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Case Report: A prenatal diagnosis of osteogenesis imperfecta in a patient with a novel pathogenic variant in COL1A2
(F1000 Research, 2023)
Osteogenesis imperfecta is considered a rare genetic condition which is characterized by bone fragility. In 85% of cases, it is caused by mutations in COL1A1 and COL1A2 genes which are essential to produce type I collagen. ...
Changes in inflammatory gene expression in brain tissue adjacent and distant to a viable cyst in a rat model for neurocysticercosis
(Public Library of Science, 2021)
BACKGROUND: The parasite Taenia solium causes neurocysticercosis (NCC) in humans and is a common cause of adult-onset epilepsy in the developing world. Hippocampal atrophy, which occurs far from the cyst, is an emerging ...
Evidence of recent interspecies horizontal gene transfer regarding nucleopolyhedrovirus infection of Spodoptera frugiperda
(BioMed Central, 2015-11)
Background: Baculoviruses are insect-associated viruses carrying large, circular double-stranded-DNA genomes with significant biotechnological applications such as biological pest control, recombinant protein production, ...
Variantes genéticas de susceptibilidad en epilepsia genética generalizada en familias colombianasSusceptibility gene variants in genetic generalized epilepsy in Colombian families
(Asociación Colombiana de NeurologíaGenética Molecular (GENMOL)Grupo de Investigación Clínica en Enfermedades del Niño y del Adolescente - PediacienciasGrupo Mapeo GenéticoBogotá, Colombia, 2021)
Small qnrB-harbouring ColE-like plasmids widespread in commensal enterobacteria from a remote Amazonas population not exposed to antibiotics
(Oxford University Press, 2011)
Sir, After a decade since discovery, a variety of qnr-type plasmid-mediated quinolone resistance genes have been reported worldwide, especially in clinical isolates of Enterobacteriaceae.1 Recently, we found that qnr genes ...
Papel del gen TP53 en la oncogénesis
(Universidad Industrial de SantanderGenética MédicaBucaramanga, Colombia, 2022)
Elucidating multi-input processing 3-node gene regulatory network topologies capable of generating striped gene expression patterns
(Public Library of ScienceFundamentos y Enseñanza de la Física y los Sistemas DinámicosSan Francisco, Estados Unidos, 2022)
Assessing duplication and loss of APETALA1/FRUITFULL homologs in Ranunculales
(Frontiers Research FoundationBiotecnologíaLausana, Suiza, 2023)
Distribution of APOE polymorphism in the ‘‘Paisa’’ population from northwest Colombia (Antioquia)
(Society for the Study of Human Biology (SSHB)Taylor & FrancisGenética Molecular (GENMOL)Grupo de Neurociencias de AntioquiaLondres, Inglaterra, 2022)