PPARD May Play a Protective Role against the Development of Schizophrenia
PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3)...
Saved in:
Published in | PPAR research Vol. 2020; no. 2020; pp. 1 - 6 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Cairo, Egypt
Hindawi Publishing Corporation
2020
Hindawi John Wiley & Sons, Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 1687-4757 1687-4765 |
DOI | 10.1155/2020/3480412 |
Cover
Abstract | PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3) 19 early onset of SCZ (EOS) patients. After that, we conducted a systematical pathway analysis to explore the potential mechanisms involved in PPARD exerting influence on the pathological development of SCZ. Compared to the HC group, the expression of PPARD was slightly decreased in the EOS group (LFC=−0.34; p=0.23) and increased in the CHR group (LFC=0.65; p=0.20). However, there was a significant difference between the EOS group and the CHR group (LFC=−0.99; p=0.015), reflecting the amount of variation in PPARD expression before and after the onset of SCZ. Pathway analysis suggested that overexpression of PPARD may regulate ten proteins or molecules to inhibit the pathological development of SCZ, including the deactivation of eight SCZ promoters and stimulation of two SCZ inhibitors. Our results support the association between PPARD and SCZ. The pathways identified may help in the understanding of the potential mechanisms by which PPARD contributes to the etiology of SCZ. |
---|---|
AbstractList | PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3) 19 early onset of SCZ (EOS) patients. After that, we conducted a systematical pathway analysis to explore the potential mechanisms involved in PPARD exerting influence on the pathological development of SCZ. Compared to the HC group, the expression of PPARD was slightly decreased in the EOS group (
LFC
=
−
0.34
;
p
=
0.23
) and increased in the CHR group (
LFC
=
0.65
;
p
=
0.20
). However, there was a significant difference between the EOS group and the CHR group (
LFC
=
−
0.99
;
p
=
0.015
), reflecting the amount of variation in PPARD expression before and after the onset of SCZ. Pathway analysis suggested that overexpression of PPARD may regulate ten proteins or molecules to inhibit the pathological development of SCZ, including the deactivation of eight SCZ promoters and stimulation of two SCZ inhibitors. Our results support the association between PPARD and SCZ. The pathways identified may help in the understanding of the potential mechanisms by which PPARD contributes to the etiology of SCZ. PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3) 19 early onset of SCZ (EOS) patients. After that, we conducted a systematical pathway analysis to explore the potential mechanisms involved in PPARD exerting influence on the pathological development of SCZ. Compared to the HC group, the expression of PPARD was slightly decreased in the EOS group (LFC=−0.34; p=0.23) and increased in the CHR group (LFC=0.65; p=0.20). However, there was a significant difference between the EOS group and the CHR group (LFC=−0.99; p=0.015), reflecting the amount of variation in PPARD expression before and after the onset of SCZ. Pathway analysis suggested that overexpression of PPARD may regulate ten proteins or molecules to inhibit the pathological development of SCZ, including the deactivation of eight SCZ promoters and stimulation of two SCZ inhibitors. Our results support the association between PPARD and SCZ. The pathways identified may help in the understanding of the potential mechanisms by which PPARD contributes to the etiology of SCZ. PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3) 19 early onset of SCZ (EOS) patients. After that, we conducted a systematical pathway analysis to explore the potential mechanisms involved in PPARD exerting influence on the pathological development of SCZ. Compared to the HC group, the expression of PPARD was slightly decreased in the EOS group (LFC = -0.34; p = 0.23) and increased in the CHR group (LFC = 0.65; p = 0.20). However, there was a significant difference between the EOS group and the CHR group (LFC = -0.99; p = 0.015), reflecting the amount of variation in PPARD expression before and after the onset of SCZ. Pathway analysis suggested that overexpression of PPARD may regulate ten proteins or molecules to inhibit the pathological development of SCZ, including the deactivation of eight SCZ promoters and stimulation of two SCZ inhibitors. Our results support the association between PPARD and SCZ. The pathways identified may help in the understanding of the potential mechanisms by which PPARD contributes to the etiology of SCZ. PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3) 19 early onset of SCZ (EOS) patients. After that, we conducted a systematical pathway analysis to explore the potential mechanisms involved in PPARD exerting influence on the pathological development of SCZ. Compared to the HC group, the expression of PPARD was slightly decreased in the EOS group (LFC = -0.34; p = 0.23) and increased in the CHR group (LFC = 0.65; p = 0.20). However, there was a significant difference between the EOS group and the CHR group (LFC = -0.99; p = 0.015), reflecting the amount of variation in PPARD expression before and after the onset of SCZ. Pathway analysis suggested that overexpression of PPARD may regulate ten proteins or molecules to inhibit the pathological development of SCZ, including the deactivation of eight SCZ promoters and stimulation of two SCZ inhibitors. Our results support the association between PPARD and SCZ. The pathways identified may help in the understanding of the potential mechanisms by which PPARD contributes to the etiology of SCZ.PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3) 19 early onset of SCZ (EOS) patients. After that, we conducted a systematical pathway analysis to explore the potential mechanisms involved in PPARD exerting influence on the pathological development of SCZ. Compared to the HC group, the expression of PPARD was slightly decreased in the EOS group (LFC = -0.34; p = 0.23) and increased in the CHR group (LFC = 0.65; p = 0.20). However, there