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Genetic relatedness of the novel human group C betacoronavirus to Tylonycteris bat coronavirus HKU4 and Pipistrellus bat coronavirus HKU5.

Emerging microbes & infections

Woo PC, Lau SK, Li KS, Tsang AK, Yuen KY.
PMID: 26038405
Emerg Microbes Infect. 2012 Nov;1(11):e35. doi: 10.1038/emi.2012.45. Epub 2012 Nov 07.

The recent outbreak of severe respiratory infections associated with a novel group C betacoronavirus (HCoV-EMC) from Saudi Arabia has drawn global attention to another highly probable "SARS-like" animal-to-human interspecies jumping event in coronavirus (CoV). The genome of HCoV-EMC is...

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Woo PC, Lau SK, Li KS, et al. Genetic relatedness of the novel human group C betacoronavirus to Tylonycteris bat coronavirus HKU4 and Pipistrellus bat coronavirus HKU5. Emerg Microbes Infect. 2012;1(11):e35doi: 10.1038/emi.2012.45.
Woo, P. C., Lau, S. K., Li, K. S., Tsang, A. K., & Yuen, K. Y. (2012). Genetic relatedness of the novel human group C betacoronavirus to Tylonycteris bat coronavirus HKU4 and Pipistrellus bat coronavirus HKU5. Emerging microbes & infections, 1(11), e35. https://doi.org/10.1038/emi.2012.45
Woo, Patrick Cy, et al. "Genetic relatedness of the novel human group C betacoronavirus to Tylonycteris bat coronavirus HKU4 and Pipistrellus bat coronavirus HKU5." Emerging microbes & infections vol. 1,11 (2012): e35. doi: https://doi.org/10.1038/emi.2012.45
Woo PC, Lau SK, Li KS, Tsang AK, Yuen KY. Genetic relatedness of the novel human group C betacoronavirus to Tylonycteris bat coronavirus HKU4 and Pipistrellus bat coronavirus HKU5. Emerg Microbes Infect. 2012 Nov;1(11):e35. doi: 10.1038/emi.2012.45. Epub 2012 Nov 07. PMID: 26038405; PMCID: PMC3630921.
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Optimization of self-catalyzed InAs Nanowires on flexible graphite for photovoltaic infrared photodetectors.

Scientific reports

Anyebe EA, Sandall I, Jin ZM, Sanchez AM, Rajpalke MK, Veal TD, Cao YC, Li HD, Harvey R, Zhuang QD.
PMID: 28393845
Sci Rep. 2017 Apr 10;7:46110. doi: 10.1038/srep46110.

The recent discovery of flexible graphene monolayers has triggered extensive research interest for the development of III-V/graphene functional hybrid heterostructures. In order to fully exploit their enormous potential in device applications, it is essential to optimize epitaxial growth for...

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Anyebe EA, Sandall I, Jin ZM, et al. Optimization of self-catalyzed InAs Nanowires on flexible graphite for photovoltaic infrared photodetectors. Sci Rep. 2017;7:46110doi: 10.1038/srep46110.
Anyebe, E. A., Sandall, I., Jin, Z. M., Sanchez, A. M., Rajpalke, M. K., Veal, T. D., Cao, Y. C., Li, H. D., Harvey, R., & Zhuang, Q. D. (2017). Optimization of self-catalyzed InAs Nanowires on flexible graphite for photovoltaic infrared photodetectors. Scientific reports, 746110. https://doi.org/10.1038/srep46110
Anyebe, Ezekiel A, et al. "Optimization of self-catalyzed InAs Nanowires on flexible graphite for photovoltaic infrared photodetectors." Scientific reports vol. 7 (2017): 46110. doi: https://doi.org/10.1038/srep46110
Anyebe EA, Sandall I, Jin ZM, Sanchez AM, Rajpalke MK, Veal TD, Cao YC, Li HD, Harvey R, Zhuang QD. Optimization of self-catalyzed InAs Nanowires on flexible graphite for photovoltaic infrared photodetectors. Sci Rep. 2017 Apr 10;7:46110. doi: 10.1038/srep46110. PMID: 28393845; PMCID: PMC5385536.
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Mitral valve repair.

