Ghostery is available here for free: https://www.ghostery.com/fr/products/
You can also visit the CNIL web site for instructions on how to configure your browser to manage cookie storage on your device.
In the case of third-party advertising cookies, you can also visit the following site: http://www.youronlinechoices.com/fr/controler-ses-cookies/, offered by digital advertising professionals within the European Digital Advertising Alliance (EDAA). From the site, you can deny or accept the cookies used by advertising professionals who are members.
It is also possible to block certain third-party cookies directly via publishers:
Means of blocking
Analytical and performance cookies
Realytics Google Analytics Spoteffects Optimizely
Targeted advertising cookies
The following types of cookies may be used on our websites:
Social media and advertising cookies
These cookies are needed to ensure the proper functioning of the site and cannot be disabled. They help ensure a secure connection and the basic availability of our website.
These cookies allow us to analyse site use in order to measure and optimise performance. They allow us to store your sign-in information and display the different components of our website in a more coherent way.
These cookies are used by advertising agencies such as Google and by social media sites such as LinkedIn and Facebook. Among other things, they allow pages to be shared on social media, the posting of comments, and the publication (on our site or elsewhere) of ads that reflect your centres of interest.
Our EZPublish content management system (CMS) uses CAS and PHP session cookies and the New Relic cookie for monitoring purposes (IP, response times).
These cookies are deleted at the end of the browsing session (when you log off or close your browser window)
Our EZPublish content management system (CMS) uses the XiTi cookie to measure traffic. Our service provider is AT Internet. This company stores data (IPs, date and time of access, length of the visit and pages viewed) for six months.
Our EZPublish content management system (CMS) does not use this type of cookie.
For more information about the cookies we use, contact INRA’s Data Protection Officer by email at email@example.com or by post at:
INRA 24, chemin de Borde Rouge –Auzeville – CS52627 31326 Castanet Tolosan CEDEX - France
Members - Endosymbiotic infection and nodule development
Dr. Fernanda de Carvalho-Niebel, DR2 CNRS, co-group leader
Fernanda obtained her PhD diploma at the University of Ghent (Belgium), while working in the in lab of Genetics under the direction of Dirk Inzé & Marc Van Montagu. During her PhD she studied the regulation by stress of a plant pathogenesis-Related ß-1,3-glucanase gene and characterized one of the first cases of Post-Transcriptional Gene Silencing (PTGS) in plants resulting in dose-dependent co-suppression of homologous ß-1,3-glucanase genes. As an EMBO post-doctoral fellow, she joined the group of P. Gamas/J. Cullimore at the LIPM to identify genes expressed during early stages of the rhizobial root nodule symbiosis using the model legume Medicago truncatula. During this period, and shortly after as a CNRS researcher, Fernanda characterized new Medigaco genes induced by purified bacterial secreted Nod factor signals, and developed promoter functional studies and tissue-specific yeast-based approaches to identify promoter cis-sequences and underlying symbiotic transcription factors regulating symbiotic host gene regulation. She has in particular characterized a new group of symbiotic ERF transcription factors that in a tissue-specific manner regulate host symbiotic signalling programs. She is currently interested in deciphering these spatio-temporal signalling programs by using adapted molecular and in vivo strategies. Fernanda is now group leader of the Endosymbiotic infection and nodule development (ENOD) team together with Andreas Niebel.
Dr. Andreas Niebel, DR2 CNRS, co-group leader
Andreas obtained his PhD at the University of Ghent in 1994 in the Lab of Marc van Montagu under the supervision of Dirk Inzé and Godelieve Gheysen. His research project involved identifying and characterizing genes such as the cell cycle regulator gene cdc2a, which are expressed in the giant feeding cells elicited in roots of potato, tobacco and Arabidopsis by plant endoparasitic nematodes. As an EMBO postdoctoral fellow he then moved to the LIPM to work on the legume-Rhizobium symbiotic interaction, where he was subsequently recruited by the CNRS (CR2). Andreas initially studied rhizobial Nod factor perception using biochemical and molecular approaches in the group of Julie Cullimore. In 2000, he joined the group of Pascal Gamas and contributed to the study of the symbiotic transcriptome of Medicago truncatula, especially during early steps of this symbiotic interaction. As a member of the Barker-Gamas team he is particularly interested in a group of transcription factors belonging to the CCAAT-box binding factor family, also known as HAP (Heme activating protein) that act as key regulators of rhizobial infection and nodule development and possibly also Nod factor signal transduction. In addition he also studies the symbiotic microtranscriptome and in particular several microRNAs that control early symbiotic signaling and/or nodule development. Andreas is now group leader of the Endosymbiotic infection and nodule development (ENOD) team together with Fernanda de Carvalho-Niebel.
