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Cemented versus Uncemented Oxford Unicompartmental Knee Arthroplasty: Is There a Difference?.

Advances in orthopedics

Akan B, Karaguven D, Guclu B, Yildirim T, Kaya A, Armangil M, Cetin I.
PMID: 24383006
Adv Orthop. 2013;2013:245915. doi: 10.1155/2013/245915. Epub 2013 Dec 09.

Purpose. The use of uncemented unicompartmental knee prostheses has recently increased. However, few studies on the outcomes of uncemented unicompartmental knee prostheses have been performed. The purpose of this study was to compare the outcomes of cemented and uncemented...

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Akan B, Karaguven D, Guclu B, et al. Cemented versus Uncemented Oxford Unicompartmental Knee Arthroplasty: Is There a Difference?. Adv Orthop. 2013;2013:245915doi: 10.1155/2013/245915.
Akan, B., Karaguven, D., Guclu, B., Yildirim, T., Kaya, A., Armangil, M., & Cetin, I. (2013). Cemented versus Uncemented Oxford Unicompartmental Knee Arthroplasty: Is There a Difference?. Advances in orthopedics, 2013245915. https://doi.org/10.1155/2013/245915
Akan, Burak, et al. "Cemented versus Uncemented Oxford Unicompartmental Knee Arthroplasty: Is There a Difference?." Advances in orthopedics vol. 2013 (2013): 245915. doi: https://doi.org/10.1155/2013/245915
Akan B, Karaguven D, Guclu B, Yildirim T, Kaya A, Armangil M, Cetin I. Cemented versus Uncemented Oxford Unicompartmental Knee Arthroplasty: Is There a Difference?. Adv Orthop. 2013;2013:245915. doi: 10.1155/2013/245915. Epub 2013 Dec 09. PMID: 24383006; PMCID: PMC3872020.
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Twisted Polycyclic Arenes from Tetranaphthyldiphenylbenzenes by Controlling the Scholl Reaction with Substituents.

Chemistry (Weinheim an der Bergstrasse, Germany)

Yang Y, Yuan L, Shan B, Liu Z, Miao Q.
PMID: 27709688
Chemistry. 2016 Dec 19;22(51):18620-18627. doi: 10.1002/chem.201604649. Epub 2016 Nov 09.

Herein, we report two new types of twisted polycyclic arenes (2 a, b and 3 a, b) with constitutionally isomeric π-backbones, which are synthesized by controlling the Scholl reaction of 1,2,4,5-tetra(naphth-2-yl)-3,6-diphenylbenzene (1) with properly positioned electron-donating substituents. With a...

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Yang Y, Yuan L, Shan B, et al. Twisted Polycyclic Arenes from Tetranaphthyldiphenylbenzenes by Controlling the Scholl Reaction with Substituents. Chemistry. 2016;22(51):18620-18627doi: 10.1002/chem.201604649.
Yang, Y., Yuan, L., Shan, B., Liu, Z., & Miao, Q. (2016). Twisted Polycyclic Arenes from Tetranaphthyldiphenylbenzenes by Controlling the Scholl Reaction with Substituents. Chemistry (Weinheim an der Bergstrasse, Germany), 22(51), 18620-18627. https://doi.org/10.1002/chem.201604649
Yang, Yong, et al. "Twisted Polycyclic Arenes from Tetranaphthyldiphenylbenzenes by Controlling the Scholl Reaction with Substituents." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,51 (2016): 18620-18627. doi: https://doi.org/10.1002/chem.201604649
Yang Y, Yuan L, Shan B, Liu Z, Miao Q. Twisted Polycyclic Arenes from Tetranaphthyldiphenylbenzenes by Controlling the Scholl Reaction with Substituents. Chemistry. 2016 Dec 19;22(51):18620-18627. doi: 10.1002/chem.201604649. Epub 2016 Nov 09. PMID: 27709688.
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Water Photo-oxidation Initiated by Surface-Bound Organic Chromophores.

Journal of the American Chemical Society

Eberhart MS, Wang D, Sampaio RN, Marquard SL, Shan B, Brennaman MK, Meyer GJ, Dares C, Meyer TJ.
PMID: 29023122
J Am Chem Soc. 2017 Nov 15;139(45):16248-16255. doi: 10.1021/jacs.7b08317. Epub 2017 Oct 31.

