Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Vincent Sater"'
Autor:
Victor Bobée, Mathieu Viennot, Vinciane Rainville, Liana Veresezan, Fanny Drieux, Pierre‐Julien Viailly, Victor Michel, Vincent Sater, Marie‐Delphine Lanic, Elodie Bohers, Vincent Camus, Hervé Tilly, Fabrice Jardin, Philippe Ruminy
Publikováno v:
HemaSphere, Vol 8, Iss 2, Pp n/a-n/a (2024)
Abstract Follicular lymphoma (FL) course is highly variable, making its clinical management challenging. In this incurable and recurring pathology, the interval between relapses tends to decrease while aggressiveness increases, sometimes resulting in
Externí odkaz:
https://doaj.org/article/b2f0a3b2f6474b0887c06b90dc53dcb5
Autor:
Pierre-Julien Viailly, Vincent Sater, Mathieu Viennot, Elodie Bohers, Nicolas Vergne, Caroline Berard, Hélène Dauchel, Thierry Lecroq, Alison Celebi, Philippe Ruminy, Vinciane Marchand, Marie-Delphine Lanic, Sydney Dubois, Dominique Penther, Hervé Tilly, Sylvain Mareschal, Fabrice Jardin
Publikováno v:
BMC Bioinformatics, Vol 22, Iss 1, Pp 1-15 (2021)
Abstract Background Recently, copy number variations (CNV) impacting genes involved in oncogenic pathways have attracted an increasing attention to manage disease susceptibility. CNV is one of the most important somatic aberrations in the genome of t
Externí odkaz:
https://doaj.org/article/b229cd4e14c749a68bcf4b30c189122a
Autor:
Vincent Sater, Pierre-Julien Viailly, Thierry Lecroq, Philippe Ruminy, Caroline Bérard, Élise Prieur-Gaston, Fabrice Jardin
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 18, Iss , Pp 2270-2280 (2020)
Motivation: With Next Generation Sequencing becoming more affordable every year, NGS technologies asserted themselves as the fastest and most reliable way to detect Single Nucleotide Variants (SNV) and Copy Number Variations (CNV) in cancer patients.
Externí odkaz:
https://doaj.org/article/d19bf484d8ca43d794f9a515e4f4f14f
Autor:
Marie-Delphine, Lanic, François, Le Loarer, Vinciane, Rainville, Vincent, Sater, Mathieu, Viennot, Ludivine, Beaussire, Pierre-Julien, Viailly, Emilie, Angot, Isabelle, Hostein, Fabrice, Jardin, Philippe, Ruminy, Marick, Laé
Publikováno v:
Modern Pathology. 35:649-663
Morphological, immunohistochemical, and molecular methods often need to be combined for accurate diagnosis and optimal clinical management of sarcomas. Here, we have developed, a new molecular diagnostic assay, for the detection of gene fusions in sa
Autor:
Marie‐Delphine Lanic, René Guérin, Vincent Sater, Pauline Durdilly, Philippe Ruminy, Alena Skálová, Marick Laé
Publikováno v:
Genes, chromosomescancer.
