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802 results on '"Herzog E"'

65. Adrenergic Nerve-Associated Lung Fibrosis Is Driven by Myeloid Netrin-1

Author

Perry, C., primary, Gao, R., additional, Peng, X., additional, Ntokou, A., additional, Ryu, C., additional, Gomez, J.L., additional, Reeves, B.C., additional, Walia, A., additional, Sun, H., additional, Black, K.E., additional, Hariri, L.P., additional, Moore, M.W., additional, Gulati, M., additional, Homer, R., additional, Greif, D., additional, Eltzschig, H., additional, and Herzog, E., additional

Published
2020
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72. The Prognostic Value of Monocyte Count in Idiopathic Pulmonary Fibrosis: A Multi-Omic Cohort Study

Author

Scott, M., primary, Quinn, K., additional, Li, Q., additional, Carroll, R., additional, Chen, S., additional, Carns, M., additional, Aren, K., additional, Sun, J., additional, Koloms, K., additional, Lee, J., additional, Kropski, J., additional, Zhao, H., additional, Herzog, E., additional, Martinez, F.J., additional, Moore, B.B., additional, Hinchcliff, M., additional, Denny, J., additional, Kaminski, N., additional, Herazo-Maya, J.D., additional, Shah, N., additional, and Khatri, P., additional

Published
2019
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78. Cocaine increases dopaminergic connectivity in the nucleus accumbens

Author

Andrianarivelo, Andry, Saint-Jour, Estefani, Trifilieff, Pierre, Cahill, Emma, Bo, Gregory Dal, Dos Santos, Marc, Salery, Marine, Forget, Benoit, Garcia Perez, Maria Alexandra, Betuing, Sandrine, Boudier, Thomas, Sakae, D, Marti, F., Lecca, S, Vorspan, F., Martín-García, E, Morel, L., Henrion, A, Gutierrez-Cuesta, J., Besnard, A., Heck, Nicolas, Herzog, E., Bolte, S., Prado, V, Prado, M., Bellivier, F., Eap, C, Crettol, S, Vanhoutte, Peter, Caboche, Jocelyne, Gratton, A, Moquin, L, Giros, Bruno, Maldonado, R, Daumas, S, Mameli, M., Jamain, S., El Mestikawy, S, Sorbonne Université (SU), Neurosciences Paris Seine (NPS), Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Biologie Paris Seine (IBPS), Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Paris Seine (IBPS), Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), University of Cambridge [UK] (CAM), McGill University = Université McGill [Montréal, Canada], Institut de Recherche Biomédicale des Armées (IRBA), Neuroscience Paris Seine (NPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Nutrition et Neurobiologie intégrée (NutriNeur0), Université Bordeaux Segalen - Bordeaux 2-Institut National de la Recherche Agronomique (INRA)-Université Sciences et Technologies - Bordeaux 1-Institut Polytechnique de Bordeaux-Ecole nationale supérieure de chimie, biologie et physique, Physiopathologie des Maladies du Système Nerveux Central, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Neuropsychopharmacologie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Signalisation Neuronale et Régulations Géniques = Neuronal Signaling and Gene Regulation (NPS-02), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Neurogénétique moléculaire, Université d'Évry-Val-d'Essonne (UEVE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Image & Pervasive Access Lab (IPAL), Institute for Infocomm Research - I²R [Singapore]-Centre National de la Recherche Scientifique (CNRS)-Agency for science, technology and research [Singapore] (A*STAR)-MATHEMATIQUES, SCIENCES ET TECHNOLOGIES DE L'INFORMATION ET DE LA COMMUNICATION (UJF)-National University of Singapore (NUS)-Université Pierre et Marie Curie - Paris 6 (UPMC), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Neuropsychopharmacologie des addictions. Vulnérabilité et variabilité expérimentale et clinique (NAVVEC - UM 81 (UMR 8206/ U705)), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Descartes - Paris 5 (UPD5)-Institut des sciences du Médicament -Toxicologie - Chimie - Environnement (IFR71), Institut National de la Santé et de la Recherche Médicale (INSERM)-Ecole Nationale Supérieure de Chimie de Paris- Chimie ParisTech-PSL (ENSCP)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Ecole Nationale Supérieure de Chimie de Paris- Chimie ParisTech-PSL (ENSCP)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Paris Descartes - Paris 5 (UPD5)-Université Paris Diderot - Paris 7 (UPD7), Unitat de Farmacologia i Farmacognòsia Facultat de Farmàcia, Nucli Universitari de Pedralbes, La Jaillière, ARVALIS - Institut du végétal [Paris], Université Pierre et Marie Curie - Paris 6 (UPMC), Institut de biologie moléculaire des plantes (IBMP), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Institut des sciences du végétal (ISV), Centre National de la Recherche Scientifique (CNRS), Paringa Mineração Limitada, Optimisation Thérapeutique en Neuropsychopharmacologie (VariaPsy - U1144), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Neurobiologie des processus adaptatifs (NPA), Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS), Physiopathologie des maladies psychiatriques = Pathophysiology of Psychiatric Disorders (NPS-07), Institut du Fer à Moulin, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Université Paris-Est Créteil Val-de-Marne - Faculté de médecine (UPEC Médecine), Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Université McGill, HAL-UPMC, Gestionnaire, Cahill, Emma [0000-0003-3054-1708], and Apollo - University of Cambridge Repository