was a significant difference between the EOS group and the CHR group (LFC = -0.99; p = 0.015), reflecting the amount of variation in PPARD expression before and after the onset of SCZ. Pathway analysis suggested that overexpression of PPARD may regulate ten proteins or molecules to inhibit the pathological development of SCZ, including the deactivation of eight SCZ promoters and stimulation of two SCZ inhibitors. Our results support the association between PPARD and SCZ. The pathways identified may help in the understanding of the potential mechanisms by which PPARD contributes to the etiology of SCZ. PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and analyzed the PPARD expression profile from three groups: (1) 18 healthy control (HC) subjects, (2) 14 clinical high-risk (CHR) patients, and (3) 19 early onset of SCZ (EOS) patients. After that, we conducted a systematical pathway analysis to explore the potential mechanisms involved in PPARD exerting influence on the pathological development of SCZ. Compared to the HC group, the expression of PPARD was slightly decreased in the EOS group (LFC = −0.34; p = 0.23) and increased in the CHR group (LFC = 0.65; p = 0.20). However, there was a significant difference between the EOS group and the CHR group (LFC = −0.99; p = 0.015), reflecting the amount of variation in PPARD expression before and after the onset of SCZ. Pathway analysis suggested that overexpression of PPARD may regulate ten proteins or molecules to inhibit the pathological development of SCZ, including the deactivation of eight SCZ promoters and stimulation of two SCZ inhibitors. Our results support the association between PPARD and SCZ. The pathways identified may help in the understanding of the potential mechanisms by which PPARD contributes to the etiology of SCZ. |
Audience | Academic |
Author | Xu, Yong Liu, Sha Li, Xinrong Kapoor, Karan |
AuthorAffiliation | 2 Department of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical University, Taiyuan, China 3 NIH Center for Macromolecular Modeling and Bioinformatics, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA 1 Shanxi Key Laboratory of Artificial Intelligence Assisted Diagnosis and Treatment for Mental Disorder, First Hospital of Shanxi Medical University, Taiyuan, China |
AuthorAffiliation_xml | – name: 1 Shanxi Key Laboratory of Artificial Intelligence Assisted Diagnosis and Treatment for Mental Disorder, First Hospital of Shanxi Medical University, Taiyuan, China – name: 3 NIH Center for Macromolecular Modeling and Bioinformatics, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA – name: 2 Department of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical University, Taiyuan, China |
Author_xml | – sequence: 1 fullname: Xu, Yong – sequence: 2 fullname: Kapoor, Karan – sequence: 3 fullname: Liu, Sha – sequence: 4 fullname: Li, Xinrong |
