What is he best known for?
The fields of study he is best known for:
- Enzyme
- Neurotransmitter
- Amino acid
Jeremy M. Henley mostly deals with Cell biology, AMPA receptor, Neuroscience, Receptor and Neurotransmission.
The various areas that Jeremy M. Henley examines in his Cell biology study include Endocytosis and Cell membrane.
He has researched AMPA receptor in several fields, including Synaptic plasticity and Synapse.
His studies deal with areas such as Long-term potentiation, Long-term depression and Postsynaptic potential as well as Neuroscience.
His Receptor study necessitates a more in-depth grasp of Biochemistry.
Jeremy M. Henley studied Neurotransmission and Kainate receptor that intersect with Kainic acid.
His most cited work include:
- Induction of LTP in the hippocampus needs synaptic activation of glutamate metabotropic receptors (661 citations)
- NSF Binding to GluR2 Regulates Synaptic Transmission (501 citations)
- NSF Binding to GluR2 Regulates Synaptic Transmission (501 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Cell biology, AMPA receptor, Neuroscience, Kainate receptor and Receptor.
His research integrates issues of Postsynaptic potential, Endocytosis, Neurotransmission and PICK1 in his study of Cell biology.
His Neurotransmission research incorporates themes from Synapse and Excitatory postsynaptic potential.
His study in AMPA receptor is interdisciplinary in nature, drawing from both Synaptic plasticity and Hippocampal formation.
The study incorporates disciplines such as Synaptic scaling, Long-term potentiation, Long-term depression and Silent synapse in addition to Neuroscience.
His Kainate receptor study incorporates themes from Kainic acid, Biophysics and CNQX.
He most often published in these fields:
- Cell biology (50.76%)
- AMPA receptor (39.21%)
- Neuroscience (27.36%)
What were the highlights of his more recent work (between 2013-2021)?
- Cell biology (50.76%)
- AMPA receptor (39.21%)
- Neurotransmission (16.72%)
In recent papers he was focusing on the following fields of study:
His main research concerns Cell biology, AMPA receptor, Neurotransmission, Neuroscience and SUMO protein.
His Cell biology research incorporates elements of Receptor, Synapse and Synaptic vesicle.
His AMPA receptor research includes themes of Synaptic plasticity and Long-term potentiation.
Jeremy M. Henley combines subjects such as Endosome, Neuron and Function with his study of Neurotransmission.
Many of his studies involve connections with topics such as Synaptic scaling and Neuroscience.
In general SUMO protein study, his work on Protein sumoylation and SUMO enzymes often relates to the realm of Lysine, Molecular biology and HEK 293 cells, thereby connecting several areas of interest.
Between 2013 and 2021, his most popular works were:
- Synaptic AMPA receptor composition in development, plasticity and disease. (216 citations)
- Neuronal SUMOylation: Mechanisms, Physiology, and Roles in Neuronal Dysfunction (107 citations)
- Ubiquitin C-terminal hydrolase L1 (UCH-L1): structure, distribution and roles in brain function and dysfunction. (86 citations)
In his most recent research, the most cited papers focused on:
- Enzyme
- Neurotransmitter
- Amino acid
His scientific interests lie mostly in Cell biology, Neurotransmission, AMPA receptor, SUMO protein and Neuroscience.
Jeremy M. Henley usually deals with Cell biology and limits it to topics linked to Biochemistry and Neurodegeneration.
Jeremy M. Henley has included themes like Exocytosis, Function, Synapsin, Synaptic vesicle and Mitochondrion in his Neurotransmission study.
His AMPA receptor research includes elements of Long-term potentiation and Endocytosis.
His work in the fields of SUMO protein, such as Protein sumoylation, overlaps with other areas such as Synapse, HEK 293 cells, Lysine and Signal transducing adaptor protein.
His research integrates issues of Synaptic plasticity, Signal transduction, Complex cell and Drug discovery in his study of Neuroscience.
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