Chios gum mastic enhance the proliferation and odontogenic differentiation of human dental pulp stem cells
Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and n...
Saved in:
Published in | The Korean journal of physiology & pharmacology Vol. 28; no. 5; pp. 423 - 433 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
The Korean Physiological Society and The Korean Society of Pharmacology
01.09.2024
대한약리학회 |
Subjects | |
Online Access | Get full text |
ISSN | 1226-4512 2093-3827 |
DOI | 10.4196/kjpp.2024.28.5.423 |
Cover
Abstract | Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and nerve regeneration. Chios gum mastic (CGM), a resin extracted from the stems and leaves of
var.
, has garnered attention for its potential in tissue regeneration. This study aims to confirm alterations in cell proliferation rates and induce differentiation in human DPSCs (hDPSCs) through CGM treatment, a substance known for effectively promoting odontogenic differentiation. Administration of CGM to hDPSC cells was followed by an assessment of cell survival, proliferation, and odontogenic differentiation through protein and gene analysis. The study revealed that hDPSCs exhibited low sensitivity to CGM toxicity. CGM treatment induced cell proliferation by activating cell-cycle proteins through the Wnt/β-catenin pathway. Additionally, the study demonstrated that CGM enhances alkaline phosphatase activation by upregulating the expression of collagen type I, a representative matrix protein of dentin. This activation of markers associated with odontogenic and bone differentiation ultimately facilitated the mineralization of hDPSCs. This study concludes that CGM, as a natural substance, fosters the cell cycle and cell proliferation in hDPSCs. Furthermore, it triggers the transcription of odontogenic and osteogenic markers, thereby facilitating odontogenic differentiation. |
---|---|
AbstractList | Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and nerve regeneration. Chios gum mastic (CGM), a resin extracted from the stems and leaves of Pistacia lentiscus var. Chia, has garnered attention for its potential in tissue regeneration. This study aims to confirm alterations in cell proliferation rates and induce differentiation in human DPSCs (hDPSCs) through CGM treatment, a substance known for effectively promoting odontogenic differentiation. Administration of CGM to hDPSC cells was followed by an assessment of cell survival, proliferation, and odontogenic differentiation through protein and gene analysis. The study revealed that hDPSCs exhibited low sensitivity to CGM toxicity. CGM treatment induced cell proliferation by activating cell-cycle proteins through the Wnt/β-catenin pathway. Additionally, the study demonstrated that CGM enhances alkaline phosphatase activation by upregulating the expression of collagen type I, a representative matrix protein of dentin. This activation of markers associated with odontogenic and bone differentiation ultimately facilitated the mineralization of hDPSCs. This study concludes that CGM, as a natural substance, fosters the cell cycle and cell proliferation in hDPSCs. Furthermore, it triggers the transcription of odontogenic and osteogenic markers, thereby facilitating odontogenic differentiation. KCI Citation Count: 0 Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and nerve regeneration. Chios gum mastic (CGM), a resin extracted from the stems and leaves of var. , has garnered attention for its potential in tissue regeneration. This study aims to confirm alterations in cell proliferation rates and induce differentiation in human DPSCs (hDPSCs) through CGM treatment, a substance known for effectively promoting odontogenic differentiation. Administration of CGM to hDPSC cells was followed by an assessment of cell survival, proliferation, and odontogenic differentiation through protein and gene analysis. The study revealed that hDPSCs exhibited low sensitivity to CGM toxicity. CGM treatment induced cell proliferation by activating