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Junle Qu

Researcher at Shenzhen University

Publications -  68
Citations -  725

Junle Qu is an academic researcher from Shenzhen University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 10, co-authored 37 publications receiving 315 citations. Previous affiliations of Junle Qu include National Research Nuclear University MEPhI.

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Photo-activated chemo-immunotherapy for metastatic cancer using a synergistic graphene nanosystem

TL;DR: It is demonstrated that rGO/MTX/SB combined with laser irradiation provided a synergistic chemo-immuno-photothermal effect against tumors by in situ vaccination and inhibition of immunosuppressive microenvironment.
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Mitochondrial dynamics quantitatively revealed by STED nanoscopy with an enhanced squaraine variant probe.

TL;DR: This study developed an enhanced squaraine variant dye (MitoESq-635) to study the dynamic structures of mitochondrial cristae in live cells with a superresolution technique, demonstrating the emerging capability of optical STED nanoscopy to investigate intracellular physiological processes with nanoscale resolution for an extended period of time.
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Dual-functional fluorescent molecular rotor for endoplasmic reticulum microviscosity imaging during reticulophagy

TL;DR: A BODIPY-arsenicate conjugate 1-based fluorescent molecular rotor was designed to covalently bind vicinal dithiol-containing proteins in the ER, exhibiting a bifunction of reticulophagy initiation and microviscosity evaluation.
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A BODIPY-based two-photon fluorescent probe validates tyrosinase activity in live cells

TL;DR: The nontoxic probe Tyro-1 provides information about H2O2-mediated upregulation of tyrosinase through Cellular imaging through cellular imaging, and its two-photon imaging ability makes it a noninvasive tool for validating the expression of tyosinase in the live cells.
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Resolution improvement in STED super-resolution microscopy at low power using a phasor plot approach.

TL;DR: A phasor plot approach combined with fluorescence lifetime imaging microscopy (FLIM) is used to resolve the problem of stimulated emission partially inhibiting the spontaneous emission in the periphery of a diffraction-limited area, providing a 86 nm higher resolution than that in traditional STED imaging at a depletion power of 20 mW.