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Exploration of CO2-Philicity of Poly(vinyl acetate-co-alkyl vinyl ether) through Molecular Modeling and Dissolution Behavior Measurement.

The journal of physical chemistry. B

Hu D, Sun S, Yuan PQ, Zhao L, Liu T.
PMID: 26332013
J Phys Chem B. 2015 Sep 24;119(38):12490-501. doi: 10.1021/acs.jpcb.5b08393. Epub 2015 Sep 10.

Hydrocarbon CO2-philes are of great interest for use in expanding CO2 applications as a green solvent. In this work, multiscale molecular modeling and dissolution behavior measurement were both applied to explore CO2-philicity of the poly(vinyl acetate) (PVAc)-based copolymer. Introduction...

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Hu D, Sun S, Yuan PQ, et al. Exploration of CO2-Philicity of Poly(vinyl acetate-co-alkyl vinyl ether) through Molecular Modeling and Dissolution Behavior Measurement. J Phys Chem B. 2015;119(38):12490-501doi: 10.1021/acs.jpcb.5b08393.
Hu, D., Sun, S., Yuan, P. Q., Zhao, L., & Liu, T. (2015). Exploration of CO2-Philicity of Poly(vinyl acetate-co-alkyl vinyl ether) through Molecular Modeling and Dissolution Behavior Measurement. The journal of physical chemistry. B, 119(38), 12490-501. https://doi.org/10.1021/acs.jpcb.5b08393
Hu, Dongdong, et al. "Exploration of CO2-Philicity of Poly(vinyl acetate-co-alkyl vinyl ether) through Molecular Modeling and Dissolution Behavior Measurement." The journal of physical chemistry. B vol. 119,38 (2015): 12490-501. doi: https://doi.org/10.1021/acs.jpcb.5b08393
Hu D, Sun S, Yuan PQ, Zhao L, Liu T. Exploration of CO2-Philicity of Poly(vinyl acetate-co-alkyl vinyl ether) through Molecular Modeling and Dissolution Behavior Measurement. J Phys Chem B. 2015 Sep 24;119(38):12490-501. doi: 10.1021/acs.jpcb.5b08393. Epub 2015 Sep 10. PMID: 26332013.
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An integrated analysis for long noncoding RNAs and microRNAs with the mediated competing endogenous RNA network in papillary renal cell carcinoma.

OncoTargets and therapy

Huang C, Yuan N, Wu L, Wang X, Dai J, Song P, Li F, Xu C, Zhao X.
PMID: 28860812
Onco Targets Ther. 2017 Aug 14;10:4037-4050. doi: 10.2147/OTT.S141951. eCollection 2017.

Papillary renal cell carcinoma (PRCC) is the second most common subtype of renal cell carcinoma, and it lacks effective therapeutic targets and prognostic molecular biomarkers. Attention has been increasingly focused on long noncoding RNAs (lncRNAs), which can act as...

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Huang C, Yuan N, Wu L, et al. An integrated analysis for long noncoding RNAs and microRNAs with the mediated competing endogenous RNA network in papillary renal cell carcinoma. Onco Targets Ther. 2017;10:4037-4050doi: 10.2147/OTT.S141951.
Huang, C., Yuan, N., Wu, L., Wang, X., Dai, J., Song, P., Li, F., Xu, C., & Zhao, X. (2017). An integrated analysis for long noncoding RNAs and microRNAs with the mediated competing endogenous RNA network in papillary renal cell carcinoma. OncoTargets and therapy, 104037-4050. https://doi.org/10.2147/OTT.S141951
Huang, Chuiguo, et al. "An integrated analysis for long noncoding RNAs and microRNAs with the mediated competing endogenous RNA network in papillary renal cell carcinoma." OncoTargets and therapy vol. 10 (2017): 4037-4050. doi: https://doi.org/10.2147/OTT.S141951
Huang C, Yuan N, Wu L, Wang X, Dai J, Song P, Li F, Xu C, Zhao X. An integrated analysis for long noncoding RNAs and microRNAs with the mediated competing endogenous RNA network in papillary renal cell carcinoma. Onco Targets Ther. 2017 Aug 14;10:4037-4050. doi: 10.2147/OTT.S141951. eCollection 2017. PMID: 28860812; PMCID: PMC5565391.
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Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients.

