221 results on '"Renard, L"'
Search Results
2. Quand le loup sème le doute, le cochon perd la foi
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Stavris, C., primary, Chiche, L., additional, Charpin, C., additional, Dukan, P., additional, Doncarli, C., additional, Drouet, H., additional, Delord, M., additional, Renard, L., additional, Allemand, J., additional, Caillères, S., additional, Talbi, N., additional, Halfon, P., additional, Retornaz, F., additional, and Servettaz, A., additional
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- 2022
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3. CTV for Lymphatics in Prostate Adenocarcinoma: an Anatomical Description and Clinical Discussion
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Scalliet, P., Renard, L., Lengelé, B., Tombal, B., Grégoire, Vincent, editor, Scalliet, Pierre, editor, and Ang, K. Kian, editor
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- 2004
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4. Radiation therapy for age-related subfoveal neovascular membranes
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Snyders, B., Renard, L., Koninckx, C., Cioffi, M., Coscas, Gabriel, editor, and Piccolino, Felice Cardillo, editor
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- 1998
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5. Vestibular evoked myogenic potentials
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Dorbeau, C., Bourget, K., Renard, L., Calais, C., and Bakhos, D.
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- 2021
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6. Potentiels évoqués vestibulaires myogéniques
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Dorbeau, C., Bourget, K., Renard, L., Calais, C., and Bakhos, D.
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- 2021
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7. Proteomic Analysis of Mouse Hypothalamus under Simulated Microgravity
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Sarkar, Poonam, Sarkar, Shubhashish, Ramesh, Vani, Kim, Helen, Barnes, Stephen, Kulkarni, Anil, Hall, Joseph C., Wilson, Bobby L., Thomas, Renard L., Pellis, Neal R., and Ramesh, Govindarajan T.
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- 2008
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8. Deep photometry of C1.2244-02 in U colour with an electronographic camera
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Wlérick, G., Vanderriest, C., Hammer, F., Lelièvre, G., Horville, D., Renard, L., Arnaud, J., Gouiffes, C., Araki, H., editor, Ehlers, J., editor, Hepp, K., editor, Kippenhahn, R., editor, Ruelle, D., editor, Weidenmüller, H. A., editor, Wess, J., editor, Zittartz, J., editor, Beiglböck, W., editor, Mellier, Yannick, editor, Fort, Bernard, editor, and Soucail, Geneviève, editor
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- 1990
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9. Activation of activator protein-1 in mouse brain regions exposed to simulated microgravity
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Sarkar, Shubhashish, Wise, Kimberly C., Manna, Sunil K., Ramesh, Vani, Yamauchi, Keiko, Thomas, Renard L., Wilson, Bobby L., Kulkarni, Anil D., Pellis, Neil R., and Ramesh, Govindarajan T.
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- 2006
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10. Manual del cazador ó arte completo de toda clase de caza / L. Renard ; traducción de R. Villalta, aficionado con 30 años de ejercicio en casa mayor y menor
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Villalta, R., Renard, L., Villalta, R., and Renard, L.
- Abstract
Tratado primero : armas, municiones, tiro, perros, caballos -- Primera parte : caza menor -- Tratado primero : caza de pelo -- Tratado segundo : caza de pluma -- Tratado tercero : pájaros de agua -- Segunda parte : caza mayor -- Tratado primero : caza de animales fieros -- Tratado segundo : animales feroces y dañinos -- Apéndices : jurisprudencia vigente sobre la caza, sección de anuncios, 210 p.
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- 2020
11. Radiation dose constraints for organs at risk in neuro-oncology; the European Particle Therapy Network consensus
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Lambrecht, M., Eekers, D.B.P., Alapetite, C., Burnet, N.G., Calugaru, V., Coremans, I.E.M., Fossati, P., Hoyer, M., Langendijk, J.A., Romero, A.M., Paulsen, F., Perpar, A., Renard, L., Ruysscher, D. de, Timmermann, B., Vitek, P., Weber, D.C., Weide, H.L. van der, Whitfield, G.A., Wiggenraad, R., Roelofs, E., Nystrom, P.W., Troost, E.G.C., Taskforce European Particle, and Radiotherapy
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medicine.medical_specialty ,Consensus ,NONPITUITARY BRAIN-TUMORS ,Neuro oncology ,medicine.medical_treatment ,Medizin ,Particle therapy ,Heavy Ion Radiotherapy ,Cochrane Library ,Dose constraints ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,INDUCED OPTIC NEUROPATHY ,EXTERNAL-BEAM IRRADIATION ,NASOPHARYNGEAL CARCINOMA ,European Particle Therapy Network ,Proton Therapy ,Humans ,Medicine ,Radiology, Nuclear Medicine and imaging ,Medical physics ,SENSORINEURAL HEARING-LOSS ,Proton therapy ,TERM-FOLLOW-UP ,Modalities ,DRY-EYE SYNDROME ,Brain Neoplasms ,business.industry ,Radiotherapy Planning, Computer-Assisted ,Radiation dose ,Radiotherapy Dosage ,Hematology ,Clinical trial ,INTENSITY-MODULATED RADIOTHERAPY ,Organs at risk ,MODEL-BASED APPROACH ,Oncology ,030220 oncology & carcinogenesis ,business ,SKULL BASE TUMORS - Abstract
Purpose: For unbiased comparison of different radiation modalities and techniques, consensus on delineation of radiation sensitive organs at risk (OARs) and on their dose constraints is warranted. Following the publication of a digital, online atlas for OAR delineation in neuro-oncology by the same group, we assessed the brain OAR-dose constraints in a follow-up study. Methods: We performed a comprehensive search to identify the current papers on OAR dose constraints for normofractionated photon and particle therapy in PubMed, Ovid Medline, Cochrane Library, Embase and Web of Science. Moreover, the included articles' reference lists were cross-checked for potential studies that met the inclusion criteria. Consensus was reached among 20 radiation oncology experts in the field of neuro-oncology. Results: For the OARs published in the neuro-oncology literature, we summarized the available literature and recommended dose constraints associated with certain levels of normal tissue complication probability (NTCP) according to the recent ICRU recommendations. For those OARs with lacking or insufficient NTCP data, a proposal for effective and efficient data collection is given. Conclusion: The use of the European Particle Therapy Network-consensus OAR dose constraints summarized in this article is recommended for the model-based approach comparing photon and proton beam irradiation as well as for prospective clinical trials including novel radiation techniques and/or modalities. (C) 2018 Elsevier B.V. All rights reserved.
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- 2018
12. Activation of nuclear transcription factor-κB in mouse brain induced by a simulated microgravity environment
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Wise, Kimberly C., Manna, Sunil K., Yamauchi, Keiko, Ramesh, Vani, Wilson, Bobby L., Thomas, Renard L., Sarkar, Shubhashish, Kulkarni, Anil D., Pellis, Neil R., and Ramesh, Govindarajan T.
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- 2005
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13. Concurrent spinal cord and vertebral bone marrow radionecrosis 8 years after therapeutic irradiation
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Warscotte, L., Duprez, T., Lonneux, M., Michaux, L., Renard, L., Sindic, C., and Lecouvet, F.
