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Evaluating Genetic Alterations in Metastatic Pancreatic Neuroendocrine Tumors with Potential Therape...

Evaluating Genetic Alterations in Metastatic Pancreatic Neuroendocrine Tumors with Potential Therape...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2955225436

Evaluating Genetic Alterations in Metastatic Pancreatic Neuroendocrine Tumors with Potential Therapeutic and Prognostic Applications: A Comparative In Silico Study with Metastatic Neuroendocrine Tumors Originating from the Small Intestine and Rectum

About this item

Full title

Evaluating Genetic Alterations in Metastatic Pancreatic Neuroendocrine Tumors with Potential Therapeutic and Prognostic Applications: A Comparative In Silico Study with Metastatic Neuroendocrine Tumors Originating from the Small Intestine and Rectum

Publisher

US: Oxford University Press

Journal title

American journal of clinical pathology, 2023-11, Vol.160 (Supplement_1), p.S100-S101

Language

English

Formats

Publication information

Publisher

US: Oxford University Press

More information

Scope and Contents

Contents

Abstract
Introduction/Objective
Pancreatic neuroendocrine tumors (P-NET) are diverse tumors with slow growth and varying levels of potential malignant behavior. The overall 5-year survival rates for P-NET are approximately 95%, 72%, and 23% if localized, and in cases of regional and distant metastasis respectively. These tumors exhibit a low...

Alternative Titles

Full title

Evaluating Genetic Alterations in Metastatic Pancreatic Neuroendocrine Tumors with Potential Therapeutic and Prognostic Applications: A Comparative In Silico Study with Metastatic Neuroendocrine Tumors Originating from the Small Intestine and Rectum

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2955225436

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2955225436

Other Identifiers

ISSN

0002-9173

E-ISSN

1943-7722

DOI

10.1093/ajcp/aqad150.221

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