Single-cell characterization of self-renewing primary trophoblast organoids as modeling of EVT differentiation and interactions with decidual natural killer cells

Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still...

Full description

Saved in:
Bibliographic Details
Published inBMC genomics Vol. 24; no. 1; pp. 1 - 18
Main Authors Zhuang, Bai-Mei, Cao, Dan-Dan, Li, Tian-Xi, Liu, Xiao-Feng, Lyu, Min-Min, Wang, Si-Dong, Cui, Xin-Yuan, Wang, Li, Chen, Xiao-Lin, Lin, Xiao-Li, Lee, Cheuk-Lun, Chiu, Philip C.N., Yeung, William S.B., Yao, Yuan-Qing
Format Journal Article
LanguageEnglish
Published London BioMed Central Ltd 18.10.2023
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still lacking. Recent trophoblast organoid (TO) has advanced the molecular and mechanistic research in placentation. Here, we firstly generated the self-renewing TO from human placental villous and differentiated it into EVTs (EVT-TO) for investigating the differentiation events. We then co-cultured EVT-TO with freshly isolated decidual NKs for further study of cell communication. TO modelling of EVT differentiation as well as EVT interaction with dNK might cast new aspect for placentation research. Single-cell RNA sequencing (scRNA-seq) was applied for comprehensive characterization and molecular exploration of TOs modelling of EVT differentiation and interaction with dNKs. Multiple distinct trophoblast states and dNK subpopulations were identified, representing CTB, STB, EVT, dNK1/2/3 and dNKp. Lineage trajectory and Seurat mapping analysis identified the close resemblance of TO and EVT-TO with the human placenta characteristic. Transcription factors regulatory network analysis revealed the cell-type specific essential TFs for controlling EVT differentiation. CellphoneDB analysis predicted the ligand-receptor complexes in dNK-EVT-TO co-cultures, which relate to cytokines, immunomodulation and angiogenesis. EVT was known to affect the immune properties of dNK. Our study found out that on the other way around, dNKs could exert effects on EVT causing expression changes which are functionally important. Our study documented a single-cell atlas for TO and its applications on EVT differentiation and communications with dNKs, and thus provide methodology and novel research cues for future study of human placentation.
AbstractList Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still lacking. Recent trophoblast organoid (TO) has advanced the molecular and mechanistic research in placentation. Here, we firstly generated the self-renewing TO from human placental villous and differentiated it into EVTs (EVT-TO) for investigating the differentiation events. We then co-cultured EVT-TO with freshly isolated decidual NKs for further study of cell communication. TO modelling of EVT differentiation as well as EVT interaction with dNK might cast new aspect for placentation research. Single-cell RNA sequencing (scRNA-seq) was applied for comprehensive characterization and molecular exploration of TOs modelling of EVT differentiation and interaction with dNKs. Multiple distinct trophoblast states and dNK subpopulations were identified, representing CTB, STB, EVT, dNK1/2/3 and dNKp. Lineage trajectory and Seurat mapping analysis identified the close resemblance of TO and EVT-TO with the human placenta characteristic. Transcription factors regulatory network analysis revealed the cell-type specific essential TFs for controlling EVT differentiation. CellphoneDB analysis predicted the ligand-receptor complexes in dNK-EVT-TO co-cultures, which relate to cytokines, immunomodulation and angiogenesis. EVT was known to affect the immune properties of dNK. Our study found out that on the other way around, dNKs could exert effects on EVT causing expression changes which are functionally important. Our study documented a single-cell atlas for TO and its applications on EVT differentiation and communications with dNKs, and thus provide methodology and novel research cues for future study of human placentation.
Abstract Background Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still lacking. Recent trophoblast organoid (TO) has advanced the molecular and mechanistic research in placentation. Here, we firstly generated the self-renewing TO from human placental villous and differentiated it into EVTs (EVT-TO) for investigating the differentiation events. We then co-cultured EVT-TO with freshly isolated decidual NKs for further study of cell communication. TO modelling of EVT differentiation as well as EVT interaction with dNK might cast new aspect for placentation research. Results Single-cell RNA sequencing (scRNA-seq) was applied for comprehensive characterization and molecular exploration of TOs modelling of EVT differentiation and interaction with dNKs. Multiple distinct trophoblast states and dNK subpopulations were identified, representing CTB, STB, EVT, dNK1/2/3 and dNKp. Lineage trajectory and Seurat mapping analysis identified the close resemblance of TO and EVT-TO with the human placenta characteristic. Transcription factors regulatory network analysis revealed the cell-type specific essential TFs for controlling EVT differentiation. CellphoneDB analysis predicted the ligand-receptor complexes in dNK-EVT-TO co-cultures, which relate to cytokines, immunomodulation and angiogenesis. EVT was known to affect the immune properties of dNK. Our study found out that on the other way around, dNKs could exert effects on EVT causing expression changes which are functionally important. Conclusion Our study documented a single-cell atlas for TO and its applications on EVT differentiation and communications with dNKs, and thus provide methodology and novel research cues for future study of human placentation.
