Pathology and biology of GISTs (notice n° 2081477)

détails MARC
000 -LEADER
fixed length control field 01307cam a2200157 4500500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260405005146.0
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Ngo, Carine
Relator term author
245 00 - TITLE STATEMENT
Title Pathology and biology of GISTs
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2026.<br/>
500 ## - GENERAL NOTE
General note 50
520 ## - SUMMARY, ETC.
Summary, etc. Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the digestive tract and most often result from activating mutations in the KIT or PDGFRA genes. Their diagnosis relies on morphology and immunohistochemistry, with characteristic expression of KIT (CD117) and DOG1. Tyrosine kinase inhibitors (TKIs), particularly imatinib, have revolutionized GIST management, significantly improving patient survival. The “wild-type” GISTs, lacking KIT or PDGFRA mutations, comprise distinct subtypes, including SDH-deficient GISTs and those harboring BRAF, NF1, or NTRK alterations.The identification of the molecular profile of GISTs is a critical step for optimal patient management, as both the choice of TKI and its dosing directly depend on the tumor mutational status.
786 0# - DATA SOURCE ENTRY
Note Hépato-Gastro & Oncologie Digestive | 33 | N° Supp 1 | 2026-02-23 | p. 7-15 | 2115-3310
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://stm.cairn.info/journal-hepato-gastro-oncologie-digestive-2026-HS1-page-7?lang=en&redirect-ssocas=7080">https://stm.cairn.info/journal-hepato-gastro-oncologie-digestive-2026-HS1-page-7?lang=en&redirect-ssocas=7080</a>

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