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dc.contributor.authorRamos Amigo, Adriana
dc.contributor.authorRodríguez-Seoane, C.
dc.contributor.authorRosa Benito, Isaac
dc.contributor.authorTrossbach, S. V.
dc.contributor.authorOrtega-Alonso, A.
dc.contributor.authorTomppo, L.
dc.contributor.authorEkelund, J.
dc.contributor.authorVeijola, J.
dc.contributor.authorJärvelin, M. R.
dc.contributor.authorAlonso Lorenzo, Jana 
dc.contributor.authorVeiga García, Sonia 
dc.contributor.authorSawa, A.
dc.contributor.authorHennah, W.
dc.contributor.authorGarcía Alonso, Ángel
dc.contributor.authorKorth, C.
dc.contributor.authorRodríguez Requena, Jesús
dc.date.accessioned2017-06-07T07:24:03Z
dc.date.available2017-06-07T07:24:03Z
dc.date.issued2014
dc.identifier.issn0964-6906
dc.identifier.urihttp://hdl.handle.net/20.500.11940/5977
dc.description.abstractIn a large Scottish pedigree, disruption of the gene coding for DISC1 clearly segregates with major depression, schizophrenia and related mental conditions. Thus, study of DISC1 may provide a clue to understand the biology of major mental illness. A neuropeptide precursor VGF has potent antidepressant effects and has been reportedly associated with bipolar disorder. Here we show that DISC1 knockdown leads to a reduction of VGF, in neurons. VGF is also downregulated in the cortices from sporadic cases with major mental disease. A positive correlation of VGF single-nucleotide polymorphisms (SNPs) with social anhedonia was also observed. We now propose that VGF participates in a common pathophysiology of major mental disease.
dc.language.isoeng
dc.subject.meshAnhedonia
dc.subject.meshBrain
dc.subject.meshCohort Studies
dc.subject.meshDown-Regulation
dc.subject.meshHumans
dc.subject.meshMental Disorders
dc.subject.meshNerve Growth Factors
dc.subject.meshNerve Tissue Proteins
dc.subject.meshNeurons
dc.subject.meshPedigree
dc.subject.meshPolymorphism, Single Nucleotide
dc.titleNeuropeptide precursor VGF is genetically associated with social anhedonia and underrepresented in the brain of major mental illness: its downregulation by DISC1
dc.typeArtigoes
dc.authorsophosRamos, A.
dc.authorsophosRodríguez-Seoane, C.
dc.authorsophosRosa, I.
dc.authorsophosTrossbach, S. V.
dc.authorsophosOrtega-Alonso, A.
dc.authorsophosTomppo, L.
dc.authorsophosEkelund, J.
dc.authorsophosVeijola, J.
dc.authorsophosJärvelin, M. R.
dc.authorsophosAlonso, J.
dc.authorsophosVeiga, S.
dc.authorsophosSawa, A.
dc.authorsophosHennah, W.
dc.authorsophosGarcía, A.
dc.authorsophosKorth, C.
dc.authorsophosRequena, J. R.
dc.identifier.doi10.1093/hmg/ddu303
dc.identifier.isi344671900001
dc.identifier.pmid24934694
dc.identifier.sophos14938
dc.issue.number22
dc.journal.titleHUMAN MOLECULAR GENETICS
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initial5859
dc.page.final65
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number23


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