Showing 13,981 - 14,000 results of 135,317 for search '(( 2 we decrease ) OR ( 5 ((((ng decrease) OR (a decrease))) OR (mean decrease)) ))', query time: 1.92s Refine Results
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    Decreased proliferation in tuft endothelium despite increased VEGFA level in N-CAM deficient retinas in OIR. by Joakim Håkansson (200855)

    Published 2011
    “…Although not significant with a 5% level of significance, there is a tendency of increase in all isoforms with the highest relative elevation in VEGFA<sub>120</sub>. …”
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  8. 13988

    A higher mean amplitude or lower standard deviation of the EOD of the swimming fish facilitates estimation of beat frequency at the receptor level. by Na Yu (151735)

    Published 2012
    “…<p>(A) The height (solid line) of the peak of at the beat frequency, , and the width (dashed line) of this peak at the coherence value of 0.15 increase and slightly decrease, respectively, with (with fixed  = 0.1). …”
  9. 13989

    Ganaxolone: A Review in Epileptic Seizures Associated with Cyclin‑Dependent Kinase‑Like 5 Deficiency Disorder by Sheridan M. Hoy (4897468)

    Published 2024
    “…While somnolence and sedation are related to the dose of ganaxolone, they appear early in treatment and may decrease with continued therapy. Thus, although current evidence is somewhat limited, adjunctive ganaxolone could be a valuable therapeutic option for patients aged 2–17 years with epileptic seizures associated with CDD.…”
  10. 13990

    Ab Initio Study of the Substituent Effects on the Relative Stability of the <i>E</i> and <i>Z</i> Conformers of Phenyl Esters. Stereoelectronic Effects on the Reactivity of the Car... by Helmi Neuvonen (2643793)

    Published 2005
    “…ED/EW substituents adjust the availability of the π*<sub>C</sub><sub></sub><sub>O</sub> antibonding orbital to interact with the lone pair orbital of the attacking nucleophile and therefore affect the reactivity:  EW substituents increase and ED substituents decrease it. Excellent correlations were observed between the rate coefficients of nucleophilic acyl substitutions and π*<sub>C</sub><sub></sub><sub>O</sub> occupancies of the ester series <b>4 </b>and <b>5</b>.…”
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