Background Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still lacking. Recent trophoblast organoid (TO) has advanced the molecular and mechanistic research in placentation. Here, we firstly generated the self-renewing TO from human placental villous and differentiated it into EVTs (EVT-TO) for investigating the differentiation events. We then co-cultured EVT-TO with freshly isolated decidual NKs for further study of cell communication. TO modelling of EVT differentiation as well as EVT interaction with dNK might cast new aspect for placentation research. Results Single-cell RNA sequencing (scRNA-seq) was applied for comprehensive characterization and molecular exploration of TOs modelling of EVT differentiation and interaction with dNKs. Multiple distinct trophoblast states and dNK subpopulations were identified, representing CTB, STB, EVT, dNK1/2/3 and dNKp. Lineage trajectory and Seurat mapping analysis identified the close resemblance of TO and EVT-TO with the human placenta characteristic. Transcription factors regulatory network analysis revealed the cell-type specific essential TFs for controlling EVT differentiation. CellphoneDB analysis predicted the ligand-receptor complexes in dNK-EVT-TO co-cultures, which relate to cytokines, immunomodulation and angiogenesis. EVT was known to affect the immune properties of dNK. Our study found out that on the other way around, dNKs could exert effects on EVT causing expression changes which are functionally important. Conclusion Our study documented a single-cell atlas for TO and its applications on EVT differentiation and communications with dNKs, and thus provide methodology and novel research cues for future study of human placentation. Keywords: Trophoblast organoid, Extravillous trophoblast, Trophoblast differentiation, Placentation, Pregnancy
BackgroundExtravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still lacking. Recent trophoblast organoid (TO) has advanced the molecular and mechanistic research in placentation. Here, we firstly generated the self-renewing TO from human placental villous and differentiated it into EVTs (EVT-TO) for investigating the differentiation events. We then co-cultured EVT-TO with freshly isolated decidual NKs for further study of cell communication. TO modelling of EVT differentiation as well as EVT interaction with dNK might cast new aspect for placentation research.ResultsSingle-cell RNA sequencing (scRNA-seq) was applied for comprehensive characterization and molecular exploration of TOs modelling of EVT differentiation and interaction with dNKs. Multiple distinct trophoblast states and dNK subpopulations were identified, representing CTB, STB, EVT, dNK1/2/3 and dNKp. Lineage trajectory and Seurat mapping analysis identified the close resemblance of TO and EVT-TO with the human placenta characteristic. Transcription factors regulatory network analysis revealed the cell-type specific essential TFs for controlling EVT differentiation. CellphoneDB analysis predicted the ligand-receptor complexes in dNK-EVT-TO co-cultures, which relate to cytokines, immunomodulation and angiogenesis. EVT was known to affect the immune properties of dNK. Our study found out that on the other way around, dNKs could exert effects on EVT causing expression changes which are functionally important.ConclusionOur study documented a single-cell atlas for TO and its applications on EVT differentiation and communications with dNKs, and thus provide methodology and novel research cues for future study of human placentation.
Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still lacking. Recent trophoblast organoid (TO) has advanced the molecular and mechanistic research in placentation. Here, we firstly generated the self-renewing TO from human placental villous and differentiated it into EVTs (EVT-TO) for investigating the differentiation events. We then co-cultured EVT-TO with freshly isolated decidual NKs for further study of cell communication. TO modelling of EVT differentiation as well as EVT interaction with dNK might cast new aspect for placentation research.BACKGROUNDExtravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK) cell are critical events for placentation. However, appropriate in vitro modelling system and regulatory programs of these two events are still lacking. Recent trophoblast organoid (TO) has advanced the molecular and mechanistic research in placentation. Here, we firstly generated the self-renewing TO from human placental villous and differentiated it into EVTs (EVT-TO) for investigating the differentiation events. We then co-cultured EVT-TO with freshly isolated decidual NKs for further study of cell communication. TO modelling of EVT differentiation as well as EVT interaction with dNK might cast new aspect for placentation research.Single-cell RNA sequencing (scRNA-seq) was applied for comprehensive characterization and molecular exploration of TOs modelling of EVT differentiation and interaction with dNKs. Multiple distinct trophoblast states and dNK subpopulations were identified, representing CTB, STB, EVT, dNK1/2/3 and dNKp. Lineage trajectory and Seurat mapping analysis identified the close resemblance of TO and EVT-TO with the human placenta characteristic. Transcription factors regulatory network analysis revealed the cell-type specific essential TFs for controlling EVT differentiation. CellphoneDB analysis predicted the ligand-receptor complexes in dNK-EVT-TO co-cultures, which relate to cytokines, immunomodulation and angiogenesis. EVT was known to affect the immune properties of dNK. Our study found out that on the other way around, dNKs could exert effects on EVT causing expression changes which are functionally important.RESULTSSingle-cell RNA sequencing (scRNA-seq) was applied for comprehensive characterization and molecular exploration of TOs modelling of EVT differentiation and interaction with dNKs. Multiple distinct trophoblast states and dNK subpopulations were identified, representing CTB, STB, EVT, dNK1/2/3 and dNKp. Lineage trajectory and Seurat mapping analysis identified the close resemblance of TO and EVT-TO with the human placenta characteristic. Transcription factors regulatory network analysis revealed the cell-type specific essential TFs for controlling EVT differentiation. CellphoneDB analysis predicted the ligand-receptor complexes in dNK-EVT-TO co-cultures, which relate to cytokines, immunomodulation and angiogenesis. EVT was known to affect the immune properties of dNK. Our study found out that on the other way around, dNKs could exert effects on EVT causing expression changes which are functionally important.Our study documented a single-cell atlas for TO and its applications on EVT differentiation and communications with dNKs, and thus provide methodology and novel research cues for future study of human placentation.CONCLUSIONOur study documented a single-cell atlas for TO and its applications on EVT differentiation and communications with dNKs, and thus provide methodology and novel research cues for future study of human placentation.
