PRISMΔDB

Analyze how specific documents activate the features of the SAE. Select a dataset, a run and a document to begin.

Active Features

1523

0.0
Details List
#1289 Feature 1289
2.8
#915 Feature 915
2.6
#2496 Feature 2496
2.4
#2006 Feature 2006
2.4
#1649 Feature 1649
2.3
#306 Feature 306
2.3
#1837 Feature 1837
2.3
#1668 Feature 1668
2.3
#241 Feature 241
2.2
#2955 Feature 2955
2.2
#506 Feature 506
2.1
#1259 Feature 1259
2.0
#2241 Feature 2241
2.0
#143 Feature 143
2.0
#604 Feature 604
1.9
#2534 Feature 2534
1.9
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1.8
#226 Feature 226
1.8
#2769 Feature 2769
1.7
#1166 Feature 1166
1.7
#1434 Feature 1434
1.7
#2615 Feature 2615
1.6
#2905 Feature 2905
1.6
#1911 Feature 1911
1.6
#1515 Feature 1515
1.6
#2359 Feature 2359
1.6
#662 Feature 662
1.6
#1620 Feature 1620
1.6
#264 Feature 264
1.5
#363 Feature 363
1.5
#536 Feature 536
1.5
#1821 Feature 1821
1.4
#146 Feature 146
1.4
#2625 Feature 2625
1.4
#2828 Feature 2828
1.4
#683 Feature 683
1.4
#209 Feature 209
1.4
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1.4
#1569 Feature 1569
1.3
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1.3
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1.3
#1223 Feature 1223
1.3
#1690 Feature 1690
1.3
#414 Feature 414
1.3
#1605 Feature 1605
1.3
#1853 Feature 1853
1.3
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1.3
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1.3
#547 Feature 547
1.3
#244 Feature 244
1.3
#2997 Feature 2997
1.3
#2522 Feature 2522
1.3
#968 Feature 968
1.3
#2658 Feature 2658
1.3
#1597 Feature 1597
1.3
#2279 Feature 2279
1.3
#2778 Hippocampal Memory and Cognitive Function
1.3
#1959 Feature 1959
1.3
#233 Feature 233
1.3
#1229 Feature 1229
1.3
#1700 Feature 1700
1.3
#2066 Feature 2066
1.3
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1.2
#1995 Feature 1995
1.2
#150 Feature 150
1.2
#2949 Feature 2949
1.2
#469 Feature 469
1.2
#1778 Feature 1778
1.2
#1512 Feature 1512
1.2
#841 Feature 841
1.2
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1.2
#2917 Feature 2917
1.2
#1347 Feature 1347
1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.2
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
#847 Feature 847
1.1
#1930 Feature 1930
1.1
#2622 Feature 2622
1.1
#23 Neuronal Circuitry and Cellular Processes
1.1
#1180 Feature 1180
1.1
#318 Feature 318
1.1
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1.1
#1919 Feature 1919
1.1
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1.1
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1.1
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1.1
#86 Feature 86
1.1
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1.1
#1237 Feature 1237
1.1
#2972 Sensory-Motor Integration
1.1
#2753 Feature 2753
1.1
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1.1
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1.1
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1.1
#2614 Feature #2614
1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
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1.1
#1348 Feature 1348
1.1
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1.1
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1.1
#2806 Feature 2806
1.1
#1888 Feature 1888
1.1
#2978 Feature 2978
1.1
#595 Feature 595
1.1
#1100 Feature 1100
1.0
#1311 Molecular Mechanisms and Biological Processes
1.0
#2505 Feature 2505
1.0
#1600 Feature 1600
1.0
#2752 Feature 2752
1.0
#1334 Feature 1334
1.0
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1.0
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1.0
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1.0
#2205 Feature 2205
1.0
#1039 Feature 1039
1.0
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1.0
#1418 Feature 1418
1.0
#1104 Feature 1104
1.0
#1011 Feature 1011
1.0
#773 Feature 773
1.0
#1379 Feature 1379
1.0
#1145 Feature 1145
1.0
#2033 Feature 2033
1.0
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1.0
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1.0
#30 Feature 30
1.0
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1.0
#2981 Feature 2981
1.0
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1.0
#418 Feature 418
1.0
#2112 Feature 2112
1.0
#1390 Feature 1390
1.0
#2458 Feature 2458
1.0
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1.0
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1.0
#3020 Feature 3020
1.0
#330 Feature 330
1.0
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1.0
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1.0
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1.0
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1.0
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1.0
#2018 Feature 2018
1.0
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1.0
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1.0
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1.0
#383 Feature 383
1.0
#2572 Feature 2572
1.0
#1473 Feature 1473
1.0
#1341 Feature 1341
1.0
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1.0
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1.0
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0.9
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0.9
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0.9
#2218 Feature 2218
0.9
#53 Feature 53
0.9
#2007 Developmental Disparities & Intervention
0.9
#267 Feature 267
0.9
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0.9
#1601 Feature 1601
0.9
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0.9
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0.9
#2513 Feature 2513
0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
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0.9
#2072 Feature 2072
0.9
#69 Feature 69
0.9
#1374 Feature 1374
0.9
#1698 Feature 1698
0.9
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0.9
#1405 Feature 1405
0.9
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0.9
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0.9
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0.9
#1117 Feature 1117
0.9
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0.9
#2227 Feature 2227
0.9
#1613 Feature 1613
0.9
#1468 Feature 1468
0.9
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0.9
#336 Feature 336
0.9
#1050 Feature 1050
0.9
#2932 Feature 2932
0.9
#2581 Feature 2581
0.9
#2765 Feature 2765
0.9
#1964 Feature 1964
0.9
#162 Feature 162
0.9
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0.9
#2372 Feature 2372
0.9
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0.9
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0.9
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0.9
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0.9
#378 Feature 378
0.9
#1695 Feature 1695
0.9
#1824 Feature 1824
0.9
#548 Feature 548
0.9
#2451 Feature #2451
0.9
#251 Feature 251
0.9
#2198 Feature 2198
0.9
#1592 Feature 1592
0.9
#1404 Feature 1404
0.9
#858 Feature 858
0.9
#2024 Feature 2024
0.9
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0.9
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0.9
#2229 Feature 2229
0.9
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0.9
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0.9
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0.9
#2529 Feature 2529
0.9
#1262 Feature 1262
0.9
#1856 Feature 1856
0.9
#1970 Feature 1970
0.9
#2010 Feature 2010
0.9
#2795 Feature 2795
0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
#954 Feature 954
0.8
#100 Feature 100
0.8
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0.8
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0.8
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0.8
#33 Feature 33
0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
#2333 Feature 2333
0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.8
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.7
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0.6
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0.6
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0.6
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0.6
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0.6
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0.6
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0.6
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Document Content

