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    Mascons as structural relief on a lunar Moho

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    Mascons as structural relief on lunar Moh

    The role of SOX family members in solid tumours and metastasis

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    Cancer is a heavy burden for humans across the world with high morbidity and mortality. Transcription factors including sex determining region Y (SRY)-related high-mobility group (HMG) box (SOX) proteins are thought to be involved in the regulation of specific biological processes. The deregulation of gene expression programs can lead to cancer development. Here, we review the role of the SOX family in breast cancer, prostate cancer, renal cell carcinoma, thyroid cancer, brain tumours, gastrointestinal and lung tumours as well as the entailing therapeutic implications. The SOX family consists of more than 20 members that mediate DNA binding by the HMG domain and have regulatory functions in development, cell-fate decision, and differentiation. SOX2, SOX4, SOX5, SOX8, SOX9, and SOX18 are up-regulated in different cancer types and have been found to be associated with poor prognosis, while the up-regulation of SOX11 and SOX30 appears to be favourable for the outcome in other cancer types. SOX2, SOX4, SOX5 and other SOX members are involved in tumorigenesis, e.g. SOX2 is markedly up-regulated in chemotherapy resistant cells. The SoxF family (SOX7, SOX17, SOX18) plays an important role in angio- and lymphangiogenesis, with SOX18 seemingly being an attractive target for anti-angiogenic therapy and the treatment of metastatic disease in cancer. In summary, SOX transcription factors play an important role in cancer progression, including tumorigenesis, changes in the tumour microenvironment, and metastasis. Certain SOX proteins are potential molecular markers for cancer prognosis and putative potential therapeutic targets, but further investigations are required to understand their physiological functions