ArticleNumber 618
Audience Academic
Author Zhuang, Bai-Mei
Cui, Xin-Yuan
Wang, Li
Li, Tian-Xi
Lyu, Min-Min
Cao, Dan-Dan
Yao, Yuan-Qing
Yeung, William S.B.
Wang, Si-Dong
Chen, Xiao-Lin
Lin, Xiao-Li
Lee, Cheuk-Lun
Liu, Xiao-Feng
Chiu, Philip C.N.
Author_xml – sequence: 1
  givenname: Bai-Mei
  surname: Zhuang
  fullname: Zhuang, Bai-Mei
– sequence: 2
  givenname: Dan-Dan
  surname: Cao
  fullname: Cao, Dan-Dan
– sequence: 3
  givenname: Tian-Xi
  surname: Li
  fullname: Li, Tian-Xi
– sequence: 4
  givenname: Xiao-Feng
  surname: Liu
  fullname: Liu, Xiao-Feng
– sequence: 5
  givenname: Min-Min
  surname: Lyu
  fullname: Lyu, Min-Min
– sequence: 6
  givenname: Si-Dong
  surname: Wang
  fullname: Wang, Si-Dong
– sequence: 7
  givenname: Xin-Yuan
  surname: Cui
  fullname: Cui, Xin-Yuan
– sequence: 8
  givenname: Li
  surname: Wang
  fullname: Wang, Li
– sequence: 9
  givenname: Xiao-Lin
  surname: Chen
  fullname: Chen, Xiao-Lin
– sequence: 10
  givenname: Xiao-Li
  surname: Lin
  fullname: Lin, Xiao-Li
– sequence: 11
  givenname: Cheuk-Lun
  surname: Lee
  fullname: Lee, Cheuk-Lun
– sequence: 12
  givenname: Philip C.N.
  surname: Chiu
  fullname: Chiu, Philip C.N.
– sequence: 13
  givenname: William S.B.
  surname: Yeung
  fullname: Yeung, William S.B.
– sequence: 14
  givenname: Yuan-Qing
  surname: Yao
  fullname: Yao, Yuan-Qing
BookMark eNp9ks1u1DAUhSNUJNrCC7CyxAYWKXHiJPYKVVWBkSoh0cLWcuzrGQ8Ze7AdOvA4PCl3fpA6FSJZ2HG-c67v1TkrTnzwUBQvaXVBKe_eJlrzjpVV3ZSV6ERVbp4Up5T1tKxpx04e7J8VZyktq4r2vG5Pi9-3zs9HKDWMI9ELFZXOEN0vlV3wJFiSYLRlBA_3CJJ1dCsVf5Icw3oRhlGlTEKcKx-cSUQlsgoGxi2J0uuvd8Q4awHl2e0dlTfEeSyBdfA7kXuXF8SAdmZSI_EqTxHXb24cIZLtrdLz4qlVY4IXh_W8-PL--u7qY3nz6cPs6vKm1G3f5lLQgWswitaCN7qHRne07gQ0VnOoObVgWMcM470eVMs6aodK1aa3jPZs4Ko5L2Z7XxPUUh46lUE5uTvANqWK2ekRpOCiqwTDUSvNhOb4tK3WFdTo1vQWvd7tvdbTsAKjcQDY1pHp8R_vFnIefkhatbxpWoYOrw8OMXyfIGW5cmk7D-UhTEnWvMcLtE3HEX31CF2GKXqcFVKiQseePqDmCjtw3gYsrLem8rLvBOOMNQKpi39Q-BpYOY2hsw7PjwRvjgTIZNjkuZpSkrPbz8cs37M6hpQiWKld3uUCi7gRm5fbNMt9miWmWe7SLDcorR9J_87yP6I_a-38hw
CitedBy_id crossref_primary_10_1093_humupd_dmaf007
crossref_primary_10_1016_j_placenta_2024_12_003
crossref_primary_10_1007_s10815_024_03036_6
crossref_primary_10_3389_fmed_2023_1304002
crossref_primary_10_1186_s40364_024_00598_6
crossref_primary_10_1038_s41421_024_00740_6
Cites_doi 10.1242/dev.199749
10.1093/humupd/dmaa062
10.1016/j.celrep.2018.10.045
10.1038/ncomms14049
10.1016/j.cels.2019.03.003
10.1093/molehr/gar053
10.1093/humupd/dmac007
10.1016/j.cell.2021.04.048
10.1016/j.gpb.2022.04.008
10.1016/j.stemcr.2018.07.004
10.1146/annurev-cellbio-100814-125620
10.1093/humrep/den178
10.1242/dev.199840
10.1186/s10020-022-00592-4
10.1038/ncb3222
10.1038/s41467-019-13032-5
10.1002/0471142735.im0740s97
10.1038/cdd.2009.1
10.1073/pnas.2204069119
10.3390/biom10030453
10.1126/sciadv.aau4788
10.1016/j.ajpath.2016.11.018
10.1111/imr.12323
10.7150/thno.72297
10.1016/j.omtn.2019.11.031
10.1038/s41586-018-0753-3
10.1038/s41586-023-05869-0
10.1093/nar/gkac963
10.1007/s00018-019-03104-6
10.1038/s41586-018-0698-6
10.1038/s41422-021-00540-7
10.1093/humupd/dms015
10.1016/j.freeradbiomed.2018.06.006
10.1038/nm1452
10.1038/s41592-019-0619-0
10.1186/s13046-021-01862-5
10.1242/dev.163428
10.1096/fj.202100925RR
10.1016/j.placenta.2021.01.002
10.1073/pnas.2120667119
10.1016/j.placenta.2023.01.005
10.1038/s41588-021-00972-2
10.1073/pnas.1612335113
10.3389/fimmu.2023.1087155
10.1038/s41596-020-0381-x
10.1038/nmeth.4463
10.1016/j.stem.2017.11.004
10.1038/nmeth.4402
10.1016/j.placenta.2020.12.013
10.1093/humupd/dmaa020
10.1210/en.2007-1282
10.1007/s00018-022-04363-6
10.1073/pnas.1517724112
10.1038/s41596-020-0292-x
ContentType Journal Article
Copyright COPYRIGHT 2023 BioMed Central Ltd.