BookMark | eNqFktuLEzEUxgdZcS_65rMM-CJod3ObTPIilF0vhRXLqs_hTHLSpkwn3cy0sv71pra6dFEkkITk930n5-ScFkdd7LAonlNyTmlVXTDCyAUXigjKHhUnVKp6JGpZHf3ZV_Vxcdr3C0Iqzhl5UhxzpjhVVJ4Uk-l0fHNVfoK7ctrmCcppigPaIWywvIktljCD0PVDOcyxvMINtnG1xG4ooy-_2Hn4EVfzhF2Ap8VjD22Pz_brWfHt_buvlx9H158_TC7H1yNbKTqMvBScOQThgEhfE1ZzyUVFmxqwEVb5ijKhHK2dolpo3VCupbdSNso5ApafFZOdr4uwMKsUlpDuTIRgfh3ENDOQhmBbNJWXkoEC1DUXpPJKaQDVaM-ly9F49nq781qtmyU6m_NK0B6YHt50YW5mcWNqwZTiIhu82hukeLvGfjDL0FtsW-gwrnvDBM9_QLVmGX35AF3EdepyqbaUEITkV95TM8gJhM7HHNduTc1Ycp2rpQnJ1PlfqDwcLoPN_eFDPj8QsJ3Aptj3Cb2xYYAhxG1aoTWUmG0zmW0zmX0zZdGbB6LfhfkH_nqHz0Pn4Hv4H_1iR2Nm0MM9zYistOQ_AeYJ3fE |
CitedBy_id | crossref_primary_10_4103_1673_5374_357908 crossref_primary_10_1016_j_pbb_2023_173706 crossref_primary_10_1038_s41598_022_05129_7 |
Cites_doi | 10.1023/A:1022034115078 10.1038/tp.2014.128 10.1016/j.schres.2012.06.031 10.1124/jpet.116.233106 10.1016/j.plipres.2005.12.002 10.1038/mp.2012.23 10.1016/j.neuroscience.2003.11.012 10.1038/npp.2013.81 10.1016/j.schres.2018.06.023 10.1093/schbul/sbl060 10.3892/ijmm.2018.3588 10.1093/schbul/sbm103 10.1016/j.schres.2007.12.348 10.1038/tp.2017.182 10.1097/BRS.0b013e3182276d88 10.1016/j.schres.2010.02.1070 10.1038/nature09563 10.1007/s12035-016-9954-7 10.1038/sj.mp.4001563 10.1002/art.38915 10.1016/0920-9964(92)90004-O 10.1146/annurev.med.53.082901.104018 10.1097/YPG.0000000000000181 10.3760/cma.j.issn.0366-6999.20132972 10.1007/s00109-016-1501-5 10.1093/schbul/22.2.353 10.1186/1471-244X-12-150 |
ContentType | Journal Article |
Copyright | Copyright © 2020 Xinrong Li et al. COPYRIGHT 2020 John Wiley & Sons, Inc. Copyright © 2020 Xinrong Li et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 Copyright © 2020 Xinrong Li et al. 2020 |
Copyright_xml | – notice: Copyright © 2020 Xinrong Li et al. – notice: COPYRIGHT 2020 John Wiley & Sons, Inc. – notice: Copyright © 2020 Xinrong Li et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 – notice: Copyright © 2020 Xinrong Li et al. 2020 |
DBID | ADJCN AHFXO RHU RHW RHX AAYXX CITATION 3V. 7X7 7XB 8AO 8FE 8FH 8FI 8FJ 8FK ABUWG AFKRA AZQEC BBNVY BENPR BHPHI CCPQU CWDGH DWQXO FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0S M7P PHGZM PHGZT PIMPY PKEHL PQEST PQGLB PQQKQ PQUKI PRINS 7X8 5PM DOA |
DOI | 10.1155/2020/3480412 |
DatabaseName | الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete Hindawi Publishing Complete Hindawi Publishing Subscription Journals Hindawi Publishing Open Access CrossRef ProQuest Central (Corporate) ProQuest Health & Medical Collection ProQuest Central (purchase pre-March 2016) ProQuest Pharma Collection ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials - QC Biological Science Collection ProQuest Central Natural Science Collection ProQuest One Community College Middle East & Africa Database ProQuest Central Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Biological Sciences ProQuest Health & Medical Collection ProQuest Biological Science ProQuest Central Premium ProQuest One Academic (New) ProQuest Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef Publicly Available Content Database ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China ProQuest Central ProQuest One Applied & Life Sciences Health Research Premium Collection Middle East & Africa Database Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Biological Science Collection ProQuest Central (New) ProQuest Biological Science Collection ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest One Academic UKI Edition ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | CrossRef MEDLINE - Academic Publicly Available Content Database |
