2004 - Fellow of the American Academy of Arts and Sciences
2003 - Fellow of the American Association for the Advancement of Science (AAAS)
1987 - Fellow of Alfred P. Sloan Foundation
Mark F. Bear mainly focuses on Neuroscience, Synaptic plasticity, Long-term potentiation, Long-term depression and Visual cortex. His Neuroscience research integrates issues from NMDA receptor and Metaplasticity. His Synaptic plasticity study incorporates themes from Hippocampus, Metabotropic glutamate receptor and Anatomy.
His biological study spans a wide range of topics, including Neurotransmission and Long-Term Synaptic Depression. His Long-term depression research is multidisciplinary, incorporating perspectives in Postsynaptic density and Silent synapse. His Visual cortex study combines topics in areas such as Cerebral cortex and Neuron.
Mark F. Bear focuses on Neuroscience, Visual cortex, Synaptic plasticity, Long-term potentiation and Fragile X syndrome. His Neuroscience research incorporates themes from Metaplasticity, Long-term depression and Metabotropic glutamate receptor. Mark F. Bear combines subjects such as NMDA receptor, Kitten, Anatomy and Neurotransmission with his study of Visual cortex.
As a part of the same scientific family, Mark F. Bear mostly works in the field of Synaptic plasticity, focusing on Hippocampus and, on occasion, Hippocampal formation. His Long-term potentiation study combines topics from a wide range of disciplines, such as Stimulus and Stimulation. His study in Fragile X syndrome is interdisciplinary in nature, drawing from both Autism and FMR1.
His primary areas of investigation include Neuroscience, Fragile X syndrome, Visual cortex, Neuroplasticity and Long-term potentiation. His studies in Neuroscience integrate themes in fields like Synaptic plasticity, Metabotropic glutamate receptor 5 and FMR1. His Fragile X syndrome research is multidisciplinary, incorporating elements of Neurodevelopmental disorder, Autism, Gene expression and Intellectual disability.
His research in Visual cortex intersects with topics in Cerebral cortex, Retinal, Interneuron and Audiology. In his study, which falls under the umbrella issue of Neuroplasticity, Neocortex is strongly linked to Recognition memory. His Metaplasticity study in the realm of Long-term potentiation connects with subjects such as Arc.
Neuroscience, Fragile X syndrome, Neuroplasticity, Synaptic plasticity and Visual cortex are his primary areas of study. Mark F. Bear is interested in Monocular deprivation, which is a branch of Neuroscience. His Monocular deprivation research includes elements of Metaplasticity and Anatomy.
His work deals with themes such as Muscarinic acetylcholine receptor, Cholinergic, Basal forebrain, Long-Term Synaptic Depression and Stimulation, which intersect with Neuroplasticity. Synaptic plasticity is frequently linked to Long-term depression in his study. His Visual cortex research is multidisciplinary, relying on both Stimulus, Cognitive psychology, Somatosensory system and Acetylcholine.
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Neuroscience: Exploring the Brain
Mark F. Bear;Barry W. Connors;Michael A. Paradiso.
LTP and LTD: an embarrassment of riches.
Robert C. Malenka;Mark F. Bear.
Homosynaptic long-term depression in area CA1 of hippocampus and effects of N-methyl-D-aspartate receptor blockade.
Serena M. Dudek;Mark F. Bear.
Proceedings of the National Academy of Sciences of the United States of America (1992)
Learning Induces Long-Term Potentiation in the Hippocampus
Jonathan R. Whitlock;Arnold J. Heynen;Marshall G. Shuler;Mark F. Bear.
The mGluR theory of fragile X mental retardation
Mark F Bear;Kimberly M Huber;Stephen T Warren.
Trends in Neurosciences (2004)
Metaplasticity: the plasticity of synaptic plasticity
Wickliffe C. Abraham;Mark F. Bear.
Trends in Neurosciences (1996)
Synaptic plasticity: LTP and LTD
Mark F. Bear;Robert C. Malenka.
Current Opinion in Neurobiology (1994)
Altered synaptic plasticity in a mouse model of fragile X mental retardation
Kimberly M. Huber;Kimberly M. Huber;Sean M. Gallagher;Stephen T. Warren;Mark F. Bear.
Proceedings of the National Academy of Sciences of the United States of America (2002)
BDNF Regulates the Maturation of Inhibition and the Critical Period of Plasticity in Mouse Visual Cortex
Z. Josh Huang;Alfredo Kirkwood;Tommaso Pizzorusso;Vittorio Porciatti.
Regulation of distinct AMPA receptor phosphorylation sites during bidirectional synaptic plasticity.
Hey Kyoung Lee;Michaela Barbarosie;Kimihiko Kameyama;Mark F. Bear.
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