    Building zeolites from precrystallized units: nanoscale architecture

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    This is the peer reviewed version of the following article: Angew. Chem. Int. Ed. 2018, 57, 15330 15353, which has been published in final form at https://doi.org/10.1002/anie.201711422. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.[EN] Since the early reports by Barrer in the 1940s on converting natural minerals into synthetic zeolites, the use of precrystallized zeolites as crucial inorganic directing agents to synthesize other crystalline zeolites with improved physicochemical properties has become a very important research field, allowing the design, particularly in recent years, of new industrial catalysts. This Review highlights how the presence of some crystalline fragments in the synthesis media, such as small secondary building units (SBUs) or layered substructures, not only favors the crystallization of other zeolites with similar SBUs or layers, but also permits control over important parameters affecting their catalytic activity (chemical composition, crystal size, or porosity, etc.). Recent advances in the preparation of 3D and 2D zeolites through seeding and zeolite-to-zeolite transformation processes will be discussed extensively in this Review, including their preparation in the presence or absence of organic structure-directing agents (OSDAs). The aim is to introduce general guidelines for more efficient approaches for target zeolites.This work has been supported by the Spanish Government (MINECO through "Severo Ochoa" (SEV-2016-0683) and MAT2015-71261-R), by the European Union through ERC-AdG-2014-671093 (SynCatMatch), and by the Fundacion Ramon Areces (through the "Life and Materials Science" program).Li, C.; Moliner Marin, M.; Corma Canós, A. (2018). Building zeolites from precrystallized units: nanoscale architecture. Angewandte Chemie International Edition. 57(47):15330-15353. https://doi.org/10.1002/anie.201711422S15330153535747Cundy, C. S., & Cox, P. A. (2005). The hydrothermal synthesis of zeolites: Precursors, intermediates and reaction mechanism. Microporous and Mesoporous Materials, 82(1-2), 1-78. doi:10.1016/j.micromeso.2005.02.016Martínez, C., & Corma, A. (2011). Inorganic molecular sieves: Preparation, modification and industrial application in catalytic processes. 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Angewandte Chemie, 125(52), 14124-14134. doi:10.1002/ange.201304713Burton, A. W., & Zones, S. I. (2007). Organic Molecules in Zeolite Synthesis: Their Preparation and Structure-Directing Effects. Introduction to Zeolite Science and Practice, 137-179. doi:10.1016/s0167-2991(07)80793-2Dorset, D. L., Kennedy, G. J., Strohmaier, K. G., Diaz-Cabañas, M. J., Rey, F., & Corma, A. (2006). P-Derived Organic Cations as Structure-Directing Agents:  Synthesis of a High-Silica Zeolite (ITQ-27) with a Two-Dimensional 12-Ring Channel System. Journal of the American Chemical Society, 128(27), 8862-8867. doi:10.1021/ja061206oSimancas, R., Dari, D., Velamazan, N., Navarro, M. T., Cantin, A., Jorda, J. L., … Rey, F. (2010). Modular Organic Structure-Directing Agents for the Synthesis of Zeolites. Science, 330(6008), 1219-1222. doi:10.1126/science.1196240Blasco, T., Corma, A., Díaz-Cabañas, M. J., Rey, F., Vidal-Moya, J. A., & Zicovich-Wilson, C. M. (2002). Preferential Location of Ge in the Double Four-Membered Ring Units of ITQ-7 Zeolite. The Journal of Physical Chemistry B, 106(10), 2634-2642. doi:10.1021/jp013302bCorma, A., Díaz-Cabañas, M. J., Rey, F., Nicolopoulus, S., & Boulahya, K. (2004). ITQ-15: The first ultralarge pore zeolite with a bi-directional pore system formed by intersecting 14- and 12-ring channels, and its catalytic implications. Chem. Commun., (12), 1356-1357. doi:10.1039/b406572gCorma, A., Díaz-Cabañas, M. J., Jordá, J. L., Martínez, C., & Moliner, M. (2006). High-throughput synthesis and catalytic properties of a molecular sieve with 18- and 10-member rings. Nature, 443(7113), 842-845. doi:10.1038/nature05238Jiang, J., Yu, J., & Corma, A. (2010). Extra-Large-Pore Zeolites: Bridging the Gap between Micro and Mesoporous Structures. Angewandte Chemie International Edition, 49(18), 3120-3145. doi:10.1002/anie.200904016Jiang, J., Yu, J., & Corma, A. (2010). Zeolithe mit sehr großen Poren als Bindeglied zwischen mikro- und mesoporösen Strukturen. Angewandte Chemie, 122(18), 3186-3212. doi:10.1002/ange.200904016Sano, T., Itakura, M., & Sadakane, M. (2013). High Potential of Interzeolite Conversion Method for Zeolite Synthesis. Journal of the Japan Petroleum Institute, 56(4), 183-197. doi:10.1627/jpi.56.183Goel, S., Zones, S. I., & Iglesia, E. (2015). Synthesis of Zeolites via Interzeolite Transformations without Organic Structure-Directing Agents. Chemistry of Materials, 27(6), 2056-2066. doi:10.1021/cm504510fMartín, N., Moliner, M., & Corma, A. (2015). High yield synthesis of high-silica chabazite by combining the role of zeolite precursors and tetraethylammonium: SCR of NOx. Chemical Communications, 51(49), 9965-9968. doi:10.1039/c5cc02670aSonoda, T., Maruo, T., Yamasaki, Y., Tsunoji, N., Takamitsu, Y., Sadakane, M., & Sano, T. (2015). Synthesis of high-silica AEI zeolites with enhanced thermal stability by hydrothermal conversion of FAU zeolites, and their activity in the selective catalytic reduction of NOx with NH3. Journal of Materials Chemistry A, 3(2), 857-865. doi:10.1039/c4ta05621cD.Xie S. I.Zones C. M.Lew T. M.Davis WO2016/003504 2016.Jon, H., Ikawa, N., Oumi, Y., & Sano, T. (2008). An Insight into the Process Involved in Hydrothermal Conversion of FAU to *BEA Zeolite. Chemistry of Materials, 20(12), 4135-4141. doi:10.1021/cm703676yGoto, I., Itakura, M., Shibata, S., Honda, K., Ide, Y., Sadakane, M., & Sano, T. (2012). Transformation of LEV-type zeolite into less dense CHA-type zeolite. Microporous and Mesoporous Materials, 158, 117-122. doi:10.1016/j.micromeso.2012.03.032Goel, S., Zones, S. I., & Iglesia, E. (2014). Encapsulation of Metal Clusters within MFI via Interzeolite Transformations and Direct Hydrothermal Syntheses and Catalytic Consequences of Their Confinement. Journal of the American Chemical Society, 136(43), 15280-15290. doi:10.1021/ja507956mZones, S. I. (1991). Conversion of faujasites to high-silica chabazite SSZ-13 in the presence of N,N,N-trimethyl-1-adamantammonium iodide. Journal of the Chemical Society, Faraday Transactions, 87(22), 3709. doi:10.1039/ft9918703709Inoue, T., Itakura, M., Jon, H., Oumi, Y., Takahashi, A., Fujitani, T., & Sano, T. (2009). Synthesis of LEV zeolite by interzeolite conversion method and its catalytic performance in ethanol to olefins reaction. Microporous and Mesoporous Materials, 122(1-3), 149-154. doi:10.1016/j.micromeso.2009.02.027Itakura, M., Goto, I., Takahashi, A., Fujitani, T., Ide, Y., Sadakane, M., & Sano, T. (2011). Synthesis of high-silica CHA type zeolite by interzeolite conversion of FAU type zeolite in the presence of seed crystals. Microporous and Mesoporous Materials, 144(1-3), 91-96. doi:10.1016/j.micromeso.2011.03.041Martín, N., Boruntea, C. R., Moliner, M., & Corma, A. (2015). Efficient synthesis of the Cu-SSZ-39 catalyst for DeNOx applications. Chemical Communications, 51(55), 11030-11033. doi:10.1039/c5cc03200hInagaki, S., Tsuboi, Y., Nishita, Y., Syahylah, T., Wakihara, T., & Kubota, Y. (2013). Rapid Synthesis of an Aluminum-Rich MSE-Type Zeolite by the Hydrothermal Conversion of an FAU-Type Zeolite. Chemistry - A European Journal, 19(24), 7780-7786. doi:10.1002/chem.201300125Zones, S. I., & Nakagawa, Y. (1995). Use of modified zeolites as reagents influencing nucleation in zeolite synthesis. Studies in Surface Science and Catalysis, 45-52. doi:10.1016/s0167-2991(06)81871-9Fan, W., Wu, P., Namba, S., & Tatsumi, T. (2004). A Titanosilicate That Is Structurally Analogous to an MWW-Type Lamellar Precursor. Angewandte Chemie International Edition, 43(2), 236-240. doi:10.1002/anie.200352723Fan, W., Wu, P., Namba, S., & Tatsumi, T. (2004). A Titanosilicate That Is Structurally Analogous to an MWW-Type Lamellar Precursor. Angewandte Chemie, 116(2), 238-242. doi:10.1002/ange.200352723De Baerdemaeker, T., Feyen, M., Vanbergen, T., Müller, U., Yilmaz, B., Xiao, F.-S., … Gies, H. (2014). From Layered Zeolite Precursors to Zeolites with a Three-Dimensional Porosity: Textural and Structural Modifications through Alkaline Treatment. Chemistry of Materials, 27(1), 316-326. doi:10.1021/cm504014dIyoki, K., Itabashi, K., & Okubo, T. (2014). Progress in seed-assisted synthesis of zeolites without using organic structure-directing agents. Microporous and Mesoporous Materials, 189, 22-30. doi:10.1016/j.micromeso.2013.08.008Honda, K., Itakura, M., Matsuura, Y., Onda, A., Ide, Y., Sadakane, M., & Sano, T. (2013). Role of Structural Similarity Between Starting Zeolite and Product Zeolite in the Interzeolite Conversion Process. Journal of Nanoscience and Nanotechnology, 13(4), 3020-3026. doi:10.1166/jnn.2013.7356Barrer, R. M. (1948). 33. Synthesis of a zeolitic mineral with chabazite-like sorptive properties. Journal of the Chemical Society (Resumed), 127. doi:10.1039/jr9480000127Barrer, R. M., & Riley, D. W. (1948). 34. Sorptive and molecular-sieve properties of a new zeolitic mineral. Journal of the Chemical Society (Resumed), 133. doi:10.1039/jr9480000133Barrer, R. M., Cole, J. F., & Sticher, H. (1968). Chemistry of soil minerals. Part V. Low temperature hydrothermal transformations of kaolinite. Journal of the Chemical Society A: Inorganic, Physical, Theoretical, 2475. doi:10.1039/j19680002475Subotić, B., Škrtić, D., Šmit, I., & Sekovanić, L. (1980). Transformation of zeolite A into hydroxysodalite. Journal of Crystal Growth, 50(2), 498-508. doi:10.1016/0022-0248(80)90099-8Subotić, B., & Sekovanić, L. (1986). Transformation of zeolite A into hydroxysodalite. Journal of Crystal Growth, 75(3), 561-572. doi:10.1016/0022-0248(86)90102-8Subotić, B., Šmit, I., Madžija, O., & Sekovanić, L. (1982). Kinetic study of the transformation of zeolite A into zeolite P. 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Factors affecting the formation of zeolites X and B. The Journal of Physical Chemistry, 72(4), 1385-1386. doi:10.1021/j100850a056Xie, B., Song, J., Ren, L., Ji, Y., Li, J., & Xiao, F.-S. (2008). Organotemplate-Free and Fast Route for Synthesizing Beta Zeolite. Chemistry of Materials, 20(14), 4533-4535. doi:10.1021/cm801167eMajano, G., Delmotte, L., Valtchev, V., & Mintova, S. (2009). Al-Rich Zeolite Beta by Seeding in the Absence of Organic Template. Chemistry of Materials, 21(18), 4184-4191. doi:10.1021/cm900462uKamimura, Y., Chaikittisilp, W., Itabashi, K., Shimojima, A., & Okubo, T. (2010). Critical Factors in the Seed-Assisted Synthesis of Zeolite Beta and «Green Beta» from OSDA-Free Na+-Aluminosilicate Gels. Chemistry - An Asian Journal, 5(10), 2182-2191. doi:10.1002/asia.201000234Xie, B., Zhang, H., Yang, C., Liu, S., Ren, L., Zhang, L., … Xiao, F.-S. (2011). Seed-directed synthesis of zeolites with enhanced performance in the absence of organic templates. Chemical Communications, 47(13), 3945. doi:10.1039/c0cc05414cKamimura, Y., Tanahashi, S., Itabashi, K., Sugawara, A., Wakihara, T., Shimojima, A., & Okubo, T. (2010). Crystallization Behavior of Zeolite Beta in OSDA-Free, Seed-Assisted Synthesis. The Journal of Physical Chemistry C, 115(3), 744-750. doi:10.1021/jp1098975Iyoki, K., Kamimura, Y., Itabashi, K., Shimojima, A., & Okubo, T. (2010). Synthesis of MTW-type Zeolites in the Absence of Organic Structure-directing Agent. Chemistry Letters, 39(7), 730-731. doi:10.1246/cl.2010.730Majano, G., Darwiche, A., Mintova, S., & Valtchev, V. (2009). Seed-Induced Crystallization of Nanosized Na-ZSM-5 Crystals. Industrial & Engineering Chemistry Research, 48(15), 7084-7091. doi:10.1021/ie8017252Zhang, H., Guo, Q., Ren, L., Yang, C., Zhu, L., Meng, X., … Xiao, F.-S. (2011). Organotemplate-free synthesis of high-silica ferrierite zeolite induced by CDO-structure zeolite building units. 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Seed-assisted, OSDA-free synthesis of MTW-type zeolite and «Green MTW» from sodium aluminosilicate gel systems. Microporous and Mesoporous Materials, 147(1), 149-156. doi:10.1016/j.micromeso.2011.05.038Kamimura, Y., Itabashi, K., Kon, Y., Endo, A., & Okubo, T. (2017). Seed-Assisted Synthesis of MWW-Type Zeolite with Organic Structure-Directing Agent-Free Na-Aluminosilicate Gel System. Chemistry -

    Chiral effective action with heavy quark symmetry

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    We derive an effective action combining chiral and heavy quark symmetry, using approximate bosonization techniques of QCD. We explicitly show that the heavy-quark limit is compatible with the large NcN_c (number of color) limit in the meson sector, and derive specific couplings between the light and heavy mesons (DD, DD^*, ...) and their chiral partners. The relevance of this effective action to solitons with heavy quarks describing heavy baryons is discussed.Comment: 14 pages, SUNY-NTG-92/2

    One Spin Trace Formalism for BK B_K

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    It has been known for some time that there are two methods to calculate BK B_K with staggered fermions: one is the two spin trace formalism and the other is the one spin trace formalism. Until now, the two spin trace formalism has been exclusively used for weak matrix element calculations with staggered fermions. Here, the one spin trace formalism to calculate BK B_K with staggered fermions is explained. It is shown that the one spin trace operators require additional chiral partner operators in order to keep the continuum chiral behavior. The renormalization of the one spin trace operators is described and compared with the two spin trace formalism.Comment: 47 pages, latex, 4 figures are available on reques

    Strong Decays of Strange Charmed P-Wave Mesons

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    Goldstone boson decays of P-wave DsD_s^{**} mesons are studied within the framework of Heavy Hadron Chiral Perturbation Theory. We first analyze the simplest single kaon decays of these strange charmed mesons. We derive a model independent prediction for the width of Ds2D_{s2} and use experimental information on Ds1D_{s1} to constrain the S-wave contribution to D10D_1^0 decay. Single and double pion decay modes are then discussed and shown to be significantly restricted by isospin conservation. We conclude that the pion channels may offer the best hope for detecting one strange member of an otherwise invisible P-wave flavor multiplet.Comment: 16 pages, 2 updated figures not included but available upon request, CALT-68-1902. (Revised estimates for error on Ds2D_{s2} width and for isospin violating neutral pion decay of Ds1D'_{s1}.

