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  • American Association for the Advancement of Science (AAAS)  (6)
  • Society of Economic Geologists (SEG)  (2)
  • Il Cigno Galileo Galilei
  • 1
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    Il Cigno Galileo Galilei
    In:  Professional Paper, Open-File Rept., Earthquake Prediction, Roma, Il Cigno Galileo Galilei, vol. 1, no. 2, pp. 317-332, (ISBN 0080419208)
    Publication Date: 1992
    Keywords: Earthquake precursor: prediction research ; Earthquake precursor: deformation or strain ; Earth tides ; Earthquake precursor: tilt ; JZSCHAU
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  • 2
    Publication Date: 2013-08-31
    Description: Invasion of microbial DNA into the cytoplasm of animal cells triggers a cascade of host immune reactions that help clear the infection; however, self DNA in the cytoplasm can cause autoimmune diseases. Biochemical approaches led to the identification of cyclic guanosine monophosphate-adenosine monophosphate (cGAMP) synthase (cGAS) as a cytosolic DNA sensor that triggers innate immune responses. Here, we show that cells from cGAS-deficient (cGas(-/-)) mice, including fibroblasts, macrophages, and dendritic cells, failed to produce type I interferons and other cytokines in response to DNA transfection or DNA virus infection. cGas(-/-) mice were more susceptible to lethal infection with herpes simplex virus 1 (HSV1) than wild-type mice. We also show that cGAMP is an adjuvant that boosts antigen-specific T cell activation and antibody production in mice.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863637/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863637/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, Xiao-Dong -- Wu, Jiaxi -- Gao, Daxing -- Wang, Hua -- Sun, Lijun -- Chen, Zhijian J -- 5T32AI070116/AI/NIAID NIH HHS/ -- AI-093967/AI/NIAID NIH HHS/ -- R01 AI093967/AI/NIAID NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2013 Sep 20;341(6152):1390-4. doi: 10.1126/science.1244040. Epub 2013 Aug 29.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23989956" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies, Viral/biosynthesis ; DNA, Viral/genetics/immunology ; Dendritic Cells/immunology ; Fibroblasts/immunology ; Herpes Simplex/*immunology ; *Herpesvirus 1, Human ; Interferon Regulatory Factor-3/genetics ; Interferon-beta/*biosynthesis/genetics ; Lymphocyte Activation ; Macrophages/immunology ; Mice ; Mice, Knockout ; Nucleotidyltransferases/genetics/*immunology ; Signal Transduction ; T-Lymphocytes/immunology ; Transfection
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-11-08
    Description: A recently assembled data set of inner core-sensitive free oscillation splitting measurements and body wave differential travel times provides constraints on the patterns of anisotropy in the Earth's inner core. Applying a formalism that allows departures from radial symmetry and cylindrical anisotropy results in models with P-wave velocity distributions whose strength and pattern are incompatible with frozen-in anisotropy, but rather suggest a simple large-scale convection regime in the inner core.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Romanowicz -- Li -- Durek -- New York, N.Y. -- Science. 1996 Nov 8;274(5289):963-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉B. Romanowicz, Seismographic Station and Department of Geology and Geophysics, University of California at Berkeley, Berkeley, CA 94720, USA. X.-D. Li and J. Durek, Seismographic Station, University of California at Berkeley, Berkeley, CA 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8875934" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2009-03-28
    Description: The spread of HIV between immune cells is greatly enhanced by cell-cell adhesions called virological synapses, although the underlying mechanisms have been unclear. With use of an infectious, fluorescent clone of HIV, we tracked the movement of Gag in live CD4 T cells and captured the direct translocation of HIV across the virological synapse. Quantitative, high-speed three-dimensional (3D) video microscopy revealed the rapid formation of micrometer-sized "buttons" containing oligomerized viral Gag protein. Electron microscopy showed that these buttons were packed with budding viral crescents. Viral transfer events were observed to form virus-laden internal compartments within target cells. Continuous time-lapse monitoring showed preferential infection through synapses. Thus, HIV dissemination may be enhanced by virological synapse-mediated cell adhesion coupled to viral endocytosis.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756521/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756521/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hubner, Wolfgang -- McNerney, Gregory P -- Chen, Ping -- Dale, Benjamin M -- Gordon, Ronald E -- Chuang, Frank Y S -- Li, Xiao-Dong -- Asmuth, David M -- Huser, Thomas -- Chen, Benjamin K -- 5R24 CA095823-04/CA/NCI NIH HHS/ -- AI074420-02/AI/NIAID NIH HHS/ -- DP1 DA028866/DA/NIDA NIH HHS/ -- R01 AI074420/AI/NIAID NIH HHS/ -- R01 AI074420-01A2/AI/NIAID NIH HHS/ -- R01 AI074420-02/AI/NIAID NIH HHS/ -- S10RR09145-01/RR/NCRR NIH HHS/ -- ULRR024146/PHS HHS/ -- New York, N.Y. -- Science. 2009 Mar 27;323(5922):1743-7. doi: 10.1126/science.1167525.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Infectious Diseases, Department of Medicine, Immunology Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19325119" target="_blank"〉PubMed〈/a〉
    Keywords: CD4-Positive T-Lymphocytes/*physiology/ultrastructure/*virology ; *Cell Adhesion ; Coculture Techniques ; Cytochalasin D/pharmacology ; Endocytosis ; HIV/*physiology/ultrastructure ; Humans ; Imaging, Three-Dimensional ; Jurkat Cells ; Microscopy, Confocal ; Microscopy, Electron, Transmission ; Microscopy, Video ; Receptors, CCR5/metabolism ; Receptors, CXCR4/metabolism ; Recombinant Fusion Proteins/metabolism ; *Virus Internalization ; gag Gene Products, Human Immunodeficiency Virus/*metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2014-12-20