Neoplasma

Yuan L, Xu B, Fan H, Yuan P, Zhao P, Suo Z.
PMID: 25591589
Neoplasma. 2015;62(2):239-49. doi: 10.4149/neo_2015_029.

UNLABELLED: This study aims to explore whether pre-operative or post-operative percentages of circulating myeloid-derived suppressor cells (MDSC) have any correlations with clinicopathological parameters in patients with rectal cancer and have any predictive values for local recurrence and disease free...

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Yuan L, Xu B, Fan H, et al. Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients. Neoplasma. 2015;62(2):239-49doi: 10.4149/neo_2015_029.
Yuan, L., Xu, B., Fan, H., Yuan, P., Zhao, P., & Suo, Z. (2015). Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients. Neoplasma, 62(2), 239-49. https://doi.org/10.4149/neo_2015_029
Yuan, L, et al. "Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients." Neoplasma vol. 62,2 (2015): 239-49. doi: https://doi.org/10.4149/neo_2015_029
Yuan L, Xu B, Fan H, Yuan P, Zhao P, Suo Z. Pre- and post-operative evaluation: percentages of circulating myeloid-derived suppressor cells in rectal cancer patients. Neoplasma. 2015;62(2):239-49. doi: 10.4149/neo_2015_029. PMID: 25591589.
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Breakdown assisted by a novel electron drift injection in the J-TEXT tokamak.

The Review of scientific instruments

Wang N, Jin H, Zhuang G, Ding Y, Pan Y, Cen Y, Chen Z, Huang H, Liu D, Rao B, Zhang M, Zou B.
PMID: 25085138
Rev Sci Instrum. 2014 Jul;85(7):073505. doi: 10.1063/1.4890287.

A novel electron drift injection (EDI) system aiming to improve breakdown behavior has been designed and constructed on the Joint Texas EXperiment Tokamak Tokamak. Electrons emitted by the system undergo the E×B drift, ∇B drift and curvature drift in...

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Wang N, Jin H, Zhuang G, et al. Breakdown assisted by a novel electron drift injection in the J-TEXT tokamak. Rev Sci Instrum. 2014;85(7):073505doi: 10.1063/1.4890287.
Wang, N., Jin, H., Zhuang, G., Ding, Y., Pan, Y., Cen, Y., Chen, Z., Huang, H., Liu, D., Rao, B., Zhang, M., & Zou, B. (2014). Breakdown assisted by a novel electron drift injection in the J-TEXT tokamak. The Review of scientific instruments, 85(7), 073505. https://doi.org/10.1063/1.4890287
Wang, Nengchao, et al. "Breakdown assisted by a novel electron drift injection in the J-TEXT tokamak." The Review of scientific instruments vol. 85,7 (2014): 073505. doi: https://doi.org/10.1063/1.4890287
Wang N, Jin H, Zhuang G, Ding Y, Pan Y, Cen Y, Chen Z, Huang H, Liu D, Rao B, Zhang M, Zou B. Breakdown assisted by a novel electron drift injection in the J-TEXT tokamak. Rev Sci Instrum. 2014 Jul;85(7):073505. doi: 10.1063/1.4890287. PMID: 25085138.
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Simultaneous Imaging of Endogenous Survivin mRNA and On-Demand Drug Release in Live Cells by Using a Mesoporous Silica Nanoquencher.

Small (Weinheim an der Bergstrasse, Germany)

Yuan P, Mao X, Chong KC, Fu J, Pan S, Wu S, Yu C, Yao SQ.
PMID: 28544466
Small. 2017 Jul;13(27). doi: 10.1002/smll.201700569. Epub 2017 May 24.

The design of multifunctional drug delivery systems capable of simultaneous target detection, imaging, and therapeutics in live mammalian cells is critical for biomedical research. In this study, by using mesoporous silica nanoparticles (MSNs) chemically modified with a small-molecule dark...

