9 results on '"Brou, M."'
Search Results
2. Communique issued at the end of a 1-day workshop organized by the International Society for the Study of Behavioural Development on Open Science and Developmental Psychology
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Youth in Changing Cultural Contexts, Leerstoel Finkenauer, Faculteit Sociale Wetenschappen, Iorfa, Steven Kotar, Maes, Marlies, Ku, S., Benitez, Y. R., Brou, M., Gönül, B., Makila, M. L., Monteoliva, J., Riberiro, A. C. L., van Aken, Marcel, Youth in Changing Cultural Contexts, Leerstoel Finkenauer, Faculteit Sociale Wetenschappen, Iorfa, Steven Kotar, Maes, Marlies, Ku, S., Benitez, Y. R., Brou, M., Gönül, B., Makila, M. L., Monteoliva, J., Riberiro, A. C. L., and van Aken, Marcel
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- 2022
3. VUV photo-ionization parameters and effective mean free path of epithermal photoelectrons in pure non-polar dielectric liquids
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Guelfucci, J.P., Brou, M., Huertas, M.L., and Casanovas, J.
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Photoionization -- Analysis ,Dielectrics -- Optical properties ,Electron mobility -- Analysis ,Business ,Electronics ,Electronics and electrical industries - Abstract
VUV photo-ionization spectra of cyclohexane, 2,2 dimethylbutane, tetramethylsilane and polydimethylsiloxane oils were experimentally obtained, using a new experimental set-up. Power laws for photocurrent were observed and photoionization thresholds, confirming our previous data, were deduced. Using a 3-parameter adjustment method and Onsager theory, parameters specific of photoionization process were extracted from curves giving the photocurrent as a function of an applied electric field, at photon excess energies between 0.5 eV and 2 eV above the corresponding ionization thresholds. Assuming the range distribution function of thermalized photoelectrons to be a modified exponential function, called PE3, an effective mean free path along the thermalization path in each liquid was deduced from [B.sub.3], the experimental range parameter associated with the range distribution function. These mean free path values, at epithermal stage, were compared to those of thermal mean free path of conduction electrons.
- Published
- 2002
4. PROCESS FOR IMPLEMENTING POLIOVIRUS ENVIRONMENTAL SURVEILLANCE IN COTE D’IVOIRE FROM DECEMBER 2016 TO DECEMBER 2017
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Adjogoua, E. V., primary, Coulibaly, F., additional, Ouattara, A., additional, Kadjo, H., additional, Guidy, F., additional, Brou, M., additional, Kra, E., additional, Tieoulou, L., additional, and Kouadio, H., additional
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- 2019
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5. V.U.V. Photoionization process in non polar dielectric liquids
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Guelfucci, J. P., primary, Brou, M., additional, and Huertas, M. L., additional
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- 1999
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6. Rab11a–Rab8a cascade regulates the formation of tunneling nanotubes through vesicle recycling
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Chiara Zurzolo, Sylvie Syan, Mitsunori Fukuda, Yoshihiko Kuchitsu, Seng Zhu, Shaarvari Bhat, Trafic membranaire et Pathogénèse, Institut Pasteur [Paris] (IP), Tohoku University [Sendai], This work was supported by the Agence Nationale de la Recherche (ANR 16 CE 16 0019 01 NEUROTUNN) and the EU Joint Programme on Neurodegenerative Diseases (JPND-NeuTARGETs-ANR-14-JPCD-0002-02) and by Equipe FRM (Fondation pour la Recherche Médicale) 2014 (DEQ 20140329557) to C.Z. S.Z. is supported by Ph.D. fellowships from the China Scholarship Council (201306170046) and by an Institute Carnot fellowship. S.B. is supported by JPND-NeuTARGETs-ANR-14-JPCD-0002-02 and INSERM (HTE201602)., The authors thank A. Echard (Institut Pasteur) and all C.Z. laboratory members for discussion and J. Y. Vargas, C. Brou, M. Henderson and D. Cordero-Cervantes for critical reading of the manuscript. We gratefully acknowledge the Imagopole–Citech of Institut Pasteur (Paris). We are also grateful for the financial support of Institut Pasteur (Paris, ANR-16-CE16-0019,Neurotunn,Role des nanotubes membranaires dans la propagation d'agrégats protéiques impliqués dans les maladie neurodégénératives(2016), ANR-14-JPCD-0002,Neutargets,Targeting the propagation of pathogenic protein assemblies in neurodegenerative disease(2014), Institut Pasteur [Paris], Zhu, S., Bhat, S., Syan, S., Kuchitsu, Y., Fukuda, M., and Zurzolo, C.