    Description: Multivalent molecules with repetitive structures including bacterial capsular polysaccharides and viral capsids elicit antibody responses through B cell receptor (BCR) crosslinking in the absence of T cell help. We report that immunization with these T cell-independent type 2 (TI-2) antigens causes up-regulation of endogenous retrovirus (ERV) RNAs in antigen-specific mouse B cells. These RNAs are detected via a mitochondrial antiviral signaling protein (MAVS)-dependent RNA sensing pathway or reverse-transcribed and detected via the cGAS-cGAMP-STING pathway, triggering a second, sustained wave of signaling that promotes specific immunoglobulin M production. Deficiency of both MAVS and cGAS, or treatment of MAVS-deficient mice with reverse transcriptase inhibitors, dramatically inhibits TI-2 antibody responses. These findings suggest that ERV and two innate sensing pathways that detect them are integral components of the TI-2 B cell signaling apparatus.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391621/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391621/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zeng, Ming -- Hu, Zeping -- Shi, Xiaolei -- Li, Xiaohong -- Zhan, Xiaoming -- Li, Xiao-Dong -- Wang, Jianhui -- Choi, Jin Huk -- Wang, Kuan-wen -- Purrington, Tiana -- Tang, Miao -- Fina, Maggy -- DeBerardinis, Ralph J -- Moresco, Eva Marie Y -- Pedersen, Gabriel -- McInerney, Gerald M -- Karlsson Hedestam, Gunilla B -- Chen, Zhijian J -- Beutler, Bruce -- P01 AI070167/AI/NIAID NIH HHS/ -- R01 AI093967/AI/NIAID NIH HHS/ -- R01 CA157996/CA/NCI NIH HHS/ -- U19 AI100627/AI/NIAID NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2014 Dec 19;346(6216):1486-92. doi: 10.1126/science.346.6216.1486.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-8502, USA. ; Department of Pediatrics and Children's Medical Center Research Institute, and McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-8502, USA. ; Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-8502, USA. Howard Hughes Medical Institute, Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9148, USA. ; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Nobels vag 16, SE-171 77 Stockholm, Sweden. ; Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-8502, USA. Bruce.Beutler@UTSouthwestern.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25525240" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/genetics/*immunology ; Animals ; Antibody Formation ; Antigens, T-Independent/*immunology ; B-Lymphocytes/*immunology ; Cytosol/immunology ; DNA/immunology ; Endogenous Retroviruses/genetics/*immunology ; Lymphocyte Activation ; Membrane Proteins/immunology ; Mice ; Mice, Inbred C57BL ; NF-kappa B/metabolism ; Nucleotides, Cyclic/immunology ; Nucleotidyltransferases/genetics/*immunology ; RNA, Viral/genetics/*immunology ; Transcription, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2015-11-10
    Description: The Handan-Xingtai district in the North China craton is one of the most important concentrations of iron skarn deposits in China, with proven reserves of 900 to 1,000 Mt at an average of 40 to 55 wt % Fe. The iron mineralization occurs predominantly along contact zones between Early Cretaceous intermediate-silicic intrusions and Middle Ordovician marine carbonates intercalated with numerous evaporite beds. In this paper, we present textural features and laser ablation ICP-MS U-Pb dating results of hydrothermal zircon from five major iron skarn deposits to place tight constraints on the timing and duration of the district-scale iron mineralization. Zircon grains from the mineralized skarns are anhedral to subhedral crystals and euhedral tetragonal bipyramids. They are closely intergrown or texturally associated with diopside, garnet, epidote, calcite, albite, and phlogopite. Other common minerals in the skarn assemblages include F-rich hornblende, wilkeite-F, F-apatite, and fluorite. Zircon grains typically contain abundant inclusions of skarn minerals and daughter mineral-rich (mostly magnetite, halite, and sylvite) fluid inclusions. Compositionally, these zircon grains have moderately to extremely high Th (518–7,477 ppm) and U (109–25,610 ppm) contents, with highly variable Th/U ratios ranging from 0.01 to 5.23. The morphological, textural, and geochemical features of the zircons confirm their hydrothermal origin and indicate that they most likely precipitated from high-temperature, F-rich, magmatic-derived ore-forming fluids. The hydrothermal zircon grains yield well-defined concordant U-Pb ages for the five studied iron skarn deposits, with weighted mean 206 Pb/ 238 U dates ranging from 133.6 ± 0.9 to 128.5 ± 1.4 Ma (2 ). These ages are remarkably consistent with U-Pb ages (134.1 ± 1.2 to 128.5 ± 0.9 Ma; 2 ) of magmatic zircon grains from the ore-related intrusions in each deposit, demonstrating that iron skarn mineralization was genetically related to the coeval magmatism. Our new geochronological data, when combined with existing isotopic ages, indicate that iron mineralization and associated magmatism in the Handan-Xingtai district took place mainly at the ca. 137–133 and 131–128 Ma intervals. Iron skarn deposits of similar ages also occur widely in other parts of the eastern North China craton, forming the only known giant Mesozoic iron skarn province in a cratonic block on the Earth. The formation of these iron skarn deposits and associated intrusions coincided in time with lithospheric thinning or destruction of the North China craton, strongly suggesting a causal link between the two processes.