Organic chromophores can be synthesized by established methods and offer an opportunity to expand overall solar spectrum utilization for dye-sensitized photoelectrosynthesis cells. However, there are complications in the use of organic chromophores arising from the instability of their oxidized...

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Eberhart MS, Wang D, Sampaio RN, et al. Water Photo-oxidation Initiated by Surface-Bound Organic Chromophores. J Am Chem Soc. 2017;139(45):16248-16255doi: 10.1021/jacs.7b08317.
Eberhart, M. S., Wang, D., Sampaio, R. N., Marquard, S. L., Shan, B., Brennaman, M. K., Meyer, G. J., Dares, C., & Meyer, T. J. (2017). Water Photo-oxidation Initiated by Surface-Bound Organic Chromophores. Journal of the American Chemical Society, 139(45), 16248-16255. https://doi.org/10.1021/jacs.7b08317
Eberhart, Michael S, et al. "Water Photo-oxidation Initiated by Surface-Bound Organic Chromophores." Journal of the American Chemical Society vol. 139,45 (2017): 16248-16255. doi: https://doi.org/10.1021/jacs.7b08317
Eberhart MS, Wang D, Sampaio RN, Marquard SL, Shan B, Brennaman MK, Meyer GJ, Dares C, Meyer TJ. Water Photo-oxidation Initiated by Surface-Bound Organic Chromophores. J Am Chem Soc. 2017 Nov 15;139(45):16248-16255. doi: 10.1021/jacs.7b08317. Epub 2017 Oct 31. PMID: 29023122.
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Ultrathin CoO.

Physical chemistry chemical physics : PCCP

Du C, Wang J, Liu X, Yang J, Cao K, Wen Y, Chen R, Shan B.
PMID: 28530305
Phys Chem Chem Phys. 2017 May 31;19(21):14178-14184. doi: 10.1039/c7cp01588g.

Photoelectrochemical water splitting holds great potential for solar energy conversion and storage with zero greenhouse gas emission. Integration of a suitable co-catalyst with an absorber material enables the realization of highly efficient photocleavage of water. Herein, nanostructured hematite film...

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Du C, Wang J, Liu X, et al. Ultrathin CoO. Phys Chem Chem Phys. 2017;19(21):14178-14184doi: 10.1039/c7cp01588g.
Du, C., Wang, J., Liu, X., Yang, J., Cao, K., Wen, Y., Chen, R., & Shan, B. (2017). Ultrathin CoO. Physical chemistry chemical physics : PCCP, 19(21), 14178-14184. https://doi.org/10.1039/c7cp01588g
Du, Chun, et al. "Ultrathin CoO." Physical chemistry chemical physics : PCCP vol. 19,21 (2017): 14178-14184. doi: https://doi.org/10.1039/c7cp01588g
Du C, Wang J, Liu X, Yang J, Cao K, Wen Y, Chen R, Shan B. Ultrathin CoO. Phys Chem Chem Phys. 2017 May 31;19(21):14178-14184. doi: 10.1039/c7cp01588g. PMID: 28530305.
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Enhanced stability of black phosphorus field-effect transistors with SiO₂ passivation.

Nanotechnology

Wan B, Yang B, Wang Y, Zhang J, Zeng Z, Liu Z, Wang W.
PMID: 26436439
Nanotechnology. 2015 Oct 30;26(43):435702. doi: 10.1088/0957-4484/26/43/435702. Epub 2015 Oct 05.

Few-layer black phosphorus (BP) has attracted much attention due to its high mobility and suitable band gap for potential applic5ations in optoelectronics and flexible devices. However, its instability under ambient conditions limits its practical applications. Our investigations indicate that...