Annals of cardiothoracic surgery

Woo YJ.
PMID: 26309822
Ann Cardiothorac Surg. 2015 May;4(3):219. doi: 10.3978/j.issn.2225-319X.2015.05.04.

No abstract available.

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Woo YJ. Mitral valve repair. Ann Cardiothorac Surg. 2015;4(3):219doi: 10.3978/j.issn.2225-319X.2015.05.04.
Woo, Y. J. (2015). Mitral valve repair. Annals of cardiothoracic surgery, 4(3), 219. https://doi.org/10.3978/j.issn.2225-319X.2015.05.04
Woo, Y Joseph. "Mitral valve repair." Annals of cardiothoracic surgery vol. 4,3 (2015): 219. doi: https://doi.org/10.3978/j.issn.2225-319X.2015.05.04
Woo YJ. Mitral valve repair. Ann Cardiothorac Surg. 2015 May;4(3):219. doi: 10.3978/j.issn.2225-319X.2015.05.04. PMID: 26309822; PMCID: PMC4533074.
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Corrigendum to "SPOP promotes SIRT2 degradation and suppresses non-small cell lung cancer cell growth" [Biochem. Biophys. Res. Commun. 483 (2017) 880-884].

Biochemical and biophysical research communications

Luo J, Bao YC, Ji XX, Chen B, Deng QF, Zhou SW.
PMID: 28292429
Biochem Biophys Res Commun. 2017 Apr 22;486(1):57. doi: 10.1016/j.bbrc.2017.02.122. Epub 2017 Mar 11.

No abstract available.

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Luo J, Bao YC, Ji XX, et al. Corrigendum to "SPOP promotes SIRT2 degradation and suppresses non-small cell lung cancer cell growth" [Biochem. Biophys. Res. Commun. 483 (2017) 880-884]. Biochem Biophys Res Commun. 2017;486(1):57doi: 10.1016/j.bbrc.2017.02.122.
Luo, J., Bao, Y. C., Ji, X. X., Chen, B., Deng, Q. F., & Zhou, S. W. (2017). Corrigendum to "SPOP promotes SIRT2 degradation and suppresses non-small cell lung cancer cell growth" [Biochem. Biophys. Res. Commun. 483 (2017) 880-884]. Biochemical and biophysical research communications, 486(1), 57. https://doi.org/10.1016/j.bbrc.2017.02.122
Luo, Jie, et al. "Corrigendum to "SPOP promotes SIRT2 degradation and suppresses non-small cell lung cancer cell growth" [Biochem. Biophys. Res. Commun. 483 (2017) 880-884]." Biochemical and biophysical research communications vol. 486,1 (2017): 57. doi: https://doi.org/10.1016/j.bbrc.2017.02.122
Luo J, Bao YC, Ji XX, Chen B, Deng QF, Zhou SW. Corrigendum to "SPOP promotes SIRT2 degradation and suppresses non-small cell lung cancer cell growth" [Biochem. Biophys. Res. Commun. 483 (2017) 880-884]. Biochem Biophys Res Commun. 2017 Apr 22;486(1):57. doi: 10.1016/j.bbrc.2017.02.122. Epub 2017 Mar 11. PMID: 28292429.
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Resistance patterns of multidrug resistant Acinetobacter baumannii in an ICU of a tertiary care hospital, Malaysia.

Pakistan journal of medical sciences

Janahiraman S, Aziz MN, Hoo FK, P'ng HS, Boo YL, Ramachandran V, Shamsuddin AF.
PMID: 26870101
Pak J Med Sci. 2015 Nov-Dec;31(6):1383-8. doi: 10.12669/pjms.316.8445.

