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You've got <font color ="red">23</font> hits!<HR width="580" align="left"> <table border='1' cellpadding="0" cellspacing="0" bordercolor="#000060" width =580>
<tr>
  <td  bgcolor = "#47589D"><font color = "white"><b>Gene 1</b></font></td>
  <td bgcolor = "#47589D"><font color = "white"><b>Gene 2</b></font></td>
  <td bgcolor = "#47589D"><font color = "white"><b>Interaction Type</b></font></td>
 <td bgcolor = "#47589D"><font color = "white"><b>Sentence</b></font></td>
 <td bgcolor = "#47589D"><font color = "white"><b>Value</b></font></td>
 <td bgcolor = "#47589D"><font color = "white"><b>Judge me</b></font></td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>Smad2</td>
  <td>interact1</td>
  <td>Phosphorylation at both sites is required to mediate association of Smad2 with Smad4 in mammalian cells , while in yeast , Smad2 interacts directly with Smad4 and does not require phosphorylation .</td>
  <td>21</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=2166">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=2166">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Smads</td>
  <td>associate2</td>
  <td>This phosphorylation induces association between these receptor-regulated Smads and Smad4 followed by translocation of the heteromeric complex to the nucleus .</td>
  <td>20</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=2160">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=2160">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>MAD</td>
  <td>complex3</td>
  <td>MEDEA is most similar to mammalian Smad4 and forms heteromeric complexes with MAD .</td>
  <td>19</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=2153">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=2153">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>D1</td>
  <td>associate2</td>
  <td>As aberrations in cell cycle regulatory genes are associated with the progression of precursor pancreatic ductal lesions to invasive adenocarcinoma , we examined expression of key cell cycle regulator</td>
  <td>18</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=484">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=484">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>p16</td>
  <td>associate3</td>
  <td>CONCLUSIONS : These data indicate that loss of p16 ( INK4A ) and Smad4 expression occur more frequently in IPMC alone , or with associated invasive carcinoma , compared with adenoma  borderline IPMT .</td>
  <td>17</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=486">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=486">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>activin</td>
  <td>interact1</td>
  <td>After TGF-beta-mediated phosphorylation and association with Smad4 , Smad2 moves to the nucleus and activates expression of specific genes through cooperative interactions with DNA-binding proteins ,</td>
  <td>16</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=1742">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=1742">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>Smad1</td>
  <td>bind1</td>
  <td>Here we show that Smad1 binds to this motif upon BMP stimulation in the presence of the common Smad , Smad4 .</td>
  <td>16</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=2118">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=2118">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Smad3</td>
  <td>associate1</td>
  <td>Activin stimulation triggered association of Dok-1 with Smad3 , as well as association of Smad3 with Smad4 .</td>
  <td>16</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=806">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=806">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>Smad2</td>
  <td>associate1</td>
  <td>These results indicate that receptor-dependent phosphorylation of Smad2 on serines 465 and 467 is required in mammalian cells to permit association with Smad4 and to propagate TGF-beta signals .</td>
  <td>15</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=2167">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=2167">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Smad3</td>
  <td>complex2</td>
  <td>Although Smad3 and Smad4 were not detectable in TGFbeta ( 3 ) -inducible AP-1 complexes at the TGFbeta ( 1 ) promoter , stable expression of dominant-negative Smad3 could significantly inhibit the abi</td>
  <td>15</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=976">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=976">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>Activin</td>
  <td>associate1</td>
  <td>Activin stimulation triggered association of Dok-1 with Smad3 , as well as association of Smad3 with Smad4 .</td>
  <td>14</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=1595">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=1595">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Delta</td>
  <td>associate1</td>
  <td>c-Fos , FosB  Delta FosB , and JunB were associated with Smad4 .</td>
  <td>14</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=1655">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=1655">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>p16</td>
  <td>associate3</td>
  <td>Aberrant p16 ( INK4A ) and DPC4  Smad4 expression in intraductal papillary mucinous tumours of the pancreas is associated with invasive ductal adenocarcinoma .</td>
  <td>14</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=482">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=482">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Smad</td>
  <td>complex3</td>
  <td>Smad proteins activated by TGF-beta form complexes with Smad4 .</td>
  <td>13</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=1995">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=1995">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>Smad2</td>
  <td>associate1</td>
  <td>These results indicate that receptor-dependent phosphorylation of Smad2 on serines 465 and 467 is required in mammalian cells to permit association with Smad4 and to propagate TGF-beta signals .</td>
  <td>13</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=203">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=203">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Smad</td>
  <td>bind1</td>
  <td>While there are two potential Smad binding elements ( SBE ' s ) in the TGFbeta ( 1 ) promoter , supershift assays suggest that at least one of these does not bind Smad4 , and the other is unable to bi</td>
  <td>12</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=1813">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=1813">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>p38</td>
  <td>associate1</td>
  <td>Our findings demonstrate that ( i ) decrease of Smad4 mRNA expression is closely associated with defective TGF-beta response and lack of growth inhibition , ( ii ) activation of PAI-1 by TGF-beta may</td>
  <td>11</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=1996">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=1996">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Dpp</td>
  <td>complex1</td>
  <td>Mad forms a heteromeric complex with Drosophila Smad4 ( Medea ) upon phosphorylation by Thick veins ( Tkv ) , a type I receptor for Dpp .</td>
  <td>10</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=169">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=169">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>p38</td>
  <td>associate1</td>
  <td>Our findings demonstrate that ( i ) decrease of Smad4 mRNA expression is closely associated with defective TGF-beta response and lack of growth inhibition , ( ii ) activation of PAI-1 by TGF-beta may</td>
  <td>10</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=1180">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=1180">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Smad1</td>
  <td>bind1</td>
  <td>Here we show that Smad1 binds to this motif upon BMP stimulation in the presence of the common Smad , Smad4 .</td>
  <td>10</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=113">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=113">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>Smad2</td>
  <td>interact1</td>
  <td>Phosphorylation at both sites is required to mediate association of Smad2 with Smad4 in mammalian cells , while in yeast , Smad2 interacts directly with Smad4 and does not require phosphorylation .</td>
  <td>10</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=201">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=201">bad</a>
                </td>
 </tr>
<tr bgcolor=#CCCCCC>
  <td>Smad4</td>
  <td>Smads</td>
  <td>associate2</td>
  <td>This phosphorylation induces association between these receptor-regulated Smads and Smad4 followed by translocation of the heteromeric complex to the nucleus .</td>
  <td>10</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=187">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=187">bad</a>
                </td>
 </tr>
<tr >
  <td>Smad4</td>
  <td>MAD</td>
  <td>complex3</td>
  <td>MEDEA is most similar to mammalian Smad4 and forms heteromeric complexes with MAD .</td>
  <td>9</td>
  <td><a href ="vote.php?vote=1&textfield=smad4&id=175">good</a>
                <a href="vote.php?vote=-1&textfield=smad4&id=175">bad</a>
                </td>
 </tr>
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      <div align="center"><i><a href="index.html">Text2Knowledge</a> <font color = "red"> ... </font><a href="http://bioinformatics.org/~hyy/index.html">Yong Huang</a> 
        2002</i></div>
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