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              <name>Title</name>
              <description>A name given to the resource</description>
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                  <text>Agricultura sostenible</text>
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              <name>Description</name>
              <description>An account of the resource</description>
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                  <text>Dominio científico: Agricultura sostenible</text>
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                <text>In vitro multiplication of ginger Zingiber officinale Roscoe, cv. ‘Grand Caiman’ in Temporary Immersion System</text>
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                <text>Juan G. Villegas Ramírez, Tomás Palma Zúñiga</text>
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            <name>Description</name>
            <description>An account of the resource</description>
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                <text>Ginger (Zingiber officinale Roscoe) is a plant of great interest for its properties and uses. Although it has been in vitro propagated in semi-solid culture media, the use of Temporary Immersion Systems (TIS) could be an alternative to increase the number of plants. The research aimed to multiply Z. officinale in TIS. Four experiments were carried out for selecting the immersion time (5, 10 and 15 minutes), the immersion frequency (four immersions every three hours, two every 12 hours and one every 24 hours), the volume of medium culture by explant (30, 40 and 50 ml) and a comparison of the TIS system, with the conventional method of propagation in semi-solid culture medium. It was found that the immersion time did not influence the evaluated variables. With immersions every six hours (four per day) the highest multiplication coefficient, shoot length and number of roots were obtained. With 20 ml of culture medium per explant, the plants were observed chlorotic and no significant differences were found between 40 and 60 ml. The use of TIS with an immersion time of 5 minutes, an immersion frequency every 6 hours and a volume of culture medium of 40 ml / explant, improved the response obtained from ginger shoots grown in semi-solid culture medium. The use of SIT for in vitro multiplication of Zingiber officinale Roscoe cv. ‘Grand Cayman’ increases the multiplication coefficient and improves the characteristics of the plants obtained. Its use is recommended as an alternative to propagate this cultivar selected by producers from the canton of Guatuso, Alajuela, Costa Rica.</text>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="200485">
                <text>2019</text>
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            <name>Subject</name>
            <description>The topic of the resource</description>
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                <text>jengibre, multiplication coefficient, organogenesis</text>
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            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
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                <text>Biotecnología Vegetal</text>
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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              <elementText elementTextId="200488">
                <text>Universidad Central Marta Abreu" de Las Villas"</text>
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            <name>Coverage</name>
            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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                <text>Agriculture, Plant culture</text>
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                <text>&lt;a href="https://revista.ibp.co.cu/index.php/BV/article/view/646" target="_blank" rel="noreferrer noopener"&gt;https://revista.ibp.co.cu/index.php/BV/article/view/646&lt;/a&gt;</text>
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              <name>Title</name>
              <description>A name given to the resource</description>
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                  <text>Coronavirus</text>
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              <name>Description</name>
              <description>An account of the resource</description>
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                  <text>Dominio científico: Coronavirus</text>
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      <name>Text</name>
      <description>A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.</description>
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        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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            <description>A name given to the resource</description>
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                <text>In vitro reconstitution of SARS-coronavirus mRNA cap methylation.</text>
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            <description>An entity primarily responsible for making the resource</description>
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                <text>Mickaël Bouvet, Claire Debarnot, Isabelle Imbert, Barbara Selisko, Eric J. Snijder, Bruno Canard, Etienne Decroly</text>
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            <description>An account of the resource</description>
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                <text>SARS-coronavirus (SARS-CoV) genome expression depends on the synthesis of a set of mRNAs, which presumably are capped at their 5' end and direct the synthesis of all viral proteins in the infected cell. Sixteen viral non-structural proteins (nsp1 to nsp16) constitute an unusually large replicase complex, which includes two methyltransferases putatively involved in viral mRNA cap formation. The S-adenosyl-L-methionine (AdoMet)-dependent (guanine-N7)-methyltransferase (N7-MTase) activity was recently attributed to nsp14, whereas nsp16 has been predicted to be the AdoMet-dependent (nucleoside-2'O)-methyltransferase. Here, we have reconstituted complete SARS-CoV mRNA cap methylation in vitro. We show that mRNA cap methylation requires a third viral protein, nsp10, which acts as an essential trigger to complete RNA cap-1 formation. The obligate sequence of methylation events is initiated by nsp14, which first methylates capped RNA transcripts to generate cap-0 (7Me)GpppA-RNAs. The latter are then selectively 2'O-methylated by the 2'O-MTase nsp16 in complex with its activator nsp10 to give rise to cap-1 (7Me)GpppA(2'OMe)-RNAs. Furthermore, sensitive in vitro inhibition assays of both activities show that aurintricarboxylic acid, active in SARS-CoV infected cells, targets both MTases with IC(50) values in the micromolar range, providing a validated basis for anti-coronavirus drug design.</text>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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                <text>2010</text>
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            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
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              <elementText elementTextId="2451">
                <text>DOI: 10.1371/journal.ppat.1000863</text>
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            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="2452">
                <text>PLoS Pathogens</text>
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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                <text>Public Library of Science (PLoS)</text>
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            <name>Coverage</name>
            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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                <text>Biology (General), Immunologic diseases. Allergy</text>