    Structural and dielectric properties of Sr2_{2}TiO4_{4} from first principles

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    We have investigated the structural and dielectric properties of Sr2_{2}TiO4_{4},the first member of the Srn+1_{n+1}Tin_{n}O3n+1_{3n+1} Ruddlesden-Popper series, within density functional theory. Motivated by recent work in which thin films of Sr2_{2}TiO4_{4} were grown by molecular beam epitaxy (MBE) on SrTiO3_{3} substrates, the in-plane lattice parameter was fixed to the theoretically optimized lattice constant of cubic SrTiO3_{3} (n=\infty), while the out-of-plane lattice parameter and the internal structural parameters were relaxed. The fully relaxed structure was also investigated. Density functional perturbation theory was used to calculate the zone-center phonon frequencies, Born effective charges, and the electronic dielectric permittivity tensor. A detailed study of the contribution of individual infrared-active modes to the static dielectric permittivity tensor was performed. The calculated Raman and infrared phonon frequencies were found to be in agreement with experiment where available. Comparisons of the calculated static dielectric permittivity with experiments on both ceramic powders and epitaxial thin films are discussed.Comment: 11 pages, 1 figure, 8 tables, submitted to Phys. Rev.

    Moving from a Product-Based Economy to a Service-Based Economy for a More Sustainable Future

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    Traditionally, economic growth and prosperity have been linked with the availability, production and distribution of tangible goods as well as the ability of consumers to acquire such goods. Early evidence regarding this connection dates back to Adam Smith's Wealth of Nations (1776), in which any activity not resulting in the production of a tangible good is characterized as unproductive of any value." Since then, this coupling of economic value and material production has been prevalent in both developed and developing economies throughout the world. One unintended consequence of this coupling has been the exponential increase in the amount of solid waste being generated. The reason is that any production and consumption of material goods eventually generates the equivalent amount of (or even more) waste. Exacerbating this problem is the fact that, with today's manufacturing and supply chain management technologies, it has become cheaper to dispose and replace most products rather than to repair and reuse them. This has given rise to what some call a disposable society." To put things in perspective: In 2012 households in the U.K. generated approximately 22 thousand tons of waste, which amounted to 411 kg of waste generated per person (Department for Environment, Food & Rural Affairs, 2015). During the same time period, households in the U.S. generated 251 million tons of waste, which is equivalent to a person generating approximately 2 kg of waste every day (U.S. Environmental Protection Agency, 2012). Out of these 251 million tons of total waste generated, approximately 20% of the discarded items were categorized as durable goods. The disposal of durable goods is particularly worrisome because they are typically produced using material from non- renewable resources such as iron, minerals, and petroleum-based raw materials

    Transfer College Quality and Student Performance

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    With escalating tuitions, the return to college quality remains an important consideration for students deciding whether to spend more money for a higher quality college education. This paper examines how students that transfer credit for an introductory-level course perform in a subsequent intermediate-level course. Using rich administrative data we estimate how college quality affects student performance, holding constant many observable student characteristics. Students taking introductory courses at higher quality institutions earn higher grades in their intermediate courses than students attending lower quality institutions. This difference is small, but statistically significant. A back of the envelope calculation suggests that, for the average student, the benefit from attending a higher quality institution is more than worth the higher tuition.cheri_wp98.pdf: 334 downloads, before Oct. 1, 2020

    Nonresonant Contributions in B->rho pi Decay

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    We consider nonresonant contributions in the Dalitz plot analysis of B->rho pi->pi^+ pi^- pi^0 decay and their potential impact on the extraction of the CKM parameter alpha. In particular, we examine the role of the heavy mesons B^* and B_0, via the process B->pi (B^*, B_0)->pi^+ pi^- pi^0, and their interference with resonant contributions in the rho-mass region. We discuss the inherent uncertainties and suggest that the effects may be substantially smaller than previously indicated.Comment: 15 pages, 3 figures; minor changes, version to appear in Phys. Rev.
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