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Wan B, Yang B, Wang Y, et al. Enhanced stability of black phosphorus field-effect transistors with SiO₂ passivation. Nanotechnology. 2015;26(43):435702doi: 10.1088/0957-4484/26/43/435702.
Wan, B., Yang, B., Wang, Y., Zhang, J., Zeng, Z., Liu, Z., & Wang, W. (2015). Enhanced stability of black phosphorus field-effect transistors with SiO₂ passivation. Nanotechnology, 26(43), 435702. https://doi.org/10.1088/0957-4484/26/43/435702
Wan, Bensong, et al. "Enhanced stability of black phosphorus field-effect transistors with SiO₂ passivation." Nanotechnology vol. 26,43 (2015): 435702. doi: https://doi.org/10.1088/0957-4484/26/43/435702
Wan B, Yang B, Wang Y, Zhang J, Zeng Z, Liu Z, Wang W. Enhanced stability of black phosphorus field-effect transistors with SiO₂ passivation. Nanotechnology. 2015 Oct 30;26(43):435702. doi: 10.1088/0957-4484/26/43/435702. Epub 2015 Oct 05. PMID: 26436439.
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Distinct and Overlapping Requirements for Cyclins A, B, and B3 in .

G3 (Bethesda, Md.)

Bourouh M, Dhaliwal R, Rana K, Sinha S, Guo Z, Swan A.
PMID: 27652889
G3 (Bethesda). 2016 Nov 08;6(11):3711-3724. doi: 10.1534/g3.116.033050.

Meiosis, like mitosis, depends on the activity of the cyclin dependent kinase Cdk1 and its cyclin partners. Here, we examine the specific requirements for the three mitotic cyclins, A, B, and B3 in meiosis of

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Bourouh M, Dhaliwal R, Rana K, et al. Distinct and Overlapping Requirements for Cyclins A, B, and B3 in . G3 (Bethesda). 2016;6(11):3711-3724doi: 10.1534/g3.116.033050.
Bourouh, M., Dhaliwal, R., Rana, K., Sinha, S., Guo, Z., & Swan, A. (2016). Distinct and Overlapping Requirements for Cyclins A, B, and B3 in . G3 (Bethesda, Md.), 6(11), 3711-3724. https://doi.org/10.1534/g3.116.033050
Bourouh, Mohammed, et al. "Distinct and Overlapping Requirements for Cyclins A, B, and B3 in ." G3 (Bethesda, Md.) vol. 6,11 (2016): 3711-3724. doi: https://doi.org/10.1534/g3.116.033050
Bourouh M, Dhaliwal R, Rana K, Sinha S, Guo Z, Swan A. Distinct and Overlapping Requirements for Cyclins A, B, and B3 in . G3 (Bethesda). 2016 Nov 08;6(11):3711-3724. doi: 10.1534/g3.116.033050. PMID: 27652889; PMCID: PMC5100870.
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A Spiking Neural Network Model of the Lateral Geniculate Nucleus on the SpiNNaker Machine.

Frontiers in neuroscience

Sen-Bhattacharya B, Serrano-Gotarredona T, Balassa L, Bhattacharya A, Stokes AB, Rowley A, Sugiarto I, Furber S.
PMID: 28848380
Front Neurosci. 2017 Aug 09;11:454. doi: 10.3389/fnins.2017.00454. eCollection 2017.

We present a spiking neural network model of the thalamic Lateral Geniculate Nucleus (LGN) developed on SpiNNaker, which is a state-of-the-art digital neuromorphic hardware built with very-low-power ARM processors. The parallel, event-based data processing in SpiNNaker makes it viable...

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Sen-Bhattacharya B, Serrano-Gotarredona T, Balassa L, et al. A Spiking Neural Network Model of the Lateral Geniculate Nucleus on the SpiNNaker Machine. Front Neurosci. 2017;11:454doi: 10.3389/fnins.2017.00454.
Sen-Bhattacharya, B., Serrano-Gotarredona, T., Balassa, L., Bhattacharya, A., Stokes, A. B., Rowley, A., Sugiarto, I., & Furber, S. (2017). A Spiking Neural Network Model of the Lateral Geniculate Nucleus on the SpiNNaker Machine. Frontiers in neuroscience, 11454. https://doi.org/10.3389/fnins.2017.00454
Sen-Bhattacharya, Basabdatta, et al. "A Spiking Neural Network Model of the Lateral Geniculate Nucleus on the SpiNNaker Machine." Frontiers in neuroscience vol. 11 (2017): 454. doi: https://doi.org/10.3389/fnins.2017.00454
Sen-Bhattacharya B, Serrano-Gotarredona T, Balassa L, Bhattacharya A, Stokes AB, Rowley A, Sugiarto I, Furber S. A Spiking Neural Network Model of the Lateral Geniculate Nucleus on the SpiNNaker Machine. Front Neurosci. 2017 Aug 09;11:454. doi: 10.3389/fnins.2017.00454. eCollection 2017. PMID: 28848380; PMCID: PMC5552764.
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Digital network of writers helps to foster spirit of collaboration.