BACKGROUNDS & OBJECTIVE: Antimicrobial resistance is a major health problem worldwide in hospitals. The main contributing factors are exposures to broad-spectrum antimicrobials and cross-infections. Understanding the extent and type of antimicrobial use in tertiary care hospitals will aid in...

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Janahiraman S, Aziz MN, Hoo FK, et al. Resistance patterns of multidrug resistant Acinetobacter baumannii in an ICU of a tertiary care hospital, Malaysia. Pak J Med Sci. 2015;31(6):1383-8doi: 10.12669/pjms.316.8445.
Janahiraman, S., Aziz, M. N., Hoo, F. K., P'ng, H. S., Boo, Y. L., Ramachandran, V., & Shamsuddin, A. F. (2015). Resistance patterns of multidrug resistant Acinetobacter baumannii in an ICU of a tertiary care hospital, Malaysia. Pakistan journal of medical sciences, 31(6), 1383-8. https://doi.org/10.12669/pjms.316.8445
Janahiraman, Sivakami, et al. "Resistance patterns of multidrug resistant Acinetobacter baumannii in an ICU of a tertiary care hospital, Malaysia." Pakistan journal of medical sciences vol. 31,6 (2015): 1383-8. doi: https://doi.org/10.12669/pjms.316.8445
Janahiraman S, Aziz MN, Hoo FK, P'ng HS, Boo YL, Ramachandran V, Shamsuddin AF. Resistance patterns of multidrug resistant Acinetobacter baumannii in an ICU of a tertiary care hospital, Malaysia. Pak J Med Sci. 2015 Nov-Dec;31(6):1383-8. doi: 10.12669/pjms.316.8445. PMID: 26870101; PMCID: PMC4744286.
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Ginsenoside Rg1 and 20(S)-Rg3 Induce IgA Production by Mouse B Cells.

Immune network

Park HY, Lee SH, Lee KS, Yoon HK, Yoo YC, Lee J, Choi JE, Kim PH, Park SR.
PMID: 26770188
Immune Netw. 2015 Dec;15(6):331-6. doi: 10.4110/in.2015.15.6.331. Epub 2015 Dec 24.

Ginsenosides are the major components of ginseng, which is known to modulate blood pressure, metabolism, and immune function, and has been used to treat various diseases. It has been reported that ginseng and several ginsenosides have immunoregulatory effects on...

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Park HY, Lee SH, Lee KS, et al. Ginsenoside Rg1 and 20(S)-Rg3 Induce IgA Production by Mouse B Cells. Immune Netw. 2015;15(6):331-6doi: 10.4110/in.2015.15.6.331.
Park, H. Y., Lee, S. H., Lee, K. S., Yoon, H. K., Yoo, Y. C., Lee, J., Choi, J. E., Kim, P. H., & Park, S. R. (2015). Ginsenoside Rg1 and 20(S)-Rg3 Induce IgA Production by Mouse B Cells. Immune network, 15(6), 331-6. https://doi.org/10.4110/in.2015.15.6.331
Park, Ha-Yan, et al. "Ginsenoside Rg1 and 20(S)-Rg3 Induce IgA Production by Mouse B Cells." Immune network vol. 15,6 (2015): 331-6. doi: https://doi.org/10.4110/in.2015.15.6.331
Park HY, Lee SH, Lee KS, Yoon HK, Yoo YC, Lee J, Choi JE, Kim PH, Park SR. Ginsenoside Rg1 and 20(S)-Rg3 Induce IgA Production by Mouse B Cells. Immune Netw. 2015 Dec;15(6):331-6. doi: 10.4110/in.2015.15.6.331. Epub 2015 Dec 24. PMID: 26770188; PMCID: PMC4700410.
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Quantification of intracellular payload release from polymersome nanoparticles.