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Yuan P, Mao X, Chong KC, et al. Simultaneous Imaging of Endogenous Survivin mRNA and On-Demand Drug Release in Live Cells by Using a Mesoporous Silica Nanoquencher. Small. 2017;13(27)doi: 10.1002/smll.201700569.
Yuan, P., Mao, X., Chong, K. C., Fu, J., Pan, S., Wu, S., Yu, C., & Yao, S. Q. (2017). Simultaneous Imaging of Endogenous Survivin mRNA and On-Demand Drug Release in Live Cells by Using a Mesoporous Silica Nanoquencher. Small (Weinheim an der Bergstrasse, Germany), 13(27), . https://doi.org/10.1002/smll.201700569
Yuan, Peiyan, et al. "Simultaneous Imaging of Endogenous Survivin mRNA and On-Demand Drug Release in Live Cells by Using a Mesoporous Silica Nanoquencher." Small (Weinheim an der Bergstrasse, Germany) vol. 13,27 (2017). doi: https://doi.org/10.1002/smll.201700569
Yuan P, Mao X, Chong KC, Fu J, Pan S, Wu S, Yu C, Yao SQ. Simultaneous Imaging of Endogenous Survivin mRNA and On-Demand Drug Release in Live Cells by Using a Mesoporous Silica Nanoquencher. Small. 2017 Jul;13(27). doi: 10.1002/smll.201700569. Epub 2017 May 24. PMID: 28544466.
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Pairwise H.

Journal of the American Chemical Society

Manz DH, Duan PC, Dechert S, Demeshko S, Oswald R, John M, Mata RA, Meyer F.
PMID: 29037034
J Am Chem Soc. 2017 Nov 22;139(46):16720-16731. doi: 10.1021/jacs.7b08629. Epub 2017 Nov 07.

A compartmental ligand scaffold HL with two β-diketiminato binding sites spanned by a pyrazolate bridge gave a series of dinuclear nickel(II) dihydride complexes M[LNi

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Manz DH, Duan PC, Dechert S, et al. Pairwise H. J Am Chem Soc. 2017;139(46):16720-16731doi: 10.1021/jacs.7b08629.
Manz, D. H., Duan, P. C., Dechert, S., Demeshko, S., Oswald, R., John, M., Mata, R. A., & Meyer, F. (2017). Pairwise H. Journal of the American Chemical Society, 139(46), 16720-16731. https://doi.org/10.1021/jacs.7b08629
Manz, Dennis-Helmut, et al. "Pairwise H." Journal of the American Chemical Society vol. 139,46 (2017): 16720-16731. doi: https://doi.org/10.1021/jacs.7b08629
Manz DH, Duan PC, Dechert S, Demeshko S, Oswald R, John M, Mata RA, Meyer F. Pairwise H. J Am Chem Soc. 2017 Nov 22;139(46):16720-16731. doi: 10.1021/jacs.7b08629. Epub 2017 Nov 07. PMID: 29037034.
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Research on ultra-fast vacuum mechanical switch driven by repulsive force actuator.

The Review of scientific instruments

Yuan Z, He J, Pan Y, Jing X, Zhong C, Zhang N, Wei X, Tang G.
PMID: 28040972
Rev Sci Instrum. 2016 Dec;87(12):125103. doi: 10.1063/1.4968578.

In order to meet the fast operation demands of DC circuit breakers, a high-speed vacuum mechanical switch (VMS) driven by a repulsive force actuator is focused. To improve the drive speed and energy conversion efficiency (ECE) of the actuators,...

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Yuan Z, He J, Pan Y, et al. Research on ultra-fast vacuum mechanical switch driven by repulsive force actuator. Rev Sci Instrum. 2016;87(12):125103doi: 10.1063/1.4968578.
Yuan, Z., He, J., Pan, Y., Jing, X., Zhong, C., Zhang, N., Wei, X., & Tang, G. (2016). Research on ultra-fast vacuum mechanical switch driven by repulsive force actuator. The Review of scientific instruments, 87(12), 125103. https://doi.org/10.1063/1.4968578
Yuan, Zhao, et al. "Research on ultra-fast vacuum mechanical switch driven by repulsive force actuator." The Review of scientific instruments vol. 87,12 (2016): 125103. doi: https://doi.org/10.1063/1.4968578
Yuan Z, He J, Pan Y, Jing X, Zhong C, Zhang N, Wei X, Tang G. Research on ultra-fast vacuum mechanical switch driven by repulsive force actuator. Rev Sci Instrum. 2016 Dec;87(12):125103. doi: 10.1063/1.4968578. PMID: 28040972.
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Geometric factors affecting capillary discharge jet length in atmospheric pressure air.

The Review of scientific instruments

Li L, Xiong J, Cheng Y, Peng M, Pan Y.
PMID: 28668013
Rev Sci Instrum. 2017 Jun;88(6):065109. doi: 10.1063/1.4983842.

The capillary discharge triggered by a pulse source can produce a certain length of plasma jet. In this paper, the physical process of the capillary discharge jet is analyzed, and it is pointed out that the capillary plasma-jet length...

