His primary scientific interests are in Cell biology, AMPA receptor, Neuroscience, PDZ domain and Glutamate receptor. The concepts of his Cell biology study are interwoven with issues in NMDA receptor and Long-term potentiation. His studies deal with areas such as Lipid bilayer fusion and Chaperone as well as AMPA receptor.
His studies in Neuroscience integrate themes in fields like Synaptic plasticity and Developmental verbal dyspraxia. Pavel Osten combines subjects such as Receptor, Protein subunit and PICK1 with his study of PDZ domain. His Protein kinase C research is multidisciplinary, incorporating perspectives in Hippocampal formation and Molecular biology.
His primary areas of investigation include Neuroscience, Cell biology, AMPA receptor, Excitatory postsynaptic potential and Cell type. The Neuroscience study combines topics in areas such as Globus pallidus and Neurotransmission. In general Cell biology study, his work on Protein kinase C often relates to the realm of N-Ethylmaleimide-Sensitive Proteins, thereby connecting several areas of interest.
His AMPA receptor study combines topics in areas such as PDZ domain and Chaperone. His research in Excitatory postsynaptic potential tackles topics such as Synaptic plasticity which are related to areas like Long-term depression and Silent synapse. His Cell type research includes elements of Brain atlas, GABAergic and Primary motor cortex.
His primary areas of study are Neuroscience, Light sheet fluorescence microscopy, Cell type, Fate mapping and Striatum. As part of his studies on Neuroscience, Pavel Osten often connects relevant subjects like Glutamatergic. His research in Light sheet fluorescence microscopy intersects with topics in Dendritic spine, Artificial intelligence and Microscopy.
His Cell type research includes themes of Mice brain, Tomography, Primary motor cortex and Photon. The various areas that he examines in his Fate mapping study include Chromatin and Epigenomics, DNA methylation. As a part of the same scientific study, Pavel Osten usually deals with the Striatum, concentrating on Cortex and frequently concerns with Parafascicular nucleus, Somatosensory system, Electrophysiology, Thalamus and Stimulation.
His main research concerns Neuroscience, Fate mapping, DNA methylation, Chromatin and Epigenomics. His research integrates issues of Tissue clearing, Light sheet fluorescence microscopy and Microscopy in his study of Neuroscience. His study in Fate mapping is interdisciplinary in nature, drawing from both Neuron, Ganglionic eminence, Striosome, Neurogenesis and Medium spiny neuron.
His research integrates issues of Reprogramming, Mutant, Cell biology, Histone and Epigenetics in his study of DNA methylation. His Chromatin research incorporates elements of Brain atlas, Computational biology, Primary motor cortex and Cell type.
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Evoked Axonal Oxytocin Release in the Central Amygdala Attenuates Fear Response
H. Sophie Knobloch;Alexandre Charlet;Lena C. Hoffmann;Marina Eliava.
Serial two-photon tomography for automated ex vivo mouse brain imaging
Timothy Ragan;Lolahon R Kadiri;Kannan Umadevi Venkataraju;Karsten Bahlmann.
Nature Methods (2012)
Persistent activation of the zeta isoform of protein kinase C in the maintenance of long-term potentiation
Todd Charlton Sacktor;Pavel Osten;Helen Valsamis;Xiaolan Jiang.
Proceedings of the National Academy of Sciences of the United States of America (1993)
Lentivirus-based genetic manipulations of cortical neurons and their optical and electrophysiological monitoring in vivo
Tanjew Dittgen;Axel Nimmerjahn;Shoji Komai;Pawel Licznerski.
Proceedings of the National Academy of Sciences of the United States of America (2004)
Mapping of Brain Activity by Automated Volume Analysis of Immediate Early Genes
Nicolas Renier;Eliza L. Adams;Christoph Kirst;Zhuhao Wu.
Incomplete and Inaccurate Vocal Imitation after Knockdown of FoxP2 in Songbird Basal Ganglia Nucleus Area X
Sebastian Haesler;Christelle Rochefort;Christelle Rochefort;Benjamin Georgi;Pawel Licznerski.
PLOS Biology (2007)
PICK1 Targets Activated Protein Kinase Cα to AMPA Receptor Clusters in Spines of Hippocampal Neurons and Reduces Surface Levels of the AMPA-Type Glutamate Receptor Subunit 2
Jose L. Perez;Latika Khatri;Craig Chang;Sapna Srivastava.
The Journal of Neuroscience (2001)
Mutagenesis reveals a role for ABP/GRIP binding to GluR2 in synaptic surface accumulation of the AMPA receptor.
Pavel Osten;Latika Khatri;Joey L. Perez;Georg Köhr.
Novel Anchorage of GluR2/3 to the Postsynaptic Density by the AMPA Receptor–Binding Protein ABP
S Srivastava;P Osten;F.S Vilim;L Khatri.
The AMPA receptor GluR2 C terminus can mediate a reversible, ATP-dependent interaction with NSF and α- and β-SNAPs
P Osten;P Osten;S Srivastava;G.J Inman;G.J Inman;F.S Vilim;F.S Vilim.
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