Differential modulation of the glutamate transporters GLT1, GLAST and EAAC1 by docosahexaenoic acid.
At present, the ability of polyunsaturated fatty acids (PUFAs) to regulate individual glutamate transporter subtypes is poorly understood and very little information exists on the mechanism(s) by which PUFAs achieve their effects on the transport process. Here we investigate the effect of cis-4,7,10,13,16,19-docosahexaenoic acid (DHA) on the activity of the mammalian glutamate transporter subtypes, GLT1, GLAST and EAAC1 individually expressed in human embryonic kidney (HEK) cells. Exposure of cells to 100 muM DHA increased the rate of d-[(3)H]aspartate uptake by over 72% of control in HEK(GLT1) cells, and by 45% of control in HEK(EAAC1) cells. In contrast, exposure of HEK(GLAST) cells to 200 muM DHA resulted in almost 40% inhibition of d-[(3)H]aspartate transport. Removal of extracellular calcium increased the inhibitory potential of DHA in HEK(GLAST) cells. In contrast, in the absence of extracellular calcium, the stimulatory effect of DHA on d-[(3)H]aspartate uptake in HEK(GLT1) and HEK(EAAC1) cells was abolished, and significant inhibition of the transport process by DHA was observed. Inhibition of CaM kinase II or PKC had no effect on the ability of DHA to inhibit transport into HEK(GLAST) cells but abolished the stimulatory effect of DHA on d-[(3)H]aspartate transport into HEK(GLT1) and HEK(EAAC1) cells. Inhibition of PKA had no effect on the modulation of d-[(3)H]aspartate transport by DHA in any of the cell lines. We conclude that DHA differentially modulates the GLT1, GLAST and EAAC1 glutamate transporter subtypes via different mechanisms. In the case of GLT1 and EAAC1, DHA appears to stimulate d-[(3)H]aspartate uptake via a mechanism requiring extracellular calcium and involving CaM kinase II and PKC, but not PKA. In contrast, the inhibitory effect of DHA on GLAST does not require extracellular calcium and does not involve CaM kinase II, PKC or PKA.