O
Olivier Bernard
Researcher at French Institute for Research in Computer Science and Automation
Publications - 830
Citations - 42407
Olivier Bernard is an academic researcher from French Institute for Research in Computer Science and Automation. The author has contributed to research in topics: Liver transplantation & Segmentation. The author has an hindex of 96, co-authored 790 publications receiving 37878 citations. Previous affiliations of Olivier Bernard include Intelligence and National Security Alliance & Institut national des sciences appliquées.
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Mutations of ASXL1 gene in myeloproliferative neoplasms
Nadine Carbuccia,Anne Murati,Virginie Trouplin,Mandy Brecqueville,José Adélaïde,Jérôme Rey,William Vainchenker,Olivier Bernard,Max Chaffanet,Norbert Vey,David Jérémie Birnbaum,M J Mozziconacci +11 more
TL;DR: It is confirmed that epoxomicin-based compounds may be subject to this type of resistance mechanism and the first report to demonstrate the acquisition of P-gP with a proteasome inhibitor is demonstrated.
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Hurdles and challenges for modelling and control of microalgae for CO2 mitigation and biofuel production
Olivier Bernard,Olivier Bernard +1 more
TL;DR: The Droop model, which has been widely used to predict microalgal behaviour under nutrient limitation, is reviewed, and a model for raceways or planar photobioreactors, when both light and nutrients are limiting is details.
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The use of fluorescent Nile red and BODIPY for lipid measurement in microalgae
Judith Rumin,Hubert Bonnefond,Bruno Saint-Jean,Catherine Rouxel,Antoine Sciandra,Olivier Bernard,Jean-Paul Cadoret,Gaël Bougaran +7 more
TL;DR: The overall conclusion of the present review study gives limitations on the use of fluorochrome for screening of lipid-rich microalgae species and suggests improved protocols for staining recalcitrantmicroalgae and recommendations for the staining quantification.
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Defect of multidrug‐resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis
J F Deleuze,E. Jacquemin,Claire Dubuisson,D Cresteil,M. Dumont,Serge Erlinger,Olivier Bernard,Michelle Hadchouel +7 more
TL;DR: The absence of the mdr3 P‐glycoprotein may be responsible for this type of PFIC, which, as in the murine model, may be due to a toxic effect of bile acids on the biliary epithelium in absence of biliary phospholipids.
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Outcome in adulthood of biliary atresia: a study of 63 patients who survived for over 20 years with their native liver.
Panayotis Lykavieris,Christophe Chardot,Maroun Sokhn,Frédéric Gauthier,Jacques Valayer,Olivier Bernard +5 more
TL;DR: In the long term, less than 18% of infants with biliary atresia who are treated with corrective surgery may avoid liver transplantation, but even these patients require assiduous lifelong care.