Common mechanisms in development and disease: BMP signaling in craniofacial development

Highlights • BMP signaling is one of the key pathways regulating craniofacial development. • BMP signaling is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. • BMP signaling regulates development of mineralized structures, such as c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cytokine & growth factor reviews 2016-02, Vol.27, p.129-139
Hauptverfasser: Graf, Daniel, Malik, Zeba, Hayano, Satoru, Mishina, Yuji
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 139
container_issue
container_start_page 129
container_title Cytokine & growth factor reviews
container_volume 27
creator Graf, Daniel
Malik, Zeba
Hayano, Satoru
Mishina, Yuji
description Highlights • BMP signaling is one of the key pathways regulating craniofacial development. • BMP signaling is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. • BMP signaling regulates development of mineralized structures, such as cranial bones, maxilla, mandible, palate, and teeth. • Targeted mutations in the mouse have been instrumental to delineate the functional involvement of BMP signaling in different aspects of craniofacial development. • Gene polymorphisms and mutations in BMP pathway genes have been associated with various non-syndromic and syndromic human craniofacial malformations. • Balanced BMP signaling and its local fine-regulation is critical to organize and maintain craniofacial tissues. This has direct implications for the development of clinical applications using recombinant BMPs or BMP antagonists for tissue engineering in situ.
doi_str_mv 10.1016/j.cytogfr.2015.11.004
format Article
fullrecord <record><control><sourceid>elsevier_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4753105</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1359610115300162</els_id><sourcerecordid>S1359610115300162</sourcerecordid><originalsourceid>FETCH-LOGICAL-c555t-65c9d3963290960a1de7bfc9399ea65803ac07d18f0be7fd24402f0f41bda0f43</originalsourceid><addsrcrecordid>eNqFkdFuEzEQRS0Eom3gE0D7A7uM1-vdmIciiKAgFYEEiMeRY49Th107stNI-Xu8SqkKLzyNJd97R3MuYy84NBx4_2rbmOM-blxqWuCy4bwB6B6xc74cVA0C5OPyFlLVfZGfsYuct1AUQsJTdtb2QzeIgZ-zn6s4TTFUE5kbHXyecuVDZelAY9xNFPaVDrayPpPO9Lp69_lrlf0m6NGHzaw0qbii08br8aHtGXvi9Jjp-d1csB8f3n9ffayvv1x9Wr29ro2Ucl_30igrVC9aBaoHzS0Na2eUUIp0L5cgtIHB8qWDNQ3Otl0HrQPX8bXVZYgFuzzl7m7XE1lTVic94i75SacjRu3x75_gb3ATD9gNUnCQJUCeAkyKOSdy914OOJPGLd6Rxpk0co4zxwV7-XDxvesP2iJ4cxJQOf_gKWE2noIh6xOZPdro_7vi8p8EU7B7o8dfdKS8jbepFJGRY24R8Ntc99w2lwJKait-AzIWqWI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Common mechanisms in development and disease: BMP signaling in craniofacial development</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Graf, Daniel ; Malik, Zeba ; Hayano, Satoru ; Mishina, Yuji</creator><creatorcontrib>Graf, Daniel ; Malik, Zeba ; Hayano, Satoru ; Mishina, Yuji</creatorcontrib><description>Highlights • BMP signaling is one of the key pathways regulating craniofacial development. • BMP signaling is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. • BMP signaling regulates development of mineralized structures, such as cranial bones, maxilla, mandible, palate, and teeth. • Targeted mutations in the mouse have been instrumental to delineate the functional involvement of BMP signaling in different aspects of craniofacial development. • Gene polymorphisms and mutations in BMP pathway genes have been associated with various non-syndromic and syndromic human craniofacial malformations. • Balanced BMP signaling and its local fine-regulation is critical to organize and maintain craniofacial tissues. This has direct implications for the development of clinical applications using recombinant BMPs or BMP antagonists for tissue engineering in situ.