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- 2002
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14. CTV for Lymphatics in Prostate Adenocarcinoma: an Anatomical Description and Clinical Discussion
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Scalliet, P., primary, Renard, L., additional, Lengelé, B., additional, and Tombal, B., additional
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- 2004
- Full Text
- View/download PDF
15. Electron conducting organic coating of mild steel by electropolymerization
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Troch-Nagels, G., Winand, R., Weymeersch, A., and Renard, L.
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- 1992
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16. Pad Over Active (POA) solutions for three metal level BCD5 mixed power process - Design and validation of ESD protections
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Andreini, A., Neva, C., Renard, L., Sironi, G., Speroni, F., Sponton, L., Tampellini, F., and Tiziani, R.
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- 2003
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17. A phase II randomized, open-label study comparing salvage radiotherapy in combination with 6 months of androgen-deprivation therapy with LHRH agonist or antagonist versus anti-androgen therapy with apalutamide in patients with biochemical progression after radical prostatectomy
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Dirix, P., primary, Strijbos, M., additional, Fransis, K., additional, Liefhooghe, N., additional, Van Bruwaene, S., additional, Uvin, P., additional, Ghysel, C., additional, Ost, D., additional, Engels, B., additional, Van den Begin, R., additional, Otte, F.-X., additional, Roumeguere, T., additional, Palumbo, S., additional, Neybuch, Y., additional, Fonteyne, V., additional, Renard, L., additional, Everaerts, W., additional, Tombal, B., additional, Ost, P., additional, and Dirix, L.Y., additional
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- 2019
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18. Final results of power conditioning of SPIRAL 2 couplers
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Gómez Martínez, Y., Baylac, M., Boge, P., Cabanel, T., De Lamberterie, P., Giraud, J., Vezzu, F., Chatelet, F., Joly, C., Lesrel, J., Longuevergne, D., Martret, R., Olry, G., Renard, L., Bosland, P., Marchand, C., Maurice, L., Piquet, O., Bernaudin, P.-E., and Ferdinand, R.
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- 2017
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19. Exhibition review : following Te Rā in Aotearoa : from Te wai pounamu to Te ika a Maui
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Renard, Lisa
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- 2024
20. The EPTN consensus-based atlas for CT- and MR-based contouring in neuro-oncology
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Eekers, D.B. (Daniëlle BP), in ‘t Ven, L. (Lieke), Roelofs, E. (Erik), Postma, A. (Alida), Alapetite, C. (Claire), Burnet, N.G. (Neil G.), Calugaru, V. (Valentin), Compter, I. (Inge), Coremans, I.E.M. (Ida E.M.), Høyer, M. (Morton), Lambrecht, M. (Maarten), Nyström, P.W. (Petra Witt), Romero, A.M. (Alejandra Méndez), Paulsen, F. (Frank), Perpar, A. (Ana), Ruysscher, D.K.M. (Dirk) de, Renard, L. (Laurette), Timmermann, B. (Beate), Vitek, P. (Pavel), Weber, D.C. (Damien C.), van der Weide, H.L. (Hiske L.), Whitfield, G.A. (Gillian A.), Wiggenraad, R. (Ruud), Troost, E.G.C. (Esther G.C.), Eekers, D.B. (Daniëlle BP), in ‘t Ven, L. (Lieke), Roelofs, E. (Erik), Postma, A. (Alida), Alapetite, C. (Claire), Burnet, N.G. (Neil G.), Calugaru, V. (Valentin), Compter, I. (Inge), Coremans, I.E.M. (Ida E.M.), Høyer, M. (Morton), Lambrecht, M. (Maarten), Nyström, P.W. (Petra Witt), Romero, A.M. (Alejandra Méndez), Paulsen, F. (Frank), Perpar, A. (Ana), Ruysscher, D.K.M. (Dirk) de, Renard, L. (Laurette), Timmermann, B. (Beate), Vitek, P. (Pavel), Weber, D.C. (Damien C.), van der Weide, H.L. (Hiske L.), Whitfield, G.A. (Gillian A.), Wiggenraad, R. (Ruud), and Troost, E.G.C. (Esther G.C.)
- Abstract
Purpose: To create a digital, online atlas for organs at risk (OAR) delineation in neuro-oncology based on high-quality computed tomography (CT) and magnetic resonance (MR) imaging. Methods: CT and 3 Tesla (3T) MR images (slice thickness 1 mm with intravenous contrast agent) were obtained from the same patient and subsequently fused. In addition, a 7T MR without intravenous contrast agent was obtained from a healthy volunteer. Based on discussion between experienced radiation oncologists, the clinically relevant organs at risk (OARs) to be included in the atlas for neuro-oncology were determined, excluding typical head and neck OARs previously published. The draft atlas was delineated by a senior radiation oncologist, 2 residents in radiation oncology, and a senior neuro-radiologist incorporating relevant available literature. The proposed atlas was then critically reviewed and discussed by European radiation oncologists until consensus was reached. Results: The online atlas includes one CT-scan at two different window settings and one MR scan (3T) showing the OARs in axial, coronal and sagittal view. This manuscript presents the three-dimensional descriptions of the fifteen consensus OARs for neuro-oncology. Among these is a new OAR relevant for neuro-cognition, the posterior cerebellum (illustrated on 7T MR images). Conclusion: In order to decrease inter- and intra-observer variability in delineating OARs relevant for neuro-oncology and thus derive consistent dosimetric data, we propose this atlas to be used in photon and particle therapy. The atlas is available online at www.cancerdata.org and will be updated whenever required.
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- 2018
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- View/download PDF
21. The EPTN consensus-based atlas for CT- and MR-based contouring in Neuro-Oncology
- Author
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Eekers, D., In 'T Ven, L., Roelofs, E., Postma, A., Alapetite, C., Burnet, N., Calugaru, V., Compter, I., Coremans, I., Hoyer, M., Lambrecht, M., Romero, A., Paulsen, F., Perpar, A., Ruysscher, D., Renard, L., Vitek, P., Weber, D., Weide, H., Whitfield, G., Wiggenraad, R., Nyström, P., Timmermann, B., Troost, E., Eekers, D., In 'T Ven, L., Roelofs, E., Postma, A., Alapetite, C., Burnet, N., Calugaru, V., Compter, I., Coremans, I., Hoyer, M., Lambrecht, M., Romero, A., Paulsen, F., Perpar, A., Ruysscher, D., Renard, L., Vitek, P., Weber, D., Weide, H., Whitfield, G., Wiggenraad, R., Nyström, P., Timmermann, B., and Troost, E.
