Showing 21 - 40 results of 224,927 for search '(( 10 ((teer decrease) OR (a decrease)) ) OR ( 5 ((mm decrease) OR (nn decrease)) ))', query time: 1.30s Refine Results
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    Table1_Open Screw Placement in a 1.5 mm LCP Over a Fracture Gap Decreases Fatigue Life.docx by Sarah G. J. Alwen (5263049)

    Published 2018
    “…Objective<p>To investigate the influence of plate and screw hole position on the stability of simulated radial fractures stabilized with a 1.5 mm condylar locking compression plate (LCP).</p>Study Design<p>In vitro mechanical testing of paired cadaveric limbs.…”
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    Flies decrease the level of aggression as the availability of food resource increases. by Rod S. Lim (622045)

    Published 2014
    “…(c) Male-male courtship normalized by locomotion shows no increase or decrease (See <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0105626#pone.0105626.s012" target="_blank">Table S4</a> for statistics). …”
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    Increasing temperature decreases oxygen concentration and decreasing oxygen content decreases neuronal excitability. by Yuguo Yu (172221)

    Published 2012
    “…Increasing temperature can dramatically decrease oxygen levels. B. Response of layer 2/3 pyramidal cells (n = 5) to the intracellular injection of a depolarizing current pulse (200 pA, 500 ms) at different temperatures (same experiments as in A). …”
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    A New Rotane Family:  Synthesis, Structure, Conformation, and Dynamics of [3.4]-, [4.4]-, [5.4]-, and [6.4]Rotane<sup>1</sup> by Lutz Fitjer (2466634)

    Published 1998
    “…All syntheses are based on bicyclobutylidene (<b>9</b>):  [2+1] cycloaddition of cyclobutylidene yields [3.4]rotane (<b>5</b>) (<b>9</b>−<b>5</b>), [2+2] cycloaddition of trimethyleneketene followed by spiroalkylation of the resulting trispiroketone <b>10</b> yields [4.4]rotane (<b>6</b>) (<b>9</b>−<b>10</b>−<b>13</b>−<b>14</b>−<b>6</b>), homologization of <b>10</b> via β-hydroxy selenides gives access to tetraspiroketone <b>11</b> and pentaspiroketone <b>12</b> (<b>10</b>−<b>15</b>−<b>11</b>−<b>16</b>−<b>12</b>), and further elaboration directed toward a cyclopropylcarbene−cyclobutene rearrangement yields [5.4]rotane (<b>7</b>) and [6.4]rotane (<b>8</b>) [<b>11</b>(<b>12</b>)−<b>18</b>(<b>24</b>)−<b>19</b>(<b>25</b>)−<b>20</b>(<b>26</b>)−<b>21</b>(<b>27</b>)−<b>22</b>(<b>28</b>)−<b>23</b>(<b>29</b>)−<b>7</b>(<b>8</b>)]. …”
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