Phenotypic and Functional Characterization of Peripheral Sensory Neurons derived from Human Embryonic Stem Cells

The dorsal root ganglia (DRG) consist of a multitude of sensory neuronal subtypes that function to relay sensory stimuli, including temperature, pressure, pain and position to the central nervous system. Our knowledge of DRG sensory neurons have been predominantly driven by animal studies and consid...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Scientific reports 2018-01, Vol.8 (1), p.603-12, Article 603
Hauptverfasser: Alshawaf, Abdullah Jawad, Viventi, Serena, Qiu, Wanzhi, D’Abaco, Giovanna, Nayagam, Bryony, Erlichster, Michael, Chana, Gursharan, Everall, Ian, Ivanusic, Jason, Skafidas, Efstratios, Dottori, Mirella
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 12
container_issue 1
container_start_page 603
container_title Scientific reports
container_volume 8
creator Alshawaf, Abdullah Jawad
Viventi, Serena
Qiu, Wanzhi
D’Abaco, Giovanna
Nayagam, Bryony
Erlichster, Michael
Chana, Gursharan
Everall, Ian
Ivanusic, Jason
Skafidas, Efstratios
Dottori, Mirella
description The dorsal root ganglia (DRG) consist of a multitude of sensory neuronal subtypes that function to relay sensory stimuli, including temperature, pressure, pain and position to the central nervous system. Our knowledge of DRG sensory neurons have been predominantly driven by animal studies and considerably less is known about the human DRG. Human embryonic stem cells (hESC) are valuable resource to help close this gap. Our previous studies reported an efficient system for deriving neural crest and DRG sensory neurons from hESC. Here we show that this differentiation system gives rise to heterogeneous populations of sensory neuronal subtypes as demonstrated by phenotypic and functional analyses. Furthermore, using microelectrode arrays the maturation rate of the hESC-derived sensory neuronal cultures was monitored over 8 weeks in culture, showing their spontaneous firing activities starting at about 12 days post-differentiation and reaching maximum firing at about 6 weeks. These studies are highly valuable for developing an in vitro platform to study the diversity of sensory neuronal subtypes found within the human DRG.
doi_str_mv 10.1038/s41598-017-19093-0
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5766621</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1989580854</sourcerecordid><originalsourceid>FETCH-LOGICAL-c577t-a7b1d457694b402c30e23ffa0bc20df499da9093188905bab1ac14dda7090d903</originalsourceid><addsrcrecordid>eNp1UU1rGzEUFCWlMan_QA9FkEsu2z59rLW6BIJJmoBpA2nPQitp4zVeaSPtBtxfX22cBCdQXfQx8-a90SD0hcA3Aqz6njgpZVUAEQWRIFkBH9CMAi8Lyig9Ojgfo3lKG8irpJIT-QkdU8kYMCFmqL9dOx-GXd8arL3FV6M3Qxu83uLlWkdtBhfbv3p6wqHBt_nWr13M8J3zKcQd_unGGHzCNkOPzuImhg5fj532-LKr4y74LH03uA4v3XabPqOPjd4mN3_eT9Cfq8vfy-ti9evHzfJiVZhSiKHQoiaWl2Ihec2BGgaOsqbRUBsKtuFSWj3ZJlUloax1TbQh3FotQIKVwE7Q-V63H-vOWeP8kKdWfWw7HXcq6Fa9RXy7VvfhUeWeiwUlWeDsWSCGh9GlQXVtMtmC9i6MSRFZybKCquSZevqOugljzH_4xFpIMRnJLLpnmRhSiq55HYaAmjJV-0xVzlQ9ZaomG18PbbyWvCSYCWxPSBny9y4e9P6_7D--dK5_</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1986974576</pqid></control><display><type>article</type><title>Phenotypic and Functional Characterization of Peripheral Sensory Neurons derived from Human Embryonic Stem Cells</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Springer Nature OA Free Journals</source><source>Nature Free</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Alshawaf, Abdullah Jawad ; Viventi, Serena ; Qiu, Wanzhi ; D’Abaco, Giovanna ; Nayagam, Bryony ; Erlichster, Michael ; Chana, Gursharan ; Everall, Ian ; Ivanusic, Jason ; Skafidas, Efstratios ; Dottori, Mirella</creator><creatorcontrib>Alshawaf, Abdullah Jawad ; Viventi, Serena ; Qiu, Wanzhi ; D’Abaco, Giovanna ; Nayagam, Bryony ; Erlichster, Michael ; Chana, Gursharan ; Everall, Ian ; Ivanusic, Jason ; Skafidas, Efstratios ; Dottori, Mirella</creatorcontrib><description>The dorsal root ganglia (DRG) consist of a multitude of sensory neuronal subtypes that function to relay sensory stimuli, including temperature, pressure, pain and position to the central nervous system. Our knowledge of DRG sensory neurons have been predominantly driven by animal studies and considerably less is known about the human DRG. Human embryonic stem cells (hESC) are valuable resource to help close this gap. Our previous studies reported an efficient system for deriving neural crest and DRG sensory neurons from hESC. Here we show that this differentiation system gives rise to heterogeneous populations of sensory neuronal subtypes as demonstrated by phenotypic and functional analyses. Furthermore, using microelectrode arrays the maturation rate of the hESC-derived sensory neuronal cultures was monitored over 8 weeks in culture, showing their spontaneous firing activities starting at about 12 days post-differentiation and reaching maximum firing at about 6 weeks. These studies are highly valuable for developing an in vitro platform to study the diversity of sensory neuronal subtypes found within the human DRG.