measurement methods such as atomic force microscopy do not capture intrinsic morphological features. …”
  17. 19937

    Conditional doxycycline-dependent Pgp-EGFP-expressing hCMEC/D3-MDR1-EGFP cells. by Andreas Noack (519906)

    Published 2014
    “…<p>(A) Representative images showing intracellular localization of Pgp-EGFP fusion protein in hCMEC/D3-MDR1-EGFP (doxycycline-on) cells. …”
  18. 19938

    3D Nanoscale Structures of Hydrated Polyamide Desalination Membranes Revealed by Cryogenic Transmission Electron Microscopy Tomography by Chenhao Yao (1569328)

    Published 2025
    “…Additionally, while the surface area decreases upon hydration for both SW and BW membranes, indicating a smoothing of surface nodules and cavities, surface roughness remains unchanged, suggesting that current roughness measurement methods such as atomic force microscopy do not capture intrinsic morphological features. …”
  19. 19939

    Supplementary file 1_Mechanical properties of 3D voxel-printed materials for cardiovascular tissue imitation.docx by Joël Illi (21449474)

    Published 2025
    “…To overcome these challenges, a novel 3D voxel-printing approach may provide an effective solution.…”
  20. 19940

    3D Nanoscale Structures of Hydrated Polyamide Desalination Membranes Revealed by Cryogenic Transmission Electron Microscopy Tomography by Chenhao Yao (1569328)

    Published 2025
    “…Additionally, while the surface area decreases upon hydration for both SW and BW membranes, indicating a smoothing of surface nodules and cavities, surface roughness remains unchanged, suggesting that current roughness measurement methods such as atomic force microscopy do not capture intrinsic morphological features. …”