J
Jun Ma
Researcher at Harbin Institute of Technology
Publications - 1523
Citations - 58397
Jun Ma is an academic researcher from Harbin Institute of Technology. The author has contributed to research in topics: Nasopharyngeal carcinoma & Medicine. The author has an hindex of 97, co-authored 1338 publications receiving 39643 citations. Previous affiliations of Jun Ma include Shenyang Aerospace University & University of Technology, Sydney.
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Nomogram to predict the benefit of additional induction chemotherapy to concurrent chemoradiotherapy in locoregionally advanced nasopharyngeal carcinoma: Analysis of a multicenter, phase III randomized trial
TL;DR: A convenient nomogram is developed to estimate the benefit of IC for individual patients with LANPC and can serve as a catalyst of individual treatment discussions and facilitator of informed decision-making.
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Preparation of polyvinylpyrrolidone/graphene oxide/epoxy resin composite coatings and the study on their anticorrosion performance
Jian Zhang,Liu Zhongyuan,Lanhe Zhang,Jun Ma,Dong Sun,Di Zhang,Jingrong Liu,Haina Bai,Bing Wang +8 more
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Prognostic Value of Neoadjuvant Chemotherapy in Locoregionally Advanced Nasopharyngeal Carcinoma with Low Pre-treatment Epstein-Barr Virus DNA: a Propensity-matched Analysis.
Hao Peng,Lei Chen,Wen Fei Li,Rui Guo,Yuan Zhang,Fan Zhang,Li Zhi Liu,Li Tian,Ai Hua Lin,Ying Sun,Jun Ma +10 more
TL;DR: NCT was not established as an independent prognostic factor, and it should not be used in locoregionally advanced NPC with low pre-DNA in the era of intensity-modulated radiotherapy.
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UV photolysis of tetrachloro-p-benzoquinone (TCBQ) in aqueous solution: Mechanistic insight from quantum chemical calculations
TL;DR: In this paper, a systematical investigation on the transformation of tetrachloro-p-benzoquinone (TCBQ) under UV irradiation (at 253.7 nm) in aqueous solution has been conducted through quantum chemical calculations.
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Oil/water separation membranes with a fluorine island structure for stable high flux
TL;DR: In this paper, the authors focus on the distribution of hydrophilic and low-surface-energy (LSE) domains on membrane surfaces to relieve the adverse side effects of LSE domains, and the stable flux is improved from 280 to 770 Lm−2 h−1 bar−1 just by the manipulation of domain distribution.