What is he best known for?
The fields of study he is best known for:
Jianhong Luo focuses on NMDA receptor, Protein subunit, Cell biology, Neuroscience and Receptor.
His NMDA receptor research incorporates themes from Glutamate receptor, Biophysics, Neuropathic pain and Excitatory postsynaptic potential.
His studies deal with areas such as Hippocampal formation, AMPA receptor and Synapse as well as Excitatory postsynaptic potential.
Jianhong Luo works mostly in the field of Protein subunit, limiting it down to concerns involving Molecular biology and, occasionally, CFLAR and MCL1.
His Cell biology research incorporates elements of Honokiol and Mitochondrial permeability transition pore.
In his study, Cell surface receptor, PDZ domain, Mutant and Binding domain is strongly linked to Transfection, which falls under the umbrella field of Receptor.
His most cited work include:
- Functional and pharmacological differences between recombinant N-methyl-D-aspartate receptors. (568 citations)
- Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3 -mutant mice (562 citations)
- The majority of N-methyl-D-aspartate receptor complexes in adult rat cerebral cortex contain at least three different subunits (NR1/NR2A/NR2B). (355 citations)
What are the main themes of his work throughout his whole career to date?
Jianhong Luo mainly focuses on Cell biology, NMDA receptor, Neuroscience, Hippocampal formation and Biochemistry.
His NMDA receptor research integrates issues from Glutamate receptor, Molecular biology and Protein subunit.
His study in Protein subunit is interdisciplinary in nature, drawing from both Endoplasmic reticulum and ER retention.
His Neuroscience study integrates concerns from other disciplines, such as Synaptic plasticity and Postsynaptic potential.
His biological study spans a wide range of topics, including Interleukin 2, Long-term potentiation, Neuron and Postsynaptic density.
His work in Biochemistry addresses issues such as Biophysics, which are connected to fields such as Alanine, Transient receptor potential channel, Ion channel, Patch clamp and C-terminus.
He most often published in these fields:
- Cell biology (34.68%)
- NMDA receptor (33.87%)
- Neuroscience (29.84%)
What were the highlights of his more recent work (between 2016-2020)?
- Neuroscience (29.84%)
- Cell biology (34.68%)
- TRPM2 (9.68%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Neuroscience, Cell biology, TRPM2, Hippocampus and NMDA receptor.
His work in Neuroscience addresses subjects such as Synaptic plasticity, which are connected to disciplines such as Postsynaptic potential and Excitatory postsynaptic potential.
His research in Cell biology intersects with topics in Membrane and Depolarization.
The various areas that he examines in his TRPM2 study include Autophagy, In vivo, Biophysics and Human brain.
His work deals with themes such as AMPA receptor and Long-term depression, which intersect with Hippocampus.
His NMDA receptor study is associated with Receptor.
Between 2016 and 2020, his most popular works were:
- BNIP3L/NIX-mediated mitophagy protects against ischemic brain injury independent of PARK2. (80 citations)
- 3D printing of conducting polymers. (74 citations)
- Depolarized GABAergic Signaling in Subicular Microcircuits Mediates Generalized Seizure in Temporal Lobe Epilepsy (58 citations)
In his most recent research, the most cited papers focused on:
His primary areas of study are Cell biology, Autophagy, Parvalbumin, Optogenetics and Neuroscience.
Jianhong Luo regularly links together related areas like Mitophagy in his Cell biology studies.
His studies deal with areas such as Ischemic brain injury, Ischemia, Mitochondrion and Phosphorylation as well as Autophagy.
His study in Parvalbumin is interdisciplinary in nature, drawing from both Novelty and Stimulation.
His research integrates issues of Photostimulation, Nerve net, Electrophysiology and Neuroligin in his study of Optogenetics.
His study in GABAergic and Hippocampus are all subfields of Neuroscience.
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