Now showing items 17044-17063 of 39571

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      Genetic turnovers and northern survival during the last glacial maximum in European brown bears 

      Ersmark, Erik; Baryshnikov, Gennady; Higham, Thomas; Argant, Alain; Castaños Ugarte, Pedro María; Döppes, Doris; Gasparik, Mihaly; Lidén, Kerstin; Germonpré, Mietje; Lipecki, Grzegorz; Marciszak, Adrian; Miller, Rebecca; Moreno García, Marta; Pacher, Martina; Robu, Marius; Rodríguez Varela, Ricardo; Rojo Guerra, Manuel; Sabol, Martin; Spassov, Nikolai; Storå, Jan; Valdiosera, Christina; Villaluenga Martínez, Aritza ORCID; Stewart, John R.; Dalén, Love (John Wiley & Sons, 2019-05-29)
      The current phylogeographic pattern of European brown bears (Ursus arctos) has commonly been explained by postglacial recolonization out of geographically distinct refugia in southern Europe, a pattern well in accordance ...
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      Genetic Variants and Hamstring Injury in Soccer: An Association and Validation Study 

      Larruskain Zabala, Jon; Celorrio Herrera, David; Barrio Beraza, Irantzu; Odriozola Martínez, Adrián;; Gil Orozko, Susana María ORCID; Fernandez-Lopez, Juan R; Nozal, Raul; Ortuzar Pérez, Isusko; Lekue Gallano, José Antonio ORCID; Aznar, José M. (American College of Sports Medicine, 2018-02)
      Purpose: This study aimed to investigate the association of candidate single nucleotide polymorphisms (SNP) with noncontact hamstring muscle injuries in elite soccer players and to create and validate a model to assess the ...
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      Genetic Variants as Predictors of the Success of Colorectal Cancer Treatments 

      García Etxebarria, Koldo; Etxart, Ane; Barrero, Maialen; Nafria, Beatriz; Segues Merino, Nerea Miren; Romero Garmendia, Irati; Goel, Ajay; Franke, Andre; D’Amato, Mauro; Bujanda Fernández de Pierola, Luis ORCID (MDPI, 2023-09-22)
      Some colorectal cancer (CRC) outcomes are partially associated with genetics, and different studies have proposed several genetic variants as predictors. However, analysis of their performance in other populations is ...
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      Genetic Variants Associated with Colorectal Adenoma Susceptibility 

      Abulí, Anna; Castells, Antoni; Bujanda Fernández de Pierola, Luis ORCID; Lozano, Juan José; Bessa, Xavier; Hernández, Cristina; Álvarez-Urturi, Cristina; Pellisé, María; Esteban-Jurado, Clara; Hijona Muruamendiaraz, Elizabeth; Burón, Andrea; Macià, Francesc; Grau, Jaume; Guayta, Rafael; Castellví-Bel, Sergi; Andreu, Montserrat; PROCOLON research group (PUBLIC LIBRARY SCIENCE, 2016-04-14)
      Background Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. Aim To determine if these genetic variants are associated also with adenoma susceptibility and may ...
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      Genetic variants associated with susceptibility to SARS CoV 2 infection and severity of COVID 19 symptoms 

      Azcárate Igarza, Daniel (2024-01-11)
      Infection with the SARS-CoV-2 coronavirus results in COVID 19 disease, which is widespread and has significant impacts on public health and the workforce. The quest for indicators that can identify individuals with a ...
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      Genetic Variants in MiRNA Processing Genes and Pre-MiRNAs Are Associated with the Risk of Chronic Lymphocytic Leukemia 

      Martín Guerrero, Idoia; Gutiérrez Camino, Ángela ORCID; López López, Elixabet ORCID; Bilbao Aldaiturriaga, Nerea; Pombar Gómez, María; Ardanaz, Maite; García-Orad Carles, África ORCID (Public Library Science, 2015-03-20)
      Genome wide association studies (GWAS) have identified several low-penetrance susceptibility alleles in chronic lymphocytic leukemia (CLL). Nevertheless, these studies scarcely study regions that are implicated in non-coding ...
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      Genetic variants involved in Childhood Acute Lymphoblastic Leukemia Susceptibility 

