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)...

Full description

Saved in:
Bibliographic Details
Published inPPAR research Vol. 2020; no. 2020; pp. 1 - 6
Main Authors Xu, Yong, Kapoor, Karan, Liu, Sha, Li, Xinrong
Format Journal Article
LanguageEnglish
Published Cairo, Egypt Hindawi Publishing Corporation 2020
Hindawi
John Wiley & Sons, Inc
Wiley
Subjects
Online AccessGet full text
ISSN1687-4757
1687-4765
DOI10.1155/2020/3480412

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