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ACS Applied Materials & Interfaces|April 25, 2023
Magnetic Moment Is an Effective Descriptor for Electrocatalytic Nitrogen Reduction Reaction on Two-Dimensional Organometallic NanosheetsDan Deng, Li-Ming Yang
Journal of the American Chemical Society|October 10, 2012
Asymmetric approach toward chiral cyclohex-2-enones from anisoles via an enantioselective isomerization by a new chiral diamine catalystJung Hwa Lee, Li Deng
Australian Endodontic Journal : the Journal of the Australian Society of Endodontology Inc|August 9, 2025
Ex Vivo Evaluation of the Fit of Matched Gutta Percha Points in Human Root Canals Prepared With the Corresponding Nickel-Titanium FilesSamuel Deng, Paul V Abbott
Environmental Science & Technology|March 12, 2024
Dynamic Regulation of Intracellular Labile Cu(I)/Cu(II) Cycle in Microalgae Chlamydomonas reinhardtii: Disrupting the Balance by Cu StressShaoxi Deng, Wen-Xiong Wang
Cureus|August 20, 2024
Multipronged Electronic Health Record Analysis of Antidepressant Effectiveness on Depression Remission in Patients With Concurrent Depression and Irritable Bowel SyndromeAshley Deng, Eduardo D Espiridion
Neurology|August 12, 2024
Pearls & Oy-sters: Use of Muscle Ultrasound as a Clinical Tool in INPP5K-Related Muscular Dystrophy: A Case ReportStella Deng, Bo Hoon Lee
Environmental Pollution (Barking, Essex : 1987)|July 21, 2026
Persistent and reversible labile Cu(I) heterogeneity reflects stress response during chronic copper exposure in microalgaeShaoxi Deng, Wen-Xiong Wang
Acta Biomaterialia|October 15, 2022
Gene editing of Duchenne muscular dystrophy using biomineralization-based spCas9 variant nanoparticlesShuojun Li, Moqing Du, Jiamin Deng, et al.
Acta Oto-Laryngologica|April 6, 2016
Compound heterozygous GJB2 mutations associated to a consanguineous Han family with autosomal recessive non-syndromic hearing lossHong Xia, Hongbo Xu, Xiong Deng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen]Jie Yan, Donghong Deng, Xuelian Deng, et al.
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