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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
(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 ... -
Genetic Variants and Hamstring Injury in Soccer: An Association and Validation Study
(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 ... -
Genetic Variants as Predictors of the Success of Colorectal Cancer Treatments
(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 ... -
Genetic Variants Associated with Colorectal Adenoma Susceptibility
(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 ... -
Genetic variants associated with susceptibility to SARS CoV 2 infection and severity of COVID 19 symptoms
(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 ... -
Genetic Variants in MiRNA Processing Genes and Pre-MiRNAs Are Associated with the Risk of Chronic Lymphocytic Leukemia
(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 ... -
Genetic variants involved in Childhood Acute Lymphoblastic Leukemia Susceptibility
(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 ... -
Genetically modified macrophages accelerate myelin repair
(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 of adult attachment: An updated review of the literature
(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 ... -
Genetics of ancestry-specific risk for relapse in acute lymphoblastic leukemia
(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 ... -
Genetics of Somatotype and Physical Fitness in Children and Adolescents
(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 ... -
Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm
(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 ... -
Genetika eta Biomedikuntzari buruzko hainbat lege
(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 ... -
Gene–Diet Interactions in Colorectal Cancer: Survey Design, Instruments, Participants and Descriptive Data of a Case–Control Study in the Basque Country
(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 ... -
Genial...: Automatic Irony Detection in Spanish Tweets
(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 ... -
El genio de un solo ojo, I: en la mitología griega, Polifemo
(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 ... -
El genio de un solo ojo, II: en la mitología vasca, Tártaro
(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 ... -
Genome of Pesxtera Muierii skull shows high diversity and low mutational load in pre-glacial Europe
(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 ... -
Genome of Peștera Muierii skull shows high diversity and low mutational load in pre-glacial Europe
(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,’’ ...