Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Charles Marcaillou"'
Autor:
Amélie Roehrig, Theo Z. Hirsch, Aurore Pire, Guillaume Morcrette, Barkha Gupta, Charles Marcaillou, Sandrine Imbeaud, Christophe Chardot, Emmanuel Gonzales, Emmanuel Jacquemin, Masahiro Sekiguchi, Junko Takita, Genta Nagae, Eiso Hiyama, Florent Guérin, Monique Fabre, Isabelle Aerts, Sophie Taque, Véronique Laithier, Sophie Branchereau, Catherine Guettier, Laurence Brugières, Brice Fresneau, Jessica Zucman-Rossi, Eric Letouzé
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Hepatoblastomas (HB) display heterogeneous cellular phenotypes that influence the clinical outcome, but the underlying mechanisms are poorly understood. Here, we use a single-cell multiomic strategy to unravel the molecular determinants of t
Externí odkaz:
https://doaj.org/article/14c4d115a5e440889f8a8405c0ba7b92
Autor:
Lucas Ramon, Catherine David, Karine Fontaine, Elodie Lallet, Charles Marcaillou, Séverine Martin-Lannerée, Virginie Decaulne, Céline Vazart, Anne-Héloise Gélibert, Raouf Ben Abdelali, Jean-Marc Costa, Francis Rousseau, Raphaële Thiébaut, Larry Yost, Yann Gaston-Mathé
Publikováno v:
Biomarker Insights, Vol 13 (2018)
MiR-31-3p expression has been shown to be a predictive biomarker for response to anti-epithelial growth factor receptor therapy in patients with RAS wild-type metastatic colorectal cancer (mCRC). To aid in the quantification of miR-31-3p expression i
Externí odkaz:
https://doaj.org/article/29d467dfb55d46a394e871291f5aab64
Autor:
Florence Koeppel, Steven Blanchard, Cécile Jovelet, Bérengère Genin, Charles Marcaillou, Emmanuel Martin, Etienne Rouleau, Eric Solary, Jean-Charles Soria, Fabrice André, Ludovic Lacroix
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0188174 (2017)
Tumor mutation load (TML) has been proposed as a biomarker of patient response to immunotherapy in several studies. TML is usually determined by tumor biopsy DNA (tDNA) whole exome sequencing (WES), therefore TML evaluation is limited by informative
Externí odkaz:
https://doaj.org/article/e2b6f738d86a4647abfc46697be49b5a
Autor:
Philippe Rameau, Sylvia Julien, Corinne Laplace-Builhé, Philippe Vielh, Karim Fizazi, Yohann Loriot, Jean-Charles Soria, Semih Dogan, Fanny Billiot, Arian Tibbe, Melissa Taylor, Marianne Oulhen, Françoise Farace, Vincent Faugeroux, Charles Marcaillou, Maud Ngo-Camus, Emma Pailler, Christophe Massard, Celine Lefebvre, Valérie Pierron, Sebastien Tourlet
Publikováno v:
European Urology Oncology. 3:498-508
Background Genomic analysis of circulating tumor cells (CTCs) could provide a unique and accessible representation of tumor diversity but remains hindered by technical challenges associated with CTC rarity and heterogeneity. Objective To evaluate CTC
Autor:
Laure Piqueret-Stephan, Aurélie Honoré, Nathalie Droin, David Gentien, Ludovic Lacroix, Charles Marcaillou, Jean-Yves Scoazec, Cécile Reyes, Philippe Vielh, Melanie Letexier
Publikováno v:
Cancer Cytopathology. 124:241-253
BACKGROUND Data generated by next-generation sequencing technologies have a pivotal role in precision medicine. These high-throughput techniques are preferentially performed on fresh tissue, but there is an increasing need for protocols adapted to ma
Autor:
Pascal Reynier, Lisa Boucret, Véronique Ferré-L’Hotellier, J.M. Chao de la Barca, Valérie Desquiret, Charles Marcaillou, Catherine Morinière, Philippe Descamps, Pascale May-Panloup, Vincent Procaccio
Publikováno v:
Human reproduction (Oxford, England)
Human reproduction (Oxford, England), 2015, 30 (7), pp.1653-64. ⟨10.1093/humrep/dev114⟩
Human reproduction (Oxford, England), 2015, 30 (7), pp.1653-64. ⟨10.1093/humrep/dev114⟩
International audience; STUDY QUESTION: What part do mitochondria play in cases of diminished ovarian reserve (DOR)?SUMMARY ANSWER: Mitochondrial biogenesis in cumulus cells may be linked with impaired oocyte competence in patients with DOR.WHAT IS K