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0301 basic medicine ,Vesicle-Associated Membrane Protein 3 ,Vesicle transfer ,GTPase ,Vesicle recycling ,Protein aggregation ,Biology ,Models, Biological ,Cell Line ,03 medical and health sciences ,Mice ,Animals ,Guanine Nucleotide Exchange Factors ,Pseudopodia ,Transport Vesicles ,[SDV.MP.MYC]Life Sciences [q-bio]/Microbiology and Parasitology/Mycology ,VAMP3 ,Nanotubes ,Animal ,Vesicle ,Cell Biology ,Guanine Nucleotide Exchange Factor ,musculoskeletal system ,Endocytosis ,Nanotube ,Vesicular transport protein ,rab GTP-Binding Protein ,030104 developmental biology ,rab GTP-Binding Proteins ,Transport Vesicle ,Biophysics ,Rab ,Guanosine Triphosphate ,Filopodia ,RAB11A ,Rab GTPase ,Tunneling nanotube - Abstract
International audience; Tunneling nanotubes (TNTs) are actin-enriched membranous channels enabling cells to communicate over long distances. TNT-like structures form between various cell types and mediate the exchange of different cargos, such as ions, vesicles, organelles and pathogens; thus, they may play a role in physiological conditions and diseases (e.g. cancer and infection). TNTs also allow the intercellular passage of protein aggregates related to neurodegenerative diseases, thus propagating protein misfolding. Understanding the mechanism of TNT formation is mandatory in order to reveal the mechanism of disease propagation and to uncover their physiological function. Vesicular transport controlled by the small GTPases Rab11a and Rab8a can promote the formation of different plasma membrane protrusions (filopodia, cilia and neurites). Here, we report that inhibiting membrane recycling reduces the number of TNT-connected cells and that overexpression of Rab11a and Rab8a increases the number of TNT-connected cells and the propagation of vesicles between cells in co-culture. We demonstrate that these two Rab GTPases act in a cascade in which Rab11a activation of Rab8a is independent of Rabin8. We also show that VAMP3 acts downstream of Rab8a to regulate TNT formation.
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- 2018
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7. Multivariable modeling: A retrospective cohort study exploring the impact of socioeconomic status and distance to a rural academic center on all-cause preterm delivery.
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Darivemula S, Kouassi-Brou M, Pollack C, Paris A, Goodman D, and Fisher T
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- Humans, Female, Retrospective Studies, Pregnancy, Adult, Infant, Newborn, Infant, Low Birth Weight, Rural Population statistics & numerical data, Young Adult, Academic Medical Centers statistics & numerical data, Logistic Models, Premature Birth epidemiology, Social Class
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Objective: Hospital-based labor and delivery units are closing at increasing rates in the rural US, significantly impacting maternal and newborn health. The objective of this study to determine if rurality-measured as distance from the hospital-and socioeconomic status-measured as insurance payor-impact both spontaneous and medically indicated preterm birth incidence at a single rural academic institution., Methods: This was a retrospective cohort study using electronic medical records of patients with singleton pregnancies delivering at a single rural academic institution between 2016-2018. The primary outcome was preterm delivery (PTD) and secondary outcomes included low birth weight (LBW) and intensive care nursery (ICN) admission. The primary exposures included (1) travel time from a patient's address to the hospital and (2) insurance carrier as a proxy for socioeconomic status. Bivariate analyses indicated that travel time, insurance status, race, ethnicity, marital status, number of prenatal visits, gravida and para, and smoking status were significant predictors of all outcomes (LBW, ICN admission, and PTD). Therefore, these predictors were included in the multivariable logistic models., Results: Within the multivariable logistic model, patients traveling 1-1.5 hours had approximately twice the odds of PTD (Odds Ratio, OR: 2.08, 95% Confidence Interval CI, 1.32, 3.29, p = .002), birth of a LBW neonate (OR: 2.15; 95% CI: 1.29-3.58, p = .005), and infant admission to the ICN (OR 1.83, 95% CI: 1.22-2.76, p = .004) compared to patients traveling under 30 minutes,. Insurance carrier status was not associated with increased odds of PTD, LBW, or ICN admission., Conclusion: Patients living 1-to-1.5 hours from the hospital had an increased risk for LBW, ICN admission, and PTD, despite living in zip codes with less social deprivation than zip codes further away from the hospital., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2024 Darivemula et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
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- 2024
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8. Piperacetazine Directly Binds to the PAX3::FOXO1 Fusion Protein and Inhibits Its Transcriptional Activity.
