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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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Patent

Solution-based methods for rna expression profiling

TL;DR: In this article, a solution-based method for RNA expression profiling, including expression of microRNAs and mRNAs, is proposed. But the method is not suitable for high-throughput, low-cost, and flexible solution.
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The events that occur when cisplatin encounters cells

TL;DR: The sequence of chemical events, platinum binding to the monomeric protein and the induced conformational change and perturbations to the self-association of the monomers, is shown to be important in the cell damaging process.
Journal Article

Recognition of prostate tumor cells by cytotoxic T lymphocytes specific for prostate-specific membrane antigen

TL;DR: Only one of the four peptides predicted, PSMA(27), induced CTLs that were effective at recognizing prostate tumor cells expressing the HLA-A2 and PSMA molecules, underline the importance of demonstrating antitumor reactivity of peptide-induced C TLs for the selection of epitopes destined to become immunotherapeutic for prostate cancer.
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A Pentacene with a 144° Twist

TL;DR: The most twisted polycyclic aromatic hydrocarbon known, with an end-to-end twist of 143.6 degrees as discussed by the authors, was obtained by the reaction of 1,3-diphenylphenanthro[9,10-c]furan with the bisaryne equivalent generated from 1,2,4,5-tetrabromo-3,6-dimethylbenzene.
Journal Article

Direct Costimulation of Tumor-reactive CTL by Helper T Cells Potentiate Their Proliferation, Survival, and Effector Function

TL;DR: In an in vitro model system, the expansion and cytolytic function of tumor-reactive human CTL can be enhanced by CD4(+) helper T lymphocytes through costimulatory signals that are mediated by cell surface molecules.