Subjects
0301 basic medicine, Male, Dendritic spine, RNA, Untranslated, [SDV]Life Sciences [q-bio], striatum, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, Dopamine, Striatum, Nucleus Accumbens, Mice, 0302 clinical medicine, Cocaine, Dopamine Uptake Inhibitors, dendritic spine, General Neuroscience, Dopaminergic, 3. Good health, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Anatomy, Locomotion, medicine.drug, Genetically modified mouse, Histology, Presynaptic Terminals, Mice, Transgenic, Nucleus accumbens, Biology, In Vitro Techniques, Statistics, Nonparametric, 03 medical and health sciences, Glutamatergic, Imaging, Three-Dimensional, 3D imaging, medicine, Animals, Dopamine transporter, Dopamine Plasma Membrane Transport Proteins, [SCCO.NEUR]Cognitive science/Neuroscience, Dopaminergic Neurons, fungi, [SDV.NEU.NB] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, Dendrites, Mice, Inbred C57BL, Luminescent Proteins, 030104 developmental biology, nervous system, Vesicular Monoamine Transport Proteins, Synapses, biology.protein, Neuroscience, 030217 neurology & neurosurgery
Abstract

International audience; The development of addictive behavior is associated with functional and structural plasticity in the mesocorticolimbic pathway. Increased connectivity upon cocaine administration has been inferred from increases in dendritic spine density, but without observations of presynaptic elements. Recently, we established a method that enables analyses of both dendritic spines and glutamatergic boutons and presented evidence that cocaine induces changes in striatal connectivity. As the pharmacological and behavioral effects of cocaine directly implicate dopaminergic neurons and their afferents, a remaining question is whether dopaminergic striatal innervations also undergo structural plasticity. To address this issue, we generated transgenic mice in which the fluorophore tdTomato is expressed under the promoter of the dopamine transporter gene. In these mice, specific labeling of dopaminergic boutons was observed in the striatum. Of note, the accordance of our results for control mice with previous electron microscopy studies confirms that our method can be used to decipher the spatial organization of boutons in relation to dendritic elements. Following repeated cocaine administration that led to behavioral locomotor sensitization, an increased density of dopaminergic boutons was observed 1 day later in the nucleus accumbens shell specifically, and not in other striatal regions. Combined labeling of dopaminergic boutons and striatal dendrites showed that cocaine significantly increased the percentage of dendritic spines associated with a dopaminergic bouton. Our results show that chronic cocaine administration induces structural plasticity of dopaminergic boutons that could participate in dopamine-dependent neuronal adaptations in the striatum.

Published
2017

79. Performance Loss Induced by LeTID in the Field

Author

Kersten, F., Fertig, F., Petter, K., Klöter, B., Herzog, E., Strobel, M.B., Heitmann, J., and Müller, J.W.