2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2023. BioMed Central Ltd., part of Springer Nature.
BioMed Central Ltd., part of Springer Nature 2023
Copyright_xml – notice: COPYRIGHT 2023 BioMed Central Ltd.
– notice: 2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2023. BioMed Central Ltd., part of Springer Nature.
– notice: BioMed Central Ltd., part of Springer Nature 2023
DBID AAYXX
CITATION
ISR
3V.
7QP
7QR
7SS
7TK
7U7
7X7
7XB
88E
8AO
8FD
8FE
8FH
8FI
8FJ
8FK
ABUWG
AEUYN
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
C1K
CCPQU
DWQXO
FR3
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0S
M1P
M7P
P64
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
RC3
7X8
5PM
DOA
DOI 10.1186/s12864-023-09690-x
DatabaseName CrossRef
Gale In Context: Science
ProQuest Central (Corporate)
Calcium & Calcified Tissue Abstracts
Chemoreception Abstracts
Entomology Abstracts (Full archive)
Neurosciences Abstracts
Toxicology Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
ProQuest Pharma Collection
Technology Research Database
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 One Sustainability
ProQuest Central UK/Ireland
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
Natural Science Collection
Environmental Sciences and Pollution Management
ProQuest One Community College
ProQuest Central Korea
Engineering Research Database
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
ProQuest Biological Science Collection
ProQuest Health & Medical Collection
Medical Database ProQuest
Biological Science Database
Biotechnology and BioEngineering Abstracts
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
Genetics Abstracts
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
Publicly Available Content Database
ProQuest Central Student
Technology Research Database
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 One Health & Nursing
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Central China
Environmental Sciences and Pollution Management
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest One Sustainability
ProQuest Health & Medical Research Collection
Genetics Abstracts
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Health & Medical Research Collection
Biological Science Collection
Chemoreception Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Biological Science Collection
Toxicology Abstracts
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
Neurosciences Abstracts
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
Entomology Abstracts
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Engineering Research Database
ProQuest One Academic
Calcium & Calcified Tissue Abstracts
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList



Publicly Available Content Database
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 1471-2164
EndPage 18
ExternalDocumentID oai_doaj_org_article_9896094096ac49c888855cc0e2f4137f
PMC10583354
A769484439
10_1186_s12864_023_09690_x
GeographicLocations China
GeographicLocations_xml – name: China
GrantInformation_xml – fundername: ;
  grantid: KQTD20190929172749226 to Y-QY.and WY
– fundername: ;
  grantid: 82271704
GroupedDBID ---
0R~
23N
2WC
2XV
53G
5VS
6J9
7X7
88E
8AO
8FE
8FH
8FI
8FJ
AAFWJ
AAHBH
AAJSJ
AASML
AAYXX
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACIWK
ACPRK
ACUHS
ADBBV
ADUKV
AEAQA
AENEX
AEUYN
AFKRA
AFPKN
AFRAH
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BBNVY
BCNDV
BENPR
BFQNJ
BHPHI
BMC
BPHCQ
BVXVI
C6C
CCPQU
CITATION
CS3
DIK
DU5
E3Z
EAD
EAP
EAS
EBD
EBLON
EBS
EMB
EMK
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HCIFZ
HMCUK
IAO
IGS
IHR
INH
INR
ISR
ITC
KQ8
LK8
M1P
M48
M7P
M~E
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SBL
SOJ
SV3
TR2
TUS
U2A
UKHRP
W2D
WOQ
WOW
XSB
PMFND
3V.
7QP
7QR
7SS
7TK
7U7
7XB
8FD
8FK
AZQEC
C1K
DWQXO
FR3
GNUQQ
K9.
