399 results on '"Chibon, Frédéric"'
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2. Special features of sarcomas developed in patients with Lynch syndrome: A systematic review
3. CINSARC signature outperforms gold-standard TNM staging and consensus molecular subtypes for clinical outcome in stage II–III colorectal carcinoma
4. A metabolic crosstalk between liposarcoma and muscle sustains tumor growth.
5. Biologie et voies de signalisations impliquées dans l’oncogenèse des tumeurs desmoïdes
6. Genomic profile analysis of leiomyomas with bizarre nuclei and fumarate hydratase deficient leiomyomas: Strengths, weaknesses, and limitations of array‐CGH interpretation
7. Genome remodeling upon mesenchymal tumor cell fusion contributes to tumor progression and metastatic spread
8. Medium levels of transcription and replication related chromosomal instability are associated with poor clinical outcome
9. Germinal GLT8D1, GATAD2A and SLC25A39 mutations in a patient with a glomangiopericytal tumor and five different sarcomas over a 10-year period
10. Acquisition of cancer stem cell capacities after spontaneous cell fusion
11. Genomic and transcriptomic comparison of post-radiation versus sporadic sarcomas
12. Gastrointestinal stromal tumor enhancers support a transcription factor network predictive of clinical outcome
13. Genome profiling is an efficient tool to avoid the STUMP classification of uterine smooth muscle lesions: a comprehensive array-genomic hybridization analysis of 77 tumors
14. Fusion-mediated chromosomal instability promotes aneuploidy patterns that resemble human tumors
15. Alternative PDGFD rearrangements in dermatofibrosarcomas protuberans without PDGFB fusions
16. Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas
17. Cell–cell fusion of mesenchymal cells with distinct differentiations triggers genomic and transcriptomic remodelling toward tumour aggressiveness
18. Value of peri-operative chemotherapy in patients with CINSARC high-risk localized grade 1 or 2 soft tissue sarcoma: study protocol of the target selection phase III CHIC-STS trial
19. Analysis of the Peritumoral Tissue Unveils Cellular Changes Associated with a High Risk of Recurrence
20. Clinical effect of molecular methods in sarcoma diagnosis (GENSARC): a prospective, multicentre, observational study
21. RNA sequencing validation of the Complexity INdex in SARComas prognostic signature
22. Leiomyosarcomas: whole genome sequencing for a whole biology characterization
23. Clinicopathologic and Molecular Features of a Series of 41 Biphenotypic Sinonasal Sarcomas Expanding Their Molecular Spectrum
24. Supplementary Figures from Recurrent TRIO Fusion in Nontranslocation–Related Sarcomas
25. Supplementary figures and tables from A Global and Integrated Analysis of CINSARC-Associated Genetic Defects
26. Supplementary Data Table from The Nanocind Signature Is an Independent Prognosticator of Recurrence and Death in Uterine Leiomyosarcomas
27. Supplementary Figures 1-4, Tables 1-5 from Mitotic Checkpoints and Chromosome Instability Are Strong Predictors of Clinical Outcome in Gastrointestinal Stromal Tumors
28. Supplementary Tables from Recurrent TRIO Fusion in Nontranslocation–Related Sarcomas
29. Supplementary Figure 3 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
30. Supplementary Table 1 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
31. Supplementary Figure 2 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
32. Supplementary Figure 1 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
33. Supplementary Table 2 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
34. Supplementary Table 3 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
35. Supplementary Figure Legend from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
36. Supplementary Figure 11 from Recurrent TRIO Fusion in Nontranslocation–Related Sarcomas
37. Supplementary Table 5 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
38. Data from A Global and Integrated Analysis of CINSARC-Associated Genetic Defects
39. Supplementary Table 4 from Genetic Profiling Identifies Two Classes of Soft-Tissue Leiomyosarcomas with Distinct Clinical Characteristics
40. MED12 and uterine smooth muscle oncogenesis: State of the art and perspectives
41. Uterine smooth muscle tumor analysis by comparative genomic hybridization: a useful diagnostic tool in challenging lesions
42. Nuclear-Receptor-Mediated Telomere Insertion Leads to Genome Instability in ALT Cancers
43. Fluorescence in situ hybridization analysis is a helpful test for the diagnosis of dermatofibrosarcoma protuberans
44. Genomic index predicts clinical outcome of intermediate-risk gastrointestinal stromal tumours, providing a new inclusion criterion for imatinib adjuvant therapy
45. Biologie moléculaire en pathologie des tissus mous : utile ou nécessaire ?
46. Sarcomas Genetics: From Point Mutation to Complex Karyotype, from Diagnosis to Therapies
47. Distinct Cellular Origins and Differentiation Process Account for Distinct Oncogenic and Clinical Behaviors of Leiomyosarcomas
48. Smooth muscle differentiation identifies two classes of poorly differentiated pleomorphic sarcomas with distinct outcome
49. Grading of soft tissue sarcomas: from histological to molecular assessment
50. YWHAE rearrangement identified by FISH and RT-PCR in endometrial stromal sarcomas: genetic and pathological correlations
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