Analyzer · Sparsifire

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

Dataset

SAE Model

Document

Active Features

1456

MIN ACTIVATION

0.0

Details List

#2887 Feature 2887

#1304 Feature 1304

#405 Feature 405

#708 Drug Resistance Mechanisms in Cancer

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#2561 Feature 2561

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#198 Feature 198

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#2481 Feature 2481

#1243 Feature 1243

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#2669 Feature 2669

#150 Feature 150

#112 Feature 112

#3007 Feature 3007

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#374 Medical Imaging and Oncology

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#1475 Feature 1475

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#2292 Feature 2292

#896 Feature 896

#1425 Feature 1425

#1037 Feature 1037

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#1965 Feature 1965

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#1496 Feature 1496

#1116 Feature 1116

#2108 Feature 2108

#2270 Feature 2270

#389 Feature 389

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#979 Feature 979

#997 Feature 997

#2583 Feature 2583

#1082 Feature 1082

#218 Feature 218

#2475 Feature 2475

#2353 Feature 2353

#1792 Metastatic Cancer

#630 Feature 630

#2201 Feature 2201

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#2250 Feature 2250

#2221 Feature 2221

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#1680 Feature 1680

#115 Feature 115

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#1121 Feature 1121

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#2415 Feature 2415

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#231 Feature 231

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#316 Feature 316

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#2199 Feature 2199

#1631 Feature #1631

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#2869 Feature 2869

#887 Feature 887

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#2069 Feature 2069

#1445 Feature 1445

#127 Feature 127

#2945 Feature 2945

#2161 Medical/Scientific Discourse with Ethical/Social Implications

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#2732 Feature 2732

#1468 Feature 1468

#2232 Medical Case Reports & Cancer Research

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#2822 Feature 2822

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#1569 Feature 1569

#3049 Feature 3049

#1457 Feature 1457

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#2261 Feature 2261

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#2033 Feature 2033

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#1090 Feature 1090

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#1867 Feature 1867

#1550 Feature 1550

#1386 Feature 1386

#2441 Feature 2441

#579 Feature 579

#2166 Feature #2166

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#675 Feature 675

#1004 Feature 1004

#2113 Feature 2113

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#315 Feature 315

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#238 Feature 238

#2668 Feature 2668

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#571 Feature 571

#2755 Feature 2755

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#2408 Feature 2408

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#424 Feature 424

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#3001 Feature 3001

#1140 Feature 1140

#1778 Feature 1778

#1198 Feature 1198

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#240 Feature 240

#2639 Feature 2639

#2018 Feature 2018

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#2599 Feature 2599

#1820 Feature 1820

#2589 Feature 2589

#2749 Feature 2749

#113 Feature 113

#2427 Feature 2427

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#475 Feature 475

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#2083 Feature 2083

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#2026 Feature 2026

#2524 Feature 2524

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#1161 Feature 1161

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#2676 Feature #2676

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#1773 Feature 1773

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#2070 Feature 2070

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#2825 Feature 2825

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#923 Feature 923

#2284 Feature 2284

#101 Feature 101

#1722 Feature 1722

#3029 Feature 3029

#143 Feature 143

#110 Feature 110

#1580 Feature 1580

#1593 Feature #1593

#1469 Feature 1469

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#611 Feature 611

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#275 Feature 275

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#2377 Feature 2377

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#1521 Feature #1521

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#1340 Feature 1340

#2772 Feature 2772

#419 Feature 419

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#583 Feature 583

#2147 Feature 2147

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#2601 Feature 2601

#2021 Feature 2021

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#139 Feature 139

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#1572 Feature 1572

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#2092 Feature 2092

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#1125 Feature 1125

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#2224 Feature 2224

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#2946 Feature 2946

#1348 Feature 1348

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#2361 Feature 2361

#2811 Feature 2811

#121 Feature 121

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#2841 Feature 2841

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#922 Feature 922

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#335 Feature 335

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#1217 Feature 1217

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#2171 Molecular and Cellular Biological Processes

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Document Content

Dysregulation of cellular signaling in gastric cancer.
The pathogenesis of gastric cancer is complex and related to multiple factors. Dysregulation of intracellular signaling pathways represents a common pathogenic mechanism and may be amenable to drug targeting. Multiple well-established oncogenic pathways, such as those mediated by cell cycle regulators, nuclear factor-kappaB, cyclooxygenase-2 and epidermal growth factor receptor are implicated in gastric carcinogenesis. Emerging evidence also underscores the importance of signaling pathways involved in the developmental process, including transforming growth factor-beta/bone morphogenetic protein signaling, Wnt/beta-catenin signaling, Hedgehog signaling and Notch signaling. Understanding their biological significance will provide a rational basis for drug development. Their relative importance and cross-talk in gastric carcinogenesis, however, are still not completely understood and warrant further investigation.

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