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            <name>Language</name>
            <description>A language of the resource</description>
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                <text>EN</text>
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            <element elementId="50">
              <name>Title</name>
              <description>A name given to the resource</description>
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                <elementText elementTextId="1">
                  <text>Coronavirus</text>
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            <element elementId="41">
              <name>Description</name>
              <description>An account of the resource</description>
              <elementTextContainer>
                <elementText elementTextId="2">
                  <text>Dominio científico: Coronavirus</text>
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      <name>Text</name>
      <description>A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.</description>
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      <elementSet elementSetId="1">
        <name>Dublin Core</name>
        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>In Vivo Antiviral Effects of U18666A Against Type I Feline Infectious Peritonitis Virus</text>
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          <element elementId="39">
            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
            <elementTextContainer>
              <elementText elementTextId="12917">
                <text>Tomoyoshi Doki, Tomoyo Tarusawa, Tsutomu Hohdatsu, Tomomi Takano</text>
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          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
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              <elementText elementTextId="12918">
                <text>Background: The cationic amphiphilic drug U18666A inhibits the proliferation of type I FIPV in vitro. In this study, we evaluated the in vivo antiviral effects of U18666A by administering it to SPF cats challenged with type I FIPV. Methods: Ten SPF cats were randomly assigned to two experimental groups. FIPV KU-2 were inoculated intraperitoneally to cats. The control group was administered PBS, and the U18666A-treated group was administered U18666A subcutaneously at 2.5 mg/kg on day 0, and 1.25 mg/kg on days 2 and 4 after viral inoculation. Results: Two of the five control cats administered PBS alone developed FIP. Four of the five cats administered U18666A developed no signs of FIP. One cat that temporarily developed fever, had no other clinical symptoms, and no gross lesion was noted on an autopsy after the end of the experiment. The FIPV gene was detected intermittently in feces and saliva regardless of the development of FIP or administration of U18666A. Conclusions: When U18666A was administered to cats experimentally infected with type I FIPV, the development of FIP might be suppressed compared with the control group. However, the number of animals with FIP is too low to establish anti-viral effect of U18666A in cats.</text>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="12919">
                <text>2020</text>
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          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
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              <elementText elementTextId="12920">
                <text>Feline coronavirus, feline infectious peritonitis, U18666A, cationic amphiphilic drug, antiviral agent</text>
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            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
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              <elementText elementTextId="12921">
                <text>DOI: 10.3390/pathogens9010067</text>
              </elementText>
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          <element elementId="48">
            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="12922">
                <text>Pathogens</text>
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          <element elementId="45">
            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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              <elementText elementTextId="12923">
                <text>MDPI AG</text>
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            <name>Coverage</name>
            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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                <text>Medicine</text>
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            <description>A language of the resource</description>
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                <text>EN</text>
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            <element elementId="50">
              <name>Title</name>
              <description>A name given to the resource</description>
              <elementTextContainer>
                <elementText elementTextId="1">
                  <text>Coronavirus</text>
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              </elementTextContainer>
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            <element elementId="41">
              <name>Description</name>
              <description>An account of the resource</description>
              <elementTextContainer>
                <elementText elementTextId="2">
                  <text>Dominio científico: Coronavirus</text>
                </elementText>
              </elementTextContainer>
            </element>
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      <name>Text</name>
      <description>A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.</description>
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        <name>Dublin Core</name>
        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>In Young Adults with COVID-19, Obesity Is Associated with Adverse Outcomes</text>
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          <element elementId="39">
            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
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              <elementText elementTextId="44866">
                <text>Eric Steinberg, Ellsworth Wright, Beth Kushner</text>
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          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
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                <text>Introduction: For patients with COVID-19, several characteristics have been identified that may be associated with adverse outcomes. However, there is a paucity of data regarding the effect of obesity on young adult patients with COVID-19. We sought to identify whether adverse outcomes are associated with obesity, particularly in COVID-19 patients 45 years and younger. Methods: This was a two-center, retrospective cohort study that included 210 patients. Eligible patients were between the ages of 18–45 years old, had tested positive for SARS-CoV-2 on real-time reverse transcription polymerase chain reaction via nasopharyngeal swab, and were not pregnant. Primary outcomes were defined as follows: 1) in-hospital mortality during the study period; 2) need for mechanical ventilation; and 3) admission to the hospital. We analyzed baseline characteristics of the cohort using descriptive statistics. Odds ratios (OR) were calculated to assess associations between outcomes and obesity, defined as body mass index (BMI) &gt;30. Results: Of those patients who tested positive, 18 died during hospitalization (9%), 36 (17%) required mechanical ventilation, and 94 (45%) were admitted. Each of the primary outcomes was significantly associated with a BMI &gt;30 (mortality OR = 6.29, 95% confidence interval [CI], 1.76–22.46, p = 0.0046; mechanical ventilation OR = 6.01, 95% CI, 2.5–14.48, p = 0.0001; admission OR 2.61, 95% CI, 1.49–4.58, p =.0008). Conclusion: Obesity appears to be an independent risk factor for poor outcomes in young patients with COVID-19. Future studies examining the clinical characteristics and risk factors of COVID-19 patients across large, diverse populations will strengthen our understanding of this novel and complex disease.</text>