- Abstract
Purpose: To create a digital, online atlas for organs at risk (OAR) delineation in neurooncology based on high-quality computed tomography (CT) and magnetic resonance (MR) imaging. Methods: CT and 3 Tesla (3T) MR images (slice thickness 1 mm with intravenous contrast agent) were obtained from the same patient and subsequently fused. In addition, a 7T MR without intravenous contrast agent was obtained from a healthy volunteer. Based on discussions between experienced radiation oncologists, the clinically relevant organs at risk (OARs) to be included in the atlas for neuro-oncology were determined, excluding typical head and neck OARs previously published. The draft atlas was delineated by a senior radiation oncologist, 2 residents in radiation oncology, and a senior neuro-radiologist incorporating relevant available literature. The proposed atlas was then critically reviewed and discussed by European radiation oncologists until consensus was reached. Results: The online atlas includes one CT-scan at two different window settings and one MR scan (3T) showing the OARs in axial, coronal and sagittal view. This manuscript presents the three-dimensional descriptions of the fifteen consensus OARs for neurooncology. Among these is a new OAR relevant for neuro-cognition, the posterior cerebellum (illustrated on 7T MR images). Conclusion: In order to decrease inter- and intra-observer variability in delineating OARs relevant for neuro-oncology and thus derive consistent dosimetric data, we propose this atlas to be used in photon and particle therapy. The atlas is available online at www.cancerdata.org and will be updated whenever required.
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- 2018
22. The EPTN consensus-based atlas for CT- and MR-based contouring in neuro-oncology
- Author
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Eekers, DBP, in 't Ven, L, Roelofs, E, Postma, A, Alapetite, C, Burnet, NG, Calugaru, V, Compter, I, Coremans, IEM, Hoyer, M, Lambrecht, M, Nystrom, PW, Mendez Romero, Alejandra, Paulsen, F, Perpar, A, De Ruysscher, D, Renard, L, Timmermann, B, Vitek, P, Weber, DC, van der Weide, HL, Whitfield, GA, Wiggenraad, R, Troost, EGC, Eekers, DBP, in 't Ven, L, Roelofs, E, Postma, A, Alapetite, C, Burnet, NG, Calugaru, V, Compter, I, Coremans, IEM, Hoyer, M, Lambrecht, M, Nystrom, PW, Mendez Romero, Alejandra, Paulsen, F, Perpar, A, De Ruysscher, D, Renard, L, Timmermann, B, Vitek, P, Weber, DC, van der Weide, HL, Whitfield, GA, Wiggenraad, R, and Troost, EGC
- Published
- 2018
23. OC-0589: Phase-II parallel non-randomized/observation study (EORTC 22042-26042) for non-benign meningiomas
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Weber, D.C., primary, Ares, C., additional, Villa, S., additional, Peerdeman, S.M., additional, Renard, L., additional, Baumert, B.G., additional, Lucas, A., additional, Stelmes, J.J., additional, Collette, S., additional, and Miralbell, R., additional
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- 2018
- Full Text
- View/download PDF
24. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma
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Stupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, Taphoorn MJB, Belanger K, Brandes AA, Marosi C, Bogdahn U, Curschmann J, Janzer RC, Ludwin SK, Gorlia T, Allgeier A, Lacombe D, Cairncross JG, Eisenhauer E, Mirimanoff RO, Van Den Weyngaert D, Kaendler S, Krauseneck P, Vinolas N, Villa S, Wurm RE, Maillot MHB, Spagnolli F, Kantor G, Malhaire JP, Renard L, De Witte O, Scandolaro L, Vecht CJ, Maingon P, Lutterbach J, Kobierska A, Bolla M, Souchon R, Mitine C, Tzuk-Shina T, Kuten A, Haferkamp G, de Greve J, Priou F, Menten J, Rutten I, Clavere P, Malmstrom A, Jancar B, Newlands E, Pigott K, Twijnstra A, Chinot O, Reni M, Boiardi A, Fabbro M, Campone M, Bozzino J, Frenay M, Gijtenbeek J, Delattre JY, De Paula U, Hanzen C, Pavanato G, Schraub S, Pfeffer R, Soffietti R, Kortmann RD, Taphoorn M, Torrecilla JL, Grisold W, Huget P, Forsyth P, Fulton D, Kirby S, Wong R, Fenton D, Cairncross G, Whitlock P, Burdette-Radoux S, Gertler S, Saunders S, Laing K, Siddiqui J, Martin LA, Gulavita S, Perry J, Mason W, Thiessen B, Pai H, Alam ZY, Eisenstat D, Mingrone W, Hofer S, Pesce G, Dietrich PY, Thum P, Baumert B, Ryan G, Stupp, R, Mason, Wp, van den Bent, Mj, Weller, M, Fisher, B, Taphoorn, Mjb, Belanger, K, Brandes, Aa, Marosi, C, Bogdahn, U, Curschmann, J, Janzer, Rc, Ludwin, Sk, Gorlia, T, Allgeier, A, Lacombe, D, Cairncross, Jg, Eisenhauer, E, Mirimanoff, Ro, Van Den Weyngaert, D, Kaendler, S, Krauseneck, P, Vinolas, N, Villa, S, Wurm, Re, Maillot, Mhb, Spagnolli, F, Kantor, G, Malhaire, Jp, Renard, L, De Witte, O, Scandolaro, L, Vecht, Cj, Maingon, P, Lutterbach, J, Kobierska, A, Bolla, M, Souchon, R, Mitine, C, Tzuk-Shina, T, Kuten, A, Haferkamp, G, de Greve, J, Priou, F, Menten, J, Rutten, I, Clavere, P, Malmstrom, A, Jancar, B, Newlands, E, Pigott, K, Twijnstra, A, Chinot, O, Reni, M, Boiardi, A, Fabbro, M, Campone, M, Bozzino, J, Frenay, M, Gijtenbeek, J, Delattre, Jy, De Paula, U, Hanzen, C, Pavanato, G, Schraub, S, Pfeffer, R, Soffietti, R, Kortmann, Rd, Taphoorn, M, Torrecilla, Jl, Grisold, W, Huget, P, Forsyth, P, Fulton, D, Kirby, S, Wong, R, Fenton, D, Cairncross, G, Whitlock, P, Burdette-Radoux, S, Gertler, S, Saunders, S, Laing, K, Siddiqui, J, Martin, La, Gulavita, S, Perry, J, Mason, W, Thiessen, B, Pai, H, Alam, Zy, Eisenstat, D, Mingrone, W, Hofer, S, Pesce, G, Dietrich, Py, Thum, P, Baumert, B, Ryan, G, Neurology, and Plastic and Reconstructive Surgery and Hand Surgery
- Subjects
