PRISMΔDB

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

Active Features

1501

0.0
Details List
#672 Feature 672
3.0
#1028 Feature 1028
2.9
#2146 Feature 2146
2.8
#115 Feature 115
2.8
#708 Drug Resistance Mechanisms in Cancer
2.7
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2.7
#548 Feature 548
2.7
#1805 Feature 1805
2.6
#2467 Feature 2467
2.6
#2758 Feature 2758
2.5
#876 Feature 876
2.5
#2848 Feature 2848
2.4
#515 Feature 515
2.4
#1229 Feature 1229
2.4
#476 Feature 476
2.3
#2790 Feature 2790
2.2
#1245 Feature 1245
2.2
#34 Feature 34
2.2
#1867 Feature 1867
2.2
#1063 Feature 1063
2.1
#1365 Feature 1365
2.1
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2.1
#2803 Feature 2803
2.1
#437 Feature 437
2.0
#112 Feature 112
2.0
#1873 Feature 1873
2.0
#411 Feature 411
2.0
#2033 Feature 2033
2.0
#1896 Feature 1896
1.9
#1596 Feature 1596
1.9
#1130 Feature 1130
1.8
#1388 Feature 1388
1.8
#1834 Feature 1834
1.8
#579 Feature 579
1.8
#84 Feature 84
1.7
#2460 Feature 2460
1.7
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1.7
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1.7
#2090 Feature 2090
1.7
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1.7
#389 Feature 389
1.7
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1.6
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1.6
#2291 Feature 2291
1.6
#2916 Feature 2916
1.6
#1205 Feature 1205
1.6
#1994 Feature 1994
1.6
#2340 Feature 2340
1.6
#1094 Feature 1094
1.6
#1728 Feature 1728
1.6
#31 Feature 31
1.5
#375 Feature 375
1.5
#1484 Feature 1484
1.5
#2199 Feature 2199
1.5
#436 Feature 436
1.5
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1.5
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1.5
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1.5
#3026 Feature 3026
1.5
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1.5
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1.5
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1.5
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1.5
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
#1946 Feature 1946
1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.4
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
#2013 Feature 2013
1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
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1.3
#2825 Feature 2825
1.3
#2309 Feature 2309
1.3
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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
#1972 Feature 1972
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
#11 Feature 11
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
#2353 Feature 2353
1.2
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1.2
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1.2
#2877 Feature 2877
1.2
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1.2
#987 Feature 987
1.2
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1.2
#971 Feature 971
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
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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
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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
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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
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1.1
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1.1
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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
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1.0
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1.0
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1.0
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1.0
#2021 Feature 2021
1.0
#1695 Feature 1695
1.0
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1.0
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1.0
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1.0
#2030 Feature 2030
1.0
#1954 Feature 1954
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
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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
#2190 Feature 2190
1.0
#1087 Feature 1087
1.0
#2471 Feature 2471
1.0
#2188 Feature 2188
1.0
#2628 Feature 2628
1.0
#431 Feature 431
1.0
#1509 Feature 1509
1.0
#639 Feature 639
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
#79 Feature 79
1.0
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1.0
#323 Feature 323
1.0
#2086 Feature 2086
1.0
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1.0
#1990 Feature 1990
1.0
#1066 Feature 1066
1.0
#2261 Feature 2261
1.0
#2561 Feature 2561
1.0
#891 Feature 891
1.0
#456 Feature 456
1.0
#350 Feature 350
1.0
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1.0
#74 Feature 74
1.0
#510 Feature 510
1.0
#597 Feature 597
1.0
#1196 Feature 1196
1.0
#3070 Spiritual and Holistic Care in Healthcare
1.0
#1459 Feature 1459
1.0
#1181 Feature 1181
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
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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
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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
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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
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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
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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
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0.9
#1792 Metastatic Cancer
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
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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
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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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0.8
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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
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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
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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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0.7
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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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Document Content

[Resistance to tumor specific therapy with imatinib by clonal selection of mutated cells].
A 60-year-old woman presented with night-sweats and increasing weakness. Physical examination revealed no abnormalities. For 27 years she had been treated for Philadelphia-positive chronic myeloid leukemia (CML). Because of progressive disease treatment with the tyrosine kinase inhibitor imatinib (STI571, Glivec (R)) had been started 9 months before. She had achieved complete hematological remission within 8 weeks, but not a cytogenetic response. Elevated WBC count (26.7/nl) with a differential displaying typical features of acceleration in bone marrow aspirate confirmed CML in accelerated phase. Sequencing of the ATP binding site of the BCR-ABL gene, which - at protein level - is the target for imatinib, revealed the clonal selection of cells harboring a point mutation leading to the exchange of amino acid 253 from tyrosine to histidine. This was considered to be the cause of resistance to imatinib. Dose increase of imatinib up to 600 mg daily and administration of cytarabine did not overcome resistance. Imatinib therapy was discontinued; hematologic remission was induced by oral therapy with hydroxyurea and mercaptopurine. In the course of the following 6 months a gradual decrease of the resistant clone from 100 % down to lower than the detection limit of the method was demonstrated. Clonal mutations are often the cause of resistance to imatinib therapy. They can be detected by sequencing of the ATP binding site of BCR-ABL in specialized laboratories. This case shows that discontinuation of imatinib therapy can significantly reduce the mutated (resistant) clone and thereby restore sensitivity to imatinib.