about
Comprehensive Molecular Profiling of Archival Bone Marrow Trephines Using a Commercially Available Leukemia Panel and Semiconductor-Based Targeted ResequencingRoutine clinical mutation profiling using next generation sequencing and a customized gene panel improves diagnostic precision in myeloid neoplasms.Molecular Analysis of Circulating Cell-Free DNA from Lung Cancer Patients in Routine Laboratory Practice: A Cross-Platform Comparison of Three Different Molecular Methods for Mutation Detection.Subclonal analysis in a lobular breast cancer with classical and solid growth pattern mimicking a solid-papillary carcinoma.Archival bone marrow trephines are suitable for high-throughput mutation analysis using next generation sequencing technology.SRSF2 and U2AF1 mutations in primary myelofibrosis are associated with JAK2 and MPL but not calreticulin mutation and may independently reoccur after allogeneic stem cell transplantation.SRSF2 mutation is present in the hypercellular and prefibrotic stage of primary myelofibrosis.Absence of MGMT promoter methylation in diffuse midline glioma, H3 K27M-mutant.Fibrotic progression in Polycythemia vera is associated with early concomitant driver-mutations besides JAK2.Next-Generation Sequencing Analysis of Laser-Microdissected Formalin-Fixed and Paraffin-Embedded (FFPE) Tissue Specimens.Evolution of chronic myelomonocytic leukemia to myeloproliferative neoplasm.CDKN2A loss and PIK3CA mutation in myoepithelial-like metaplastic breast cancer.Analysis of Mutational Hotspots in Routinely Processed Bone Marrow Trephines by Pyrosequencing®.Comprehensive mutation profiling and mRNA expression analysis in atypical chronic myeloid leukemia in comparison with chronic myelomonocytic leukemiaDe novo CSF3R mutation associated with transformation of myeloproliferative neoplasm to atypical CMLMolecular defects in BRAF wild-type ameloblastomas and craniopharyngiomas-differences in mutation profiles in epithelial-derived oropharyngeal neoplasmsEstrogen receptor (ESR1) mutation in bone metastases from breast cancerHotspot mutations in cancer genes may be missed in routine diagnostics due to neighbouring sequence variantsERBB2 mutation frequency in lobular breast cancer with pleomorphic histology or high-risk characteristics by molecular expression profilingActivating human epidermal growth factor receptor 2 (HER2) gene mutation in bone metastases from breast cancerRNA-binding protein (RBFOX1) inherited polymorphism rs8051518 is not associated with splice factor mutations in myelodysplastic syndromes and myeloproliferative neoplasmsMutations associated with age-related clonal hematopoiesis in PMF patients with rapid progression to myelofibrosis[Liquid biopsy in tumor diagnostics : Applications, perspectives, and limitations of the "cancer liquidome"]
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
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հետազոտող
@hy
name
Stephan Bartels
@ast
Stephan Bartels
@en
Stephan Bartels
@es
Stephan Bartels
@nl
Stephan Bartels
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type
label
Stephan Bartels
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Stephan Bartels
@en
Stephan Bartels
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Stephan Bartels
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Stephan Bartels
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prefLabel
Stephan Bartels
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Stephan Bartels
@en
Stephan Bartels
@es
Stephan Bartels
@nl
Stephan Bartels
@sl
P106
P21
P31
P496
0000-0002-8903-2345