    Print ISSN: 0361-0128
    Topics: Geosciences
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  • 7
    Publication Date: 2019
    Description: 〈p〉Cancer cells often encounter oxidative stress. However, it is unclear whether normal and cancer cells differentially respond to oxidative stress. Here, we demonstrated that under oxidative stress, hepatocellular carcinoma (HCC) cells exhibit increased antioxidative response and survival rates compared to normal hepatocytes. Oxidative stimulation induces HCC-specifically expressed fructokinase A (KHK-A) phosphorylation at S80 by 5'-adenosine monophosphate-activated protein kinase. KHK-A in turn acts as a protein kinase to phosphorylate p62 at S28, thereby blocking p62 ubiquitination and enhancing p62’s aggregation with Keap1 and Nrf2 activation. Activated Nrf2 promotes expression of genes involved in reactive oxygen species reduction, cell survival, and HCC development in mice. In addition, phosphorylation of KHK-A S80 and p62 S28 and nuclear accumulation of Nrf2 are positively correlated in human HCC specimens and with poor prognosis of patients with HCC. These findings underscore the role of the protein kinase activity of KHK-A in antioxidative stress and HCC development.〈/p〉
    Electronic ISSN: 2375-2548
    Topics: Natural Sciences in General
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  • 8
    Publication Date: 2013-08-14
    Description: The Kangdian iron oxide copper-gold (IOCG) metallogenic province contains a number of economically important Fe-Cu deposits in South China and northern Vietnam. Due to the lack of precise mineralization ages, the metallogenesis of this province has long been a matter of debate. In this study, molybdenite Re-Os, pyrite Re-Os, and Rb-Sr isotope methods are used to date the Yinachang and E’touchang Fe-Cu deposits in the central part of this province. Fine-grained (〈0.1 mm) molybdenite occurs as veinlets along bandings or fractures of magnetite ores and hydrothermal veins in the Yinachang deposit. Molybdenite separates from magnetite ores have highly reproducible Re-Os model ages of 1654 ± 7 Ma, whereas those from hydrothermal veins have a much younger Re-Os model age of 1451 ± 6 Ma. Euhedral pyrite grains occur locally along foliations of hematite ores and their proximal alteration assemblages in the E’touchang deposit. Pyrite separates have an Re-Os isochron age of 1487 ± 110 Ma and a single-grain Rb-Sr isochron age of 1453 ± 28 Ma, both of which are compatible with the molybdenite Re-Os age of hydrothermal veins from the Yinachang deposit. The molybdenite age of magnetite ores is in good agreement with zircon U-Pb ages of dolerite intrusions in the region, and is considered to represent the timing of a major ore formation event at ~1655 Ma. The younger Re-Os and Rb-Sr ages likely record a secondary hydrothermal overprint event at ~1450 Ma, which has not been recognized before. The mineralization potential and implications of this event need to be investigated in future studies. Our new isotopic data set hence demonstrates that the Kangdian IOCG deposits were likely formed at ~1655 Ma, synchronous with the late Paleoproterozoic intracontinental rifting event of the western Yangtze block.
    Print ISSN: 0361-0128
    Topics: Geosciences
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  • 9
    Publication Date: 2019
    Description: 〈p〉How somatic mutations accumulate in normal cells is poorly understood. A comprehensive analysis of RNA sequencing data from ~6700 samples across 29 normal tissues revealed multiple somatic variants, demonstrating that macroscopic clones can be found in many normal tissues. We found that sun-exposed skin, esophagus, and lung have a higher mutation burden than other tested tissues, which suggests that environmental factors can promote somatic mosaicism. Mutation burden was associated with both age and tissue-specific cell proliferation rate, highlighting that mutations accumulate over both time and number of cell divisions. Finally, normal tissues were found to harbor mutations in known cancer genes and hotspots. This study provides a broad view of macroscopic clonal expansion in human tissues, thus serving as a foundation for associating clonal expansion with environmental factors, aging, and risk of disease.〈/p〉
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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