P64
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQUKI
PRINS
RC3
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c575t-91b8ceda12983c7e3c61269e3fc8e281fed464d487cba5461fb0a2d7f4174b8a3
IEDL.DBID M48
ISSN 1471-2164
IngestDate Wed Aug 27 01:20:15 EDT 2025
Thu Aug 21 18:36:04 EDT 2025
Fri Jul 11 12:44:22 EDT 2025
Sat Aug 23 12:40:21 EDT 2025
Tue Jun 17 22:25:50 EDT 2025
Tue Jun 10 21:21:05 EDT 2025
Fri Jun 27 05:49:15 EDT 2025
Tue Jul 01 00:39:25 EDT 2025
Thu Apr 24 23:00:01 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
License Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c575t-91b8ceda12983c7e3c61269e3fc8e281fed464d487cba5461fb0a2d7f4174b8a3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://doaj.org/article/9896094096ac49c888855cc0e2f4137f
PQID 2890058718
PQPubID 44682
PageCount 18
ParticipantIDs doaj_primary_oai_doaj_org_article_9896094096ac49c888855cc0e2f4137f
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10583354
proquest_miscellaneous_2879405368
proquest_journals_2890058718
gale_infotracmisc_A769484439
gale_infotracacademiconefile_A769484439
gale_incontextgauss_ISR_A769484439
crossref_citationtrail_10_1186_s12864_023_09690_x
crossref_primary_10_1186_s12864_023_09690_x
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2023-10-18
PublicationDateYYYYMMDD 2023-10-18
PublicationDate_xml – month: 10
  year: 2023
  text: 2023-10-18
  day: 18
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
PublicationTitle BMC genomics
PublicationYear 2023
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References CP Chen (9690_CR33) 2018; 124
S Haider (9690_CR19) 2022; 119
WL Thuya (9690_CR39) 2023; 13
S Haider (9690_CR3) 2018; 11
P Rascle (9690_CR41) 2023; 14
T Tilburgs (9690_CR43) 2015; 112
GX Zheng (9690_CR45) 2017; 8
9690_CR2
MY Turco (9690_CR4) 2018; 564
HL LaMarca (9690_CR22) 2008; 23
M Efremova (9690_CR55) 2020; 15
9690_CR6
AK Wakeland (9690_CR23) 2017; 187
MA Sheridan (9690_CR12) 2020; 15
9690_CR29
Y Hao (9690_CR46) 2021; 184
S Io (9690_CR7) 2020; 26
X Zhang (9690_CR42) 2019; 10
T Wu (9690_CR52) 2021; 2
H Papuchova (9690_CR31) 2022; 79
L Garcia-Alonso (9690_CR49) 2021; 53
U Schmidt (9690_CR38) 2021; 40
Y Yi (9690_CR17) 2021; 35
S Haider (9690_CR8) 2016; 113
9690_CR35
S Suo (9690_CR16) 2018; 25
H Suryawanshi (9690_CR24) 2018; 4
Y Chen (9690_CR32) 2020; 19
D Baczyk (9690_CR18) 2009; 16
A Moffett (9690_CR40) 2015; 267
I Fischer (9690_CR14) 2011; 17
S Ray (9690_CR34) 2022; 119
AE Wallace (9690_CR10) 2012; 18
Y Duan (9690_CR20) 2022; 28
S Aibar (9690_CR56) 2017; 14
9690_CR44
CS McGinnis (9690_CR47) 2019; 8
Y Mao (9690_CR15) 2021; 104
B Dietrich (9690_CR37) 2023; 133
X Qiu (9690_CR54) 2017; 14
S Gao (9690_CR26) 2022; 32
B Dietrich (9690_CR36) 2021; 104
I Korsunsky (9690_CR48) 2019; 16
H Okae (9690_CR28) 2018; 22
M Knofler (9690_CR5) 2019; 76
LL Nilsson (9690_CR27) 2022; 28
E Maltepe (9690_CR1) 2015; 31
A Arutyunyan (9690_CR30) 2023; 616
I Diaz-Hernandez (9690_CR9) 2021; 27
R Vento-Tormo (9690_CR13) 2018; 563
J Prast (9690_CR21) 2008; 149
J Hanna (9690_CR11) 2006; 12
9690_CR50
9690_CR53
M Kanehisa (9690_CR51) 2022; 51
Y Zheng (9690_CR25) 2015; 17
References_xml – ident: 9690_CR2
  doi: 10.1242/dev.199749
– volume: 27
  start-page: 720
  issue: 4
  year: 2021
  ident: 9690_CR9
  publication-title: Hum Reprod Update
  doi: 10.1093/humupd/dmaa062
– volume: 25
  start-page: 1436
  issue: 6
  year: 2018
  ident: 9690_CR16
  publication-title: Cell Rep
  doi: 10.1016/j.celrep.2018.10.045
– volume: 8
  start-page: 14049
  year: 2017
  ident: 9690_CR45
  publication-title: Nat Commun
  doi: 10.1038/ncomms14049
– volume: 8
  start-page: 329
  issue: 4
  year: 2019
  ident: 9690_CR47
  publication-title: Cell Syst
  doi: 10.1016/j.cels.2019.03.003
– volume: 2
  start-page: 100141
  issue: 3
  year: 2021
  ident: 9690_CR52
  publication-title: Innov (Camb)
– ident: 9690_CR50
– volume: 17
  start-page: 747
  issue: 12
  year: 2011
  ident: 9690_CR14
  publication-title: Mol Hum Reprod
  doi: 10.1093/molehr/gar053
– volume: 28
  start-page: 435
  issue: 3
  year: 2022
  ident: 9690_CR27
  publication-title: Hum Reprod Update
  doi: 10.1093/humupd/dmac007
– volume: 184
  start-page: 3573
  issue: 13
  year: 2021
  ident: 9690_CR46
  publication-title: Cell
  doi: 10.1016/j.cell.2021.04.048
– ident: 9690_CR53
  doi: 10.1016/j.gpb.2022.04.008
– volume: 11
  start-page: 537
  issue: 2
  year: 2018
  ident: 9690_CR3
  publication-title: Stem Cell Reports
  doi: 10.1016/j.stemcr.2018.07.004
– volume: 31
  start-page: 523
  year: 2015
  ident: 9690_CR1
  publication-title: Annu Rev Cell Dev Biol
  doi: 10.1146/annurev-cellbio-100814-125620
– volume: 23
  start-page: 1733
  issue: 8
  year: 2008
  ident: 9690_CR22
  publication-title: Hum Reprod
  doi: 10.1093/humrep/den178
– ident: 9690_CR29
  doi: 10.1242/dev.199840
– volume: 28
  start-page: 165
  issue: 1
  year: 2022
  ident: 9690_CR20
  publication-title: Mol Med
  doi: 10.1186/s10020-022-00592-4
– volume: 17
  start-page: 1348
  issue: 10
  year: 2015
  ident: 9690_CR25
  publication-title: Nat Cell Biol
  doi: 10.1038/ncb3222
– volume: 10
  start-page: 5010
  issue: 1
  year: 2019
  ident: 9690_CR42
  publication-title: Nat Commun
