Showing 19,681 - 19,700 results of 110,054 for search '(( a point decrease ) OR ( 5 ((fold decrease) OR (((mean decrease) OR (a decrease)))) ))', query time: 1.89s Refine Results
  1. 19681
  2. 19682
  3. 19683

    Point Mutations in FimH Adhesin of Crohn's Disease-Associated Adherent-Invasive <em>Escherichia coli</em> Enhance Intestinal Inflammatory Response by Nicolas Dreux (277061)

    Published 2013
    “…Point mutations in FimH, some of a unique AIEC-associated nature, confer AIEC bacteria a significantly higher ability to adhere to CEACAM-expressing T84 intestinal epithelial cells. …”
  4. 19684
  5. 19685

    XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease - Fig 3 by Katarzyna A. Piróg (490536)

    Published 2019
    “…(B) The incorporation of the labelling agent (purple staining) into the proliferating cells was also decreased in the <i>Xbp1</i><sup>Col2CreΔex2</sup> <i>Matn3</i><sup>V194D</sup> chondrocytes indicating a slowed down cell cycle. …”
  6. 19686
  7. 19687

    Image_2_A Mutation in VWA1, Encoding von Willebrand Factor A Domain-Containing Protein 1, Is Associated With Hemifacial Microsomia.TIF by Yibei Wang (5321825)

    Published 2020
    “…Background<p>Hemifacial microsomia (HFM) is a type of rare congenital syndrome caused by developmental disorders of the first and second pharyngeal arches that occurs in one out of 5,600 live births. …”
  8. 19688

    Image_1_A Mutation in VWA1, Encoding von Willebrand Factor A Domain-Containing Protein 1, Is Associated With Hemifacial Microsomia.TIF by Yibei Wang (5321825)

    Published 2020
    “…Background<p>Hemifacial microsomia (HFM) is a type of rare congenital syndrome caused by developmental disorders of the first and second pharyngeal arches that occurs in one out of 5,600 live births. …”
  9. 19689

    Table_1_A Mutation in VWA1, Encoding von Willebrand Factor A Domain-Containing Protein 1, Is Associated With Hemifacial Microsomia.DOCX by Yibei Wang (5321825)

    Published 2020
    “…Background<p>Hemifacial microsomia (HFM) is a type of rare congenital syndrome caused by developmental disorders of the first and second pharyngeal arches that occurs in one out of 5,600 live births. …”
  10. 19690

    Figure S1 - Decrease in Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) Enhanced Disease with RSV G Glycoprotein Peptide Immunization in BALB/c Mice by Gertrud U. Rey (501694)

    Published 2013
    “…<p><b>Decreased pulmonary cell inflammatory response in FI-A2 or FI-B1 and RSV G-CH17 or G-B1 peptide vaccinated mice after RSV challenge.…”
  11. 19691
  12. 19692
  13. 19693

    Effects of Calcium and Natural Organic Matter on the Transport and Remobilization of Colloidal Activated Carbon in Saturated Porous Media: Insights from Force Spectroscopy by Xun Guan (3842929)

    Published 2025
    “…Our results showed that the presence of Ca<sup>2+</sup> (e.g., >5 mM) under high ionic strength conditions (100 mM) enhanced CAC deposition and subsequently reduced its remobilization upon the introduction of a low ionic strength solution (i.e., DI water). …”
  14. 19694
  15. 19695
  16. 19696
  17. 19697
  18. 19698
  19. 19699

    17- and 19-Electron Complexes [Fe<sup>III</sup>(η<sup>5</sup>-C<sub>5</sub>R<sub>5</sub>)(S<sub>2</sub>CNMe<sub>2</sub>)L]<sup><i>n</i>+</sup> (<i>n</i> = 1, 0):  Electronic Struct... by Marie-Hélène Delville-Desbois (2995521)

    Published 1996
    “…Oxidation of [FeCp*(η<sup>1</sup>-dtc)(CO)<sub>2</sub>], <b>1</b> (Cp* = η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>, dtc = S<sub>2</sub>CNMe<sub>2</sub>), or [FeCp*(η<sup>2</sup>-dtc)(CO)], <b>2</b>, using [Fe<sup>III</sup>Cp<sub>2</sub>]<sup>+</sup>X<sup>-</sup> (X<sup>-</sup> = PF<sub>6</sub><sup>-</sup> or BF<sub>4</sub><sup>-</sup>, Cp = η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>) in THF cleanly gives [Fe<sup>III</sup>Cp*(η<sup>2</sup>-dtc)(CO)]<sup>+</sup>X<sup>-</sup>, <b>2</b><sup>+</sup><b>X</b><sup>-</sup>, as microcrystalline green, thermally stable, but substitution labile, salts. …”
  20. 19700