Database_xml | – sequence: 1 dbid: RHX name: Hindawi Publishing Open Access url: http://www.hindawi.com/journals/ sourceTypes: Publisher – sequence: 2 dbid: DOA name: DOAJ Open Access Full Text url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 3 dbid: BENPR name: ProQuest Central url: http://www.proquest.com/pqcentral?accountid=15518 sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1687-4765 |
Editor | Nesterova, Anastasia |
Editor_xml | – sequence: 1 givenname: Anastasia surname: Nesterova fullname: Nesterova, Anastasia |
EndPage | 6 |
ExternalDocumentID | oai_doaj_org_article_5f662a8ae973405f889aa8b9f36daeb3 PMC7428834 A639273900 10_1155_2020_3480412 1206596 |
GeographicLocations | China |
GeographicLocations_xml | – name: China |
GrantInformation_xml | – fundername: Scientific Research Project of Shanxi Health Commission grantid: 201601034 – fundername: National Key Research and Development Program of China grantid: 2016YFC1307004 – fundername: Support Program of the Youth Sanjin Scholars – fundername: National Natural Science Foundation of China grantid: 81701326; 81971601 – fundername: Youth Science and Technology Research Fund of Shanxi grantid: 201801D221418 – fundername: Multidisciplinary Team for Cognitive Impairment of Shanxi Science and Technology Innovation Training Team grantid: 201705D131027 – fundername: 136 Medical Rejuvenation Project of Shanxi Province |
GroupedDBID | --- 0R~ 123 188 24P 29O 2UF 2WC 4.4 53G 7X7 8AO 8FE 8FH 8FI 8FJ 8R4 8R5 AAFWJ AAMMB ABDBF ABUWG ACCMX ACPRK ACUHS ADBBV ADJCN ADRAZ AEFGJ AENEX AFKRA AFPKN AGXDD AHFXO AHMBA AIDQK AIDYY ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BBNVY BCNDV BENPR BHPHI BPHCQ BVXVI C1A CCPQU CS3 CWDGH DIK E3Z EBD EBS EJD ESX F5P FYUFA GROUPED_DOAJ GX1 H13 HCIFZ HMCUK HYE IAO IGS IHR IL9 ITC KQ8 LK8 M48 M7P O5R O5S OK1 OVT P2P PGMZT PHGZM PHGZT PIMPY PQGLB PQQKQ PROAC PUEGO Q2X RHU RNS RPM TR2 TUS UKHRP UZ3 WOQ WOW ~8M 3V. AAJEY AINHJ RHW RHX AAYXX ALIPV CITATION PMFND 7XB 8FK AZQEC DWQXO GNUQQ K9. PKEHL PQEST PQUKI PRINS 7X8 5PM |
ID | FETCH-LOGICAL-c581t-f6432dea4da06f7027363451b7aeb4c8f51248d17d819499b1396fc66b8dd0ac3 |
IEDL.DBID | M48 |
ISSN | 1687-4757 |
IngestDate | Wed Aug 27 01:32:00 EDT 2025 Thu Aug 21 13:57:16 EDT 2025 Fri Sep 05 05:22:42 EDT 2025 Fri Jul 25 19:00:59 EDT 2025 Tue Jun 17 22:02:50 EDT 2025 Tue Jun 10 21:01:55 EDT 2025 Tue Jul 01 01:29:04 EDT 2025 Thu Apr 24 23:05:20 EDT 2025 Sun Jun 02 18:55:03 EDT 2024 Thu Sep 25 15:10:09 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2020 |
Language | English |
License | This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c581t-f6432dea4da06f7027363451b7aeb4c8f51248d17d819499b1396fc66b8dd0ac3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Guest Editor: Anastasia Nesterova |
