Institution
Tokyo Institute of Technology
Education•Tokyo, Tôkyô, Japan•
About: Tokyo Institute of Technology is a education organization based out in Tokyo, Tôkyô, Japan. It is known for research contribution in the topics: Thin film & Catalysis. The organization has 46775 authors who have published 101656 publications receiving 2357893 citations. The organization is also known as: Tokyo Tech & Tokodai.
Topics: Thin film, Catalysis, Polymerization, Laser, Phase (matter)
Papers published on a yearly basis
Papers
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TL;DR: This paper presents a short overview of the changes to the trigger and data acquisition systems during the first long shutdown of the LHC and shows the performance of the trigger system and its components based on the 2015 proton–proton collision data.
Abstract: During 2015 the ATLAS experiment recorded 3.8 fb(-1) of proton-proton collision data at a centre-of-mass energy of 13 TeV. The ATLAS trigger system is a crucial component of the experiment, respons ...
488 citations
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TL;DR: In this paper, a general formula is given that expresses frequency chirping in some types of external intensity modulators, such as the loss modulator, directional-coupler-type modulator and total-internal-reflection type modulator.
Abstract: A general formula is given that expresses frequency chirping in some types of external intensity modulators, such as the loss modulator, directional-coupler-type modulator, Mach-Zehnder interferometry-type modulator, and total-internal-reflection-type modulator. The chirping phenomenon treated is caused by the phase modulation due to an accompanied refractive index change. It is uniquely expressed in terms of an alpha -parameter that contributes to frequency chirping in the same manner as in the direct modulation of a semiconductor laser. In addition, the transmission bandwidth of a single-mode fiber system using an external modulator is discussed and compared with the results obtained utilizing direct laser modulation. >
487 citations
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TL;DR: The MAXI (Monitor of All-sky X-ray Image) mission is the first astronomical payload to be installed on the Japanese Experiment Module-Exposed Facility (JEM-EF) on the ISS as discussed by the authors.
Abstract: The MAXI (Monitor of All-sky X-ray Image) mission is the first astronomical payload to be installed on the Japanese Experiment Module-Exposed Facility (JEM-EF) on the ISS. It is scheduled for launch in the middle of 2009 to monitor all-sky X-ray objects on every ISS orbit. MAXI will be more powerful than any previous X-ray All Sky Monitor (ASM) payloads, being able to monitor hundreds of AGN. MAXI will provide all sky images of X-ray sources of about 20 mCrab in the energy band of 2-30 keV from observation on one ISS orbit (90 min), about 4.5 mCrab for one day, and about 1 mCrab for one month. A final detectability of MAXI could be 0.2 mCrab for 2 year observations.
486 citations
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TL;DR: The identification of two novel proteins, Atg39 and Atg40, as receptors specific to selective autophagy of the endoplasmic reticulum and nucleus in the yeast Saccharomyces cerevisiae provides fundamental insight into the pathophysiological roles and mechanisms of ‘ER-phagy’ and ‘nucleophagy” in other organisms.
Abstract: Macroautophagy (hereafter referred to as autophagy) degrades various intracellular constituents to regulate a wide range of cellular functions, and is also closely linked to several human diseases. In selective autophagy, receptor proteins recognize degradation targets and direct their sequestration by double-membrane vesicles called autophagosomes, which transport them into lysosomes or vacuoles. Although recent studies have shown that selective autophagy is involved in quality/quantity control of some organelles, including mitochondria and peroxisomes, it remains unclear how extensively it contributes to cellular organelle homeostasis. Here we describe selective autophagy of the endoplasmic reticulum (ER) and nucleus in the yeast Saccharomyces cerevisiae. We identify two novel proteins, Atg39 and Atg40, as receptors specific to these pathways. Atg39 localizes to the perinuclear ER (or the nuclear envelope) and induces autophagic sequestration of part of the nucleus. Atg40 is enriched in the cortical and cytoplasmic ER, and loads these ER subdomains into autophagosomes. Atg39-dependent autophagy of the perinuclear ER/nucleus is required for cell survival under nitrogen-deprivation conditions. Atg40 is probably the functional counterpart of FAM134B, an autophagy receptor for the ER in mammals that has been implicated in sensory neuropathy. Our results provide fundamental insight into the pathophysiological roles and mechanisms of 'ER-phagy' and 'nucleophagy' in other organisms.
486 citations
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TL;DR: It is shown from two examples that the successive identification method of a fuzzy model is very useful for modeling complex systems.
485 citations
Authors
Showing all 46967 results
Name | H-index | Papers | Citations |
---|---|---|---|
Matthew Meyerson | 194 | 553 | 243726 |
Yury Gogotsi | 171 | 956 | 144520 |
Masayuki Yamamoto | 171 | 1576 | 123028 |
H. Eugene Stanley | 154 | 1190 | 122321 |
Takashi Taniguchi | 152 | 2141 | 110658 |
Shu-Hong Yu | 144 | 799 | 70853 |
Kazunori Kataoka | 138 | 908 | 70412 |
Osamu Jinnouchi | 135 | 885 | 86104 |
Hector F. DeLuca | 133 | 1303 | 69395 |
Shlomo Havlin | 131 | 1013 | 83347 |
Hiroyuki Iwasaki | 131 | 1009 | 82739 |
Kazunari Domen | 130 | 908 | 77964 |
Hideo Hosono | 128 | 1549 | 100279 |
Hideyuki Okano | 128 | 1169 | 67148 |
Andreas Strasser | 128 | 509 | 66903 |