The Opportunities and Challenges in the Molecular Mechanism Research of Congenital Heart Disease: A Review

Background: Advanced molecular mechanism research incorporated with multidisciplinary collaborations on congenital heart disease has prompted new insight into its cause, development, and outcomes. Summary: This literature review aims to comprehensively examine the genetic molecular mechanisms of con...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular syndromology 2024-10, p.1-7
Hauptverfasser: Li, Mingwei, Wang, Shuangxing, Zhang, Hui, Meng, Bing, Wu, Yongjie
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 7
container_issue
container_start_page 1
container_title Molecular syndromology
container_volume
creator Li, Mingwei
Wang, Shuangxing
Zhang, Hui
Meng, Bing
Wu, Yongjie
description Background: Advanced molecular mechanism research incorporated with multidisciplinary collaborations on congenital heart disease has prompted new insight into its cause, development, and outcomes. Summary: This literature review aims to comprehensively examine the genetic molecular mechanisms of congenital heart disease and explain current prospects and challenges in this field. Through a systematic exploration of etiology, embryology, clinical outcomes, algorithms, and ethics, we seek to shed light on the path toward improved diagnostics, treatments, and outcomes for patients. Key Message: Collaboration among genetic researchers, clinicians, data scientists, ethicists, and policymakers is crucial to address challenges and translate research findings into tangible benefits for CHD patients.
doi_str_mv 10.1159/000541266
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1159_000541266</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1159_000541266</sourcerecordid><originalsourceid>FETCH-LOGICAL-c119t-7030786401640e883459ea00f4cbff8e120d0ea92fda845f21ba5e24a412ec8a3</originalsourceid><addsrcrecordid>eNo9kE9Lw0AQxRdRsNQe_AZ79RCdyd-NtxK1FVoKUs9hupk1W9Kk7KaK394VpYdh5s38eDBPiFuEe8SsfACALMU4zy_EBPMcI1UUxeV5zstrMfN-HzBIylghTsR-27LcHI-DG0-9HS17SX0jq5a6jvuPIG0vx8Csh471qSMn16xb6q0_yDf2TE63cjCyGgIdHKiTy7Ac5ZMNR8-Pch64T8tfN-LKUOd59t-n4v3leVsto9Vm8VrNV5FGLMeogAQKlaeAoVipJM1KJgCT6p0xijGGBpjK2DSk0szEuKOM45TC56wVJVNx9-er3eC9Y1MfnT2Q-64R6t-c6nNOyQ_0SlnN</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Opportunities and Challenges in the Molecular Mechanism Research of Congenital Heart Disease: A Review</title><source>Alma/SFX Local Collection</source><creator>Li, Mingwei ; Wang, Shuangxing ; Zhang, Hui ; Meng, Bing ; Wu, Yongjie</creator><creatorcontrib>Li, Mingwei ; Wang, Shuangxing ; Zhang, Hui ; Meng, Bing ; Wu, Yongjie</creatorcontrib><description>Background: Advanced molecular mechanism research incorporated with multidisciplinary collaborations on congenital heart disease has prompted new insight into its cause, development, and outcomes. Summary: This literature review aims to comprehensively examine the genetic molecular mechanisms of congenital heart disease and explain current prospects and challenges in this field. Through a systematic exploration of etiology, embryology, clinical outcomes, algorithms, and ethics, we seek to shed light on the path toward improved diagnostics, treatments, and outcomes for patients. Key Message: Collaboration among genetic researchers, clinicians, data scientists, ethicists, and policymakers is crucial to address challenges and translate research findings into tangible benefits for CHD patients.</description><identifier>ISSN: 1661-8769</identifier><identifier>EISSN: 1661-8777</identifier><identifier>DOI: 10.1159/000541266</identifier><language>eng</language><ispartof>Molecular syndromology, 2024-10, p.1-7</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c119t-7030786401640e883459ea00f4cbff8e120d0ea92fda845f21ba5e24a412ec8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Li, Mingwei</creatorcontrib><creatorcontrib>Wang, Shuangxing</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Meng, Bing</creatorcontrib><creatorcontrib>Wu, Yongjie</creatorcontrib><title>The Opportunities and Challenges in the Molecular Mechanism Research of Congenital Heart Disease: A Review</title><title>Molecular syndromology</title><description>Background: Advanced molecular mechanism research incorporated