Autor:
Simon Girard, Charles Marcaillou, Amandine Campan-Fournier, Jean-Claude Bernard, Shunmoogum A. Patten, Florina Moldovan, Charlotte Zaouter, Bernard Biot, Alicia Besson, Nicolas Fraisse, Rita Menassa, Guy A. Rouleau, Raphaelle Lamy, Kariman Abelin-Genevois, Meijiang Liao, Jérôme Berard, Vincent Cunin, Gaetan Lesca, Patrick Edery, Françoise Clerget-Darpoux, Khaled Fendri, Audrey Labalme, Pierre Drapeau, Patricia Margaritte-Jeannin, Eudeline Alix, Melanie Letexier, Coline Poizat, Damien Sanlaville
Publikováno v:
Journal of Clinical Investigation. 125:1124-1128
Idiopathic scoliosis (IS) is a spine deformity that affects approximately 3% of the population. The underlying causes of IS are not well understood, although there is clear evidence that there is a genetic component to the disease. Genetic mapping st
Autor:
Charles Marcaillou, Etienne Rouleau, Steven B. Blanchard, Fabrice Andre, Emmanuel Martin, Jean-Charles Soria, Eric Solary, Cécile Jovelet, Bérengère Genin, Ludovic Lacroix, Florence Koeppel
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 11, p e0188174 (2017)
PLoS ONE, Vol 12, Iss 11, p e0188174 (2017)
Tumor mutation load (TML) has been proposed as a biomarker of patient response to immunotherapy in several studies. TML is usually determined by tumor biopsy DNA (tDNA) whole exome sequencing (WES), therefore TML evaluation is limited by informative
Autor:
Christine Petit, Eberhart Zrenner, Shzeena Dad, Martina Jarc-Vidmar, Maria Antonia Claveria, Alberto Auricchio, Ana Fakin, Marko Hawlina, Gaelle M. Lefèvre, Susanne Kohl, Anne Kurtenbach, Aziz El-Amraoui, Loreto Martorell Sampol, Jesus Rodriguez Jorge, Ditta Zobor, Saddek Mohand-Said, Crystel Bonnet, Ieva Sliesoraityte, Charles Marcaillou, Francesco Testa, Saba Battelino, Jaume Mora, Mélanie Letexier, José-Alain Sahel, Francesca Simonelli, Lisbeth Birk Møller, Sandra Chantot-Bastaraud, Jean-Pierre Hardelin, Isabelle Audo, Zied Riahi, Andrej Zupan, Luce Smagghe, Amrit Singh-Estivalet, Damjan Glavač, Souad Gherbi, Sandro Banfi, Sandrine Marlin
Publikováno v:
European Journal of Human Genetics
European Journal of Human Genetics, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩
EUROPEAN JOURNAL OF HUMAN GENETICS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
European Journal of Human Genetics, Nature Publishing Group, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
European Journal of Human Genetics, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩
EUROPEAN JOURNAL OF HUMAN GENETICS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
European Journal of Human Genetics, Nature Publishing Group, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
International audience; Usher syndrome (USH), the most prevalent cause of hereditary deafness-blindness, is an autosomal recessive and genetically heterogeneous disorder. Three clinical subtypes (USH1-3) are distinguishable based on the severity of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4afcf7a92c79aeed388ac2681d75dd57
https://hal-pasteur.archives-ouvertes.fr/pasteur-03215026/document
https://hal-pasteur.archives-ouvertes.fr/pasteur-03215026/document
Autor:
Chris Ottolenghi, Anne-Paule Gimenez-Roqueplo, Nelly Burnichon, Pierre Rustin, Maxime Janin, Aurélien de Reyniès, Charles Marcaillou, N. Abermil, Judith Favier, Alexandre Buffet, Laurence Amar, Jérôme Bertherat, Eric Letouzé, Paule Bénit, Mélanie Menara, Cosimo Martinelli, Céline Loriot, An Thach Nguyen
Publikováno v:
Cancer Cell
Cancer Cell; Vol 23
Cancer Cell; Vol 23
SummaryParagangliomas are neuroendocrine tumors frequently associated with mutations in RET, NF1, VHL, and succinate dehydrogenase (SDHx) genes. Methylome analysis of a large paraganglioma cohort identified three stable clusters, associated with dist