cell-cycle proteins through the Wnt/β-catenin pathway. Additionally, the study demonstrated that CGM enhances alkaline phosphatase activation by upregulating the expression of collagen type I, a representative matrix protein of dentin. This activation of markers associated with odontogenic and bone differentiation ultimately facilitated the mineralization of hDPSCs. This study concludes that CGM, as a natural substance, fosters the cell cycle and cell proliferation in hDPSCs. Furthermore, it triggers the transcription of odontogenic and osteogenic markers, thereby facilitating odontogenic differentiation. Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and nerve regeneration. Chios gum mastic (CGM), a resin extracted from the stems and leaves of Pistacia lentiscus var. Chia, has garnered attention for its potential in tissue regeneration. This study aims to confirm alterations in cell proliferation rates and induce differentiation in human DPSCs (hDPSCs) through CGM treatment, a substance known for effectively promoting odontogenic differentiation. Administration of CGM to hDPSC cells was followed by an assessment of cell survival, proliferation, and odontogenic differentiation through protein and gene analysis. The study revealed that hDPSCs exhibited low sensitivity to CGM toxicity. CGM treatment induced cell proliferation by activating cell-cycle proteins through the Wnt/β-catenin pathway. Additionally, the study demonstrated that CGM enhances alkaline phosphatase activation by upregulating the expression of collagen type I, a representative matrix protein of dentin. This activation of markers associated with odontogenic and bone differentiation ultimately facilitated the mineralization of hDPSCs. This study concludes that CGM, as a natural substance, fosters the cell cycle and cell proliferation in hDPSCs. Furthermore, it triggers the transcription of odontogenic and osteogenic markers, thereby facilitating odontogenic differentiation.Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and nerve regeneration. Chios gum mastic (CGM), a resin extracted from the stems and leaves of Pistacia lentiscus var. Chia, has garnered attention for its potential in tissue regeneration. This study aims to confirm alterations in cell proliferation rates and induce differentiation in human DPSCs (hDPSCs) through CGM treatment, a substance known for effectively promoting odontogenic differentiation. Administration of CGM to hDPSC cells was followed by an assessment of cell survival, proliferation, and odontogenic differentiation through protein and gene analysis. The study revealed that hDPSCs exhibited low sensitivity to CGM toxicity. CGM treatment induced cell proliferation by activating cell-cycle proteins through the Wnt/β-catenin pathway. Additionally, the study demonstrated that CGM enhances alkaline phosphatase activation by upregulating the expression of collagen type I, a representative matrix protein of dentin. This activation of markers associated with odontogenic and bone differentiation ultimately facilitated the mineralization of hDPSCs. This study concludes that CGM, as a natural substance, fosters the cell cycle and cell proliferation in hDPSCs. Furthermore, it triggers the transcription of odontogenic and osteogenic markers, thereby facilitating odontogenic differentiation. Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow mesenchymal stem cells. Their ease of collection from patients makes them well-suited for tissue engineering applications, such as tooth and nerve regeneration. Chios gum mastic (CGM), a resin extracted from the stems and leaves of Pistacia lentiscus var. Chia , has garnered attention for its potential in tissue regeneration. This study aims to confirm alterations in cell proliferation rates and induce differentiation in human DPSCs (hDPSCs) through CGM treatment, a substance known for effectively promoting odontogenic differentiation. Administration of CGM to hDPSC cells was followed by an assessment of cell survival, proliferation, and