Dr. Pascal Gamas, DR1 CNRS
The first seven years of Pascal’s scientific career were devoted to studies on bacterial transposable elements. His PhD (Michael Chandler’s lab, Toulouse University), focused on the insertion sequence IS1, after which he was recruited by the CNRS (CR2) in 1986. He then studied the transposon Tn7 as a post-doc in Nancy L. Craig’s lab at the University of California, San Francisco, USA. Returning to France, Pascal switched to plant biology to work on the Rhizobium-legume symbiosis. He joined Julie Cullimore’s group at the LIPM in 1990 (co-PI from 1997 to 2007) in order to develop global approaches aimed at identifying Medicago truncatula genes transcriptionally activated by Sinorhizobium meliloti or purified rhizobial Nod factors. He thus established with co-workers a collection of transcriptomics tools in M. truncatula, including standard cDNA sequencing, differential display analysis, subtractive probes or libraries, macro and microarrays and most recently RNA-seq approaches. Pascal is particularly interested in identifying and characterizing transcriptional regulators, notably transcription factors that control early to late nodulation stages, as well as their regulation networks. Pascal was the LIPM Director from 2003 to 2010.
Dr. Joëlle Fournier, CRCN CNRS
During her PhD at Toulouse University, Joëlle worked on the role of lipoxygenases in defense responses of tobacco upon infection by the oomycete Phytophthora parasitica in the group of Marie-Thérèse Esquerré-Tugayé. She joined the CNRS in 1992 to continue her work in this group on the participation of lipoxygenases and the oxylipin pathway in plant defense and resistance against pathogens. In 2005, Joëlle moved to the field of symbiotic plant-microbe interactions in David Barker’s group, where she initiated a project on the cellular mechanisms and dynamics associated with the initial stages of Medicago truncatula root entry by the N-fixing endosymbiont Sinorhizobium meliloti. Rhizobial infection involves the de novo formation of apoplastic compartments called infection threads which host the microsymbiont. Joëlle has developed in vivo approaches for time-lapse studies on infection thread formation in root hairs using laser confocal microscopy associated with ER- or PM-targeted fluorescent markers and fluorescent S. meliloti strains. Her current research is focused on the dynamics of cell wall deposition/modification at infection initiation sites and she is also involved in studies of the in vivo spatio-temporal dynamics of early nodulins during endosymbiotic interface construction.
Dr. M-Françoise Jardinaud, MCF ENSAT-INPT
Françoise obtained her PhD at the Graduate School of Life Sciences of Toulouse in 1994 in the Biotechnology and Plant Improvement Department under the supervision of André Souvré and Gilbert Alibert. She developed new methods for genetic transformation of Brassica and maize microspores. She then moved to CSIRO (Plant Industry, Canberra Australia) where she worked from 1994 to 1995 as post doctoral fellow on the Arabidopsis thaliana flowering gene FLF in Liz Denis’ lab. In 1996, she initiated a new research program funded by the “Australian Rice Growers company” aimed at increasing the iron content of rice seeds. In 2000, she was recruited by CIMMYT (El Batan, Mexico DF) as an associate scientist to study maize drought tolerance in Jean Marcel Ribaut’s group. In 2001, she returned to France after being recruited as an associate professor by the Graduate School of Life Sciences of Toulouse. Françoise first worked on the molecular characterization of sunflower embryogenesis in the Biotechnology and Plant Improvement Department. In 2005, her interest shifted to plant-microbe interactions and in particular the association between the soil-born pathogen Ralstonia solanacearum and Medicago truncatula. Françoise focused her research activities on the relationships between symbiotic and pathogenic plant-microbe interactions. She then joined the Barker-Gamas team in 2009 to work on transcriptional regulators common to both symbiotic and pathogenic interactions.
Lisa Frances, TCN INRA
In 1999, Lisa obtained a two-year bioengineering University diploma in Agronomy (DUT) at the Technological University Institute in Perpignan and in 2000 a Plant Biotechnology degree at ENFA/Paul Sabatier University. Lisa then worked as a technician in the molecular biology laboratories of BIOGEMMA Biotech Company (Clermont-Ferrand, France) and RAGT GENETIQUE (Rodez, France). Lisa was recruited as a technician by INRA in 2005 and joined the LIPM to take charge of the DNA sequencing service of the laboratory. Lisa also joined the Barker-Gamas team to work on the research project run by Fernanda de Carvalho-Niebel on the functional characterization of ERN transcription factors. Lisa is involved in different aspects of this research project but has particularly contributed to the study of the transcription properties of ERN factors using both N. benthamiana- and M. truncatula-based assays, and to the study of protein interactions using yeast two-hybrid and BiFC approaches.
Agnès Lepage, TCE CNRS
Agnès joined the CNRS in 1990. She first worked in the Lab of Cell Physiology in Paris attempting to identify a vaccine against the HIV virus. In 1992 she joined the Institut Jacques Monod (Paris) where she was in charge of the production and microinjection of different animal cell cultures. In 1996 she moved to Toulouse where she joined the Centre for Developmental Biology (CBD) and developed her skills in molecular biology and cytology studying Drosophila melanogaster development. In 2007 she joined the Barker-Gamas team at the LIPM where she studies the role of HAP (CCAAT-box binding factor) transcription factors during the legume-Rhizobium symbiosis under the direction of Andreas Niebel.