Adult ,Male ,medicine.medical_specialty ,medicine.medical_treatment ,Adrenal Cortex Hormones ,Adrenal Cortex Hormones/therapeutic use Adult Aged Antineoplastic Agents, Alkylating/adverse effects/*therapeutic use Brain Neoplasms/*drug therapy/mortality/*radiotherapy Chemotherapy, Adjuvant Dacarbazine/adverse effects/*analogs & derivatives/*therapeutic use Disease Progression Female Glioblastoma/*drug therapy/mortality/*radiotherapy Humans Male Middle Aged Proportional Hazards Models Radiotherapy, Computer-Assisted/adverse effects Survival Analysis ,medicine ,Temozolomide ,Humans ,Survival rate ,Pseudoprogression ,Antineoplastic Agents, Alkylating ,Aged ,Proportional Hazards Models ,business.industry ,Brain Neoplasms ,Hazard ratio ,General Medicine ,Middle Aged ,Debulking ,medicine.disease ,Survival Analysis ,Radiotherapy, Computer-Assisted ,Surgery ,Radiation therapy ,Dacarbazine ,Chemotherapy, Adjuvant ,Concomitant ,Disease Progression ,Female ,business ,Glioblastoma ,medicine.drug ,Anaplastic astrocytoma - Abstract
BACKGROUND: Glioblastoma, the most common primary brain tumor in adults, is usually rapidly fatal. The current standard of care for newly diagnosed glioblastoma is surgical resection to the extent feasible, followed by adjuvant radiotherapy. In this trial we compared radiotherapy alone with radiotherapy plus temozolomide, given concomitantly with and after radiotherapy, in terms of efficacy and safety. METHODS: Patients with newly diagnosed, histologically confirmed glioblastoma were randomly assigned to receive radiotherapy alone (fractionated focal irradiation in daily fractions of 2 Gy given 5 days per week for 6 weeks, for a total of 60 Gy) or radiotherapy plus continuous daily temozolomide (75 mg per square meter of body-surface area per day, 7 days per week from the first to the last day of radiotherapy), followed by six cycles of adjuvant temozolomide (150 to 200 mg per square meter for 5 days during each 28-day cycle). The primary end point was overall survival. RESULTS: A total of 573 patients from 85 centers underwent randomization. The median age was 56 years, and 84 percent of patients had undergone debulking surgery. At a median follow-up of 28 months, the median survival was 14.6 months with radiotherapy plus temozolomide and 12.1 months with radiotherapy alone. The unadjusted hazard ratio for death in the radiotherapy-plus-temozolomide group was 0.63 (95 percent confidence interval, 0.52 to 0.75; P
- Published
- 2005
25. Anatase Titanium Dioxide Coated Single Wall Carbon Nanotubes Manufactured by Sonochemical-Hydrothermal Technique
- Author
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Xin Wei, Paul Clemens, Renard L. Thomas, and Bobby L. Wilson
- Subjects
Materials science ,Scanning electron microscope ,Nanoparticle ,Nanotechnology ,Carbon nanotube ,Hydrothermal circulation ,law.invention ,Characterization (materials science) ,Crystal ,symbols.namesake ,law ,symbols ,Raman spectroscopy ,Deposition (law) - Abstract
A novel, cost effective, sonochemical-hydrothermal technique was used for the deposition of nanosized anatase titanium dioxide (TiO2) onto single wall carbon nanotubes (SWCNTs). This technique is described and the characterization of the synthesized TiO2-SWCNTs is reported. The characterization techniques employed include scanning electron microscopy (SEM), Raman spectroscopy, and X-ray diffraction (XRD). From the characterization the size and morphology of the synthesized TiO2 nanoparticles (deposited on the SWCNTs) are reported. Furthermore, it is demonstrated that the created TiO2 nanoparticles are chemically attached to the SWCNTs. Also, an important correlation between calculated TiO2 crystal size and the red shifts in the lowest Raman TiO2 (E.g.) predominate peak is reported. The synthesized TiO2-SWCNTs have potential for large scale production and application in a variety of new technologies such as clean energy power generation devices, electrical storage devices, photocatalysts, and sensors.
- Published
- 2013
26. NOTES BRÈVES
- Author
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Demalsy-Feller, P., Demalsy-Feller, M.-L., Lambinon, J., Sougnez, N., Renard, L., and Lawalrée, A.
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- 1957
27. AUGUSTE VISÉ 1879-1957 NOTE BIOGRAPHIQUE
- Author
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RENARD, L.
- Published
- 1957
28. Uranium induces apoptosis in lung epithelial cells
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Prabakaran Ravichandran, Govindarajan T. Ramesh, Shubhashish Sarkar, Adaikkappan Periyakaruppan, Bobby L. Wilson, Joseph C. Hall, Chidananda S. Sharma, Bindu Sadanandan, Renard L. Thomas, and Vani Ramesh
- Subjects
Programmed cell death ,Time Factors ,Membrane permeability ,Health, Toxicology and Mutagenesis ,Apoptosis ,Caspase 3 ,Biology ,Toxicology ,medicine.disease_cause ,Permeability ,Article ,Cell Line ,Electron Transport Complex IV ,In Situ Nick-End Labeling ,Organometallic Compounds ,medicine ,Animals ,Lung ,Caspase 8 ,TUNEL assay ,Dose-Response Relationship, Drug ,Cytochrome c ,Epithelial Cells ,General Medicine ,Molecular biology ,Rats ,Oxidative Stress ,Cytosol ,Biochemistry ,Mitochondrial Membranes ,biology.protein ,Oxidative stress ,Signal Transduction - Abstract
Uranium is a naturally occurring radioactive material present everywhere in the environment. It is toxic because of its chemical or radioactive properties. Uranium enters environment mainly from mines and industry and cause threat to human health by accumulating in lungs as a result of inhalation. In our previous study, we have shown the effectiveness of antioxidant system response to the oxidative stress induced by uranyl acetate (UA) in rat lung epithelial (LE) cells. As part of our continuing studies; here, we investigated the mechanism underlying when LE cells are exposed to different concentration of UA. Oxidative stress may lead to apoptotic signaling pathways. LE cells treated with 0.25, 0.5 and 1 mM of UA results in dose and time-dependent increase in activity of both caspases-3 and -8. Increase in the concentration of cytochrome-c oxidase in cytosol was seen in LE cells treated with 1 mM UA as a result of mitochondria membrane permeability. The cyto-chrome-c leakage may trigger the apoptotic pathway. TUNEL assay performed in LE cells treated with 1 mM of UA showed significant incorporation of dNTPs in the nucleus after 24 h. In the presence of the caspase inhibitors, we observed the significant decrease in the activity of caspases-8 and -3 in 0.5 and 1 mM UA-treated LE cells.