  doi: 10.1038/s41467-019-13032-5
– ident: 9690_CR44
  doi: 10.1002/0471142735.im0740s97
– volume: 16
  start-page: 719
  issue: 5
  year: 2009
  ident: 9690_CR18
  publication-title: Cell Death Differ
  doi: 10.1038/cdd.2009.1
– volume: 119
  start-page: e2204069119
  issue: 36
  year: 2022
  ident: 9690_CR34
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.2204069119
– ident: 9690_CR35
  doi: 10.3390/biom10030453
– volume: 4
  start-page: eaau4788
  issue: 10
  year: 2018
  ident: 9690_CR24
  publication-title: Sci Adv
  doi: 10.1126/sciadv.aau4788
– volume: 187
  start-page: 767
  issue: 4
  year: 2017
  ident: 9690_CR23
  publication-title: Am J Pathol
  doi: 10.1016/j.ajpath.2016.11.018
– volume: 267
  start-page: 283
  issue: 1
  year: 2015
  ident: 9690_CR40
  publication-title: Immunol Rev
  doi: 10.1111/imr.12323
– volume: 13
  start-page: 621
  issue: 2
  year: 2023
  ident: 9690_CR39
  publication-title: Theranostics
  doi: 10.7150/thno.72297
– volume: 19
  start-page: 1237
  year: 2020
  ident: 9690_CR32
  publication-title: Mol Ther Nucleic Acids
  doi: 10.1016/j.omtn.2019.11.031
– volume: 564
  start-page: 263
  issue: 7735
  year: 2018
  ident: 9690_CR4
  publication-title: Nature
  doi: 10.1038/s41586-018-0753-3
– volume: 616
  start-page: 143
  issue: 7955
  year: 2023
  ident: 9690_CR30
  publication-title: Nature
  doi: 10.1038/s41586-023-05869-0
– volume: 51
  start-page: D587
  issue: D1
  year: 2022
  ident: 9690_CR51
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gkac963
– volume: 76
  start-page: 3479
  issue: 18
  year: 2019
  ident: 9690_CR5
  publication-title: Cell Mol Life Sci
  doi: 10.1007/s00018-019-03104-6
– volume: 563
  start-page: 347
  issue: 7731
  year: 2018
  ident: 9690_CR13
  publication-title: Nature
  doi: 10.1038/s41586-018-0698-6
– volume: 32
  start-page: 38
  issue: 1
  year: 2022
  ident: 9690_CR26
  publication-title: Cell Res
  doi: 10.1038/s41422-021-00540-7
– volume: 18
  start-page: 458
  issue: 4
  year: 2012
  ident: 9690_CR10
  publication-title: Hum Reprod Update
  doi: 10.1093/humupd/dms015
– volume: 124
  start-page: 189
  year: 2018
  ident: 9690_CR33
  publication-title: Free Radic Biol Med
  doi: 10.1016/j.freeradbiomed.2018.06.006
– volume: 12
  start-page: 1065
  issue: 9
  year: 2006
  ident: 9690_CR11
  publication-title: Nat Med
  doi: 10.1038/nm1452
– volume: 16
  start-page: 1289
  issue: 12
  year: 2019
  ident: 9690_CR48
  publication-title: Nat Methods
  doi: 10.1038/s41592-019-0619-0
– volume: 40
  start-page: 69
  issue: 1
  year: 2021
  ident: 9690_CR38
  publication-title: J Exp Clin Cancer Res
  doi: 10.1186/s13046-021-01862-5
– ident: 9690_CR6
  doi: 10.1242/dev.163428
– volume: 35
  start-page: e22028
  issue: 12
  year: 2021
  ident: 9690_CR17
  publication-title: FASEB J
  doi: 10.1096/fj.202100925RR
– volume: 104
  start-page: 253
  year: 2021
  ident: 9690_CR15
  publication-title: Placenta
  doi: 10.1016/j.placenta.2021.01.002
– volume: 119
  start-page: e2120667119
  issue: 28
  year: 2022
  ident: 9690_CR19
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.2120667119
– volume: 133
  start-page: 19
  year: 2023
  ident: 9690_CR37
  publication-title: Placenta
  doi: 10.1016/j.placenta.2023.01.005
– volume: 53
  start-page: 1698
  issue: 12
  year: 2021
  ident: 9690_CR49
  publication-title: Nat Genet
  doi: 10.1038/s41588-021-00972-2
– volume: 113
  start-page: E7710
  issue: 48
  year: 2016
  ident: 9690_CR8
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1612335113
– volume: 14
  start-page: 1087155
  year: 2023
  ident: 9690_CR41
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2023.1087155
– volume: 15
  start-page: 3441
  issue: 10
  year: 2020
  ident: 9690_CR12
  publication-title: Nat Protoc
  doi: 10.1038/s41596-020-0381-x
– volume: 14
  start-page: 1083
  issue: 11
  year: 2017
  ident: 9690_CR56
  publication-title: Nat Methods
  doi: 10.1038/nmeth.4463
– volume: 22
  start-page: 50
  issue: 1
  year: 2018
  ident: 9690_CR28
  publication-title: Cell Stem Cell
  doi: 10.1016/j.stem.2017.11.004
– volume: 14
  start-page: 979
  issue: 10
  year: 2017
  ident: 9690_CR54
  publication-title: Nat Methods
  doi: 10.1038/nmeth.4402
– volume: 104
  start-page: 243
  year: 2021
  ident: 9690_CR36
  publication-title: Placenta
  doi: 10.1016/j.placenta.2020.12.013
– volume: 26
  start-page: 611
  issue: 5
  year: 2020
  ident: 9690_CR7
  publication-title: Hum Reprod Update
  doi: 10.1093/humupd/dmaa020
– volume: 149
  start-page: 979
  issue: 3
  year: 2008
  ident: 9690_CR21
  publication-title: Endocrinology
  doi: 10.1210/en.2007-1282
– volume: 79
  start-page: 337
  issue: 6
  year: 2022
  ident: 9690_CR31
  publication-title: Cell Mol Life Sci
  doi: 10.1007/s00018-022-04363-6
– volume: 112
  start-page: 13312
  issue: 43
  year: 2015
  ident: 9690_CR43
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1517724112
– volume: 15
  start-page: 1484
  issue: 4
  year: 2020
  ident: 9690_CR55
  publication-title: Nat Protoc
  doi: 10.1038/s41596-020-0292-x
SSID ssj0017825
Score 2.464158
Snippet Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural killer (NK)...
