7 research outputs found
QCD and strongly coupled gauge theories : challenges and perspectives
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- Field of study
We highlight the progress, current status, and open challenges of QCD-driven physics, in theory and in experiment. We discuss how the strong interaction is intimately connected to a broad sweep of physical problems, in settings ranging from astrophysics and cosmology to strongly coupled, complex systems in particle and condensed-matter physics, as well as to searches for physics beyond the Standard Model. We also discuss how success in describing the strong interaction impacts other fields, and, in turn, how such subjects can impact studies of the strong interaction. In the course of the work we offer a perspective on the many research streams which flow into and out of QCD, as well as a vision for future developments.Peer reviewe
Comparative characteristics of biosynthesis of polyhydroxybutyrate from methanol by Methylobacteria extorquens G10 and Methyloligella halotolerans C2
- Author
- Publication venue
- 'Pleiades Publishing Ltd'
- Publication date
- Field of study
Genetic modification of Methylobacterium extorquens G10 producer strain of polyhydroxybutyrate
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- Publication venue
- 'Pleiades Publishing Ltd'
- Publication date
- Field of study
Liquid Crystalline Polymers as Tools for the Formation of Nanohybrids
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- A Garcia-Marquez
- A Kaiser
- A Mertelj
- A Taubert
- AA Ezhov
- D Dasgupta
- EB Barmatov
- F Brochard
- F Li
- GA Shandryuk
- HH Nguyen
- HM Song
- I Gascon
- JE Marshall
- JM Haberl
- JM Haberl
- JW Lee
- L Zadoina
- L Zadoina
- M Chambers
- NE Domracheva
- O Riou
- O Riou
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- S Saliba
- S Saliba
- S Saliba
- T Hegman
- V Domenici
- V Domenici
- VA Mallia
- VN Vasilets
- W Dobbs
- YQ Shi
- Publication venue
- Springer International Publishing
- Publication date
- 01/01/2015
- Field of study
International audienceThis chapter reviews the results obtained for the use of liquid crystalline polymers for the stabilization or the in situ synthesis of nanoparticles. It aims at giving the reader an insight into incorporating different types of nanoparticles, e.g. metallic or metal oxides, in various types of liquid crystalline polymers. In particular, this review highlights the importance of the nanoparticles-liquid crystalline polymers interaction in order to access new materials exhibiting synergetic properties. Of special interest is the case of liquid crystalline materials embedding magnetic or photoluminescent nanoparticles
Current advance in bioconversion of methanol to chemicals
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Queueing theory
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- M. F. Neuts
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- N. U. Prabhu
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- S. Sugawara
- S. V. Zhak
- S. Yu. Ruderman
- S. Yu. Ruderman
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- Sharda
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- Shunji Osaki
- Shunji Osaki
- Shunro Takamatsu
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- T. C. Kotiah
- T. G. Trushko
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- T. Lewis
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- Takeji Suzuki
- Takeji Suzuki
- Takeji Suzuki
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- Toitsu Watanabe
- Toji Makino
- Toji Makino
- Tokumasa Yottani
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- Toshio Nishida
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- V. Rudlovchak
- V. Rudlovchak
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- V. V. Konyukhovskii
- V. V. Naumchenko
- V. Vladimirov
- V. Ya. Rozenberg
- Van'an'
- W. A. Horn
- W. Bisi
- W. Fieger
- W. H. Pierce
- W. Henderson
- W. J. Gordon
- W. Lampkin
- W. P. Pierskalla
- W. R. Allen
- W. Schneeweiss
- W. Schneeweiss
- W. Voigt
- W. Whitt
- Wei Chang
- Wei Chang
- Wei Chang
- Y. K. Belyaev
- Ya. Ya. Sedol
- Ya. Ya. Sedol
- Ya. Ya. Sedol
- Yoshiro Tumura
- Yoshiro Tumura
- Yoshiro Tumura
- Yu. A. Vasil'ev
- Yu. A. Vasil'ev
- Yu. F. Yakushev
- Yu. K. Belyaev
- Yu. K. Belyaev
- Yu. K. Belyaev
- Yu. K. Belyaev
- Yu. K. Belyaev
- Yu. N. Shul'ga
- Yu. V. Gusev
- Yu. V. Gusev
- Yu. V. Gusev
- Yu. V. Prokhorov
- Yu. V. Prokhorov
- Z. S. Khalil'
- Zh. B. Linkovskii
- É. A. Danielyan
- É. G. Samandarov
- É. G. Samandarov
- É. G. Samandarov
- É. G. Samandarov
- É. G. Samandarov
- É. L. Presman
- É. L. Presman
- É. L. Presman
- É. M. Baskin
- É. M. Musaev
- É. Ya. Grinberg
- É. Ya. Grinberg
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1974
- Field of study
Evolocumab and clinical outcomes in patients with cardiovascular disease
- Author
- Abelson M
- Aboufakher R
- Abrahamsen Te
- Accini Mendoza Jl
- Acheatel R
- Ackermann D
- Adamkova V
- Adams M
- Adlam D
- Aggarwal R
- Aggarwal S
- Ahsan A
- Ainsworth P
- Airody Govinda R
- Akai A
- Ako J
- Al-Bahrani A
- Al-Joundi T
- Aldegather J
- Aldrete Velasco Ja
- Alfieri A
- Alt I
- Alzohaili O
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- Wöhrle J
- Xu P
- Xue L
- Yakhontova P
- Yamamoto K
- Yamashita K
- Yan J
- Yang E
- Yang P
- Yang X
- Yang Y
- Yang Z
- Yao Z
- Yasumura Y
- Yataco A
- Yeh H
- Yena L
- Yeoman G
- Yigit Z
- Yilmaz Mb
- Yokoya K
- Yoshimichi G
- Yotov Y
- Youngman D
- Younis L
- Yuge M
- Zabowka M
- Zahn L
- Zamorano Gomez Jl
- Zarich S
- Zateyshchikov D
- Zdrenghea D
- Zechowicz T
- Zeig S
- Zemanek J
- Zeng X
- Zhang L
- Zhang X
- Zhao S
- Zheng Y
- Zheng Z
- Zhou C
- Zhu Y
- Zhurba S
- Zidkova E
- Zieba B
- Ziegler O
- Zilahi Z
- Zrazhevskiy K
- Östergren J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets