Showing 19,161 - 19,180 results of 109,953 for search '(( 5 ((a decrease) OR (mean decrease)) ) OR ( a ((nn decrease) OR (point decrease)) ))', query time: 1.71s Refine Results
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    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. …”
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    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. …”
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    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. 19168

    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. 19169

    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. 19170

    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.…”
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    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). …”
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    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. …”
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