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

1460

MIN ACTIVATION

0.0

Details List

#2475 Feature 2475

#559 Feature 559

#2676 Feature 2676

#1317 Feature 1317

#1203 Feature 1203

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#2293 Feature 2293

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#2561 Feature 2561

#2453 Feature 2453

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#812 Feature 812

#2788 Feature 2788

#2199 Feature 2199

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#1792 Metastatic Cancer

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#1604 Feature 1604

#1037 Feature 1037

#463 Feature 463

#350 Feature 350

#2117 Feature 2117

#708 Drug Resistance Mechanisms in Cancer

#2455 Feature 2455

#1155 Feature 1155

#317 Feature 317

#525 Feature 525

#2848 Feature 2848

#798 Feature 798

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#1996 Feature 1996

#1844 Feature 1844

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#374 Medical Imaging and Oncology

#1965 Feature 1965

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#1126 Feature 1126

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#787 Feature 787

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#191 Feature 191

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#1106 Feature 1106

#1024 Feature 1024

#1080 Feature 1080

#515 Feature 515

#279 Feature 279

#2414 Feature 2414

#1216 Feature 1216

#428 Feature 428

#1838 Feature 1838

#1311 Molecular Mechanisms and Biological Processes

#2010 Feature 2010

#2024 Feature 2024

#160 Feature 160

#2598 Feature 2598

#1773 Feature 1773

#225 Feature 225

#2161 Medical/Scientific Discourse with Ethical/Social Implications

#1387 Feature 1387

#2411 Feature 2411

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#2181 Feature 2181

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#3061 Feature 3061

#2874 Feature 2874

#1584 Feature 1584

#23 Neuronal Circuitry and Cellular Processes

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#2232 Medical Case Reports & Cancer Research

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Document Content

Diabetes does not influence oral oncogenesis through fibroblast growth factor receptors.
Increased expression of fibroblast growth factors and their receptors (FGFRs) has recently been described in oral squamous cell carcinoma. In addition, we have previously described a molecular basis for an association between oral cancer and diabetes. The expression of FGFR-2 and FGFR-3 investigated in an experimental model of chemically induced carcinogenesis in normal and diabetic (type I) rats. Tissue sections ranging from normal mucosa to moderately-differentiated oral squamous cell carcinoma were studied using monoclonal antibodies against FGFR-2 and FGFR-3 proteins. A similar pattern of elevated FGFR-2 and FGFR-3 expression was observed in the initial stages of oncogenesis for both diabetic and non-diabetic animals. In the last stages of oral oncogenesis, the expression of both proteins remained relatively stable. It seems that diabetes does not affect the FGFR-2 and FGFR-3 pattern of expression throughout the various stages of oral oncogenesis.

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