- Published
- 2008
29. Proteomic Analysis of Mouse Hypothalamus under Simulated Microgravity
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Shubhashish Sarkar, Joseph C. Hall, Renard L. Thomas, Helen Kim, Bobby L. Wilson, Poonam Sarkar, Neal R. Pellis, Vani Ramesh, Anil D. Kulkarni, Stephen Barnes, and Govindarajan T. Ramesh
- Subjects
Proteomics ,Pituitary gland ,medicine.medical_specialty ,Hypothalamus ,Oxidative phosphorylation ,Biochemistry ,Article ,Superoxide dismutase ,Mice ,Cellular and Molecular Neuroscience ,chemistry.chemical_compound ,Malate Dehydrogenase ,Internal medicine ,medicine ,Animals ,Electrophoresis, Gel, Two-Dimensional ,biology ,Superoxide Dismutase ,Weightlessness ,General Medicine ,Glutathione ,medicine.anatomical_structure ,Endocrinology ,chemistry ,Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ,Proteome ,biology.protein ,Peroxiredoxin VI ,Hormone - Abstract
Exposure to altered microgravity during space travel induces changes in the brain and these are reflected in many of the physical behavior seen in the astronauts. The vulnerability of the brain to microgravity stress has been reviewed and reported. Identifying microgravity-induced changes in the brain proteome may aid in understanding the impact of the microgravity environment on brain function. In our previous study we have reported changes in specific proteins under simulated microgravity in the hippocampus using proteomics approach. In the present study the profiling of the hypothalamus region in the brain was studied as a step towards exploring the effect of microgravity in this region of the brain. Hypothalamus is the critical region in the brain that strictly controls the pituitary gland that in turn is responsible for the secretion of important hormones. Here we report a 2-dimensional gel electrophoretic analysis of the mouse hypothalamus in response to simulated microgravity. Lowered glutathione and differences in abundance expression of seven proteins were detected in the hypothalamus of mice exposed to microgravity. These changes included decreased superoxide dismutase-2 (SOD-2) and increased malate dehydrogenase and peroxiredoxin-6, reflecting reduction of the antioxidant system in the hypothalamus. Taken together the results reported here indicate that oxidative imbalance occurred in the hypothalamus in response to simulated microgravity.
- Published
- 2008
30. Simulated microgravity activates apoptosis and NF-κB in mice testis
- Author
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Adaikkappan Periyakaruppan, Chidananda S. Sharma, Vani Ramesh, Bobby L. Wilson, Shubhashish Sarkar, Renard L. Thomas, Joseph C. Hall, Bindu Sadanandan, Govindarajan T. Ramesh, and Prabakaran Ravichandran
- Subjects
Male ,medicine.medical_specialty ,Clinical Biochemistry ,Apoptosis ,Caspase 3 ,Caspase 8 ,Article ,Mice ,chemistry.chemical_compound ,Internal medicine ,Testis ,medicine ,Animals ,Testosterone ,Molecular Biology ,Transcription factor ,Caspase ,Mice, Inbred BALB C ,biology ,Weightlessness ,Body Weight ,NF-kappa B ,NF-κB ,Organ Size ,Cell Biology ,General Medicine ,NFKB1 ,Cell biology ,Endocrinology ,chemistry ,biology.protein - Abstract
Microgravity is known to have significant effect on all aspects of reproductive function in animal models. Recent studies have also shown that microgravity induces changes at the cellular level, including apoptosis. Our effort here was to study the effect of simulated microgravity on caspase-8 and the caspase-3 activities, the effectors of the apoptotic pathway and on the transcription factor NF-kappaB a signaling molecule in mouse testis. Morey-Holton hind limb suspension model was used to simulate microgravity. Caspase-8 and 3 fluorometric assays were carried out and HLS mice testis exhibited a 51% increase in caspase-8 and caspase-3 compared to the controls. A sandwich ELISA-based immunoassay was carried out for detection of NF-kappaB which again significantly increased in the test mice. Testosterone levels were measured using an ELISA kit and in HLS mice the decrease was significant. There was also a significant decrease in testis weight in the test mice. Simulated microgravity activates caspase 8, 3 and NF-kappaB necessary to stimulate the apoptotic pathway in mice testis. This may account for the drop in testis weight and testosterone level further affecting testicular physiology and function.
- Published
- 2008
31. OC-0546: Video Launching during Irradiation – an alternative to anesthesia in pediatric patients?
- Author
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Palhetinha Aguas, C., primary, Humblet, P., additional, Renard, L., additional, Vaandering, A., additional, Roosen, V., additional, and Coevoet, M., additional
- Published
- 2017
- Full Text
- View/download PDF
32. Single-Walled Carbon Nanotubes Induces Oxidative Stress in Rat Lung Epithelial Cells
- Author
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Renard L. Thomas, Govindarajan T. Ramesh, Johnny Barr, Chidananda S. Sharma, Shubhashish Sarkar, Adaikkappan Periyakaruppan, Bobby L. Wilson, and Kimberly Wise
- Subjects
Materials science ,Biomedical Engineering ,Bioengineering ,Respiratory Mucosa ,Mitochondrion ,medicine.disease_cause ,Article ,Cell Line ,Superoxide dismutase ,chemistry.chemical_compound ,In vivo ,medicine ,Animals ,General Materials Science ,Lung ,chemistry.chemical_classification ,Reactive oxygen species ,biology ,Nanotubes, Carbon ,Epithelial Cells ,General Chemistry ,Glutathione ,Condensed Matter Physics ,In vitro ,Rats ,Oxidative Stress ,Biochemistry ,chemistry ,Cell culture ,Biophysics ,biology.protein ,Reactive Oxygen Species ,Oxidative stress - Abstract
Single-walled carbon nanotubes (SWCNT) show unique properties find applications in micro devices; electronics to biological systems specially drug delivery and gene therapy. However the manufacture and extensive use of nanotubes raises concern about its safe use and human health. Very few studies have been carried out on toxicity of carbon nanotubes in experimental animals and humans, thus resulted in limiting their use. The extensive toxicological studies using in vitro and in vivo models are necessary and are required to establish safe manufacturing guidelines and also the use of SWCNT. These studies also help the chemists to prepare derivative of SWCNT with less or no toxicity. The present study was undertaken to determine the toxicity exhibited by SWCNT in rat lung epithelial cells as a model system. Lung epithelial cells (LE cells) were cultured with or without SWCNT and reactive oxygen species (ROS) produced were measured by change in fluorescence using dichloro fluorescein (DCF). The results show increased ROS on exposure to SWCNT in a dose and time dependent manner. The decrease in glutathione content suggested the depletion and loss of protective mechanism against ROS in SWCNT treated cells. Use of rotenone, the inhibitor of mitochondrial function have no effect on ROS levels suggested that mitochondria is not involved in SWCNT induced ROS production. Studies carried out on the effect of SWCNT on superoxide dismutase (SOD-1 and SOD-2) levels in LE cells, indicates that these enzyme levels decreased by 24 hours. The increased ROS induced by SWCNT on LE cells decreased by treating the cells with 1 mM of glutathione, N-Acetyl Cysteine, and Vitamin C. These results further prove that SWCNT induces oxidative stress in LE cells and shows loss of antioxidants.
