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dc.contributor.authorOmidi, Y
dc.contributor.authorBarar, J
dc.date.accessioned2018-08-26T09:32:03Z
dc.date.available2018-08-26T09:32:03Z
dc.date.issued2008
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57241
dc.description.abstractMaintenance of the amino acids (AAs) levels within the central nervous system (CNS) is of importance for the formation of neurotransmitters. Alterations of the l-tryptophan and l-tyrosine (precursors of serotonin and dopamine, respectively) in brain parenchyma may result in serious CNS disorders such as depression. Malfunction of the system L (in particular LAT1/4F2hc) transporter can result in inevitable fluctuation of the large neutral amino acids (NAAs). From our preliminary mutation detection analyses, we hypothesize that the light chain LAT1 (SLC7A5) polymorphisms may change functionality of the system L resulting in fluctuation of key large NAAs levels in CNS. Also, mutations in 4F2hc (SLC3A2), the heavy chain of various AAs transporters, may alter the functions of some key transporters and cause changes in AAs concentrations of the brain. If proven, this hypothesis would grant new insights in molecular biology of the large neutral amino acid transporters in relevance to CNS disorders. © 2008 Elsevier Ltd. All rights reserved.
dc.language.isoEnglish
dc.relation.ispartofBioscience Hypotheses
dc.subjectamino acid transporter
dc.subjectdopamine
dc.subjectneurotransmitter
dc.subjectprotein 4F2hc
dc.subjectprotein lat1
dc.subjectserotonin
dc.subjecttryptophan
dc.subjecttyrosine
dc.subjectamino acid brain level
dc.subjectamino acid metabolism
dc.subjectarticle
dc.subjectcentral nervous system disease
dc.subjectdepression
dc.subjectgenetic association
dc.subjectgenetic polymorphism
dc.subjectheavy chain
dc.subjecthuman
dc.subjectlight chain
dc.subjectmolecular biology
dc.subjectmolecular interaction
dc.subjectmutational analysis
dc.subjectneurotransmission
dc.subjectprotein function
dc.titlePolymorphisms in large neutral amino acids transporter, system L, in association with CNS disorders
dc.typeArticle
dc.citation.volume1
dc.citation.issue2
dc.citation.spage109
dc.citation.epage111
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1016/j.bihy.2008.02.005


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