odontogenic differentiation through protein and gene analysis. The study revealed that hDPSCs exhibited low sensitivity to CGM toxicity. CGM treatment induced cell proliferation by activating cell-cycle proteins through the Wnt/β-catenin pathway. Additionally, the study demonstrated that CGM enhances alkaline phosphatase activation by upregulating the expression of collagen type I, a representative matrix protein of dentin. This activation of markers associated with odontogenic and bone differentiation ultimately facilitated the mineralization of hDPSCs. This study concludes that CGM, as a natural substance, fosters the cell cycle and cell proliferation in hDPSCs. Furthermore, it triggers the transcription of odontogenic and osteogenic markers, thereby facilitating odontogenic differentiation. |
Author | Kim, In-Ryoung Lee, Eun-Gyung Kim, Yong-Il Park, Se-Jin Baek, Hyun-Su |
AuthorAffiliation | 1 Department of Oral Anatomy, School of Dentistry, Pusan National University, Yangsan 50612, Korea 2 Department of Pediatric Dentistry, School of Dentistry, Pusan National University, Yangsan 50612, Korea 3 Department of Orthodontics, School of Dentistry, Pusan National University, Yangsan 50612, Korea 4 Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Korea |
AuthorAffiliation_xml | – name: 1 Department of Oral Anatomy, School of Dentistry, Pusan National University, Yangsan 50612, Korea – name: 2 Department of Pediatric Dentistry, School of Dentistry, Pusan National University, Yangsan 50612, Korea – name: 3 Department of Orthodontics, School of Dentistry, Pusan National University, Yangsan 50612, Korea – name: 4 Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Korea |
Author_xml | – sequence: 1 givenname: Hyun-Su surname: Baek fullname: Baek, Hyun-Su organization: Department of Oral Anatomy, School of Dentistry, Pusan National University, Yangsan 50612, Korea – sequence: 2 givenname: Se-Jin surname: Park fullname: Park, Se-Jin organization: Department of Oral Anatomy, School of Dentistry, Pusan National University, Yangsan 50612, Korea – sequence: 3 givenname: Eun-Gyung surname: Lee fullname: Lee, Eun-Gyung organization: Department of Pediatric Dentistry, School of Dentistry, Pusan National University, Yangsan 50612, Korea, Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Korea – sequence: 4 givenname: Yong-Il surname: Kim fullname: Kim, Yong-Il organization: Department of Orthodontics, School of Dentistry, Pusan National University, Yangsan 50612, Korea, Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Korea – sequence: 5 givenname: In-Ryoung surname: Kim fullname: Kim, In-Ryoung organization: Department of Oral Anatomy, School of Dentistry, Pusan National University, Yangsan 50612, Korea, Dental and Life Science Institute, School of Dentistry, Pusan National University, Yangsan 50612, Korea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39198223$$D View this record in MEDLINE/PubMed https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART003113103$$DAccess content in National Research Foundation of Korea (NRF) |
BookMark | eNpVkVtr3DAQhUVJaLbb_IE-FD2Wgh1dbemphKWXQCAQ0mchS_JaWVtyJTvQf19tNg3t08Ccb87McN6BsxCDA-ADRjXDsrk6PM5zTRBhNRE1rxmhb8CGIEkrKkh7BjaYkKZiHJMLcJmz7xASHHGB5FtwQSWWghC6AY-7wccM9-sEJ50Xb6ALgw7GwWVwcE5x9L1LevExQB0sjDaGJe5dKKT1fdFcWPxJjz0c1kkHaEtPj3BexxnmxU3QuHHM78F5r8fsLl_qFvz89vVh96O6vft-s7u-rQwVcqmsY4jTVnCNGet439qWdlr3jbC05aYhzEljNO-R0abVXWdFRzhyWBrrSpNuweeTb0i9OhivovbPdR_VIanr-4cbhRGXLSOywF9O8Lx2k7OmXJ70qObkJ51-P4_-rwQ_FKMnhTFtCCqXbsGnF4cUf60uL2ry-fiwDi6uWVEkJWaIloS24OO_y163_I2jAOQEmBRzTq5_RTBSx9jVMXZ1jF0RobgqpvQPpV2jrQ |