- Published
- 2007
33. Analysis of Stress Responsive Genes Induced by Single-Walled Carbon Nanotubes in BJ Foreskin Cells
- Author
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Renard L. Thomas, Enrique V. Barrera, Allison C. Rice-Ficht, Olufisayo Jejelowo, Shubhashish Sarkar, Govindarajan T. Ramesh, Chidananda S. Sharma, Rajeshwari Yog, Bobby L. Wilson, and Adaikkappan Periakaruppan
- Subjects
Keratinocytes ,Male ,HMOX1 ,Materials science ,Foreskin ,Biomedical Engineering ,Gene Expression ,Bioengineering ,Nanotechnology ,Carbon nanotube ,medicine.disease_cause ,Article ,Cell Line ,law.invention ,Nanomaterials ,law ,medicine ,Humans ,General Materials Science ,chemistry.chemical_classification ,Reactive oxygen species ,Nanotubes, Carbon ,Reverse Transcriptase Polymerase Chain Reaction ,Dimethylformamide ,General Chemistry ,Condensed Matter Physics ,Cell biology ,Kinetics ,Oxidative Stress ,medicine.anatomical_structure ,chemistry ,Cell culture ,Solvents ,Signal transduction ,Reactive Oxygen Species ,Oxidative stress - Abstract
Nanotechnology is finding its use as a potential technology in consumer products, defense, electronics, and medical applications by exploiting the properties of nanomaterials. Single-walled carbon nanotubes are novel forms of these nanomaterials with potential for large applications. However, the toxicity studies on this material are not explored in detail and therefore limiting its use. It has been earlier reported that single-walled carbon nanotubes induces oxidative stress and also dictates activation of specific signaling pathway in keratinocytes. The present study explores the effect of single-walled carbon nanotubes on stress genes in human BJ Foreskin cells. The results show induction of oxidative stress in BJ Foreskin cells by single-walled carbon nanotubes and increase in stress responsive genes. The genes included inducible genes like HMOX1, HMOX2, and Cyp1B1. In addition we validated increase for four genes by SWCNT, namely ATM, CCNC, DNAJB4, and GADD45A by RT-PCR. Moreover results of the altered stress related genes have been discussed and that partially explains some of the toxic responses induced by single-walled carbon nanotubes.
- Published
- 2007
34. Proteomic Analysis of Mice Hippocampus in Simulated Microgravity Environment
- Author
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Bobby L. Wilson, Shubhashish Sarkar, Barbara E. Hayes, Neal R. Pellis, Helen Kim, Stephen Barnes, Renard L. Thomas, Poonam Sarkar, Vani Ramesh, Govindarajan T. Ramesh, and Anil D. Kulkarni
- Subjects
Male ,Proteomics ,Proteome ,Immunoblotting ,Hippocampus ,Pyruvate Dehydrogenase Complex ,Fluid shift ,Biochemistry ,Article ,Mice ,beta-Synuclein ,Animals ,Weightlessness Simulation ,Mice, Inbred BALB C ,biology ,General Chemistry ,Metabolism ,Molecular biology ,Cell biology ,Tubulin ,Simulated microgravity ,Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ,biology.protein ,sense organs ,Beta-synuclein - Abstract
Space travel induces many deleterious effects on the flight crew due to the ‘0’ g environment. The brain experiences a tremendous fluid shift, which is responsible for many of the detrimental changes in physical behavior seen in astronauts. It therefore indicates that the brain may undergo major changes in its protein levels in a ‘0’ g environment to counteract the stress. Analysis of these global changes in proteins may explain to better understand the functioning of brain in a ‘0’ g condition. Toward such an effort, we have screened proteins in the hippocampus of mice kept in simulated microgravity environment for 7 days and have observed a few changes in major proteins as compared to control mice. Essentially, the results show a major loss of proteins in the hippocampus of mice subjected to simulated microgravity. These changes occur in structural proteins such as tubulin, coupled with the loss of proteins involved in metabolism. This preliminary investigation leads to an understanding of the alteration of proteins in the hippocampus in response to the microgravity environment.
- Published
- 2006
35. Effects of carbon nanotube fillers on the curing processes of epoxy resin-based composites
- Author
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Shuying Yang, Xin Wei, Yuanjian Deng, Renard L. Thomas, Yeon Seok Kim, Kun Tao, Bobby L. Wilson, Bachlien Dang, and Jaime C. Grunlan
- Subjects
Nanocomposite ,Materials science ,Polymers and Plastics ,Scanning electron microscope ,Thermosetting polymer ,General Chemistry ,Epoxy ,Carbon nanotube ,Surfaces, Coatings and Films ,law.invention ,Differential scanning calorimetry ,law ,visual_art ,Materials Chemistry ,visual_art.visual_art_medium ,Composite material ,Glass transition ,Curing (chemistry) - Abstract
The effects of different grades of carbon nanotubes on the curing of a typical epoxy resin (EPIKOTE™ resin 862 and EPIKURE™ curing agent W) were examined via differential scanning calorimetry. It was found that nanotubes could initiate cure at lower temperatures, while the overall curing process was slowed as evidenced by lower total heat of reaction and lower glass transition temperatures of the cured nanocomposites compared to neat epoxy. This finding is practically important as it is essential to have a consistent degree of cure when the properties of thermosets with nanoinclusions are compared to neat resins. It was also found that the inclusion of carbon nanotubes might induce the thermal degradation of epoxy composites at lower temperatures. Morphological analysis done with scanning electron microscopy revealed good dispersion of nanotubes within the epoxy matrix. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:5248–5254, 2006
- Published
- 2006
36. Short Androgen Suppression and Radiation Dose Escalation for Intermediate- and High-Risk Localized Prostate Cancer: Results of EORTC Trial 22991
- Author
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Bolla, M., Maingon, P., Carrie, C., Villa, S., Kitsios, P., Poortmans, P.M.P., Sundar, S., Steen-Banasik, E.M. van der, Armstrong, J., Bosset, J.F., Herrera, F.G., Pieters, B., Slot, A., Bahl, A., Ben-Yosef, R., Boehmer, D., Scrase, C., Renard, L., Shash, E., Coens, C., Bergh, A.C. van den, Collette, L., Bolla, M., Maingon, P., Carrie, C., Villa, S., Kitsios, P., Poortmans, P.M.P., Sundar, S., Steen-Banasik, E.M. van der, Armstrong, J., Bosset, J.F., Herrera, F.G., Pieters, B., Slot, A., Bahl, A., Ben-Yosef, R., Boehmer, D., Scrase, C., Renard, L., Shash, E., Coens, C., Bergh, A.C. van den, and Collette, L.