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Nakazawa K, Shaw T, Song YK, Kouassi-Brou M, Molotkova A, Tiwari PB, Chou HC, Wen X, Wei JS, Deniz E, Toretsky JA, Keller C, Barr FG, Khan J, and Üren A
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- Humans, Forkhead Box Protein O1 genetics, Paired Box Transcription Factors genetics, PAX3 Transcription Factor metabolism, Translocation, Genetic, Rhabdomyosarcoma genetics, Rhabdomyosarcoma, Alveolar genetics
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The tumor-specific chromosomal translocation product, PAX3::FOXO1, is an aberrant fusion protein that plays a key role for oncogenesis in the alveolar subtype of rhabdomyosarcoma (RMS). PAX3::FOXO1 represents a validated molecular target for alveolar RMS and successful inhibition of its oncogenic activity is likely to have significant clinical applications. Even though several PAX3::FOXO1 function-based screening studies have been successfully completed, a directly binding small-molecule inhibitor of PAX3::FOXO1 has not been reported. Therefore, we screened small-molecule libraries to identify compounds that were capable of directly binding to PAX3::FOXO1 protein using surface plasmon resonance technology. Compounds that directly bound to PAX3::FOXO1 were further evaluated in secondary transcriptional activation assays. We discovered that piperacetazine can directly bind to PAX3::FOXO1 protein and inhibit fusion protein-derived transcription in multiple alveolar RMS cell lines. Piperacetazine inhibited anchorage-independent growth of fusion-positive alveolar RMS cells but not embryonal RMS cells. On the basis of our findings, piperacetazine is a molecular scaffold upon which derivatives could be developed as specific inhibitors of PAX3::FOXO1. These novel inhibitors could potentially be evaluated in future clinical trials for recurrent or metastatic alveolar RMS as novel targeted therapy options., Significance: RMS is a malignant soft-tissue tumor mainly affecting the pediatric population. A subgroup of RMS with worse prognosis harbors a unique chromosomal translocation creating an oncogenic fusion protein, PAX3::FOXO1. We identified piperacetazine as a direct inhibitor of PAX3::FOXO1, which may provide a scaffold for designing RMS-specific targeted therapy., (© 2023 The Authors; Published by the American Association for Cancer Research.)
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- 2023
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9. SPRD: a surface plasmon resonance database of common factors for better experimental planning.
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Tiwari PB, Bencheqroun C, Lemus M, Shaw T, Kouassi-Brou M, Alaoui A, and Üren A
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- Kinetics, Ligands, Protein Binding, Proteins metabolism, Statistics as Topic, Protein Interaction Mapping methods, Proteins chemistry, Surface Plasmon Resonance methods
- Abstract
Background: Surface plasmon resonance is a label-free biophysical technique that is widely used in investigating biomolecular interactions, including protein-protein, protein-DNA, and protein-small molecule binding. Surface plasmon resonance is a very powerful tool in different stages of small molecule drug development and antibody characterization. Both academic institutions and pharmaceutical industry extensively utilize this method for screening and validation studies involving direct molecular interactions. In most applications of the surface plasmon resonance technology, one of the studied molecules is immobilized on a microchip, while the second molecule is delivered through a microfluidic system over the immobilized molecules. Changes in total mass on the chip surface is recorded in real time as an indicator of the molecular interactions., Main Body: Quality and accuracy of the surface plasmon resonance data depend on experimental variables, including buffer composition, type of sensor chip, coupling chemistry of molecules on the sensor surface, and surface regeneration conditions. These technical details are generally included in materials and methods sections of published manuscripts and are not easily accessible using the common internet browser search engines or PubMed. Herein, we introduce a surface plasmon resonance database, www.sprdatabase.info that contains technical details extracted from 5140 publications with surface plasmon resonance data. We also provide an analysis of experimental conditions preferred by different laboratories. These experimental variables can be searched within the database and help future users of this technology to design better experiments., Conclusion: Amine coupling and CM5 chips were the most common methods used for immobilizing proteins in surface plasmon resonance experiments. However, number of different chips, capture methods and buffer conditions were used by multiple investigators. We predict that the database will significantly help the scientific community using this technology and hope that users will provide feedback to improve and expand the database indefinitely. Publicly available information in the database can save a great amount of time and resources by assisting initial optimization and troubleshooting of surface plasmon resonance experiments.
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- 2021
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