Hyalinizing clear cell carcinoma (HCCC) is a rare salivary gland carcinoma with a generally indolent behavior, characterized by recurrent chromosomal translocation involving EWSR1 (22q12.2) leading to two fusion genes EWSR1::ATF1 or EWSR1::CREM. We r
Autor:
Vincent, Sater, Pierre-Julien, Viailly, Thierry, Lecroq, Élise, Prieur-Gaston, Élodie, Bohers, Mathieu, Viennot, Philippe, Ruminy, Hélène, Dauchel, Pierre, Vera, Fabrice, Jardin
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2493
The rapid transition from traditional sequencing methods to Next-Generation Sequencing (NGS) has allowed for a faster and more accurate detection of somatic variants (Single-Nucleotide Variant (SNV) and Copy Number Variation (CNV)) in tumor cells. NG
Autor:
Caroline Bérard, Thierry Lecroq, Fabrice Jardin, Vincent Sater, Pierre-Julien Viailly, Philippe Ruminy, Élise Prieur-Gaston
Publikováno v:
Computational and Structural Biotechnology Journal
Computational and Structural Biotechnology Journal, Elsevier, 2020, 18, pp.2270-2280. ⟨10.1016/j.csbj.2020.08.011⟩
Computational and Structural Biotechnology Journal, Vol 18, Iss, Pp 2270-2280 (2020)
Computational and Structural Biotechnology Journal, Elsevier, 2020, 18, pp.2270-2280. ⟨10.1016/j.csbj.2020.08.011⟩
Computational and Structural Biotechnology Journal, Vol 18, Iss, Pp 2270-2280 (2020)
MotivationWith Next Generation Sequencing becoming more affordable every year, NGS technologies asserted themselves as the fastest and most reliable way to detect Single Nucleotide Variants (SNV) and Copy Number Variations (CNV) in cancer patients. T
Autor:
Vincent Sater, Pierre-Julien Viailly, Thierry Lecroq, Élise Prieur-Gaston, Élodie Bohers, Mathieu Viennot, Philippe Ruminy, Hélène Dauchel, Pierre Vera, Fabrice Jardin
Publikováno v:
Variant Calling ISBN: 9781071622926
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d739e9746a457881d5e8a5312c4289ce
https://doi.org/10.1007/978-1-0716-2293-3_14
https://doi.org/10.1007/978-1-0716-2293-3_14
Autor:
Mathieu Viennot, Fabrice Jardin, Nouhoum Sako, Vinciane Marchand, Virginie Fataccioli, Philippe Ruminy, Liana Veresezan, Marie Parrens, David Vallois, Cyrielle Robe, Jean-Michel Picquenot, Fanny Drieux, Philippe Gaulard, Vincent Sater, A. Dupuy, Pierre-Julien Viailly, Marie-Delphine Lanic, Laurence de Leval, François Lemonnier, Elsa Poullot, Céline Bossard
Publikováno v:
The Journal of molecular diagnostics : JMD. 23(8)
The genetic basis of peripheral T-cell lymphoma (PTCL) is complex and encompasses several recurrent fusion transcripts discovered over the past years by means of massive parallel sequencing. However, there is currently no affordable and rapid technol
Autor:
Philippe Gaulard, Fabrice Jardin, Fanny Drieux, Vinciane Marchand, Corinne Haioun, Pierre-Julien Viailly, Victor Bobée, Marie-Delphine Lanic, Liana Veresezan, Christiane Copie-Bergman, Gilles Salles, Thierry Jo Molina, Elodie Bohers, Vincent Sater, Philippe Ruminy, Jean-Michel Picquenot, Lucie Oberic, Hervé Tilly, Mathieu Viennot
Publikováno v:
Blood Cancer Journal
Blood Cancer Journal, Nature Publishing Group, 2020, 10 (5), ⟨10.1038/s41408-020-0322-5⟩
Blood Cancer Journal, 2020, 10 (5), ⟨10.1038/s41408-020-0322-5⟩
Blood Cancer Journal, Vol 10, Iss 5, Pp 1-13 (2020)
Blood Cancer Journal, Nature Publishing Group, 2020, 10 (5), ⟨10.1038/s41408-020-0322-5⟩
Blood Cancer Journal, 2020, 10 (5), ⟨10.1038/s41408-020-0322-5⟩
Blood Cancer Journal, Vol 10, Iss 5, Pp 1-13 (2020)
Non-Hodgkin B-cell lymphomas (B-NHLs) are a highly heterogeneous group of mature B-cell malignancies. Their classification thus requires skillful evaluation by expert hematopathologists, but the risk of error remains higher in these tumors than in ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55bb3f55c0c2706550dd53986ff8e6df
https://hal-normandie-univ.archives-ouvertes.fr/hal-02733467
https://hal-normandie-univ.archives-ouvertes.fr/hal-02733467