ORCID | 0000-0002-7138-8706 0000-0001-9679-2273 |
OpenAccessLink | https://dx.doi.org/10.1155/2020/3480412 |
PMID | 32831816 |
PQID | 2434400973 |
PQPubID | 237771 |
PageCount | 6 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_5f662a8ae973405f889aa8b9f36daeb3 pubmedcentral_primary_oai_pubmedcentral_nih_gov_7428834 proquest_miscellaneous_2436871992 proquest_journals_2434400973 gale_infotracmisc_A639273900 gale_infotracacademiconefile_A639273900 crossref_citationtrail_10_1155_2020_3480412 crossref_primary_10_1155_2020_3480412 hindawi_primary_10_1155_2020_3480412 emarefa_primary_1206596 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2020-00-00 |
PublicationDateYYYYMMDD | 2020-01-01 |
PublicationDate_xml | – year: 2020 text: 2020-00-00 |
PublicationDecade | 2020 |
PublicationPlace | Cairo, Egypt |
PublicationPlace_xml | – name: Cairo, Egypt – name: New York |
PublicationTitle | PPAR research |
PublicationYear | 2020 |
Publisher | Hindawi Publishing Corporation Hindawi John Wiley & Sons, Inc Wiley |
Publisher_xml | – name: Hindawi Publishing Corporation – name: Hindawi – name: John Wiley & Sons, Inc – name: Wiley |
References | 22 23 24 25 26 27 (21) 2014; 127 10 11 12 13 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 |
References_xml | – ident: 14 doi: 10.1023/A:1022034115078 – ident: 22 doi: 10.1038/tp.2014.128 – ident: 23 doi: 10.1016/j.schres.2012.06.031 – ident: 18 doi: 10.1124/jpet.116.233106 – ident: 10 doi: 10.1016/j.plipres.2005.12.002 – ident: 7 doi: 10.1038/mp.2012.23 – ident: 27 doi: 10.1016/j.neuroscience.2003.11.012 – ident: 17 doi: 10.1038/npp.2013.81 – ident: 19 doi: 10.1016/j.schres.2018.06.023 – ident: 3 doi: 10.1093/schbul/sbl060 – ident: 16 doi: 10.3892/ijmm.2018.3588 – ident: 8 doi: 10.1093/schbul/sbm103 – ident: 11 doi: 10.1016/j.schres.2007.12.348 – ident: 12 doi: 10.1038/tp.2017.182 – ident: 26 doi: 10.1097/BRS.0b013e3182276d88 – ident: 15 doi: 10.1016/j.schres.2010.02.1070 – ident: 2 doi: 10.1038/nature09563 – ident: 24 doi: 10.1007/s12035-016-9954-7 – ident: 1 doi: 10.1038/sj.mp.4001563 – ident: 20 doi: 10.1002/art.38915 – ident: 5 doi: 10.1016/0920-9964(92)90004-O – ident: 9 doi: 10.1146/annurev.med.53.082901.104018 – ident: 13 doi: 10.1097/YPG.0000000000000181 – volume: 127 start-page: 2129 issue: 11 year: 2014 ident: 21 publication-title: Chinese Medical Journal doi: 10.3760/cma.j.issn.0366-6999.20132972 – ident: 25 doi: 10.1007/s00109-016-1501-5 – ident: 4 doi: 10.1093/schbul/22.2.353 – ident: 6 doi: 10.1186/1471-244X-12-150 |
SSID | ssj0053320 |
Score | 2.2069182 |
Snippet | PPARD has been suggested to contribute to the etiology of schizophrenia (SCZ) with the underlying mechanisms largely unknown. Here, we first collected and... |
SourceID | doaj pubmedcentral proquest gale crossref hindawi emarefa |
SourceType | Open Website Open Access Repository Aggregation Database Enrichment Source Index Database Publisher |
StartPage | 1 |