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            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="44868">
                <text>2020</text>
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            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
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              <elementText elementTextId="44869">
                <text>10.5811/westjem.2020.5.47972</text>
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            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="44870">
                <text>Western Journal of Emergency Medicine</text>
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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                <text>eScholarship Publishing, University of California</text>
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            <name>Coverage</name>
            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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                <text>Medicine, Medical emergencies. Critical care. Intensive care. First aid</text>
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              <name>Title</name>
              <description>A name given to the resource</description>
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                  <text>Coronavirus</text>
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                <text>The SARS-CoV-2 virus has caused a pandemic and is public health emergency of international concern. As of now, no registered therapies are available for treatment of coronavirus infection. The viral infection depends on the attachment of spike (S) glycoprotein to human cell receptor angiotensin-converting enzyme 2 (ACE2). We have designed a protein inhibitor (ΔABP-D25Y) targeting S protein using computational approach. The inhibitor consists of two α helical peptides homologues to protease domain (PD) of ACE2. Docking studies and molecular dynamic simulation revealed that the inhibitor binds exclusively at the ACE2 binding site of S protein. The computed binding affinity of the inhibitor is higher than the ACE2 and thus will likely out compete ACE2 for binding to S protein. Hence, the proposed inhibitor ΔABP-D25Y could be a potential blocker of S protein and receptor binding domain (RBD) attachment.</text>
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                <text>I propose a reading of the Royal Commentaries (1609 and 1617) in contemporary code, that is, finding in the work meanings pertinent to social and historical problems of the beginnings of the 21st century. In contrast to the traditional readings of the Inca Garcilaso, based on philological and historicist criteria, I offer an interpretation towards the future of the Inca, that is, according to his validity to understand and contribute to the solution of current crises such as global warming and neocolonialism.</text>
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                <text>French literature - Italian literature - Spanish literature - Portuguese literature, Romanic languages</text>
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        <name>Dublin Core</name>
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          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Incertidumbre en la evaluación del impacto del cambio climático en dos cuencas mexicanas / Uncertainty in the evaluation of climate change impacts over two Mexican catchments</text>
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            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
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                <text>Juan Alberto Velázquez Zapata, Magali Troin</text>
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          </element>
          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
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              <elementText elementTextId="204728">
                <text>Este estudio investiga la incertidumbre asociada con el modelo de circulación general (MCG) al escenario de emisión y a la variabilidad natural del clima en la estimación del impacto del cambio climático en dos cuencas mexicanas. Las cuencas seleccionadas tienen diferentes climas y regímenes hidrológicos. Las simulaciones climáticas de tres MCG bajo tres escenarios de emisión (B1, A1B y A2) se usan para alimentar el modelo hidrológico SWAT, de tipo físico y semidistribuido. Las simulaciones cubren 30 años en un periodo de referencia (1971-2000) y dos periodos de 20 años en el futuro (2046-2065 y 2081-2100). Los resultados muestran que los caudales altos son más propensos a ser influenciados por la incertidumbre asociada con el MCG; además, los indicadores hidrológicos tienen una sensibilidad menor al escenario de emisión para las cuencas de estudio. Por último, la incertidumbre vinculada con la variabilidad natural no debe pasarse por alto en los estudios de cambio climático, ya que hasta cierto punto y para caudales altos puede ser tan crítica como la incertidumbre ligada con MCG y el escenario de emisión.</text>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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                <text>2020</text>
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          <element elementId="49">
            <name>Subject</name>
            <description>The topic of the resource</description>
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              <elementText elementTextId="204730">
                <text>Escurrimiento, Incertidumbre, México, SWAT, cadena de modelación, impacto del cambio climático, variabilidad natural</text>
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            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
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              <elementText elementTextId="204731">
                <text>10.24850/j-tyca-2020-01-01</text>
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          </element>
          <element elementId="48">
            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
            <elementTextContainer>
              <elementText elementTextId="204732">
                <text>Tecnología y ciencias del agua</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="45">
            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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              <elementText elementTextId="204733">
                <text>Instituto Mexicano de Tecnología del Agua</text>
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          </element>
          <element elementId="38">
            <name>Coverage</name>
            <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
            <elementTextContainer>
              <elementText elementTextId="204734">
                <text>Hydraulic engineering, Water supply for domestic and industrial purposes</text>
              </elementText>
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          </element>
          <element elementId="46">
            <name>Relation</name>
            <description>A related resource</description>
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              <elementText elementTextId="204735">
                <text>&lt;a href="http://www.revistatyca.org.mx/ojs/index.php/tyca/article/view/1848" target="_blank" rel="noreferrer noopener"&gt;http://www.revistatyca.org.mx/ojs/index.php/tyca/article/view/1848&lt;/a&gt;</text>
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