What is he best known for?
The fields of study he is best known for:
His primary areas of study are Cell biology, Biochemistry, Biophysics, PDZ domain and Protein structure.
His studies in Cell biology integrate themes in fields like Synaptic plasticity, Membrane and Programmed cell death.
His Biochemistry research incorporates elements of Dynein and Molecular motor.
The Biophysics study combines topics in areas such as Amino acid, Antiparallel and Dimer.
His PDZ domain study incorporates themes from Peptide, Scaffold protein and Postsynaptic density.
His Protein structure study integrates concerns from other disciplines, such as Crystallography and Plasma protein binding.
His most cited work include:
- Calcium-induced conformational transition revealed by the solution structure of apo calmodulin. (559 citations)
- Organization and dynamics of PDZ-domain-related supramodules in the postsynaptic density. (286 citations)
- Phase Transition in Postsynaptic Densities Underlies Formation of Synaptic Complexes and Synaptic Plasticity. (205 citations)
What are the main themes of his work throughout his whole career to date?
Cell biology, Biophysics, Biochemistry, PDZ domain and Scaffold protein are his primary areas of study.
Mingjie Zhang has researched Cell biology in several fields, including Receptor and Guanylate kinase.
Mingjie Zhang has included themes like Crystallography, Membrane, Dimer and Postsynaptic density in his Biophysics study.
His biological study spans a wide range of topics, including AMPA receptor, Signal transduction and Protein–protein interaction.
His work is dedicated to discovering how Peptide, Calmodulin are connected with Myosin light-chain kinase and other disciplines.
His Protein structure research includes themes of Structural biology, Peptide sequence and Membrane protein.
He most often published in these fields:
- Cell biology (37.46%)
- Biophysics (28.09%)
- Biochemistry (28.09%)
What were the highlights of his more recent work (between 2017-2021)?
- Cell biology (37.46%)
- Biophysics (28.09%)
- Postsynaptic density (10.03%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Cell biology, Biophysics, Postsynaptic density, Scaffold protein and Postsynaptic potential.
His works in Plasma protein binding and Structural biology are all subjects of inquiry into Cell biology.
His work deals with themes such as Ca2+/calmodulin-dependent protein kinase, Protein subunit, Membrane, Synaptic vesicle and Organelle, which intersect with Biophysics.
His Postsynaptic density research focuses on Long-term potentiation and how it connects with Phosphatase, Neuroplasticity, Compartment and Signalling.
His studies deal with areas such as Regulator, PDZ domain, Binding site and Synaptic signaling as well as Scaffold protein.
The concepts of his PDZ domain study are interwoven with issues in CASK and Ligand.
Between 2017 and 2021, his most popular works were:
- Reconstituted Postsynaptic Density as a Molecular Platform for Understanding Synapse Formation and Plasticity. (110 citations)
- RIM and RIM-BP Form Presynaptic Active-Zone-like Condensates via Phase Separation. (60 citations)
- Formation of biological condensates via phase separation: Characteristics, analytical methods, and physiological implications. (46 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Postsynaptic density, Cell biology, Biophysics, Postsynaptic potential and Scaffold protein.
His work carried out in the field of Cell biology brings together such families of science as Autophagy, Cell fate determination and Guanylate kinase.
His Biophysics research is multidisciplinary, incorporating perspectives in Membrane and Lipid bilayer.
His Postsynaptic potential research includes elements of Inhibitory postsynaptic potential and Excitatory postsynaptic potential.
His research integrates issues of Mutation and Synaptic signaling in his study of Scaffold protein.
Plasma protein binding is often connected to Protein structure in his work.
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