Nursing standard (Royal College of Nursing (Great Britain) : 1987)

Klimas J, Swan D, McCombe G, Henihan AM.
PMID: 26219803
Nurs Stand. 2015 Jul 29;29(48):30-1. doi: 10.7748/ns.29.48.30.s38.

No abstract available.

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Klimas J, Swan D, McCombe G, et al. Digital network of writers helps to foster spirit of collaboration. Nurs Stand. 2015;29(48):30-1doi: 10.7748/ns.29.48.30.s38.
Klimas, J., Swan, D., McCombe, G., & Henihan, A. M. (2015). Digital network of writers helps to foster spirit of collaboration. Nursing standard (Royal College of Nursing (Great Britain) : 1987), 29(48), 30-1. https://doi.org/10.7748/ns.29.48.30.s38
Klimas, J, et al. "Digital network of writers helps to foster spirit of collaboration." Nursing standard (Royal College of Nursing (Great Britain) : 1987) vol. 29,48 (2015): 30-1. doi: https://doi.org/10.7748/ns.29.48.30.s38
Klimas J, Swan D, McCombe G, Henihan AM. Digital network of writers helps to foster spirit of collaboration. Nurs Stand. 2015 Jul 29;29(48):30-1. doi: 10.7748/ns.29.48.30.s38. PMID: 26219803.
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Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.

Organic letters

Xin X, Wang H, Li X, Wang D, Wan B.
PMID: 26251020
Org Lett. 2015 Aug 21;17(16):3944-7. doi: 10.1021/acs.orglett.5b01474. Epub 2015 Aug 07.

A base-catalyzed selective cycloisomerization of 3-aza-1,5-enynes is developed. This transformation provides a facile access to highly functionalized 2-azabicyclo[3.2.0]hept-2-enes and sulfonyl vinyl-substituted pyrroles. The chemoselectivity was controlled by the substituent pattern of the substrates.

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Xin X, Wang H, Li X, et al. Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Org Lett. 2015;17(16):3944-7doi: 10.1021/acs.orglett.5b01474.
Xin, X., Wang, H., Li, X., Wang, D., & Wan, B. (2015). Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Organic letters, 17(16), 3944-7. https://doi.org/10.1021/acs.orglett.5b01474
Xin, Xiaoyi, et al. "Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes." Organic letters vol. 17,16 (2015): 3944-7. doi: https://doi.org/10.1021/acs.orglett.5b01474
Xin X, Wang H, Li X, Wang D, Wan B. Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes. Org Lett. 2015 Aug 21;17(16):3944-7. doi: 10.1021/acs.orglett.5b01474. Epub 2015 Aug 07. PMID: 26251020.
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Ruthenium-Catalyzed C-C Bond Cleavage of 2H-Azirines: A Formal [3+2+2] Cycloaddition to Fused Azepine Skeletons.

Angewandte Chemie (International ed. in English)

Li T, Xu F, Li X, Wang C, Wan B.
PMID: 26800151
Angew Chem Int Ed Engl. 2016 Feb 18;55(8):2861-5. doi: 10.1002/anie.201510820. Epub 2016 Jan 22.

2H-azirines can serve as three-atom synthons by C-C bond cleavage, however, it involves a high energy barrier under thermal conditions (>50.0 kcal mol(-1) ). Reported is a ruthenium-catalyzed [3+2+2] cycloaddition reaction of 2H-azirines with diynes, thus leading to the...

