Institution
University of Tokyo
Education•Tokyo, Japan•
About: University of Tokyo is a education organization based out in Tokyo, Japan. It is known for research contribution in the topics: Population & Gene. The organization has 134564 authors who have published 337567 publications receiving 10178620 citations. The organization is also known as: Todai & Universitas Tociensis.
Topics: Population, Gene, Catalysis, Magnetic field, Galaxy
Papers published on a yearly basis
Papers
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TL;DR: Molecular substrates can be viewed as computational devices that process physical or chemical 'inputs' to generate 'outputs' based on a set of logical operators, which aid chemical (especially intracellular) sensing, small object recognition and intelligent diagnostics.
Abstract: Molecular substrates can be viewed as computational devices that process physical or chemical 'inputs' to generate 'outputs' based on a set of logical operators. By recognizing this conceptual crossover between chemistry and computation, it can be argued that the success of life itself is founded on a much longer-term revolution in information handling when compared with the modern semiconductor computing industry. Many of the simpler logic operations can be identified within chemical reactions and phenomena, as well as being produced in specifically designed systems. Some degree of integration can also be arranged, leading, in some instances, to arithmetic processing. These molecular logic systems can also lend themselves to convenient reconfiguring. Their clearest application area is in the life sciences, where their small size is a distinct advantage over conventional semiconductor counterparts. Molecular logic designs aid chemical (especially intracellular) sensing, small object recognition and intelligent diagnostics.
759 citations
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TL;DR: The onset of long-term potentiation, spine-volume growth and an increase in receptor trafficking are coincident, enabling a 'functional readout' of spine structure that links the age, size, strength and lifetime of a synapse.
759 citations
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TL;DR: In this article, it was shown that the factorization of disconnected Wilson loop amplitudes implies a major reduction in the dynamical degrees of freedom in the large-$N$ limit of lattice gauge theory; the original model may be replaced by a much simpler one.
Abstract: It is pointed out that the factorization of disconnected Wilson loop amplitudes implies a major reduction in the dynamical degrees of freedom in the large-$N$ limit of lattice gauge theory; the original model may be replaced by a much simpler one ($d$ is the space-time dimensionality), $Z=\ensuremath{\Pi}\stackrel{}{\ensuremath{\mu}}[\ensuremath{\int} d {U}_{\ensuremath{\mu}}\mathrm{exp}({\ensuremath{\beta}}_{\ensuremath{
u}\ensuremath{
e}}\ensuremath{\Sigma}\stackrel{d}{\ensuremath{\mu}\ensuremath{
e}\ensuremath{
u}=1}\mathrm{tr}{U}_{\ensuremath{\mu}}{U}_{v}{{U}_{\ensuremath{\mu}}}^{\ifmmode\dagger\else\textdagger\fi{}}{{U}_{\ensuremath{
u}}}^{\ifmmode\dagger\else\textdagger\fi{}})]$ Thus the field theory may be reduced to an integration over a finite number of matrices in large-$N$ limit.
757 citations
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TL;DR: The Event Horizon Telescope (EHT) as mentioned in this paper is a very long baseline interferometry (VLBI) array that comprises millimeter and submillimeter-wavelength telescopes separated by distances comparable to the diameter of the Earth.
Abstract: The Event Horizon Telescope (EHT) is a very long baseline interferometry (VLBI) array that comprises millimeter- and submillimeter-wavelength telescopes separated by distances comparable to the diameter of the Earth. At a nominal operating wavelength of ~1.3 mm, EHT angular resolution (λ/D) is ~25 μas, which is sufficient to resolve nearby supermassive black hole candidates on spatial and temporal scales that correspond to their event horizons. With this capability, the EHT scientific goals are to probe general relativistic effects in the strong-field regime and to study accretion and relativistic jet formation near the black hole boundary. In this Letter we describe the system design of the EHT, detail the technology and instrumentation that enable observations, and provide measures of its performance. Meeting the EHT science objectives has required several key developments that have facilitated the robust extension of the VLBI technique to EHT observing wavelengths and the production of instrumentation that can be deployed on a heterogeneous array of existing telescopes and facilities. To meet sensitivity requirements, high-bandwidth digital systems were developed that process data at rates of 64 gigabit s^(−1), exceeding those of currently operating cm-wavelength VLBI arrays by more than an order of magnitude. Associated improvements include the development of phasing systems at array facilities, new receiver installation at several sites, and the deployment of hydrogen maser frequency standards to ensure coherent data capture across the array. These efforts led to the coordination and execution of the first Global EHT observations in 2017 April, and to event-horizon-scale imaging of the supermassive black hole candidate in M87.
756 citations
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TL;DR: Trichostatin A and trapoxin are useful in analyzing the role of histone acetylation in chromatin structure and function as well as in determining the genes whose activities are regulated by histoneacetylation.
Abstract: Reversible acetylation at the epsilon-amino group of lysines located at the conserved domain of core histones is supposed to play an important role in the regulation of chromatin structure and its transcriptional activity. One promising strategy for analyzing the precise function of histone acetylation is to block the activities of acetylating or deacetylating enzymes by specific inhibitors. Recently, two microbial metabolites, trichostatin A and trapoxin, were found to be potent inhibitors of histone deacetylases. Trichostatin A reversibly inhibits the mammalian histone deacetylase, whereas trapoxin causes inhibition through irreversible binding to the enzyme. The histone deacetylase from a trichostatin A-resistant cell line is resistant to trichostatin A, indicating that the enzyme is the primary target. Both of the agents induce a variety of biological responses of cells such as induction of differentiation and cell cycle arrest. Trichostatin A and trapoxin are useful in analyzing the role of histone acetylation in chromatin structure and function as well as in determining the genes whose activities are regulated by histone acetylation.
756 citations
Authors
Showing all 135252 results
Name | H-index | Papers | Citations |
---|---|---|---|
Ronald C. Kessler | 274 | 1332 | 328983 |
Donald P. Schneider | 242 | 1622 | 263641 |
George M. Whitesides | 240 | 1739 | 269833 |
Jing Wang | 184 | 4046 | 202769 |
Tadamitsu Kishimoto | 181 | 1067 | 130860 |
Yusuke Nakamura | 179 | 2076 | 160313 |
Dennis J. Selkoe | 177 | 607 | 145825 |
David L. Kaplan | 177 | 1944 | 146082 |
D. M. Strom | 176 | 3167 | 194314 |
Masayuki Yamamoto | 171 | 1576 | 123028 |
Krzysztof Matyjaszewski | 169 | 1431 | 128585 |
Yang Yang | 164 | 2704 | 144071 |
Qiang Zhang | 161 | 1137 | 100950 |
Kenji Kangawa | 153 | 1117 | 110059 |
Takashi Taniguchi | 152 | 2141 | 110658 |