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Institution

Nanjing University

EducationNanjing, China
About: Nanjing University is a education organization based out in Nanjing, China. It is known for research contribution in the topics: Catalysis & Adsorption. The organization has 85961 authors who have published 105504 publications receiving 2289036 citations. The organization is also known as: NJU & Nanking University.


Papers
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Journal ArticleDOI
24 Aug 2020
TL;DR: In this paper, a review of the basic physical principles of these various techniques on the engineering of quasi-particle and optical bandgaps, their bandgap tunability, potentials and limitations in practical 2D device technologies are provided.
Abstract: Semiconductors are the basis of many vital technologies such as electronics, computing, communications, optoelectronics, and sensing. Modern semiconductor technology can trace its origins to the invention of the point contact transistor in 1947. This demonstration paved the way for the development of discrete and integrated semiconductor devices and circuits that has helped to build a modern society where semiconductors are ubiquitous components of everyday life. A key property that determines the semiconductor electrical and optical properties is the bandgap. Beyond graphene, recently discovered two-dimensional (2D) materials possess semiconducting bandgaps ranging from the terahertz and mid-infrared in bilayer graphene and black phosphorus, visible in transition metal dichalcogenides, to the ultraviolet in hexagonal boron nitride. In particular, these 2D materials were demonstrated to exhibit highly tunable bandgaps, achieved via the control of layers number, heterostructuring, strain engineering, chemical doping, alloying, intercalation, substrate engineering, as well as an external electric field. We provide a review of the basic physical principles of these various techniques on the engineering of quasi-particle and optical bandgaps, their bandgap tunability, potentials and limitations in practical realization in future 2D device technologies.

434 citations

Journal ArticleDOI
TL;DR: The structural and genetic diversity that exists among NBS-LRR proteins in rice is remarkable, and suggests that diversifying selection has played an important role in the evolution of R genes in this agronomically important species.
Abstract: A complete set of candidate disease resistance ( R) genes encoding nucleotide-binding sites (NBSs) was identified in the genome sequence of japonica rice ( Oryza sativa L. var. Nipponbare). These putative R genes were characterized with respect to structural diversity, phylogenetic relationships and chromosomal distribution, and compared with those in Arabidopsis thaliana. We found 535 NBS-coding sequences, including 480 non-TIR (Toll/IL-1 receptor) NBS-LRR (Leucine Rich Repeat) genes. TIR NBS-LRR genes, which are common in A. thaliana, have not been identified in the rice genome. The number of non-TIR NBS-LRR genes in rice is 8.7 times higher than that in A. thaliana, and they account for about 1% of all of predicted ORFs in the rice genome. Some 76% of the NBS genes were located in 44 gene clusters or in 57 tandem arrays, and 16 apparent gene duplications were detected in these regions. Phylogenetic analyses based both NBS and N-terminal regions classified the genes into about 200 groups, but no deep clades were detected, in contrast to the two distinct clusters found in A. thaliana. The structural and genetic diversity that exists among NBS-LRR proteins in rice is remarkable, and suggests that diversifying selection has played an important role in the evolution of R genes in this agronomically important species. (Supplemental material is available online at http://gattaca.nju.edu.cn .)

434 citations

Journal ArticleDOI
TL;DR: This paper proposes a method called Mlnb which adapts the traditional naive Bayes classifiers to deal with multi-label instances and achieves comparable performance to other well-established multi- label learning algorithms.

433 citations

Journal ArticleDOI
TL;DR: The results obtained allowed us to assess the importance of knowing the carrier and removal status of Na6(CO3)(SO4)2, as a raw material for high-performance liquid chromatography, and their applications in materials science and engineering.
Abstract: [*] Dr. F. Li Department of Chemistry University of New Orleans New Orleans, LA 70148 (USA) Fax: (+1)504-280-6860 E-mail: fli@uno.edu Dr. Y. Ding, P. Gao, Prof. Dr. Z. L. Wang School of Materials Science and Engineering Georgia Institute of Technology Atlanta, GA 30332-0245 (USA) Fax: (+1)404-894-9140 E-mail: zhong.wang@mse.gatech.edu Prof. X. Xin Department of Chemistry Nanjing University Nanjing 20093 (P. R. China) [**] The authors gratefully acknowledge the financial support of the National Science Foundation of China (No.90101028) and the National Science Foundation. Zuschriften

433 citations

Journal ArticleDOI
01 Jul 2020-Gut
TL;DR: Elevated METTL3 expression promotes tumour angiogenesis and glycolysis in GC, indicating that METTL 3 expression is a potential prognostic biomarker and therapeutic target for human GC.
Abstract: Objective N6-methyladenosine (m6A) RNA methylation and its associated methyltransferase METTL3 are involved in tumour initiation and progression via the regulation of RNA function. This study explored the biological function and clinical significance of METTL3 in gastric cancer (GC). Design The prognostic value of METTL3 expression was evaluated using tissue microarray and immunohistochemical staining analyses in a human GC cohort. The biological role and mechanism of METTL3 in GC tumour growth and liver metastasis were determined in vitro and in vivo. Results The level of m6A RNA was significantly increased in GC, and METTL3 was the main regulator involved in the abundant m6A RNA modification. METTL3 expression was significantly elevated in GC tissues and associated with poor prognosis. Multivariate Cox regression analysis revealed that METTL3 expression was an independent prognostic factor and effective predictor in human patients with GC. Moreover, METTL3 overexpression promoted GC proliferation and liver metastasis in vitro and in vivo. Mechanistically, P300-mediated H3K27 acetylation activation in the promoter of METTL3 induced METTL3 transcription, which stimulated m6A modification of HDGF mRNA, and the m6A reader IGF2BP3 then directly recognised and bound to the m6A site on HDGF mRNA and enhanced HDGF mRNA stability. Secreted HDGF promoted tumour angiogenesis, while nuclear HDGF activated GLUT4 and ENO2 expression, followed by an increase in glycolysis in GC cells, which was correlated with subsequent tumour growth and liver metastasis. Conclusions Elevated METTL3 expression promotes tumour angiogenesis and glycolysis in GC, indicating that METTL3 expression is a potential prognostic biomarker and therapeutic target for human GC.

433 citations


Authors

Showing all 86514 results

NameH-indexPapersCitations
Yi Chen2174342293080
H. S. Chen1792401178529
Zhenan Bao169865106571
Gang Chen1673372149819
Peter G. Schultz15689389716
Xiang Zhang1541733117576
Rui Zhang1512625107917
Yi Yang143245692268
Markku Kulmala142148785179
Jian Yang1421818111166
Wei Huang139241793522
Bin Liu138218187085
Jun Lu135152699767
Hui Li1352982105903
Lei Zhang135224099365
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20242
2023276
20221,089
20219,130
20208,684
20198,203