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Ding Li

Researcher at Sun Yat-sen University

Publications -  90
Citations -  2500

Ding Li is an academic researcher from Sun Yat-sen University. The author has contributed to research in topics: G-quadruplex & Transcription (biology). The author has an hindex of 27, co-authored 90 publications receiving 2084 citations.

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Turning off Transcription of the bcl-2 Gene by Stabilizing the bcl-2 Promoter Quadruplex with Quindoline Derivatives

TL;DR: It is demonstrated that the G-quadruplex structure was disrupted when partial mutation of G --> A was made, resulting in a 2-fold increase in basal transcriptional activity of bcl-2 promoter, and G- quadruplex specific ligands could regulate the transcription of bCl-2 through stabilization of quadruplex structure.
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Inhibition of Cell Proliferation by Quindoline Derivative (SYUIQ-05) through its Preferential Interaction with c-myc Promoter G-Quadruplex

TL;DR: The results showed that the effect of G-quadruplex ligand SYUIQ-05 on tumor cell lines and the mechanism of this effect showed that it preferred to bind with G- quadruplex in c-myc and had rather insignificant effect on G- quadruplex in telomere.
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Conformation Selective Antibody Enables Genome Profiling and Leads to Discovery of Parallel G-Quadruplex in Human Telomeres

TL;DR: A novel single-chain variable fragment antibody, D1, with high binding selectivity for parallel G-quadruplexes in vitro and in vivo is reported, finding it to be a valuable tool for determination of G- quadruplex and its conformation.
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Design, synthesis and evaluation of novel tacrine-multialkoxybenzene hybrids as dual inhibitors for cholinesterases and amyloid beta aggregation.

TL;DR: A new series of tacrine-multialkoxybenzene hybrids (9a-9n) were designed, synthesized and evaluated as dual inhibitors of cholinesterases (ChEs) and self-induced β-amyloid aggregation and showed higher self- induced Aβ aggregation inhibitory activity than a reference compound, curcumin.
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Cp*Rh(III) and Cp*Ir(III)-catalysed redox-neutral C–H arylation with quinone diazides: quick and facile synthesis of arylated phenols

TL;DR: The reaction represents the first example of Cp*Ir(III)-catalysed C-H direct arylation reaction, and offers a facile, operationally simple and environmentally benign access to arylated phenols.