5 results match your criteria: "Faculty of Biology Universitat de Barcelona[Affiliation]"
Mitochondrion
September 2024
Molecular Neurobiology laboratory. Department of Biochemistry and Molecular Biomedicine, Faculty of Biology. Universitat de Barcelona. Barcelona. Spain; CiberNed. Network Center for Neurodegenerative diseases. National Spanish Health Institute Carlos III. Madrid. Spain; School of Chemistry. Universitat de Barcelona. Barcelona. Spain. Electronic address:
Environ Pollut
December 2023
Department of Instrumental Analysis and Environmental Chemistry, Institute of Organic Chemistry, IQOG-CSIC, 28006, Madrid, Spain.
Poly- and Perfluoroalkyl Substances (PFAS) are a well-known class of pollutants which can bioaccumulate and biomagnify with a vast majority being highly persistent. This study aims to determine the biomagnification rates of PFAS in sexually mature striped dolphins and to assess temporal trends on PFAS concentrations over the past three decades (1990-2021) in the North-Western Mediterranean Sea. Thirteen and 17 of the 19 targeted PFAS were detected in the samples of the dolphins' digestive content and liver, respectively, at concentrations ranging between 43 and 1609 ng/g wet weight, and 254 and 7010 ng/g wet weight, respectively.
View Article and Find Full Text PDFAttention-deficit/hyperactivity disorder (ADHD) often co-occurs with other psychiatric and physical diseases. However, available evidence on associations between ADHD and cardiovascular diseases (CVDs) is mixed. To systematically review, quantitatively synthesize, and appraise available evidence on the link between ADHD with CVDs, we searched relevant articles in PubMed, Embase, PsycINFO, and Web of Science from inception to May 1, 2022.
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April 2022
Department of Genetics, Microbiology and Statistics, Faculty of Biology Universitat de Barcelona, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), instituto de investigación biomédica básica de la Universidad de Barcelona (IBUB), Institut de Recerca Sant Joan de Déu (IRSJD) Barcelona Spain.
Osteoporosis is the most common bone disease, characterized by a low bone mineral density (BMD) and increased risk of fracture. At the other end of the BMD spectrum, some individuals present strong, fracture-resistant, bones. Both osteoporosis and high BMD are heritable and their genetic architecture encompasses polygenic inheritance of common variants and some cases of monogenic highly penetrant variants in causal genes.
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December 2020
Department of Genetics, Microbiology and Statistics, Faculty of Biology Universitat de Barcelona, Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Institut de Biomedicina de la Universitat de Barcelona (IBUB), Institut de Recerca Sant Joan de Déu (IRSJD) Barcelona Spain.
The gene encodes an extracellular inhibitor of the Wnt pathway with an important role in bone tissue development, bone homeostasis, and different critical aspects of bone biology. Several BMD genome-wide association studies (GWASs) have consistently found association with SNPs in the genomic region. For these reasons, it is important to assess the functionality of coding and regulatory variants in the gene.
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