Cites_doi | 10.1016/j.biomaterials.2014.11.007 10.1038/embor.2010.23 10.1186/s13018-019-1507-0 10.2174/0929867325666180831144344 10.1002/term.2397 10.1016/j.tcb.2010.05.002 10.1038/emboj.2012.124 10.1016/j.progpolymsci.2013.05.005 10.2147/SCCAA.S166759 10.1016/j.archoralbio.2011.09.008 10.1038/s41392-021-00762-6 10.1111/etp.12037 10.3892/etm.2018.5982 10.1007/s12015-016-9661-9 10.1097/BCO.0b013e3282630851 10.1002/9780470515303.ch8 10.3390/app11125360 10.1016/j.actbio.2012.02.022 10.1016/j.addr.2010.09.012 10.1016/j.biopha.2016.12.017 10.1038/sj.onc.1210217 10.1042/CS20170047 10.1089/jmf.2014.0021 10.1111/cga.12169 10.11620/IJOB.2016.41.2.053 10.1038/embor.2009.45 10.1111/iej.13843 10.1016/j.joen.2017.10.012 10.1016/j.tibs.2005.09.005 10.1111/iej.12954 10.2741/e281 10.1016/j.dental.2015.02.004 10.2174/092986712800229014 10.1177/154405910808700206 10.1016/j.bone.2019.06.027 10.1155/2018/7571363 10.3389/fcell.2016.00025 10.1177/0022034511408426 |
ContentType | Journal Article |
Copyright | Copyright © Korean J Physiol Pharmacol 2024 |
Copyright_xml | – notice: Copyright © Korean J Physiol Pharmacol 2024 |
DBID | AAYXX CITATION NPM 7X8 5PM ACYCR |
DOI | 10.4196/kjpp.2024.28.5.423 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) Korean Citation Index |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology |
EISSN | 2093-3827 |
EndPage | 433 |
ExternalDocumentID | oai_kci_go_kr_ARTI_10597429 PMC11362005 39198223 10_4196_kjpp_2024_28_5_423 |
Genre | Journal Article |
GroupedDBID | --- 5-W 5GY 8JR 8XY 9ZL AAYXX ABDBF ACUHS ADBBV AENEX ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL CITATION DIK E3Z EBD EF. ESX F5P GX1 HYE MK0 OK1 P2P P5Y P6G RPM TR2 TUS NPM 7X8 5PM .UV 53G ACYCR KVFHK |
ID | FETCH-LOGICAL-c389t-de4053785a144b5f7d73baaf68d375c624e9cca5f0cac7abbd8b250e19cdef0c3 |
ISSN | 1226-4512 |
IngestDate | Tue Sep 03 03:13:38 EDT 2024 Thu Aug 21 18:31:53 EDT 2025 Fri Jul 11 03:56:10 EDT 2025 Thu Apr 03 07:08:33 EDT 2025 Tue Jul 01 02:33:18 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 5 |
Keywords | Cell proliferation Chios gum mastic Dental pulp stem cells Odontogenic differentiation |
Language | English |
License | This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c389t-de4053785a144b5f7d73baaf68d375c624e9cca5f0cac7abbd8b250e19cdef0c3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: I.R.K. designed this study. H.S.B. and S.J.P. performed the relevant analyses. H.S.B., E.G.L., Y.I.K., and I.R.K. wrote the manuscript. I.R.K. edited the English in this manuscript. All authors read and approved the final version of the manuscript. |
OpenAccessLink | https://pubmed.ncbi.nlm.nih.gov/PMC11362005 |
PMID | 39198223 |
PQID | 3099140342 |
PQPubID | 23479 |
PageCount | 11 |
ParticipantIDs | nrf_kci_oai_kci_go_kr_ARTI_10597429 pubmedcentral_primary_oai_pubmedcentral_nih_gov_11362005 proquest_miscellaneous_3099140342 pubmed_primary_39198223 crossref_primary_10_4196_kjpp_2024_28_5_423 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2024-09-01 2024-Sep-01 20240901 2024-09 |
PublicationDateYYYYMMDD | 2024-09-01 |
PublicationDate_xml | – month: 09 year: 2024 text: 2024-09-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | Korea (South) |
PublicationPlace_xml | – name: Korea (South) |
PublicationTitle | The Korean journal of physiology & pharmacology |
PublicationTitleAlternate | Korean J Physiol Pharmacol |
PublicationYear | 2024 |
Publisher | The Korean Physiological Society and The Korean Society of Pharmacology 대한약리학회 |
Publisher_xml | – name: The Korean Physiological Society and The Korean Society of Pharmacology – name: 대한약리학회 |
References | ref13 ref35 ref12 ref34 ref15 ref37 ref14 ref36 ref31 ref30 ref11 ref33 ref10 ref32 ref2 ref1 ref17 ref39 ref16 ref38 ref19 ref18 ref24 ref23 ref26 ref25 ref20 ref42 ref41 ref22 ref21 ref43 ref28 ref27 ref29 ref8 ref7 ref9 ref4 ref3 ref6 ref5 ref40 |