- Abstract
Item does not contain fulltext, PURPOSE: Up to 30% of patients who undergo radiation for intermediate- or high-risk localized prostate cancer relapse biochemically within 5 years. We assessed if biochemical disease-free survival (DFS) is improved by adding 6 months of androgen suppression (AS; two injections of every-3-months depot of luteinizing hormone-releasing hormone agonist) to primary radiotherapy (RT) for intermediate- or high-risk localized prostate cancer. PATIENTS AND METHODS: A total of 819 patients staged: (1) cT1b-c, with prostate-specific antigen (PSA) >/= 10 ng/mL or Gleason >/= 7, or (2) cT2a (International Union Against Cancer TNM 1997), with no involvement of pelvic lymph nodes and no clinical evidence of metastatic spread, with PSA = 50 ng/mL, were centrally randomized 1:1 to either RT or RT plus AS started on day 1 of RT. Centers opted for one dose (70, 74, or 78 Gy). Biochemical DFS, the primary end point, was defined from entry until PSA relapse (Phoenix criteria) and clinical relapse by imaging or death of any cause. The trial had 80% power to detect hazard ratio (HR), 0.714 by intent-to-treat analysis stratified by dose of RT at the two-sided alpha = 5%. RESULTS: The median patient age was 70 years. Among patients, 74.8% were intermediate risk and 24.8% were high risk. In the RT arm, 407 of 409 patients received RT; in the RT plus AS arm, 403 patients received RT plus AS and three patients received RT only. At 7.2 years median follow-up, RT plus AS significantly improved biochemical DFS (HR, 0.52; 95% CI, 0.41 to 0.66; P < .001, with 319 events), as well as clinical progression-free survival (205 events, HR, 0.63; 95% CI, 0.48 to 0.84; P = .001). In exploratory analysis, no statistically significant interaction between treatment effect and dose of RT could be evidenced (heterogeneity P = .79 and P = .66, for biochemical DFS and progression-free survival, respectively). Overall survival data are not mature yet. CONCLUSION: Six months of concomitant and adjuvant AS improve
- Published
- 2016
37. 900TiP - A phase II randomized, open-label study comparing salvage radiotherapy in combination with 6 months of androgen-deprivation therapy with LHRH agonist or antagonist versus anti-androgen therapy with apalutamide in patients with biochemical progression after radical prostatectomy
- Author
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Dirix, P., Strijbos, M., Fransis, K., Liefhooghe, N., Van Bruwaene, S., Uvin, P., Ghysel, C., Ost, D., Engels, B., Van den Begin, R., Otte, F.-X., Roumeguere, T., Palumbo, S., Neybuch, Y., Fonteyne, V., Renard, L., Everaerts, W., Tombal, B., Ost, P., and Dirix, L.Y.
- Published
- 2019
- Full Text
- View/download PDF
38. A novel mutation in the SDHD gene in a family with inherited paragangliomas
- Author
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Renard, L., Godfraind, C., Boon, L.M., and Vikkula, M.
- Subjects
Human genetics -- Research ,Genetic disorders -- Research ,Carotid body -- Abnormalities ,Tumors -- Genetic aspects ,Biological sciences - Published
- 2001
39. Analysis of persistent organic compounds and metals in urine samples of young adults (844.5)
- Author
-
Chioma Ihemadu, Renard L. Thomas, Momoh A. Yakubu, and Naga Naidu
- Subjects
business.industry ,Genetics ,Medicine ,Physiology ,Urine ,Young adult ,business ,Molecular Biology ,Biochemistry ,Biotechnology - Published
- 2014
40. Spiral2 cryomodules B tests results
- Author
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Olry, G., Chatelet, F., Commeaux, C., Gandolfo, N., Grolet, D., Joly, C., Lesrel, J., Longuevergne, D., Martret, R., Michel, G., Renard, L., Stephen, A., Szott, P., Bernaudin, P.E., Beunard, R., Ferdinand, R., Lefèvre, A., Gomez-Martinez, Y., Institut de Physique Nucléaire d'Orsay (IPNO), Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Paris-Sud - Paris 11 (UP11), Grand Accélérateur National d'Ions Lourds (GANIL), Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Laboratoire de Physique Subatomique et de Cosmologie (LPSC), Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Institut Polytechnique de Grenoble - Grenoble Institute of Technology-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Joseph Fourier - Grenoble 1 (UJF)-Centre National de la Recherche Scientifique (CNRS), SPIRAL2, Université Paris-Sud - Paris 11 (UP11)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Institut Polytechnique de Grenoble - Grenoble Institute of Technology-Centre National de la Recherche Scientifique (CNRS), and Vernay, Emmanuelle
- Subjects
[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph] ,[PHYS.PHYS.PHYS-ACC-PH] Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph] - Abstract
MOP010; International audience; Assembly and tests of the SPIRAL2 superconducting linac's cryomodules at CEA/Saclay and IPN/Orsay have now reached cruising speed after having faced a series of problems, among them contamination. 19 cryomodules are composing the whole Linac and IPN Orsay is in charge of the 7 cryomodules B, housing two 88 MHz, beta 0.12 Quarter-Wave Resonators. Threecryomodules have been assembled and successfullytested up to the nominal gradient of 6.5 MV/m for all cavities with also cryogenic losses withinspecifications. Two of them are fully qualified and already delivered to GANIL. The thirdone showed misalignment ofone cavity which could lead to partial disassembly if needed. This paper presents the results of those cryomodules tests as well as the status of the remaining ones.
- Published
- 2013
41. [Fever with skin rash and polyarthralgia in a genetically black-skinned woman]
- Author
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Maza A, Renard L, Monestier S, Jean-Jacques Grob, and Ma, Richard
- Subjects
Adult ,Fever ,Humans ,Female ,Exanthema ,Arthralgia ,Still's Disease, Adult-Onset - Abstract
Adult onset Still's disease (AOSD) is a systemic disorder characterized by intermittent fever, evanescent rash, polyarthralgia or arthritis, and neutrophilic leucocytoclasis. Appearance of skin rash during fever episodes is the characteristic feature. An atypical form of AOSD with a fixed pigmented skin rash was described in 1994. Prognosis of the atypical form is thought to be more severe than that of the classic form. The purpose of this report is to describe the first case of atypical AOSD in a genetically black-skinned woman. Treatment required administration of high-dose systemic corticosteroids.