Subjects
PV Module Performance and Reliability, Performance, Reliability and Sustainability of Photovoltaic Modules and Balance of System Components
Abstract

33rd European Photovoltaic Solar Energy Conference and Exhibition; 1418-1421, If not adequately suppressed, Light and elevated Temperature Induced Degradation (LeTID) has been shown to cause severe degradation of crystalline silicon solar cells and modules with passivated emitter and rear cell (PERC). Within this work, the system performance of LeTID-sensitive multicrystalline silicon (mc-Si) modules is investigated when operated in temperate (Germany) and Mediterranean (Cyprus) climates, and a correlation to predict the observed field performance based on accelerated laboratory testing is presented. Severe degradation of LeTID-sensitive modules of more than 7% in maximum output power is detected after one thousand hours of laboratory testing, which is shown to correspond to ~ 3 years of field installation time in Cyprus. In contrast, LeTID-sensitive modules installed in Germany show a degradation of 2.5% within the same time period. Due to lower irradiance and module temperatures in Germany LeTID is less pronounced than in Cyprus. Hence, a significant dependence of system performance and energy yield loss of LeTIDsensitive modules on installation site is shown, which affects one-to-one the levelized cost of electricity (LCOE). By applying Hanwha Q CELLS’ Q.ANTUM technology, it is shown that LeTID in the field is suppressed, independently of installation site.

Published
2017
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80. Investigating the Ocular Surface Microbiome: What Can It Tell Us?

Author

Peter VG, Morandi S C, Herzog EL, Zinkernagel MS, and Zysset-Burri DC

Subjects
ocular surface ocular surface microbiome 16s rrna gene sequencing whole metagenome shotgun sequencing, Ophthalmology, RE1-994
Abstract

Virginie G Peter,1 Sophia C Morandi,1,2 Elio L Herzog,1– 3 Martin S Zinkernagel,1,2 Denise C Zysset-Burri1,2 1Department of Ophthalmology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland; 2Department for BioMedical Research, University of Bern, Bern, Switzerland; 3Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, SwitzerlandCorrespondence: Virginie G Peter, Department of Ophthalmology, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse 15, Bern, 3010, Switzerland, Email virginie.peter@insel.chAbstract: While pathogens of the eye have been studied for a very long time, the existence of resident microbes on the surface of healthy eyes has gained interest only recently. It appears that commensal microbes are a normal feature of the healthy eye, whose role and properties are currently the subject of extensive research. This review provides an overview of studies that have used 16s rRNA gene sequencing and whole metagenome shotgun sequencing to characterize microbial communities associated with the healthy ocular surface from kingdom to genus level. Bacteria are the primary colonizers of the healthy ocular surface, with three predominant phyla: Proteobacteria, Actinobacteria, and Firmicutes, regardless of the host, environment, and method used. Refining the microbial classification to the genus level reveals a highly variable distribution from one individual and study to another. Factors accounting for this variability are intriguing - it is currently unknown to what extent this is attributable to the individuals and their environment and how much is artifactual. Clearly, it is technically challenging to accurately describe the microorganisms of the ocular surface because their abundance is relatively low, thus, permitting substantial contaminations. More research is needed, including better experimental standards to prevent biases, and the exploration of the ocular surface microbiome’s role in a spectrum of healthy to pathological states. Outcomes from such research include the opportunity for therapeutic interventions targeting the microbiome.Keywords: ocular surface, ocular surface microbiome, 16s rRNA gene sequencing, whole metagenome shotgun sequencing

Published
2023

94. Serumdigoxinspiegel in der operativen Intensivmedizin

Author

Franke, N., van Ackern, H., Herzog, E., Hohlbach, G., Inthorn, B., Reiser, M., Bergmann, H., editor, Brückner, J. B., editor, Gemperle, M., editor, Mayrhofer, O., editor, Frey, R., editor, Henschel, W. F., editor, Peter, K., editor, Weis, Karl-Heinz, editor, and Cunitz, Günther, editor

Published
1980
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