</description><identifier>ISSN: 1359-6101</identifier><identifier>EISSN: 1879-0305</identifier><identifier>DOI: 10.1016/j.cytogfr.2015.11.004</identifier><identifier>PMID: 26747371</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Advanced Basic Science ; Animals ; BMP signaling ; Bone Morphogenetic Proteins - metabolism ; Cleft palate ; Congenital malformations ; Craniofacial Abnormalities - embryology ; Craniofacial Abnormalities - pathology ; Craniofacial development ; Craniofacial malformations ; Epithelial-Mesenchymal Transition ; Face - abnormalities ; Face - embryology ; Face - pathology ; Gene targeting ; Humans ; Mice ; Neural Crest - embryology ; Neural Crest - pathology ; Signal Transduction ; Tooth morphogenesis</subject><ispartof>Cytokine &amp; growth factor reviews, 2016-02, Vol.27, p.129-139</ispartof><rights>Elsevier Ltd</rights><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c555t-65c9d3963290960a1de7bfc9399ea65803ac07d18f0be7fd24402f0f41bda0f43</citedby><cites>FETCH-LOGICAL-c555t-65c9d3963290960a1de7bfc9399ea65803ac07d18f0be7fd24402f0f41bda0f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cytogfr.2015.11.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26747371$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Graf, Daniel</creatorcontrib><creatorcontrib>Malik, Zeba</creatorcontrib><creatorcontrib>Hayano, Satoru</creatorcontrib><creatorcontrib>Mishina, Yuji</creatorcontrib><title>Common mechanisms in development and disease: BMP signaling in craniofacial development</title><title>Cytokine &amp; growth factor reviews</title><addtitle>Cytokine Growth Factor Rev</addtitle><description>Highlights • BMP signaling is one of the key pathways regulating craniofacial development. • BMP signaling is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. • BMP signaling regulates development of mineralized structures, such as cranial bones, maxilla, mandible, palate, and teeth. • Targeted mutations in the mouse have been instrumental to delineate the functional involvement of BMP signaling in different aspects of craniofacial development. • Gene polymorphisms and mutations in BMP pathway genes have been associated with various non-syndromic and syndromic human craniofacial malformations. • Balanced BMP signaling and its local fine-regulation is critical to organize and maintain craniofacial tissues. This has direct implications for the development of clinical applications using recombinant BMPs or BMP antagonists for tissue engineering in situ.</description><subject>Advanced Basic Science</subject><subject>Animals</subject><subject>BMP signaling</subject><subject>Bone Morphogenetic Proteins - metabolism</subject><subject>Cleft palate</subject><subject>Congenital malformations</subject><subject>Craniofacial Abnormalities - embryology</subject><subject>Craniofacial Abnormalities - pathology</subject><subject>Craniofacial development</subject><subject>Craniofacial malformations</subject><subject>Epithelial-Mesenchymal Transition</subject><subject>Face - abnormalities</subject><subject>Face - embryology</subject><subject>Face - pathology</subject><subject>Gene targeting</subject><subject>Humans</subject><subject>Mice</subject><subject>Neural Crest - embryology</subject><subject>Neural Crest - pathology</subject><subject>Signal Transduction</subject><subject>Tooth morphogenesis</subject><issn>1359-6101</issn><issn>1879-0305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkdFuEzEQRS0Eom3gE0D7A7uM1-vdmIciiKAgFYEEiMeRY49Th107stNI-Xu8SqkKLzyNJd97R3MuYy84NBx4_2rbmOM-blxqWuCy4bwB6B6xc74cVA0C5OPyFlLVfZGfsYuct1AUQsJTdtb2QzeIgZ-zn6s4TTFUE5kbHXyecuVDZelAY9xNFPaVDrayPpPO9Lp69_lrlf0m6NGHzaw0qbii08br8aHtGXvi9Jjp-d1csB8f3n9ffayvv1x9Wr29ro2Ucl_30igrVC9aBaoHzS0Na2eUUIp0L5cgtIHB8qWDNQ3Otl0HrQPX8bXVZYgFuzzl7m7XE1lTVic94i75SacjRu3x75_gb3ATD9gNUnCQJUCeAkyKOSdy914OOJPGLd6Rxpk0co4zxwV7-XDxvesP2iJ4cxJQOf_gKWE2noIh6xOZPdro_7vi8p8EU7B7o8dfdKS8jbepFJGRY24R8Ntc99w2lwJKait-AzIWqWI</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Graf, Daniel</creator><creator>Malik, Zeba</creator><creator>Hayano, Satoru</creator><creator>Mishina, Yuji</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20160201</creationdate><title>Common mechanisms in development and disease: BMP signaling in craniofacial development</title><author>Graf, Daniel ; Malik, Zeba ; Hayano, Satoru ; Mishina, Yuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c555t-65c9d3963290960a1de7bfc9399ea65803ac07d18f0be7fd24402f0f41bda0f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>BMP signaling</topic><topic>Bone Morphogenetic Proteins - metabolism</topic><topic>Cleft palate</topic><topic>Congenital malformations</topic><topic>Craniofacial Abnormalities - embryology</topic><topic>Craniofacial Abnormalities - pathology</topic><topic>Craniofacial development</topic><topic>Craniofacial malformations</topic><topic>Epithelial-Mesenchymal Transition</topic><topic>Face - abnormalities</topic><topic>Face - embryology</topic><topic>Face - pathology</topic><topic>Gene targeting</topic><topic>Humans</topic><topic>Mice</topic><topic>Neural Crest - embryology</topic><topic>Neural Crest - pathology</topic><topic>Signal Transduction</topic><topic>Tooth morphogenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Graf, Daniel</creatorcontrib><creatorcontrib>Malik, Zeba</creatorcontrib><creatorcontrib>Hayano, Satoru</creatorcontrib><creatorcontrib>Mishina, Yuji</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cytokine &amp; growth factor reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Graf, Daniel</au><au>Malik, Zeba</au><au>Hayano, Satoru</au><au>Mishina, Yuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Common mechanisms in development and disease: BMP signaling in craniofacial development</atitle><jtitle>Cytokine &amp; growth factor reviews</jtitle><addtitle>Cytokine Growth Factor Rev</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>27</volume><spage>129</spage><epage>139</epage><pages>129-139</pages><issn>1359-6101</issn><eissn>1879-0305</eissn><abstract>Highlights • BMP signaling is one of the key pathways regulating craniofacial development. • BMP signaling is involved in the early patterning of the head, the development of cranial neural crest cells, and facial patterning. • BMP signaling regulates development of mineralized structures, such as cranial bones, maxilla, mandible, palate, and teeth. • Targeted mutations in the mouse have been instrumental to delineate the functional involvement of BMP signaling in different aspects of craniofacial development. • Gene polymorphisms and mutations in BMP pathway genes have been associated with various non-syndromic and syndromic human craniofacial malformations. • Balanced BMP signaling and its local fine-regulation is critical to organize and maintain craniofacial tissues. This has direct implications for the development of clinical applications using recombinant BMPs or BMP antagonists for tissue engineering in situ.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26747371</pmid><doi>10.1016/j.cytogfr.2015.11.004</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1359-6101
ispartof Cytokine & growth factor reviews, 2016-02, Vol.27, p.129-139
issn 1359-6101
1879-0305
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4753105
source MEDLINE; Elsevier ScienceDirect Journals
subjects Advanced Basic Science
Animals
BMP signaling
Bone Morphogenetic Proteins - metabolism
Cleft palate
Congenital malformations
Craniofacial Abnormalities - embryology
Craniofacial Abnormalities - pathology
Craniofacial development
Craniofacial malformations
Epithelial-Mesenchymal Transition
Face - abnormalities
Face - embryology
Face - pathology
Gene targeting
Humans
Mice
Neural Crest - embryology
Neural Crest - pathology
Signal Transduction
Tooth morphogenesis
title Common mechanisms in development and disease: BMP signaling in craniofacial development
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T01%3A43%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Common%20mechanisms%20in%20development%20and%20disease:%20BMP%20signaling%20in%20craniofacial%20development&rft.jtitle=Cytokine%20&%20growth%20factor%20reviews&rft.au=Graf,%20Daniel&rft.date=2016-02-01&rft.volume=27&rft.spage=129&rft.epage=139&rft.pages=129-139&rft.issn=1359-6101&rft.eissn=1879-0305&rft_id=info:doi/10.1016/j.cytogfr.2015.11.004&rft_dat=%3Celsevier_pubme%3ES1359610115300162%3C/elsevier_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/26747371&rft_els_id=S1359610115300162&rfr_iscdi=true