References_xml | – ident: ref29 doi: 10.1016/j.biomaterials.2014.11.007 – ident: ref32 doi: 10.1038/embor.2010.23 – ident: ref3 – ident: ref14 doi: 10.1186/s13018-019-1507-0 – ident: ref22 doi: 10.2174/0929867325666180831144344 – ident: ref33 doi: 10.1002/term.2397 – ident: ref24 doi: 10.1016/j.tcb.2010.05.002 – ident: ref25 doi: 10.1038/emboj.2012.124 – ident: ref35 doi: 10.1016/j.progpolymsci.2013.05.005 – ident: ref9 doi: 10.2147/SCCAA.S166759 – ident: ref36 doi: 10.1016/j.archoralbio.2011.09.008 – ident: ref27 doi: 10.1038/s41392-021-00762-6 – ident: ref6 doi: 10.1111/etp.12037 – ident: ref7 doi: 10.3892/etm.2018.5982 – ident: ref8 doi: 10.1007/s12015-016-9661-9 – ident: ref34 doi: 10.1097/BCO.0b013e3282630851 – ident: ref38 doi: 10.1002/9780470515303.ch8 – ident: ref19 – ident: ref16 doi: 10.3390/app11125360 – ident: ref37 doi: 10.1016/j.actbio.2012.02.022 – ident: ref17 doi: 10.1016/j.addr.2010.09.012 – ident: ref12 doi: 10.1016/j.biopha.2016.12.017 – ident: ref30 doi: 10.1038/sj.onc.1210217 – ident: ref10 doi: 10.1042/CS20170047 – ident: ref11 doi: 10.1089/jmf.2014.0021 – ident: ref1 doi: 10.1111/cga.12169 – ident: ref15 doi: 10.11620/IJOB.2016.41.2.053 – ident: ref31 doi: 10.1038/embor.2009.45 – ident: ref40 doi: 10.1111/iej.13843 – ident: ref2 doi: 10.1016/j.joen.2017.10.012 – ident: ref26 doi: 10.1016/j.tibs.2005.09.005 – ident: ref4 doi: 10.1111/iej.12954 – ident: ref21 – ident: ref39 doi: 10.2741/e281 – ident: ref23 – ident: ref41 doi: 10.1016/j.dental.2015.02.004 – ident: ref13 doi: 10.2174/092986712800229014 – ident: ref42 doi: 10.1177/154405910808700206 – ident: ref43 doi: 10.1016/j.bone.2019.06.027 – ident: ref18 – ident: ref20 doi: 10.1155/2018/7571363 – ident: ref28 doi: 10.3389/fcell.2016.00025 – ident: ref5 doi: 10.1177/0022034511408426 |
SSID | ssib008505809 ssj0064464 |
Score | 2.3142 |
Snippet | Dental pulp stem cells (DPSCs) are a type of adult stem cell present in the dental pulp tissue. They possess a higher proliferative capacity than bone marrow... |
SourceID | nrf pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database |
StartPage | 423 |
SubjectTerms | Original 약리학 |
Title | Chios gum mastic enhance the proliferation and odontogenic differentiation of human dental pulp stem cells |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39198223 https://www.proquest.com/docview/3099140342 https://pubmed.ncbi.nlm.nih.gov/PMC11362005 https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART003113103 |
Volume | 28 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
ispartofPNX | The Korean Journal of Physiology & Pharmacology, 2024, 28(5), , pp.423-433 |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELZ2l8teELA8ujxkBOZSpbSJndjHJC1aQCAOu9LeojzcbfeRVN30AL-eGTtN07JCC5fI8iN2-s1MxlPPF0LeuyC58J7WTu75hcMz33dUoV1H5TwvgqGvA_NXzLfv_skZ_3Iuzvf2DzunllZ1Nsh_3ZlX8j-oQh3gilmy_4Bse1OogDLgC1dAGK73wjiezavb_sXqpn-TIt9yX5czkwJg85-qazy3YhHG-DjsQMu6grtBz_WHUer5xmc08fzC5kcuVteLPpI89zG0f9v1YVGyvlbLdQi_cWdNiMQSOqE0LTaU2G3Qnk0iFg1ZNGKTMVOSSc4mMZOSKbnTRQnTwlkksRAGTPJNl5ipMYt4U5BDNglZ5LJovOkCFcq0QJeQhWo9KO5GOVzeHuOycomzy9iMG-MaVGzGCbg1NoU-C-N1kzKFEPp37Dp4mQ4XzYltbercofIcT1pqgsZ-c5v83LgC3HJ07L5lOFgtEI2rywUSnrp84MqBGLRDu5TeO6_aLVLvq3yeXFTJ1TKBrcvnBB3dALyDffLADcAPxMT1843tleCqGqo162WAG2uo0doHswlhuLSPfy5sy-naL5fTu_ZTu8eCO37W6SPysNkg0dBK-2Oyp8sn5Cgs07q6-Uk_0B-tnB2RS6MAFBSAWgWgjQJQUAC6pQAUFIB2FIDuKACtptQoALUKQFEBKCoANQrwlJx9mpzGJ07z8RCwOlLVTqE5UhVJkY44z8Q0KAIvS9OpLwsvELkP9kmB9RLTYZ7mQZplhcxgO6BHKi80VHrPyEFZlfoFoUIBHG6qpxlYtXwo01QLoXnuC6ULcMF7pL_-dZOF5YgBNBPEIkEsEsQicWUiEsCiR94BAAb9v0hBj7xdA5SAwccnTUtdrW4TD_Z0SLLJ3R55bgFrZ_XUCPk4YQ65BWXbAWfcbinnM0Mqj992wgjz8b2W95IcbrT0FTmolyv9GrzzOntjxPY37YrUrg |
linkProvider | Geneva Foundation for Medical Education and Research |
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=Chios+gum+mastic+enhance+the+proliferation+and+odontogenic+differentiation+of+human+dental+pulp+stem+cells&rft.jtitle=The+Korean+journal+of+physiology+%26+pharmacology&rft.au=%EB%B0%B1%ED%98%84%EC%88%98&rft.au=%EB%B0%95%EC%84%B8%EC%A7%84&rft.au=%EC%9D%B4%EC%9D%80%EA%B2%BD&rft.au=%EA%B9%80%EC%9A%A9%EC%9D%BC&rft.date=2024-09-01&rft.pub=%EB%8C%80%ED%95%9C%EC%95%BD%EB%A6%AC%ED%95%99%ED%9A%8C&rft.issn=1226-4512&rft.eissn=2093-3827&rft.spage=423&rft.epage=433&rft_id=info:doi/10.4196%2Fkjpp.2024.28.5.423&rft.externalDBID=n%2Fa&rft.externalDocID=oai_kci_go_kr_ARTI_10597429 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1226-4512&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1226-4512&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1226-4512&client=summon |