Comprehensive targeted next‐generation sequencing approach in the molecular diagnosis of gastrointestinal stromal tumor
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Title
Comprehensive targeted next‐generation sequencing approach in the molecular diagnosis of
gastrointestinal stromal tumor
Authors
Keywords
-
Journal
GENES CHROMOSOMES & CANCER
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2020-12-01
DOI
10.1002/gcc.22923
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Note: Only part of the references are listed.- Gain of FGF4 is a frequent event in KIT/PDGFRA/SDH/RAS‐P WT GIST
- (2019) Milena Urbini et al. GENES CHROMOSOMES & CANCER
- Gastrointestinal Stromal Tumors
- (2018) Margaret von Mehren et al. JOURNAL OF CLINICAL ONCOLOGY
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- (2018) Lindsey M. Charo et al. Journal of the National Comprehensive Cancer Network
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- (2017) Hildegard Kehrer-Sawatzki et al. HUMAN GENETICS
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- (2017) Lawrence J. Jennings et al. JOURNAL OF MOLECULAR DIAGNOSTICS
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- (2017) Maria A. Pantaleo et al. MOLECULAR CANCER RESEARCH
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- (2016) Daniela Gasparotto et al. CLINICAL CANCER RESEARCH
- Transcriptome sequencing identifiesETV6-NTRK3as a gene fusion involved in GIST
- (2016) Monica Brenca et al. JOURNAL OF PATHOLOGY
- FGFR1 and NTRK3 actionable alterations in “Wild-Type” gastrointestinal stromal tumors
- (2016) Eileen Shi et al. Journal of Translational Medicine
- Activity of Selumetinib in Neurofibromatosis Type 1–Related Plexiform Neurofibromas
- (2016) Eva Dombi et al. NEW ENGLAND JOURNAL OF MEDICINE
- “Wild type” GIST: Clinicopathological features and clinical practice
- (2016) Ryuichi Wada et al. PATHOLOGY INTERNATIONAL
- Hybridization Capture-Based Next-Generation Sequencing to Evaluate Coding Sequence and Deep Intronic Mutations in the NF1 Gene
- (2016) Karin Cunha et al. Genes
- Molecular Subtypes ofKIT/PDGFRAWild-Type Gastrointestinal Stromal Tumors
- (2016) Sosipatros A. Boikos et al. JAMA Oncology
- Somatic loss of function mutations in neurofibromin 1 and MYC associated factor X genes identified by exome-wide sequencing in a wild-type GIST case
- (2015) Martin G. Belinsky et al. BMC CANCER
- Incidence and Mortality of Neurofibromatosis: A Total Population Study in Finland
- (2015) Elina Uusitalo et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- A point mutation in the extracellular domain of KIT promotes tumorigenesis of mast cells via ligand-independent auto-dimerization
- (2015) Yosuke Amagai et al. Scientific Reports
- Gastrointestinal stromal tumors: what do we know now?
- (2014) Christopher L Corless MODERN PATHOLOGY
- Anchored multiplex PCR for targeted next-generation sequencing
- (2014) Zongli Zheng et al. NATURE MEDICINE
- Quadruplewild-type (WT) GIST: defining the subset of GIST that lacks abnormalities of KIT, PDGFRA, SDH, or RAS signaling pathways
- (2014) Maria A. Pantaleo et al. Cancer Medicine
- Succinate Dehydrogenase-Deficient GISTs
- (2011) Markku Miettinen et al. AMERICAN JOURNAL OF SURGICAL PATHOLOGY
- Fast and accurate long-read alignment with Burrows–Wheeler transform
- (2010) Heng Li et al. BIOINFORMATICS
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations
- (2010) K. A. Janeway et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions
- (2008) Katharina Steinmann et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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