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dc.creatorMartínez-Levy, G. A.es_ES
dc.creatorRocha, L.es_ES
dc.creatorRodríguez-Pineda, F.es_ES
dc.creatorAlonso-Vanegas, M. A.es_ES
dc.creatorNani, A.es_ES
dc.creatorBuentello-García, R. M.es_ES
dc.creatorBriones-Velasco, M.es_ES
dc.creatorSan-Juan, D.es_ES
dc.creatorCienfuegos, J.es_ES
dc.creatorCruz-Fuentes, C. S.es_ES
dc.date2018
dc.date.accessioned2022-11-29T16:59:52Z
dc.date.available2022-11-29T16:59:52Z
dc.date.issued2018
dc.identifierMT07IC22
dc.identifier.issn0893-7648
dc.identifier.urihttp://repositorio.inprf.gob.mx/handle/123456789/7641
dc.identifier.urihttps://doi.org/10.1007/s12035-017-0597-0
dc.descriptionA body of evidence supports a relevant role of brain-derived neurotrophic factor (BDNF) in temporal lobe epilepsy (TLE). Magnetic resonance data reveal that the cere bral atrophy extends to regions that are functionally and ana tomically connected with the hippocampus, especially the temporal cortex. We previously reported an increased expres sion of BDNF messenger for the exon VI in the hippocampus of temporal lobe epilepsy patients compared to an autopsy control group. Altered levels of this particular transcript were also associated with pre-surgical use of certain psychotropic. We extended here our analysis of transcripts I, II, IV, and VI to the temporal cortex since this cerebral region holds intrinsic communication with the hippocampus and is structurally af fected in patients with TLE. We also assayed the cyclic aden osine monophosphate response element-binding (CREB) and glucocorticoid receptor (GR) genes as there is experimental evidence of changes in their expression associated with BDNF and epilepsy. TLE and pre-surgical pharmacological treatment were considered as the primary clinical independent variables.
dc.formatPDF
dc.language.isoeng
dc.publisherHumana Press
dc.relation55(5)3698-3708
dc.rightsAcceso Cerrado
dc.titleIncreased expression of brain-derived neurotrophic factor transcripts I and VI, cAMP response element binding, and glucocorticoid receptor in the cortex of patients with temporal lobe epilepsyes_ES
dc.typeArtículo
dc.contributor.affiliationDepartment of Genetics, National Institute of Psychiatry Ramón de la Fuente Muñiz (INPRFM), Mexico City, Mexico
dc.contributor.emailcruz@imp.edu.mx (Cruz-Fuentes, C.S.)
dc.relation.jnabreviadoMOL NEUROBIOL
dc.relation.journalMolecular Neurobiology
dc.identifier.placeEstados Unidos
dc.date.published2018
dc.identifier.organizacionInstituto Nacional de Psiquiatría Ramón de la Fuente Muñiz
dc.identifier.eissn1559-1182
dc.identifier.doi10.1007/s12035-017-0597-0
dc.subject.kwPharmacoresistant epilepsy
dc.subject.kwTemporal cortex
dc.subject.kwBDNF
dc.subject.kwCREB


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