Scientific reports

Scarpa E, Bailey JL, Janeczek AA, Stumpf PS, Johnston AH, Oreffo RO, Woo YL, Cheong YC, Evans ND, Newman TA.
PMID: 27404770
Sci Rep. 2016 Jul 11;6:29460. doi: 10.1038/srep29460.

Polymersome nanoparticles (PMs) are attractive candidates for spatio-temporal controlled delivery of therapeutic agents. Although many studies have addressed cellular uptake of solid nanoparticles, there is very little data available on intracellular release of molecules encapsulated in membranous carriers, such...

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Scarpa E, Bailey JL, Janeczek AA, et al. Quantification of intracellular payload release from polymersome nanoparticles. Sci Rep. 2016;6:29460doi: 10.1038/srep29460.
Scarpa, E., Bailey, J. L., Janeczek, A. A., Stumpf, P. S., Johnston, A. H., Oreffo, R. O., Woo, Y. L., Cheong, Y. C., Evans, N. D., & Newman, T. A. (2016). Quantification of intracellular payload release from polymersome nanoparticles. Scientific reports, 629460. https://doi.org/10.1038/srep29460
Scarpa, Edoardo, et al. "Quantification of intracellular payload release from polymersome nanoparticles." Scientific reports vol. 6 (2016): 29460. doi: https://doi.org/10.1038/srep29460
Scarpa E, Bailey JL, Janeczek AA, Stumpf PS, Johnston AH, Oreffo RO, Woo YL, Cheong YC, Evans ND, Newman TA. Quantification of intracellular payload release from polymersome nanoparticles. Sci Rep. 2016 Jul 11;6:29460. doi: 10.1038/srep29460. PMID: 27404770; PMCID: PMC4941396.
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Densely charged polyelectrolyte-stuffed nanochannel arrays for power generation from salinity gradient.

Scientific reports

Kwak SH, Kwon SR, Baek S, Lim SM, Joo YC, Chung TD.
PMID: 27194475
Sci Rep. 2016 May 19;6:26416. doi: 10.1038/srep26416.

We devised anodized aluminium oxide (AAO) frame-supported polyelectrolytic ion-exchange membranes for the application of electrical power generation systems where salinity differences are present. A series of polyelectrolytic AAO membranes (PAMs) were fabricated as a function of concentration of monomers...

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Kwak SH, Kwon SR, Baek S, et al. Densely charged polyelectrolyte-stuffed nanochannel arrays for power generation from salinity gradient. Sci Rep. 2016;6:26416doi: 10.1038/srep26416.
Kwak, S. H., Kwon, S. R., Baek, S., Lim, S. M., Joo, Y. C., & Chung, T. D. (2016). Densely charged polyelectrolyte-stuffed nanochannel arrays for power generation from salinity gradient. Scientific reports, 626416. https://doi.org/10.1038/srep26416
Kwak, Su Hong, et al. "Densely charged polyelectrolyte-stuffed nanochannel arrays for power generation from salinity gradient." Scientific reports vol. 6 (2016): 26416. doi: https://doi.org/10.1038/srep26416
Kwak SH, Kwon SR, Baek S, Lim SM, Joo YC, Chung TD. Densely charged polyelectrolyte-stuffed nanochannel arrays for power generation from salinity gradient. Sci Rep. 2016 May 19;6:26416. doi: 10.1038/srep26416. PMID: 27194475; PMCID: PMC4872233.
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Analysis of oxygen vacancy in Co-doped ZnO using the electron density distribution obtained using MEM.

Nanoscale research letters

Park JH, Lee YJ, Bae JS, Kim BS, Cho YC, Moriyoshi C, Kuroiwa Y, Lee S, Jeong SY.
PMID: 25977658
Nanoscale Res Lett. 2015 Apr 18;10:186. doi: 10.1186/s11671-015-0887-2. eCollection 2015.

Oxygen vacancy (VO) strongly affects the properties of oxides. In this study, we used X-ray diffraction (XRD) to study changes in the VO concentration as a function of the Co-doping level of ZnO. Rietveld refinement yielded a different result...