      Gutiérrez Camino, Ángela ORCID (2016-12-15)
      La Leucemia linfoblástica aguda (LLA) infantil es el cáncer pediátrico más común. El hecho de que se desarrolle a una edad temprana sugiere que para su aparición debe existir un fuerte componente genético. Recientes GWAS ...
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      Genetically modified macrophages accelerate myelin repair 

      Aigrot, Marie Stephane; Barthelemy, Clara; Moyon, Sarah; Dufayet-Chaffaud, Gaelle; Izagirre Urizar, Leire; Gillet-Legrand, Beatrix; Tada, Satoru; Bayón Cordero, Laura; Chara Ventura, Juan Carlos; Matute Almau, Carlos José; Cartier, Nathalie; Lubetzki, Catherine; Tepavcevic, Vanja (Wiley, 2022-08-08)
      [EN] Preventing neurodegeneration-associated disability progression in patients with multiple sclerosis (MS) remains an unmet therapeutic need. As remyelination prevents axonal degeneration, promoting this process in ...
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      Genetics and Epigenetics in Complex Diseases 

      López López, Elixabet ORCID (MDPI, 2023-05-03)
      ...
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      Genetics of adult attachment: An updated review of the literature 

      Erkoreka González, Leire ORCID; Zumarraga Ortiz, Mercedes; Arrue, Aurora; Zamalloa, María Isabel; Arnaiz Muñoz, Ainara; Olivas Gallego, Olga; Moreno Calle, Teresa; Sáez, Estela; García Ormaza, Jon; Marín Díaz-Guardaminio, Elena; Varela Gómez, Noemí; González Pinto Arrillaga, Ana María ORCID (Baishideng Publishing Group, 2021-09-19)
      Attachment style, which has been theorized to be rooted in childhood bonding experiences, influences adult cognitive, emotional and interpersonal functioning. Despite its relationship with early experiences, research ...
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      Genetics of ancestry-specific risk for relapse in acute lymphoblastic leukemia 

      Karol, S. E.; Larsen, E.; Yang, W.; Cheng, C.; Cao, X.; Ramsey, L. B.; Fernandez, C. A.; McCorkle, J. R.; Paugh, S. W.; Autry, R. J.; López López, Elixabet ORCID; Diouf, B.; Jeha, S.; Pui, C-H.; Raetz, E. A.; Winick, N. J.; Carroll, W. L.; Hunger, S. P.; Loh, M. L.; Devidas, M.; Evans, W. E.; Yang, J. J.; Relling, M. V. (Springer Nature, 2017-01-18)
      The causes of individual relapses in children with acute lymphoblastic leukemia (ALL) remain incompletely understood. We evaluated the contribution of germline genetic factors to relapse in 2225 children treated on Children's ...
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      Genetics of Somatotype and Physical Fitness in Children and Adolescents 

      Silventoinen, Karri; Maia, José Antonio; Jelenkovic Moreno, Aline; Pereira, Sara; Gouveia, Elvio; Antunes, Antonio; Thomis, Martine; Lefevre, Johan; Kaprio, Jaakko; Freitas, Duarte L. (Wiley, 2021-05)
      Objectives To analyze the influence of genetic and environmental factors on the variation in somatotype, physical fitness, and their mutual associations. Methods Twins from 214 pairs (87 monozygotic) of the Autonomous ...
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      Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm 

      García Castaño, Alejandro; Pérez de Nanclares, Gustavo; Madariaga Domínguez, Leire ORCID; Aguirre, Mireia; Madrid, Alvaro; Nadal, Inmaculada; Navarro, Mercedes; Lucas, Elena; Fijo, Julia; Espino, Mar; Espitaletta, Zilac; Castaño González, Luis Antonio ORCID; Ariceta, Gema; RenalTube Group (Public Library of Science, 2013-09-18)
      The p.Ala204Thr mutation (exon 7) of the CLCNKB gene is a "founder" mutation that causes most of type III Bartter syndrome cases in Spain. We performed genetic analysis of the CLCNKB gene, which encodes for the chloride ...
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      Genetika eta Biomedikuntzari buruzko hainbat lege 

