Bardoni, Barbara
Centre National de la Recherche Scientifique · Université Côte d'Azur · Institut de Pharmacologie Moléculaire et Cellulaire
17 papers on CoChatORCID 0000-0001-6411-1517
Most cited papers
- Verified
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita
Zanaria, E., Muscatelli, F., Bardoni, B., Strom, T. M., Guioli, S., Guo, W., Lalli, E., Moser, C., Walker, A. P., McCabe, E. R. B., et al. (1994) · Nature
Adrenal Hormones and DisordersSexual Differentiation and Disorders
Cited by 858
- Verified
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
Franco, B., Guioli, S., Pragliola, A., Incerti, B., Bardoni, B., Tonlorenzi, R., Carrozzo, R., Maestrini, E., Pieretti, M., Taillon-Miller, P., et al. (1991) · Nature
Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies
Cited by 846
- Verified
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif
Schaeffer, C., Bardoni, B., Mandel, J., Ehresmann, B., Ehresmann, C., & Moine, H. (2001) · The EMBO Journal
Genetics and Neurodevelopmental DisordersRNA Research and Splicing
Cited by 471
- Verified
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P
Schenck, A., Bardoni, B., Moro, A., Bagni, C., & Mandel, J.-L. (2001) · Proceedings of the National Academy of Sciences
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 356
- Verified
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.
Schenck, A., Bardoni, B., Langmann, C., Harden, N., Mandel, J.-L., & Giangrande, A. (2003) · Neuron
Genetics and Neurodevelopmental DisordersNeurobiology and Insect Physiology Research
Cited by 316
- Verified
Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology
Kim, Y., Sung, J. Y., Ceglia, I., Lee, K.-W., Ahn, J.-H., Halford, J. M., Kim, A. M., Kwak, S. P., Park, J. B., Ho Ryu, S., et al. (2006) · Nature
Neuroscience and Neuropharmacology ResearchCellular Mechanics and Interactions
Cited by 307
- Verified
A novel function for fragile X mental retardation protein in translational activation
Bechara, E. G., Didiot, M. C., Melko, M., Davidovic, L., Bensaid, M., Martin, P., Castets, M., Pognonec, P., Khandjian, E. W., Moine, H., et al. (2009) · PLoS Biology
Genetics and Neurodevelopmental DisordersRNA and protein synthesis mechanisms
Cited by 206
- Verified
Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles
Khandjian, E. W., Huot, M.-E., Tremblay, S., Davidovic, L., Mazroui, R., & Bardoni, B. (2004) · Proceedings of the National Academy of Sciences
Genetics and Neurodevelopmental DisordersRNA and protein synthesis mechanisms
Cited by 178
- Verified
FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts
Castets, M., Schaeffer, C., Bechara, E., Schenck, A., Khandjian, E. W., Luche, S., Moine, H., Rabilloud, T., Mandel, J.-L., & Bardoni, B. (2005) · Human Molecular Genetics
Genetics and Neurodevelopmental DisordersRNA Research and Splicing
Cited by 162
- Verified
A novel RNA binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein
Bardoni, B., Schenck, A., & Louis Mandel, J. (1999) · Human Molecular Genetics
Genetics and Neurodevelopmental DisordersRNA Research and Splicing
Cited by 136
- Verified
A metabolomic and systems biology perspective on the brain of the fragile X syndrome mouse model
Davidovic, L., Navratil, V., Bonaccorso, C. M., Catania, M. V., Bardoni, B., & Dumas, M.-E. (2011) · Genome Research
Genetics and Neurodevelopmental DisordersMetabolomics and Mass Spectrometry Studies
Cited by 118
- Verified
Fragile X Syndrome: from molecular pathology to therapy
Maurin, T., Zongaro, S., & Bardoni, B. (2014) · Neuroscience & Biobehavioral Reviews
Genetics and Neurodevelopmental DisordersRNA Research and Splicing
Cited by 113
- Verified
CYFIP family proteins between autism and intellectual disability: links with Fragile X syndrome
Abekhoukh, S., & Bardoni, B. (2014) · Frontiers in Cellular Neuroscience
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 110
- Verified
WAVE/SCAR, a multifunctional complex coordinating different aspects of neuronal connectivity
Schenck, A., Qurashi, A., Carrera, P., Bardoni, B., Diebold, C., Schejter, E., Mandel, J.-L., & Giangrande, A. (2004) · Developmental Biology
Axon Guidance and Neuronal SignalingNeurobiology and Insect Physiology Research
Cited by 76
- Verified
The role of G-quadruplex in RNA metabolism: involvement of FMRP and FMR2P
Melko, M., & Bardoni, B. (2010) · Biochimie
RNA Research and SplicingRNA and protein synthesis mechanisms
Cited by 74
- Verified
New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes
Abekhoukh, S., Sahin, H. B., Grossi, M., Zongaro, S., Maurin, T., Madrigal, I., Kazue-Sugioka, D., Raas-Rothschild, A., Doulazmi, M., Carrera, P., et al. (2017) · Disease Models & Mechanisms
Genetics and Neurodevelopmental DisordersNeurobiology and Insect Physiology Research
Cited by 59
- Verified
Fragile X mental retardation protein (FMRP) interacting proteins exhibit different expression patterns during development
Bonaccorso, C. M., Spatuzza, M., Di Marco, B., Gloria, A., Barrancotto, G., Cupo, A., Musumeci, S. A., D'Antoni, S., Bardoni, B., & Catania, M. V. (2015) · International Journal of Developmental Neuroscience
Genetics and Neurodevelopmental DisordersRNA Research and Splicing
Cited by 52
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free