Background Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural...
BackgroundExtravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type natural...
Abstract Background Extravillous trophoblast cell (EVT) differentiation and its communication with maternal decidua especially the leading immune cell type...
SourceID doaj
pubmedcentral
proquest
gale
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Enrichment Source
Index Database
StartPage 1
SubjectTerms Achievement tests
Angiogenesis
Cell differentiation
Cell interactions
Cells
Cytokines
Decidua
DNA binding proteins
Extravillous trophoblast
Fibroblasts
Gene sequencing
Genetic aspects
Genomics
Growth
Health aspects
Immune system
Immunomodulation
Killer cells
Methods
Modelling
Natural killer cells
Network analysis
Organoids
Placentation
Pregnancy
RNA
RNA sequencing
Subpopulations
Trajectory analysis
Transcription factors
Trophoblast
Trophoblast differentiation
Trophoblast organoid
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3Ni9UwEA-yIHgRP7G6ShTBg4TtR5qmx1V2WQU9uLuyt5Ckibvso11e-3D9d_xLnUnSx1ZBL54eNJNHOzOZj3bmN4S89oUr26KyzDguGNdesNbnNfO5LqUpdFc02OD86bM4OuUfz-qzG6O-sCYswgNHxu21EjHRIAsR2vLWQsIm69ra3JUe7G_j0fqCz5uTqfT9APxePbfISLE3ghUWnIF_YvBHbc6uF24ooPX_aZN_r5O84XgO75G7KWKk-_FO75Nbrn9AbscZkj8ekp_H4HxWjuEbeGq38Muxu5IOno5u5RkCV34HQnoV0SXotB6uzgcDsfNEw2Sn4aIbqR5pGI2DlLD14OsJnSeoTFGGVPcdRYyJdeyIGCm-yaWds6GriwagUPi9DD2GFO9qfERODw9O3h-xNHiBWYjeJjCARlrXaYgFZGUbV1mIg0TrKm-lK2XhXccF7yDXsUbXXBTegGi7BiTScCN19Zjs9EPvnhDqsNk1185A4sitb4wVPgcj4iABNrqtMlLMclA2oZLjcIyVCtmJFCrKToHsVJCdus7I2-2exLW_Ur9D8W4pEU87XADmqqRl6l9alpFXqBwKETN6LMn5pjfjqD4cf1H7jWi55BDYZeRNIvIDPIPVqcMBOIEgWwvK3QUlHGm7XJ51UCWTMir8IpzXkN_KjLzcLuNOLJPr3bBBGjCvYFYF0MiF7i4ef7nSX5wHWHGItLEDjz_9Hwx7Ru6UeNyw9kfukp1pvXHPIXybzItwUn8BHStFBA
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELagCIkL4imWFmQQEgdkNQ_HcU6ooFYFCQ60RXuzbMemFatku8mK8nf4pcw4TiAgdS8rrcfa2ON5OTPfEPLKpy6r0twy47hgXHvBKp8UzCc6kybVdVpigfOnz-L4jH9cFst44dbFtMpRJwZFXbcW78j38YVYUoB7L9-uLxl2jcK3q7GFxk1yC6HLMKWrXE4BVwrWrxgLZaTY70AXC87ASjFw3KuEXc2MUcDs_18z_5st-Zf5ObpH7ka_kR4MjL5PbrjmAbk9dJL8-ZD8OgETtHIM7-GpnUCYhxpL2nrauZVnCF_5AwjpesCYoP2mXZ-3Bjzonob-Tu1F3VHd0dAgBylh6uHXUzr2UekHTlLd1BSRJjZDXURH8T6X1s6G2i4a4ELh-3uoNKT4VN0jcnZ0ePr-mMX2C8yCD9eDGjTSulqDRyBzW7rcgjckKpd7K10mU-9qLngNEY81uuAi9QYYXJeeQ5RjpM4fk52mbdwTQh2WvCbaGQgfufWlscInoEochMFGV_mCpCMflI3Y5NgiY6VCjCKFGningHcq8E5dLcibaU7ctWup3yF7J0pE1Q4_wOaqKKSqkoi_BxGv0JZXVsKnKKxNXAZryku_IC_xcCjEzWgwMeeb3nad-nDyRR2UouKSg3u3IK8jkW9hDVbHOgfYCYTamlHuzShBsO18eDyDKiqWTv0RgwV5MQ3jTEyWa1y7RRpQsqBcBdDI2dmdLX8-0lycB3Bx8LexDo8_vf7fd8mdDAUJc3vkHtnpN1v3DNyz3jwPMvgbc1I9uw
  priority: 102
  providerName: ProQuest
Title Single-cell characterization of self-renewing primary trophoblast organoids as modeling of EVT differentiation and interactions with decidual natural killer cells