SubjectTerms | Age Bioinformatics Comparative analysis Deactivation Development and progression Disease Etiology Gene expression Hybridization Labeling Mental disorders Neurophysiology Peroxisome proliferator-activated receptors Proteins Roles Schizophrenia |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1LaxsxEBYlEOilNH1u4xYVUnooS7S7eu3RfYRQSAlpA7mJkVZqDGZdWoeSf9-ZXdn1HkouvRhsDaw1Go2-zx59w9hRq0KTVA1lVRlfSk95MHaiNHi4VDY1USi6nHz2RZ9eys9X6mqn1RfVhI3ywKPjjlXSugYLsTUNgotkbQtgfZsa3QEyQcq-ohUbMjXmYMQwgyBjpXELSaPMpuRdKWL74riRpLtTTw6jQbN_uJgL-B62OXr_mtjx78UEg04rKHeOpJOH7EHGknw-zuGA3Yv9I7Y_dpe8fcyQss8vPvIzuOXnS3wBfj6KMmCC4xerZeTwHRYIDzmCQL5TPcRXiX_dLcZ7wi5PPn37cFrmzgllULZalwlxRt1FkB0InQxp1uhGqsobdJkMNuFKSNtVpkNAgJzHIw7UKWjtbdcJCM1Tttev-vic8YCcsJHIMnFcxiB8q2ObbPIREijRFezdxoUuZFlx6m6xdAO9UMqRw112eMHebK1_jHIa_7B7T6uxtSER7OEDDA2XQ8PdFRoFe5bX8u-zavofWRfsLa2to02MXzZAvouAUyY5LDdH3IY-a4Uo2GxiiZsvTIaPcnTcMZ3ZJnRczhG_XC3JrySXVLDX22F6ANW99XF1M9hgCFOJcMHMJOQmrpmO9IvrQSfcSGolLV_8D18esvs0ofHHpxnbW_-8iS8Rjq39q2Hn_QENziwm priority: 102 providerName: Directory of Open Access Journals – databaseName: Hindawi Publishing Open Access dbid: RHX link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1bi9NAFB50YcEXcb1Gq4yw4oMEk8w1j_WyFGFlqS70bZirWyipuF1k__2ek0xro4i-FNI5JZkz5_Kd5sw3hBy3wrMkGlvWtXIldxgHY6hKBcml1onFSuDm5NPPcnbOPy3EIpMkXf75Ch-yHZbn1VvGkSgHYu1tLdF457PFNuACYOnZF2sJ_sKVUNv-9t9-O8o8PUF_vwvXwrXdBeTDCyyFfy5HgHPcLrmXf07ukbsZONLpsNJH5Fbs7pPD4SjJ6wcE6vPp_AM9tdf0bAUflp4NDAwQzeh8vYrUfrNLwIIUEB_daxWi60S_7HfePSTnJx-_vp-V-ZiE0gtdb8oEoKIJ0fJgK5kUEtRIxkXtlI2Oe51A7VyHWgXI_lDgOAB9MnkpnQ6hsp49IgfduotPCPVQADIOJSWM8-gr18rYJp1ctMmKKhTkzVaFxmcOcTzKYmX6WkIIgwo3WeEFebWT_j5wZ_xF7h2uxk4GGa_7L8AKTHYgI5KUjdU2tooByExat9Zq1yYmA8yTFeRxXstf92rwpbEsyGtcW4MeCw_rbd54AFNG7iszBZAGOmurqiCTkSR4mh8NH2fr-Md0JlvTMTkgXJqGo16RG6kgL3fDeANscuvi-qqXARPGfuCCqJHJjVQzHumWFz0puOJ4bjR_-n_P-Izcwcvhv6QJOdj8uIrPAV1t3Ivet24AMHMYtA priority: 102 providerName: Hindawi Publishing – databaseName: ProQuest Health & Medical Collection dbid: 7X7 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1La9wwEBZtSqCX0nfdbosKKT0UEz_08qlsHyEUUkLawN6ErEeysNhpsqHk33dG1jrrQ9vLglcDskaj0Tfy6BtC9hpu68Ark5elbHPWoh_0rsglbC6lCrUvOF5OPvouDk_ZtwVfpAO3q5RWufGJ0VG73uIZ-X7FasYiuczHi185Vo3Cr6uphMZdcq8EJIKlG-RiDLgAyURaxlLAQmKSy03iO-cY8xf7NUP2nWqyJUXm_ng918CzGT317jnGyL-XEyQ6zaPc2pgOHpIHCVHS-WACj8gd3z0mu0ONyZsnBAL3-ckXemRu6PEKfgw9HqgZwM3Rk37lqTkzSwCJFKAg3cohon2gP7ZT8p6S04OvPz8f5ql-Qm65Ktd5ALRROW-YM4UIEplrRM142UrjW2ZVgPlgypXSASyAyKcFNCiCFaJVzhXG1s_ITtd3_gWhFiJD1H8F7czbom2Eb4IKrTfB8MJl5MNGhdomcnGscbHSMcjgXKPCdVJ4Rt6N0hcDqcZf5D7hbIwySIUd_-gvz3RaWZoHISqjjAfTAPQZlGqMUW0TauFgnHVGnqe5vO2rwq_JIiPvcW41LmV4WWvSjQQYMpJi6TmgN9BZUxQZmU0kYQnaSfNeso7_DGe2MR2dPMWVvrXrjLwdm7EDzH7rfH8dZcCEMVE4I3JichPVTFu65XlkC5cMC0qzl__u_BW5j686HC7NyM768tq_Bri1bt_ENfUHsnsi9A priority: 102 providerName: ProQuest |
Title | PPARD May Play a Protective Role against the Development of Schizophrenia |
URI | https://search.emarefa.net/detail/BIM-1206596 https://dx.doi.org/10.1155/2020/3480412 https://www.proquest.com/docview/2434400973 https://www.proquest.com/docview/2436871992 https://pubmed.ncbi.nlm.nih.gov/PMC7428834 https://doaj.org/article/5f662a8ae973405f889aa8b9f36daeb3 |
