Institution
École Polytechnique Fédérale de Lausanne
Facility•Lausanne, Switzerland•
About: École Polytechnique Fédérale de Lausanne is a facility organization based out in Lausanne, Switzerland. It is known for research contribution in the topics: Population & Catalysis. The organization has 44041 authors who have published 98296 publications receiving 4372092 citations. The organization is also known as: EPFL & ETHL.
Topics: Population, Catalysis, Computer science, Laser, Context (language use)
Papers published on a yearly basis
Papers
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TL;DR: In this paper, the authors review the underlying science and describes the technological advances in the field of solar thermochemical production of hydrogen that uses concentrated solar radiation as the energy source of high-temperature process heat.
1,170 citations
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TL;DR: Newly available surface observations from 1990 to the present, primarily from the Northern Hemisphere, show that the dimming at land surfaces did not persist into the 1990s, and instead, a widespread brightening has been observed since the late 1980s.
Abstract: Variations in solar radiation incident at Earth's surface profoundly affect the human and terrestrial environment. A decline in solar radiation at land surfaces has become apparent in many observational records up to 1990, a phenomenon known as global dimming. Newly available surface observations from 1990 to the present, primarily from the Northern Hemisphere, show that the dimming did not persist into the 1990s. Instead, a widespread brightening has been observed since the late 1980s. This reversal is reconcilable with changes in cloudiness and atmospheric transmission and may substantially affect surface climate, the hydrological cycle, glaciers, and ecosystems.
1,167 citations
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TL;DR: It is shown that in response to treatment of mice with interferon-α (IFNα), HSCs efficiently exit G0 and enter an active cell cycle, raising the possibility for new applications of type I interferons to target cancer stem cells.
Abstract: Maintenance of the blood system is dependent on dormant haematopoietic stem cells (HSCs) with long-term self-renewal capacity. After injury these cells are induced to proliferate to quickly re-establish homeostasis. The signalling molecules promoting the exit of HSCs out of the dormant stage remain largely unknown. Here we show that in response to treatment of mice with interferon-alpha (IFNalpha), HSCs efficiently exit G(0) and enter an active cell cycle. HSCs respond to IFNalpha treatment by the increased phosphorylation of STAT1 and PKB/Akt (also known as AKT1), the expression of IFNalpha target genes, and the upregulation of stem cell antigen-1 (Sca-1, also known as LY6A). HSCs lacking the IFNalpha/beta receptor (IFNAR), STAT1 (ref. 3) or Sca-1 (ref. 4) are insensitive to IFNalpha stimulation, demonstrating that STAT1 and Sca-1 mediate IFNalpha-induced HSC proliferation. Although dormant HSCs are resistant to the anti-proliferative chemotherapeutic agent 5-fluoro-uracil, HSCs pre-treated (primed) with IFNalpha and thus induced to proliferate are efficiently eliminated by 5-fluoro-uracil exposure in vivo. Conversely, HSCs chronically activated by IFNalpha are functionally compromised and are rapidly out-competed by non-activatable Ifnar(-/-) cells in competitive repopulation assays. Whereas chronic activation of the IFNalpha pathway in HSCs impairs their function, acute IFNalpha treatment promotes the proliferation of dormant HSCs in vivo. These data may help to clarify the so far unexplained clinical effects of IFNalpha on leukaemic cells, and raise the possibility for new applications of type I interferons to target cancer stem cells.
1,167 citations
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TL;DR: A ptychographic imaging method is demonstrated that bridges the gap between CDI and STXM by measuring complete diffraction patterns at each point of a STXM scan.
Abstract: Coherent diffractive imaging (CDI) and scanning transmission x-ray microscopy (STXM) are two popular microscopy techniques that have evolved quite independently. CDI promises to reach resolutions below 10 nanometers, but the reconstruction procedures put stringent requirements on data quality and sample preparation. In contrast, STXM features straightforward data analysis, but its resolution is limited by the spot size on the specimen. We demonstrate a ptychographic imaging method that bridges the gap between CDI and STXM by measuring complete diffraction patterns at each point of a STXM scan. The high penetration power of x-rays in combination with the high spatial resolution will allow investigation of a wide range of complex mesoscopic life and material science specimens, such as embedded semiconductor devices or cellular networks.
1,164 citations
Authors
Showing all 44420 results
Name | H-index | Papers | Citations |
---|---|---|---|
Michael Grätzel | 248 | 1423 | 303599 |
Ruedi Aebersold | 182 | 879 | 141881 |
Eliezer Masliah | 170 | 982 | 127818 |
Richard H. Friend | 169 | 1182 | 140032 |
G. A. Cowan | 159 | 2353 | 172594 |
Ian A. Wilson | 158 | 971 | 98221 |
Johan Auwerx | 158 | 653 | 95779 |
Menachem Elimelech | 157 | 547 | 95285 |
A. Artamonov | 150 | 1858 | 119791 |
Melody A. Swartz | 148 | 1304 | 103753 |
Henry J. Snaith | 146 | 511 | 123155 |
Kurt Wüthrich | 143 | 739 | 103253 |
Richard S. J. Frackowiak | 142 | 309 | 100726 |
Jean-Paul Kneib | 138 | 805 | 89287 |
Kevin J. Tracey | 138 | 561 | 82791 |