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Li T, Xu F, Li X, et al. Ruthenium-Catalyzed C-C Bond Cleavage of 2H-Azirines: A Formal [3+2+2] Cycloaddition to Fused Azepine Skeletons. Angew Chem Int Ed Engl. 2016;55(8):2861-5doi: 10.1002/anie.201510820.
Li, T., Xu, F., Li, X., Wang, C., & Wan, B. (2016). Ruthenium-Catalyzed C-C Bond Cleavage of 2H-Azirines: A Formal [3+2+2] Cycloaddition to Fused Azepine Skeletons. Angewandte Chemie (International ed. in English), 55(8), 2861-5. https://doi.org/10.1002/anie.201510820
Li, Tengfei, et al. "Ruthenium-Catalyzed C-C Bond Cleavage of 2H-Azirines: A Formal [3+2+2] Cycloaddition to Fused Azepine Skeletons." Angewandte Chemie (International ed. in English) vol. 55,8 (2016): 2861-5. doi: https://doi.org/10.1002/anie.201510820
Li T, Xu F, Li X, Wang C, Wan B. Ruthenium-Catalyzed C-C Bond Cleavage of 2H-Azirines: A Formal [3+2+2] Cycloaddition to Fused Azepine Skeletons. Angew Chem Int Ed Engl. 2016 Feb 18;55(8):2861-5. doi: 10.1002/anie.201510820. Epub 2016 Jan 22. PMID: 26800151.
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Hepatic adenomatosis in liver cirrhosis.

European journal of radiology open

Gordic S, Thung SN, Roayaie S, Wagner M, Taouli B.
PMID: 28932768
Eur J Radiol Open. 2017 Sep 09;4:115-117. doi: 10.1016/j.ejro.2017.08.001. eCollection 2017.

Hepatocellular adenoma (HCA) is a benign liver tumor most frequently occurring in women using oral contraception. HCA develops in normal or nearly normal livers and is extremely rare in cirrhosis. The authors present magnetic resonance imaging and histopathologic findings...

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Gordic S, Thung SN, Roayaie S, et al. Hepatic adenomatosis in liver cirrhosis. Eur J Radiol Open. 2017;4:115-117doi: 10.1016/j.ejro.2017.08.001.
Gordic, S., Thung, S. N., Roayaie, S., Wagner, M., & Taouli, B. (2017). Hepatic adenomatosis in liver cirrhosis. European journal of radiology open, 4115-117. https://doi.org/10.1016/j.ejro.2017.08.001
Gordic, Sonja, et al. "Hepatic adenomatosis in liver cirrhosis." European journal of radiology open vol. 4 (2017): 115-117. doi: https://doi.org/10.1016/j.ejro.2017.08.001
Gordic S, Thung SN, Roayaie S, Wagner M, Taouli B. Hepatic adenomatosis in liver cirrhosis. Eur J Radiol Open. 2017 Sep 09;4:115-117. doi: 10.1016/j.ejro.2017.08.001. eCollection 2017. PMID: 28932768; PMCID: PMC5597816.
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Using Chironomus dilutus to identify toxicants and evaluate the ecotoxicity of sediments in the Haihe River Basin.

Scientific reports

Zhu X, Shan B, Tang W, Zhang C.
PMID: 28469260
Sci Rep. 2017 May 03;7(1):1438. doi: 10.1038/s41598-017-01631-5.

To effectively manage a watershed and successfully restore a river system, it is very important to assess the toxicity of sediments and identify the substances causing the toxicity. Seventy-six sediments collected in the Haihe River Basin (HRB) in China...

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Zhu X, Shan B, Tang W, et al. Using Chironomus dilutus to identify toxicants and evaluate the ecotoxicity of sediments in the Haihe River Basin. Sci Rep. 2017;7(1):1438doi: 10.1038/s41598-017-01631-5.
Zhu, X., Shan, B., Tang, W., & Zhang, C. (2017). Using Chironomus dilutus to identify toxicants and evaluate the ecotoxicity of sediments in the Haihe River Basin. Scientific reports, 7(1), 1438. https://doi.org/10.1038/s41598-017-01631-5
Zhu, Xiaolei, et al. "Using Chironomus dilutus to identify toxicants and evaluate the ecotoxicity of sediments in the Haihe River Basin." Scientific reports vol. 7,1 (2017): 1438. doi: https://doi.org/10.1038/s41598-017-01631-5
Zhu X, Shan B, Tang W, Zhang C. Using Chironomus dilutus to identify toxicants and evaluate the ecotoxicity of sediments in the Haihe River Basin. Sci Rep. 2017 May 03;7(1):1438. doi: 10.1038/s41598-017-01631-5. PMID: 28469260; PMCID: PMC5431094.
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Showing 25 to 36 of 1177 entries