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dc.contributor.authorSmirnova, Liudmila-
dc.contributor.authorSeregin, Alexander-
dc.contributor.authorBoksha, Irina-
dc.contributor.authorDmitrieva, Elena-
dc.contributor.authorSimutkin, German-
dc.contributor.authorKornetova, Elena-
dc.contributor.authorSavushkina, Olga-
dc.contributor.authorLetova, Anastasia-
dc.contributor.authorBokhan, Nikolay-
dc.contributor.authorIvanova, Svetlana-
dc.contributor.authorZgoda, Victor-
dc.date.accessioned2022-03-18T04:30:02Z-
dc.date.available2022-03-18T04:30:02Z-
dc.date.issued2019-07-11-
dc.identifier.urihttps://doi.org/10.1186/s12864-019-5848-1-
dc.identifier.urihttp://hdl.handle.net/20.500.12701/1689-
dc.description.abstractBackground Purpose of study is revealing significant differences in serum proteomes in schizophrenia and bipolar disorder (BD). Results Quantitative mass-spectrometry based proteomic analysis was used to quantify proteins in the blood serum samples after the depletion of six major blood proteins. Comparison of proteome profiles of different groups revealed 27 proteins being specific for schizophrenia, and 18 – for BD. Protein set in schizophrenia was mostly associated with immune response, cell communication, cell growth and maintenance, protein metabolism and regulation of nucleic acid metabolism. Protein set in BD was mostly associated with immune response, regulating transport processes across cell membrane and cell communication, development of neurons and oligodendrocytes and cell growth. Concentrations of ankyrin repeat domain-containing protein 12 (ANKRD12) and cadherin 5 in serum samples were determined by ELISA. Significant difference between three groups was revealed in ANKRD12 concentration (p = 0.02), with maximum elevation of ANKRD12 concentration (median level) in schizophrenia followed by BD. Cadherin 5 concentration differed significantly (p = 0.035) between schizophrenic patients with prevailing positive symptoms (4.78 [2.71, 7.12] ng/ml) and those with prevailing negative symptoms (1.86 [0.001, 4.11] ng/ml). Conclusions Our results are presumably useful for discovering the new pathways involved in endogenous psychotic disorders.ru_RU
dc.language.isoenru_RU
dc.publisherBMCru_RU
dc.relation.ispartofseriesBMC Genomics;Volume 20, Article number: 535 (2019)-
dc.subjectBiomarkerru_RU
dc.subjectBipolar disorderru_RU
dc.subjectSchizophreniaru_RU
dc.subjectProteomeru_RU
dc.subjectMass spectrometryru_RU
dc.subjectSerumru_RU
dc.titleThe difference in serum proteomes in schizophrenia and bipolar disorderru_RU
dc.typeArticleru_RU
Располагается в коллекциях:BMC Genomics

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