- Published
- 2008
42. A method for quantifying vertical displacements of the back and gait symmetry in horses trotting at high speed
- Author
-
Chateau, Henry, Renard, L, Falala, Sylvain, Valette, JP, Audigié, Fabrice, Pourcelot, Philippe, Ravary, Bérangère, Paquet, L, Denoix, Jean-Marie, Crevier-Denoix, Nathalie, ProdInra, Migration, Biomécanique et Pathologie Locomotrice du Cheval (BPLC), École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA), and Inconnu
- Subjects
[SDV] Life Sciences [q-bio] ,[SDV]Life Sciences [q-bio] - Published
- 2007
43. Installation d'une Camera Electronique Grand Champ au Telescope Canada-France-Hawaii
- Author
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Servan, B., primary, Wlérick, G., additional, Renard, L., additional, Lelièvre, G., additional, Cayatte, V., additional, Horville, D., additional, and Fromage, J., additional
- Published
- 1986
- Full Text
- View/download PDF
44. Utilisation Astronomique de la Caméra Electronique Grand Champ,–II
- Author
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Wlerick, G., primary, Lelievre, G., additional, Renard, L., additional, Servan, B., additional, Horville, D., additional, Fromage, J., additional, Le Flohic, J.M., additional, Bauduin, D., additional, Bijaoui, A., additional, and Courtes, G., additional
- Published
- 1988
- Full Text
- View/download PDF
45. Environnement Du Noyau De 3C 120
- Author
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Wlérick, G., primary, Soubeyran, A., additional, Servan, B., additional, Renard, L., additional, Horville, D., additional, Bijaoui, A., additional, Lelièvre, G., additional, and Bouchet, P., additional
- Published
- 1986
- Full Text
- View/download PDF
46. 3C 120. Properties of 4 Condensations Neighbouring the Nucleus and Emitting in the Continuum
- Author
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Soubeyran, A., primary, Wlérick, G., additional, Lelièvre, G., additional, Servan, B., additional, Renard, L., additional, Horville, D., additional, Bijaoui, A., additional, and Bouchet, P., additional
- Published
- 1989
- Full Text
- View/download PDF
47. Activation of activator protein-1 in mouse brain regions exposed to simulated microgravity
- Author
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Shubhashish Sarkar, Kimberly Wise, N. R. Pellis, Renard L. Thomas, Bobby L. Wilson, Vani Ramesh, Keiko Yamauchi, Anil D. Kulkarni, Sunil K. Manna, and Govindarajan T. Ramesh
- Subjects
Male ,Biology ,Article ,Enzyme activator ,Mice ,Animals ,Mitogen-Activated Protein Kinase 8 ,Kinase activity ,Transcription factor ,Weightlessness Simulation ,Regulation of gene expression ,Mice, Inbred BALB C ,Activator (genetics) ,JNK Mitogen-Activated Protein Kinases ,Brain ,Cell Biology ,General Medicine ,Cell biology ,Enzyme Activation ,Transcription Factor AP-1 ,Gene Expression Regulation ,Cell culture ,Immunology ,Stem cell ,Developmental biology ,Proto-Oncogene Proteins c-fos ,Developmental Biology - Abstract
Microgravity induces stress, and the brain is one of the targets that is more influenced in this environment. Alteration in transcription factors can have enormous effect because of discrepancy in the signaling process of the cells. Activator protein-1 (AP-1) is a stress-regulated transcription factor and is involved in the regulation of physiological and pathological stimuli that include cytokines, growth factors, and stress signals. In the present study, an attempt has been made to observe the effect of a microgravity environment on the activation of AP-1 in the mouse brain. Our results show that AP-1 transcription factor is activated in simulated microgravity conditions in different regions of the brain. The activation of the AP-1 is dependent upon the increased kinase activity of c-Jun NH-terminal2 kinase-1. These results suggest that microgravity stress in the brain can elicit AP-1 activity.
- Published
- 2006
48. Measurement of volatile organic compounds in the urban atmosphere of Harris County, Texas, USA
- Author
-
Bobby L. Wilson, Renard L. Thomas, and Felicia L. Conley
- Subjects
Environmental Engineering ,Air pollution ,Industrial Waste ,medicine.disease_cause ,Troposphere ,Atmosphere ,chemistry.chemical_compound ,Environmental monitoring ,medicine ,Volatile organic compound ,Organic Chemicals ,Vehicle Emissions ,chemistry.chemical_classification ,Air Pollutants ,Waste management ,Air ,Urbanization ,Butane ,General Medicine ,Texas ,Hydrocarbon ,Petrochemical ,chemistry ,Environmental science ,Volatilization ,Environmental Monitoring - Abstract
Volatile organic compounds (VOCs) are a major component of urban air pollution. It is well documented that exposure to certain types of VOCs can cause adverse health effects such as cancer, immune and neurological damage, and reproductive and endocrine disorders. Urban air samples were collected at five locations in Harris County, Texas to determine the measurement of VOCs in the ambient air of residential areas in close proximity to industrial facilities that emit toxic air pollutants into the air. Three locations used in this study were located along the Houston Ship Channel (HSC), in the heart of one of the largest petrochemical complexes in the nation. Two other sampling locations were located many miles away from the ship channel and any industrial facilities that are required to report toxic air emissions. Air samples were collected daily over an 8-h period from December 2002 to March 2003. The samples were collected in 6-L stainless steel Silonite-coated canisters and analyzed using a modified version of EPA Method TO-15. A total of 53 compounds was quantitated using a gas chromatograph mass spectrometer system coupled to a cryogenic preconcentrator. Eighteen alkanes and oxygenated compounds were identified, along with 7 alkenes and 5 aromatic compounds. Several alkanes such as butane, isobutane, 2-methyl butane, and pentane were detected at all five sites. The total VOC concentrations determined were highest at two of the industrial sites and lowest at the site farthest away from the ship channel and any industrial facilities. This study concluded that the atmosphere near Harris County's industrial complex had higher concentrations of VOCs than the atmosphere in areas farther away from the HSC. The atmosphere of areas downwind from emission sources were found to be directly affected by toxic air emissions from industrial process but not at the levels seen in areas closer to the HSC.
- Published
- 2005
49. Altered cytokine expression in tissues of mice subjected to simulated microgravity
- Author
-
Keiko Yamauchi, Renard L. Thomas, Kimberly Wise, Sunil K. Manna, Bobby L. Wilson, Govindarajan T. Ramesh, N. R. Pellis, Anil D. Kulkarni, and K. Felix
- Subjects
Male ,medicine.medical_treatment ,Clinical Biochemistry ,Spleen ,Biology ,Andrology ,Mice ,Immune system ,In vivo ,Interferon ,medicine ,Animals ,Molecular Biology ,Weightlessness Simulation ,Mice, Inbred BALB C ,Cell Biology ,General Medicine ,medicine.anatomical_structure ,Cytokine ,Gene Expression Regulation ,Organ Specificity ,Immunology ,Cytokines ,Tumor necrosis factor alpha ,Lymph ,Ex vivo ,medicine.drug - Abstract
Space flight is known to induce microgravity-associated immune dysfunction in humans, non-human primates and rodents. To understand the mechanism underlying these defects, several studies in rodents have been conducted in a ground-based antiorthostatic suspension (AOS) model that would mimic the effects of microgravity. In all these in vivo studies that showed the effects on cytokine profiles actually investigated the ex vivo production from culturing the cells isolated from whole organism that was exposed to space flight and/or microgravity. So, the purpose of the study was to examine the in vivo expression of cytokines in mice in immunologically important tissue environments of mice that were subjected to AOS. Cytokines such as Interleukin-1β (IL-1β), IL-2, IL-3, IL-6, Interferon-γ (IFN-γ) and Tumor Necrosis Factor-α (TNF-α) were measured by Enzyme Linked Immunosorbent Assay (ELISA) in the homogenates of spleen tissue, lymph nodes and also in serum of AOS mice and compared with that of control mice. AOS induced no change in the IL-3 levels, but IL-1β was increased significantly whereas IL-2 levels decreased in spleen, lymph nodes and serum. IL-6 levels did not differ in spleen but were significantly increased in lymph nodes and serum of AOS mice. IFN-γ levels in spleen did not change but showed nonsignificant reduction in lymph nodes and significant reduction in serum in response to AOS. TNF-α levels in spleen and serum were unchanged and increased in lymph nodes. This in vivo cytokine study confirms the earlier findings that microgravity-simulated conditions induce tissue-specific immune response (Mol Cell Biochem 266: 79–85, 2004)
- Published
- 2005
50. Deep photometry of C1.2244-02 in U colour with an electronographic camera
- Author
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Wlérick, G., primary, Vanderriest, C., additional, Hammer, F., additional, Lelièvre, G., additional, Horville, D., additional, Renard, L., additional, Arnaud, J., additional, and Gouiffes, C., additional
- Full Text
- View/download PDF
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