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Li L, Xiong J, Cheng Y, et al. Geometric factors affecting capillary discharge jet length in atmospheric pressure air. Rev Sci Instrum. 2017;88(6):065109doi: 10.1063/1.4983842.
Li, L., Xiong, J., Cheng, Y., Peng, M., & Pan, Y. (2017). Geometric factors affecting capillary discharge jet length in atmospheric pressure air. The Review of scientific instruments, 88(6), 065109. https://doi.org/10.1063/1.4983842
Li, Lee, et al. "Geometric factors affecting capillary discharge jet length in atmospheric pressure air." The Review of scientific instruments vol. 88,6 (2017): 065109. doi: https://doi.org/10.1063/1.4983842
Li L, Xiong J, Cheng Y, Peng M, Pan Y. Geometric factors affecting capillary discharge jet length in atmospheric pressure air. Rev Sci Instrum. 2017 Jun;88(6):065109. doi: 10.1063/1.4983842. PMID: 28668013.
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Zanos et al. reply.

Nature

Zanos P, Moaddel R, Morris PJ, Georgiou P, Fischell J, Elmer GI, Alkondon M, Yuan P, Pribut HJ, Singh NS, Dossou KSS, Fang Y, Huang XP, Mayo CL, Albuquerque EX, Thompson SM, Thomas CJ, Zarate CA, Gould TD.
PMID: 28640272
Nature. 2017 Jun 21;546(7659):E4-E5. doi: 10.1038/nature22085.

No abstract available.

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Zanos P, Moaddel R, Morris PJ, et al. Zanos et al. reply. Nature. 2017;546(7659):E4-E5doi: 10.1038/nature22085.
Zanos, P., Moaddel, R., Morris, P. J., Georgiou, P., Fischell, J., Elmer, G. I., Alkondon, M., Yuan, P., Pribut, H. J., Singh, N. S., Dossou, K. S. S., Fang, Y., Huang, X. P., Mayo, C. L., Albuquerque, E. X., Thompson, S. M., Thomas, C. J., Zarate, C. A., & Gould, T. D. (2017). Zanos et al. reply. Nature, 546(7659), E4-E5. https://doi.org/10.1038/nature22085
Zanos, Panos, et al. "Zanos et al. reply." Nature vol. 546,7659 (2017): E4-E5. doi: https://doi.org/10.1038/nature22085
Zanos P, Moaddel R, Morris PJ, Georgiou P, Fischell J, Elmer GI, Alkondon M, Yuan P, Pribut HJ, Singh NS, Dossou KSS, Fang Y, Huang XP, Mayo CL, Albuquerque EX, Thompson SM, Thomas CJ, Zarate CA, Gould TD. Zanos et al. reply. Nature. 2017 Jun 21;546(7659):E4-E5. doi: 10.1038/nature22085. PMID: 28640272; PMCID: PMC5638119.
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Expansion of CD14(+)CD16(+) monocytes is related to acute leukemia.

International journal of clinical and experimental medicine

Jiang XQ, Zhang L, Liu HA, Yuan N, Hou PQ, Zhang RQ, Wu T.
PMID: 26550139
Int J Clin Exp Med. 2015 Aug 15;8(8):12297-306. eCollection 2015.

OBJECTIVE: Aim to investigate the proportion of CD14(+)CD16(+) monocytes and understand the pathogenesis of this monocyte subset in acute leukemia.METHODS: Flow cytometry was utilized to study the phenotype expression of CD14(+)CD16(+) monocytes and CD3(+) T lymphocytes in peripheral blood...

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Jiang XQ, Zhang L, Liu HA, et al. Expansion of CD14(+)CD16(+) monocytes is related to acute leukemia. Int J Clin Exp Med. 2015;8(8):12297-306
Jiang, X. Q., Zhang, L., Liu, H. A., Yuan, N., Hou, P. Q., Zhang, R. Q., & Wu, T. (2015). Expansion of CD14(+)CD16(+) monocytes is related to acute leukemia. International journal of clinical and experimental medicine, 8(8), 12297-306.
Jiang, Xin-Quan, et al. "Expansion of CD14(+)CD16(+) monocytes is related to acute leukemia." International journal of clinical and experimental medicine vol. 8,8 (2015): 12297-306.
Jiang XQ, Zhang L, Liu HA, Yuan N, Hou PQ, Zhang RQ, Wu T. Expansion of CD14(+)CD16(+) monocytes is related to acute leukemia. Int J Clin Exp Med. 2015 Aug 15;8(8):12297-306. eCollection 2015. PMID: 26550139; PMCID: PMC4612824.
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A boron-centered radical: a potassium-crown ether stabilized boryl radical anion.