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Park JH, Lee YJ, Bae JS, et al. Analysis of oxygen vacancy in Co-doped ZnO using the electron density distribution obtained using MEM. Nanoscale Res Lett. 2015;10:186doi: 10.1186/s11671-015-0887-2.
Park, J. H., Lee, Y. J., Bae, J. S., Kim, B. S., Cho, Y. C., Moriyoshi, C., Kuroiwa, Y., Lee, S., & Jeong, S. Y. (2015). Analysis of oxygen vacancy in Co-doped ZnO using the electron density distribution obtained using MEM. Nanoscale research letters, 10186. https://doi.org/10.1186/s11671-015-0887-2
Park, Ji Hun, et al. "Analysis of oxygen vacancy in Co-doped ZnO using the electron density distribution obtained using MEM." Nanoscale research letters vol. 10 (2015): 186. doi: https://doi.org/10.1186/s11671-015-0887-2
Park JH, Lee YJ, Bae JS, Kim BS, Cho YC, Moriyoshi C, Kuroiwa Y, Lee S, Jeong SY. Analysis of oxygen vacancy in Co-doped ZnO using the electron density distribution obtained using MEM. Nanoscale Res Lett. 2015 Apr 18;10:186. doi: 10.1186/s11671-015-0887-2. eCollection 2015. PMID: 25977658; PMCID: PMC4414861.
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Metabolomic profiling of Burkholderia pseudomallei using UHPLC-ESI-Q-TOF-MS reveals specific biomarkers including 4-methyl-5-thiazoleethanol and unique thiamine degradation pathway.

Cell & bioscience

Lau SK, Lam CW, Curreem SO, Lee KC, Chow WN, Lau CC, Sridhar S, Wong SC, Martelli P, Hui SW, Yuen KY, Woo PC.
PMID: 26097677
Cell Biosci. 2015 Jun 02;5:26. doi: 10.1186/s13578-015-0018-x. eCollection 2015.

BACKGROUND: Burkholderia pseudomallei is an emerging pathogen that causes melioidosis, a serious and potentially fatal disease which requires prolonged antibiotics to prevent relapse. However, diagnosis of melioidosis can be difficult, especially in culture-negative cases. While metabolomics represents an uprising...

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Lau SK, Lam CW, Curreem SO, et al. Metabolomic profiling of Burkholderia pseudomallei using UHPLC-ESI-Q-TOF-MS reveals specific biomarkers including 4-methyl-5-thiazoleethanol and unique thiamine degradation pathway. Cell Biosci. 2015;5:26doi: 10.1186/s13578-015-0018-x.
Lau, S. K., Lam, C. W., Curreem, S. O., Lee, K. C., Chow, W. N., Lau, C. C., Sridhar, S., Wong, S. C., Martelli, P., Hui, S. W., Yuen, K. Y., & Woo, P. C. (2015). Metabolomic profiling of Burkholderia pseudomallei using UHPLC-ESI-Q-TOF-MS reveals specific biomarkers including 4-methyl-5-thiazoleethanol and unique thiamine degradation pathway. Cell & bioscience, 526. https://doi.org/10.1186/s13578-015-0018-x
Lau, Susanna K P, et al. "Metabolomic profiling of Burkholderia pseudomallei using UHPLC-ESI-Q-TOF-MS reveals specific biomarkers including 4-methyl-5-thiazoleethanol and unique thiamine degradation pathway." Cell & bioscience vol. 5 (2015): 26. doi: https://doi.org/10.1186/s13578-015-0018-x
Lau SK, Lam CW, Curreem SO, Lee KC, Chow WN, Lau CC, Sridhar S, Wong SC, Martelli P, Hui SW, Yuen KY, Woo PC. Metabolomic profiling of Burkholderia pseudomallei using UHPLC-ESI-Q-TOF-MS reveals specific biomarkers including 4-methyl-5-thiazoleethanol and unique thiamine degradation pathway. Cell Biosci. 2015 Jun 02;5:26. doi: 10.1186/s13578-015-0018-x. eCollection 2015. PMID: 26097677; PMCID: PMC4475313.
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Comparison between a center of mass and a foot pressure sensor system for measuring gait parameters in healthy adults.