Volume | 2020 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV3db9MwED-NTZN4QXyTUSojDfGAAvnwR_KAUAcbFdKmqlCpb5Hj2FulqoGuE_S_585JS4P4eLGU2FHi8539u_j8O4DjXJjUiUSHcazKkJc0D9oqChUuLnHmUhsJOpx8fiGHE_5pKqZ7sMk22grw-o-uHeWTmiznr398W79Dg3_rDV4I8t-jNyknJh2cjA_8ThEF8fHtfgJiGk_QGEs0Ka6E2oTA__Z0Z3HyHP7-oK7Ga72dsw-vyFv-Putg0m5E5c4SdXYX7rTYkg0aZbgHe3ZxHw6bbJPrB4Au_GD8gZ3rNRvNsdBs1JA04ITHxvXcMn2pZwgXGYJCthNNxGrHPu8G5z2Eydnpl_fDsM2kEBqRxavQIe5IKqt5pSPpFHHYyJSLuFTaltxkDkeGZ1WsKgQI6AOViAulM1KWWVVF2qSPYH9RL-wTYAZ9xJSj14n13JqozKXNXeZKq50WURXAq40IC9PSjFO2i3nh3Q0hChJ40Qo8gBfb1l8beo2_tDuh0di2IVJsf6NeXhatjRXCSZnoTNtcpYhDXZblWmdl7lJZYT_TAB63Y_nrXQntK8sAXtLYFqRm-LFGt2cTsMtEj1UMEMehzPIoCqDXaYnGaDrVx612_Kc7vY3qFBuVLxJOciX6pACeb6vpBRQHt7D1jW-DKkwhwwGojsp1RNOtWcyuPG-44pRamh_9uwtP4TZ9avObqQf7q-WNfYbAa1X24Zaaqj4cnJxejMZ9__sCy4_TuO-tDcvxcPoTHcAp5g |
linkProvider | Scholars Portal |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3dT9swED-xIrS9oH0vrNs8CbSHKSIftpM8oKkMUDtoVXUg8RacxIZKVcOgCPWf29-2u9QpzcO2J14qpbZi-3y-D-fudwDbichDIwLl-n6UuTwjOagLz41QufixCbUnKDm5P5DdM_7jXJyvwe86F4bCKmuZWAnqoszpjnw34CHnFbjMt-tfLlWNoq-rdQkNZUsrFHsVxJhN7DjW83t04W73ege43ztBcHR4-r3r2ioDbi5if-Ya1MlBoRUvlCdNRPguMuTCzyKlM57HBmfN48KPClSe6B9kaDNJk0uZxUXhqTzE9z6BdU4XKC1Y3z8cDEe1LkBbqgKG9CUeZR6JqA69F4JuHbzdkBP-T9BQilXtgCpBWOGzWuqKjSvy0u_HDVu4Gcm5ohqPnsOmtWlZZ8GEL2BNT1_CxqLK5fwV9IbDzuiA9dWcDSf4o9hwAQ6BgpaNyolm6lKN0UxlaIyylSgmVhr2czUo8DWcPQpt30BrWk71O2A5-qbEAQG2c517WSJ1YmKTaWWU8AoHvtYkTHMLb05VNiZp5eYIkRLBU0twB3aWva8XsB5_6bdPu7HsQ2Dc1R_lzWVqz3YqjJSBipVG5kT718RxolScJSaUBa4zdOCt3cuHsQL6ni0d-EJ7m5IwwcnmyuZE4JIJlivtoP2INEs8z4F2oycKgbzRvG254z_Ladesk1pZdZs-nCwHPi-baQCKv5vq8q7qgyxMocoORA2Wa5Cm2TIdX1V45RGnktZ869-Df4Kn3dP-SXrSGxy_h2c07cVVVxtas5s7_QGNv1n20Z4wBhePfaj_AJScZeg |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3Nb9MwFLfGpiEuiG8CBYy0iQOKmg_bSQ4T6uiqlbEqKkzazXNie6tUNWPrNPVf5K_ivdTpmgNw2qVSa6uOn9-n897vEbKT8TK2PFJ-GCaFzwrUg0YHfgLGJUxtbAKOxcnHI3F4wr6d8tMN8ruphcG0ykYn1opaVyXekXcjFjNWg8t0rUuLyPuDL5e_fOwghW9am3YayrVZ0Hs13Jgr8jgyi1sI5673hn04-90oGhz8_Hrou44DfsnTcO5bsM-RNoppFQibINaLiBkPi0SZgpWphR2wVIeJBkMKsUIB_pOwpRBFqnWgyhj-9wHZSsDqQyC4tX8wyseNXQC_qgaJDAWINUt40qThc443EEE3ZogFFLUMZN1HoC4WVvBdrezG9gVG7LeTll_czupcM5ODJ-Sx829pb8mQT8mGmT0j28uOl4vnZJjnvXGfHqsFzafwoWi-BIoApUvH1dRQda4m4LJScEzpWkYTrSz9sZ4g-IKc3AttX5LNWTUzrwktIU5FbohgnJkyKDJhMpvawiireKA98rkhoSwd1Dl23JjKOuThXCLBpSO4R3ZXsy-XEB9_mbePp7Gag8Dc9Q_V1bl0ci65FSJSqTLAqOAL2zTNlEqLzMZCwz5jj7xyZ3m3VoTvtoVHPuHZSlQs8LClcvURsGWE6JI98CWBZlkQeKTTmgkKoWwN7zju-M92Og3rSKe3ruWdlHnk42oYF8BcvJmpbuo5wMKYtuyRpMVyLdK0R2aTixq7PGHY3pq9-ffiH8hDEG75fTg6ekse4VMvb706ZHN-dWPegR84L947AaPk7L5l-g_bEmos |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=PPARD+May+Play+a+Protective+Role+against+the+Development+of+Schizophrenia&rft.jtitle=PPAR+research&rft.au=Li%2C+Xinrong&rft.au=Liu%2C+Sha&rft.au=Kapoor%2C+Karan&rft.au=Xu%2C+Yong&rft.date=2020&rft.pub=John+Wiley+%26+Sons%2C+Inc&rft.issn=1687-4757&rft.volume=2020&rft_id=info:doi/10.1155%2F2020%2F3480412&rft.externalDocID=A639273900 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1687-4757&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1687-4757&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1687-4757&client=summon |