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Jun Lu

Researcher at Chinese Academy of Sciences

Publications -  3187
Citations -  131399

Jun Lu is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Medicine & Computer science. The author has an hindex of 135, co-authored 1526 publications receiving 99767 citations. Previous affiliations of Jun Lu include Drexel University & Argonne National Laboratory.

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Development of TiO2 electrical insulation coating on Ag-alloy sheathed Bi2Sr2CaCu2O8−x round-wire

TL;DR: In this paper, the authors have developed a TiO2 coating on Ag-alloy sheathed Bi2Sr2CaCu2O8−x (Bi-2212) round-wire conductor for electrical insulation in Bi-22 12 magnets.
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Synthesis-Microstructure-Performance Relationship of Layered Transition Metal Oxides as Cathode for Rechargeable Sodium Batteries Prepared by High-Temperature Calcination

TL;DR: A novel cathode material, layered Na1+x(Fey/2Niy/2Mn1-y)1-xO2 (x = 0.1-0.5), synthesized through a facile coprecipitation process combined with subsequent calcination would make layered transition metal oxides a strong candidate for the Na-ion battery cathode.
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Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia

TL;DR: It is proposed that structural damages in the thalamus and cortex are mostly responsible for clinical manifestations of FFI, which is typically characterized by organic sleep related symptoms, rapidly progressive dementia and sympathetic symptoms.
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Observations from the Analyses of Magnetic Field and AC Loss Distributions in the NHMFL 32 T All-Superconducting Magnet HTS Insert

TL;DR: In this paper, the distribution of AC losses in the two-coil superconducting magnet windings during the magnet charging/discharging process is computed and analyzed with due regard for the AC loss density dependence on the magnetic field and the field angle.
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The Effects of Synthetically Modified Natural Compounds on ABC Transporters

TL;DR: This review evaluates whether synthetically modifying natural compounds is a viable strategy to generate potent, nontoxic, ABC transporter inhibitors which may potentially reverse MDR.