      Escajedo San Epifanio, Leire; Gorrotxategi Azurmendi, Miren (Servicio Editorial de la Universidad del País Vasco/Euskal Herriko Unibertsitatearen Argitalpen Zerbitzua, 2015)
      [EU] I. Hitzaurrea, Itziar Alkorta Idiakez. II. Aurkezpena, Leire Escajedo San Epifenio, Miren Gorrotxategi Azurmendi: - Giza eskubideak eta gizakiaren duintasuna biologiaren eta medikuntzaren aplikazioak direla-eta ...
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      Gene–Diet Interactions in Colorectal Cancer: Survey Design, Instruments, Participants and Descriptive Data of a Case–Control Study in the Basque Country 

      Alegría Lertxundi, Iker; Aguirre Gómez, Carmelo; Bujanda Fernández de Pierola, Luis ORCID; Fernández Pablos, Francisco Javier; Polo, Francisco; Ordovás, José María; Etxezarraga Zuluaga, María Carmen; Zabalza Estévez, Ignacio; Larzabal, Mikel; Portillo Villares, María Isabel; Martínez de Pancorbo Gómez, María de los Angeles ORCID; Palencia Madrid, Leire ORCID; García Etxebarria, Koldo; Rocandio Pablo, Ana María ORCID; Arroyo Izaga, Marta (MDPI, 2020)
      Epidemiologic studies have revealed inconsistent evidence of gene-diet interaction in relation to colorectal cancer (CRC). The aim of this study was to analyze them in a sample of cases and controls from the population-based ...
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      Genial...: Automatic Irony Detection in Spanish Tweets 

      Diez Ibarbia, Paula (2023-06-30)
      Irony is a form of non-literal speech that can alter the meaning of an utterance. Understanding irony may greatly impact Natural Language Processing (NLP) tasks such as sentiment analysis or stance detection. While a ...
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      El genio de un solo ojo, I: en la mitología griega, Polifemo 

      Redondo Moyano, Elena ORCID (Levante Editori, 1997)
      En este trabajo se estudia la figura de Polifemo, el hijo de Poseidón y la ninfa Toosa, como ejemplo de las sucesivas reinterpretaciones que la mitología griega hacía de temas populares que resultaban de su interés: se ...
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      El genio de un solo ojo, II: en la mitología vasca, Tártaro 

      Redondo Moyano, Elena ORCID (Levante Editori, 2002)
      En la mitología vasca existen numerosas narraciones cuyo protagonista presenta rasgos de similitud con el Polifemo de la mitología griega. En este trabajo se recopilan y analizan las diferentes populares o legendarias en ...
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      Genome of Pesxtera Muierii skull shows high diversity and low mutational load in pre-glacial Europe 

      Svensson, Emma; Günther, Torsten; Hoischen, Alexander; Hervella Afonso, Montserrat ORCID; Munters, Arielle R.; Ioana, Mihai; Ridiche, Florin; Edlund, Hanna; Van Deuren, Rosanne C.; Soficaru, Andrei; De la Rúa Vaca, Concepción ORCID; Netea, Mihai G.; Jakobsson, Mattias (Elsevier, 2021-07-26)
      Few complete human genomes from the European Early Upper Palaeolithic (EUP) have been sequenced. Using novel sampling and DNA extraction approaches, we sequenced the genome of a woman from "Pesxtera Muierii,"Romania who ...
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      Genome of Peștera Muierii skull shows high diversity and low mutational load in pre-glacial Europe 

      Svensson, Emma; Günther, Torsten; Hoischen, Alexander; Hervella Afonso, Montserrat ORCID; Munters, Arielle R.; Ioana, Mihai; Ridiche, Florin; Edlund, Hanna; Van Deuren, Rosanne C.; Soficaru, Andrei Dorian; De la Rúa Vaca, Concepción ORCID; Netea, Mihai G.; Jakobsson, Mattias (Elsevier, 2021-07-26)
      [EN] Few complete human genomes from the European Early Upper Palaeolithic (EUP) have been sequenced. Using novel sampling and DNA extraction approaches, we sequenced the genome of a woman from ‘‘Pesxtera Muierii,’’ ...