Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pauline Bouret"'
Autor:
Boris Dmitrenko, Vincent Gatinois, Morgana D’Ottavi, Ahmed El Mouatani, Pauline Bouret, Ségolène Debiesse, Michel Mondain, Mohamed Akkari, Maxime Dallemagne, Franck Pellestor, Philippe Vande Perre, Jean-Pierre Molès
Publikováno v:
Cells, Vol 12, Iss 16, p 2116 (2023)
The factors influencing mother-to-child cell trafficking and persistence over children’s lives have yet to be established. The quantification of maternal microchimerism was previously reported through HLA-based approaches, which introduced bias reg
Externí odkaz:
https://doaj.org/article/dbc3dfc05d6d458a8b582ddbd130b2e5
Autor:
Kevin Yauy, Anouck Schneider, Bee Ling Ng, Jean-Baptiste Gaillard, Satish Sati, Christine Coubes, Constance Wells, Magali Tournaire, Thomas Guignard, Pauline Bouret, David Geneviève, Jacques Puechberty, Franck Pellestor, Vincent Gatinois
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract Background Balanced structural variants are mostly described in disease with gene disruption or subtle rearrangement at breakpoints. Case presentation Here we report a patient with mild intellectual deficiency who carries a de novo balanced
Externí odkaz:
https://doaj.org/article/af431e66ab844436af04e46b042eb9d4
Autor:
Nejla Erkilic, Vincent Gatinois, Simona Torriano, Pauline Bouret, Carla Sanjurjo-Soriano, Valerie De Luca, Krishna Damodar, Nicolas Cereso, Jacques Puechberty, Rocio Sanchez-Alcudia, Christian P. Hamel, Carmen Ayuso, Isabelle Meunier, Franck Pellestor, Vasiliki Kalatzis
Publikováno v:
Cells, Vol 8, Iss 9, p 1068 (2019)
Induced pluripotent stem cells (iPSCs) have revolutionized the study of human diseases as they can renew indefinitely, undergo multi-lineage differentiation, and generate disease-specific models. However, the difficulty of working with iPSCs is that
Externí odkaz:
https://doaj.org/article/58696ef3e8e64d819ea17608c3d767c6
Autor:
Vincent Gatinois, Boris Dmitrenko, Ahmed El Mouatani, Ségolène Debiesse, Pauline Bouret, Jacques Puechberty, Joris Vermeesch, Jean-Pierre Moles, Franck Pellestor
Publikováno v:
Morphologie. 106:S11-S12
Autor:
Franck Pellestor, Jean-Marc Lemaitre, Quentin Szabo, Giorgio L. Papadopoulos, Juan Carlos Rivera-Mulia, Satish Sati, Pauline Bouret, Giacomo Cavalli, Daniel Jost, Modesto Orozco, Frédéric Bantignies, François Serra, Boyan B. Bonev, Lauriane Fritsch, David Castillo, David M. Gilbert, Paul Bensadoun, Josep Ll. Gelpi, Vincent Loubiere, Cédric Vaillant, Marc A. Marti-Renom
Publikováno v:
Molecular Cell
Molecular Cell, 2020, 78 (3), pp.522-538.e9. ⟨10.1016/j.molcel.2020.03.007⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Molecular Cell, Elsevier, 2020, 78 (3), pp.522-538.e9. ⟨10.1016/j.molcel.2020.03.007⟩
Molecular Cell, 2020, 78 (3), pp.522-538.e9. ⟨10.1016/j.molcel.2020.03.007⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Molecular Cell, Elsevier, 2020, 78 (3), pp.522-538.e9. ⟨10.1016/j.molcel.2020.03.007⟩
To understand the role of the extensive senescence-associated 3D genome reorganization, we generated genome-wide chromatin interaction maps, epigenome, replication-timing, whole-genome bisulfite sequencing, and gene expression profiles from cells ent
Autor:
Bee Ling Ng, Jacques Puechberty, Bruno Dumont, Magali Tournaire, Pauline Bouret, Christine Coubes, David Geneviève, Amaria Baghdadli, Franck Pellestor, Manon Girard, Vincent Gatinois, Julia Magnetto, Anouck Schneider
Publikováno v:
American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, Wiley, 2015, 167 (12), pp.3031-3037. ⟨10.1002/ajmg.a.37350⟩
American Journal of Medical Genetics Part A, Wiley, 2015, 167 (12), pp.3031-3037. ⟨10.1002/ajmg.a.37350⟩
International audience; Intellectual disability (ID) is a frequent feature but is highly clinically and genetically heterogeneous. The establishment of the precise diagnosis in patients with ID is challenging due to this heterogeneity but crucial for