URI https://www.proquest.com/docview/2890058718
https://www.proquest.com/docview/2879405368
https://pubmed.ncbi.nlm.nih.gov/PMC10583354
https://doaj.org/article/9896094096ac49c888855cc0e2f4137f
Volume 24
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3da9UwFA9zQ_BF_MSr8xJF8EGi_UjT9EFkkzumsCHbruwtJGnihpd23vbi9u_4l3pO2l6tDrEvheakNDk5X2nO7xDywscuKeLUMuO4YFx7wQofZcxHOpEm1mWcY4LzwaHYn_OPp9npBhnKHfUT2Fwb2mE9qfly8fry29U7EPi3QeCleNOAjhWcgfVh4JAXEQOfcgssU46CesB__VUAa5iFbKM8ZgnECUMSzbXvGBmqgOf_t9b-8yTlb6Zp7w653fuUdKdbBHfJhqvukZtdlcmr--THMZinhWO4R0_tGqC5y7-ktaeNW3iG0JbfgZBedPgTtF3WF2e1Ae-6paH2U31eNlQ3NBTPQUroOvt8QocaK23HZaqrkiIKxbLLmWgo7vXS0tmQ90UDlCjcv4YsRIpf1Twg873Zyft91pdmYBb8uxZUpJHWlRq8BZna3KUWPCVRuNRb6RIZe1dywUuIhqzRGRexN8D8MvfAFW6kTh-Szaqu3CNCHabDRtoZCC259bmxwkegZhyEyEYX6YTEAx-U7XHLsXzGQoX4RQrV8U4B71TgnbqckFfrPv2s_ZN6F9m7pkTE7fAAJlf1AqwKidh8EA0LbXlhJVxZZm3kEhhTmvsJeY6LQyGmRoWHdr7oVdOoD8dHaicXBZccXL8JedkT-RrGYHWfAwEzgTBcI8rtESUIvR03D2tQDTKj8J9xlEEELCfk2boZe-JBusrVK6QBBQyKVwCNHK3d0fDHLdX5WQAeB18cc_T44_8Z6xNyK0FxwtM_cptstsuVewoOXGum5EZ-mk_J1u7s8NPRNGyDTIOk_gQVmUiG
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1LbxMxELZKKgQXxFMEChgE4oCs7sPreA8ItZAqoW2E2hT15nq9Nq2IdkN2o7Z_hx_Ab2RmH4EFqbfmEikeZ9ee8TxszzeEvHa-DWI_NCyxXDCunWCx8yLmPB3IxNepP8AE5_2JGB3xz8fR8Rr51ebC4LXKVidWijrNDe6Rb-KBmBeBey8_zH8wrBqFp6ttCY1aLHbt5TmEbMX78Sfg75sg2BlOP45YU1WAGXBNSljdiTQ21WDoZGgGNjRg5EVsQ2ekDaTvbMoFT8GRN4mOuPBdAu-dDhwH5z2ROoT_vUHWeQihTI-sbw8nXw5W5xZgb6M2NUeKzQK0v-AM7CKDUCH22EXH_FVVAv63Bf_ez_zL4O3cJXcaT5Vu1aJ1j6zZ7D65WdeuvHxAfh6C0ZtZhjv_1Kxgn-usTpo7WtiZYwiYeQ6EdF6jWtBykc9P8wR89pJWFaXys7SguqBVSR6khK7Dr1PaVm4pa9mhOkspYlss6kyMguIOMk2tqbLJaAVQCt_fq9xGim9VPCRH18KaR6SX5Zl9TKjFJFtP2wQCVm7cIDHCeaC8LATeiY7DPvFbPijToKFjUY6ZqqIiKVTNOwW8UxXv1EWfvFv1aWbtSuptZO-KEnG8qx9gclWjFlQsEfEPYmyhDY-NhE8UGePZAMYUDlyfvELhUIjUkeFVoG96WRRqfHigtgYi5pKDQ9knbxsil8MYjG4yK2AmENyrQ7nRoQRVYrrNrQyqRpUV6s_C65OXq2bsidfzMpsvkQbUOqhzATSyI7ud4XdbsrPTCs4cPHzM_ONPrn76C3JrNN3fU3vjye5TcjvARYU3i-QG6ZWLpX0GzmGZPG9WJCUn160EfgNwQnye
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=Single-cell+characterization+of+self-renewing+primary+trophoblast+organoids+as+modeling+of+EVT+differentiation+and+interactions+with+decidual+natural+killer+cells&rft.jtitle=BMC+genomics&rft.au=Zhuang%2C+Bai-Mei&rft.au=Cao%2C+Dan-Dan&rft.au=Li%2C+Tian-Xi&rft.au=Liu%2C+Xiao-Feng&rft.date=2023-10-18&rft.pub=BioMed+Central+Ltd&rft.issn=1471-2164&rft.eissn=1471-2164&rft.volume=24&rft.issue=1&rft_id=info:doi/10.1186%2Fs12864-023-09690-x&rft.externalDBID=ISR&rft.externalDocID=A769484439
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-2164&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-2164&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-2164&client=summon