with multidisciplinary collaborations on congenital heart disease has prompted new insight into its cause, development, and outcomes. Summary: This literature review aims to comprehensively examine the genetic molecular mechanisms of congenital heart disease and explain current prospects and challenges in this field. Through a systematic exploration of etiology, embryology, clinical outcomes, algorithms, and ethics, we seek to shed light on the path toward improved diagnostics, treatments, and outcomes for patients. Key Message: Collaboration among genetic researchers, clinicians, data scientists, ethicists, and policymakers is crucial to address challenges and translate research findings into tangible benefits for CHD patients.</description><issn>1661-8769</issn><issn>1661-8777</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kE9Lw0AQxRdRsNQe_AZ79RCdyd-NtxK1FVoKUs9hupk1W9Kk7KaK394VpYdh5s38eDBPiFuEe8SsfACALMU4zy_EBPMcI1UUxeV5zstrMfN-HzBIylghTsR-27LcHI-DG0-9HS17SX0jq5a6jvuPIG0vx8Csh471qSMn16xb6q0_yDf2TE63cjCyGgIdHKiTy7Ac5ZMNR8-Pch64T8tfN-LKUOd59t-n4v3leVsto9Vm8VrNV5FGLMeogAQKlaeAoVipJM1KJgCT6p0xijGGBpjK2DSk0szEuKOM45TC56wVJVNx9-er3eC9Y1MfnT2Q-64R6t-c6nNOyQ_0SlnN</recordid><startdate>20241030</startdate><enddate>20241030</enddate><creator>Li, Mingwei</creator><creator>Wang, Shuangxing</creator><creator>Zhang, Hui</creator><creator>Meng, Bing</creator><creator>Wu, Yongjie</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20241030</creationdate><title>The Opportunities and Challenges in the Molecular Mechanism Research of Congenital Heart Disease: A Review</title><author>Li, Mingwei ; Wang, Shuangxing ; Zhang, Hui ; Meng, Bing ; Wu, Yongjie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c119t-7030786401640e883459ea00f4cbff8e120d0ea92fda845f21ba5e24a412ec8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Mingwei</creatorcontrib><creatorcontrib>Wang, Shuangxing</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Meng, Bing</creatorcontrib><creatorcontrib>Wu, Yongjie</creatorcontrib><collection>CrossRef</collection><jtitle>Molecular syndromology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Mingwei</au><au>Wang, Shuangxing</au><au>Zhang, Hui</au><au>Meng, Bing</au><au>Wu, Yongjie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Opportunities and Challenges in the Molecular Mechanism Research of Congenital Heart Disease: A Review</atitle><jtitle>Molecular syndromology</jtitle><date>2024-10-30</date><risdate>2024</risdate><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>1661-8769</issn><eissn>1661-8777</eissn><abstract>Background: Advanced molecular mechanism research incorporated with multidisciplinary collaborations on congenital heart disease has prompted new insight into its cause, development, and outcomes. Summary: This literature review aims to comprehensively examine the genetic molecular mechanisms of congenital heart disease and explain current prospects and challenges in this field. Through a systematic exploration of etiology, embryology, clinical outcomes, algorithms, and ethics, we seek to shed light on the path toward improved diagnostics, treatments, and outcomes for patients. Key Message: Collaboration among genetic researchers, clinicians, data scientists, ethicists, and policymakers is crucial to address challenges and translate research findings into tangible benefits for CHD patients.</abstract><doi>10.1159/000541266</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1661-8769
ispartof Molecular syndromology, 2024-10, p.1-7
issn 1661-8769
1661-8777
language eng
recordid cdi_crossref_primary_10_1159_000541266
source Alma/SFX Local Collection
title The Opportunities and Challenges in the Molecular Mechanism Research of Congenital Heart Disease: A Review
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T22%3A20%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Opportunities%20and%20Challenges%20in%20the%20Molecular%20Mechanism%20Research%20of%20Congenital%20Heart%20Disease:%20A%20Review&rft.jtitle=Molecular%20syndromology&rft.au=Li,%20Mingwei&rft.date=2024-10-30&rft.spage=1&rft.epage=7&rft.pages=1-7&rft.issn=1661-8769&rft.eissn=1661-8777&rft_id=info:doi/10.1159/000541266&rft_dat=%3Ccrossref%3E10_1159_000541266%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true