Journal of physical therapy science

Park G, Woo Y.
PMID: 26644674
J Phys Ther Sci. 2015 Oct;27(10):3199-202. doi: 10.1589/jpts.27.3199. Epub 2015 Oct 30.

[Purpose] The purpose of this study was to determine the relationship between an accelerometer system and a foot pressure sensor system for measuring gait characteristics during walking in healthy adults. [Subjects and Methods] Thirty-five healthy participants with no neurological,...

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Park G, Woo Y. Comparison between a center of mass and a foot pressure sensor system for measuring gait parameters in healthy adults. J Phys Ther Sci. 2015;27(10):3199-202doi: 10.1589/jpts.27.3199.
Park, G., & Woo, Y. (2015). Comparison between a center of mass and a foot pressure sensor system for measuring gait parameters in healthy adults. Journal of physical therapy science, 27(10), 3199-202. https://doi.org/10.1589/jpts.27.3199
Park, Gunoh. "Comparison between a center of mass and a foot pressure sensor system for measuring gait parameters in healthy adults." Journal of physical therapy science vol. 27,10 (2015): 3199-202. doi: https://doi.org/10.1589/jpts.27.3199
Park G, Woo Y. Comparison between a center of mass and a foot pressure sensor system for measuring gait parameters in healthy adults. J Phys Ther Sci. 2015 Oct;27(10):3199-202. doi: 10.1589/jpts.27.3199. Epub 2015 Oct 30. PMID: 26644674; PMCID: PMC4668165.
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Comparative analysis of the activation of unfolded protein response by spike proteins of severe acute respiratory syndrome coronavirus and human coronavirus HKU1.

Cell & bioscience

Siu KL, Chan CP, Kok KH, Woo PC, Jin DY.
PMID: 24410900
Cell Biosci. 2014 Jan 13;4(1):3. doi: 10.1186/2045-3701-4-3.

BACKGROUND: Whereas severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) is associated with severe disease, human coronavirus HKU1 (HCoV-HKU1) commonly circulates in the human populations causing generally milder illness. Spike (S) protein of SARS-CoV activates the unfolded protein response (UPR)....

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Siu KL, Chan CP, Kok KH, et al. Comparative analysis of the activation of unfolded protein response by spike proteins of severe acute respiratory syndrome coronavirus and human coronavirus HKU1. Cell Biosci. 2014;4(1):3doi: 10.1186/2045-3701-4-3.
Siu, K. L., Chan, C. P., Kok, K. H., Woo, P. C., & Jin, D. Y. (2014). Comparative analysis of the activation of unfolded protein response by spike proteins of severe acute respiratory syndrome coronavirus and human coronavirus HKU1. Cell & bioscience, 4(1), 3. https://doi.org/10.1186/2045-3701-4-3
Siu, Kam-Leung, et al. "Comparative analysis of the activation of unfolded protein response by spike proteins of severe acute respiratory syndrome coronavirus and human coronavirus HKU1." Cell & bioscience vol. 4,1 (2014): 3. doi: https://doi.org/10.1186/2045-3701-4-3
Siu KL, Chan CP, Kok KH, Woo PC, Jin DY. Comparative analysis of the activation of unfolded protein response by spike proteins of severe acute respiratory syndrome coronavirus and human coronavirus HKU1. Cell Biosci. 2014 Jan 13;4(1):3. doi: 10.1186/2045-3701-4-3. PMID: 24410900; PMCID: PMC3930072.
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Showing 1 to 12 of 629 entries