Chemical communications (Cambridge, England)

Yuan N, Wang W, Wu Z, Chen S, Tan G, Sui Y, Wang X, Jiang J, Power PP.
PMID: 27722270
Chem Commun (Camb). 2016 Oct 20;52(86):12714-12716. doi: 10.1039/c6cc06918e.

A boron radical contact ion-pair Mes

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Yuan N, Wang W, Wu Z, et al. A boron-centered radical: a potassium-crown ether stabilized boryl radical anion. Chem Commun (Camb). 2016;52(86):12714-12716doi: 10.1039/c6cc06918e.
Yuan, N., Wang, W., Wu, Z., Chen, S., Tan, G., Sui, Y., Wang, X., Jiang, J., & Power, P. P. (2016). A boron-centered radical: a potassium-crown ether stabilized boryl radical anion. Chemical communications (Cambridge, England), 52(86), 12714-12716. https://doi.org/10.1039/c6cc06918e
Yuan, Ningning, et al. "A boron-centered radical: a potassium-crown ether stabilized boryl radical anion." Chemical communications (Cambridge, England) vol. 52,86 (2016): 12714-12716. doi: https://doi.org/10.1039/c6cc06918e
Yuan N, Wang W, Wu Z, Chen S, Tan G, Sui Y, Wang X, Jiang J, Power PP. A boron-centered radical: a potassium-crown ether stabilized boryl radical anion. Chem Commun (Camb). 2016 Oct 20;52(86):12714-12716. doi: 10.1039/c6cc06918e. PMID: 27722270.
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T-lymphokine-activated killer cell-originated protein kinase (TOPK) as a prognostic factor and a potential therapeutic target in glioma.

Oncotarget

Quan C, Xiao J, Duan Q, Yuan P, Xue P, Lu H, Yan M, Guo D, Xu S, Zhang X, Lin X, Wang Y, Dogan S, Zhang J, Zhu F, Ke C, Liu L.
PMID: 29487691
Oncotarget. 2017 Dec 26;9(8):7782-7795. doi: 10.18632/oncotarget.23674. eCollection 2018 Jan 30.

TOPK is overexpressed in various types of cancer and associated with poor outcomes in different types of cancer. In this study, we first found that the expression of T-lymphokine-activated killer cell-originated protein kinase (TOPK) was significantly higher in Grade...

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Quan C, Xiao J, Duan Q, et al. T-lymphokine-activated killer cell-originated protein kinase (TOPK) as a prognostic factor and a potential therapeutic target in glioma. Oncotarget. 2017;9(8):7782-7795doi: 10.18632/oncotarget.23674.
Quan, C., Xiao, J., Duan, Q., Yuan, P., Xue, P., Lu, H., Yan, M., Guo, D., Xu, S., Zhang, X., Lin, X., Wang, Y., Dogan, S., Zhang, J., Zhu, F., Ke, C., & Liu, L. (2018). T-lymphokine-activated killer cell-originated protein kinase (TOPK) as a prognostic factor and a potential therapeutic target in glioma. Oncotarget, 9(8), 7782-7795. https://doi.org/10.18632/oncotarget.23674
Quan, Chuntao, et al. "T-lymphokine-activated killer cell-originated protein kinase (TOPK) as a prognostic factor and a potential therapeutic target in glioma." Oncotarget vol. 9,8 (2018): 7782-7795. doi: https://doi.org/10.18632/oncotarget.23674
Quan C, Xiao J, Duan Q, Yuan P, Xue P, Lu H, Yan M, Guo D, Xu S, Zhang X, Lin X, Wang Y, Dogan S, Zhang J, Zhu F, Ke C, Liu L. T-lymphokine-activated killer cell-originated protein kinase (TOPK) as a prognostic factor and a potential therapeutic target in glioma. Oncotarget. 2017 Dec 26;9(8):7782-7795. doi: 10.18632/oncotarget.23674. eCollection 2018 Jan 30. PMID: 29487691; PMCID: PMC5814258.
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Showing 1 to 12 of 985 entries