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-017-19093-0</identifier><identifier>PMID: 29330377</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/100 ; 13/106 ; 14/19 ; 38 ; 38/77 ; 631/136/142 ; 631/378/1959/2605 ; 631/378/3917 ; 631/532/1360 ; 82/51 ; 9/30 ; Biomarkers - metabolism ; Cell culture ; Cell Culture Techniques - methods ; Cell Differentiation ; Cell Line ; Central nervous system ; Dorsal root ganglia ; Embryo cells ; Gene expression ; Human Embryonic Stem Cells - cytology ; Human Embryonic Stem Cells - metabolism ; Humanities and Social Sciences ; Humans ; Microelectrodes ; multidisciplinary ; Neural crest ; Pain ; Peripheral Nervous System - cytology ; Phenotype ; Science ; Science (multidisciplinary) ; Sensory neurons ; Sensory Receptor Cells - cytology ; Sensory Receptor Cells - metabolism ; Sensory stimuli ; Stem cell transplantation ; Stem cells</subject><ispartof>Scientific reports, 2018-01, Vol.8 (1), p.603-12, Article 603</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published 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.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c577t-a7b1d457694b402c30e23ffa0bc20df499da9093188905bab1ac14dda7090d903</citedby><cites>FETCH-LOGICAL-c577t-a7b1d457694b402c30e23ffa0bc20df499da9093188905bab1ac14dda7090d903</cites><orcidid>0000-0003-4263-9972 ; 0000-0003-0598-4195</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766621/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766621/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29330377$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alshawaf, Abdullah Jawad</creatorcontrib><creatorcontrib>Viventi, Serena</creatorcontrib><creatorcontrib>Qiu, Wanzhi</creatorcontrib><creatorcontrib>D’Abaco, Giovanna</creatorcontrib><creatorcontrib>Nayagam, Bryony</creatorcontrib><creatorcontrib>Erlichster, Michael</creatorcontrib><creatorcontrib>Chana, Gursharan</creatorcontrib><creatorcontrib>Everall, Ian</creatorcontrib><creatorcontrib>Ivanusic, Jason</creatorcontrib><creatorcontrib>Skafidas, Efstratios</creatorcontrib><creatorcontrib>Dottori, Mirella</creatorcontrib><title>Phenotypic and Functional Characterization of Peripheral Sensory Neurons derived from Human Embryonic Stem Cells</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The dorsal root ganglia (DRG) consist of a multitude of sensory neuronal subtypes that function to relay sensory stimuli, including temperature, pressure, pain and position to the central nervous system. Our knowledge of DRG sensory neurons have been predominantly driven by animal studies and considerably less is known about the human DRG. Human embryonic stem cells (hESC) are valuable resource to help close this gap. Our previous studies reported an efficient system for deriving neural crest and DRG sensory neurons from hESC. Here we show that this differentiation system gives rise to heterogeneous populations of sensory neuronal subtypes as demonstrated by phenotypic and functional analyses. Furthermore, using microelectrode arrays the maturation rate of the hESC-derived sensory neuronal cultures was monitored over 8 weeks in culture, showing their spontaneous firing activities starting at about 12 days post-differentiation and reaching maximum firing at about 6 weeks. These studies are highly valuable for developing an in vitro platform to study the diversity of sensory neuronal subtypes found within the human DRG.</description><subject>13/100</subject><subject>13/106</subject><subject>14/19</subject><subject>38</subject><subject>38/77</subject><subject>631/136/142</subject><subject>631/378/1959/2605</subject><subject>631/378/3917</subject><subject>631/532/1360</subject><subject>82/51</subject><subject>9/30</subject><subject>Biomarkers - metabolism</subject><subject>Cell culture</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Central nervous system</subject><subject>Dorsal root ganglia</subject><subject>Embryo cells</subject><subject>Gene expression</subject><subject>Human Embryonic Stem Cells - cytology</subject><subject>Human Embryonic Stem Cells - metabolism</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Microelectrodes</subject><subject>multidisciplinary</subject><subject>Neural crest</subject><subject>Pain</subject><subject>Peripheral Nervous System - cytology</subject><subject>Phenotype</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sensory neurons</subject><subject>Sensory Receptor Cells - cytology</subject><subject>Sensory Receptor Cells - metabolism</subject><subject>Sensory stimuli</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1UU1rGzEUFCWlMan_QA9FkEsu2z59rLW6BIJJmoBpA2nPQitp4zVeaSPtBtxfX22cBCdQXfQx8-a90SD0hcA3Aqz6njgpZVUAEQWRIFkBH9CMAi8Lyig9Ojgfo3lKG8irpJIT-QkdU8kYMCFmqL9dOx-GXd8arL3FV6M3Qxu83uLlWkdtBhfbv3p6wqHBt_nWr13M8J3zKcQd_unGGHzCNkOPzuImhg5fj532-LKr4y74LH03uA4v3XabPqOPjd4mN3_eT9Cfq8vfy-ti9evHzfJiVZhSiKHQoiaWl2Ihec2BGgaOsqbRUBsKtuFSWj3ZJlUloax1TbQh3FotQIKVwE7Q-V63H-vOWeP8kKdWfWw7HXcq6Fa9RXy7VvfhUeWeiwUlWeDsWSCGh9GlQXVtMtmC9i6MSRFZybKCquSZevqOugljzH_4xFpIMRnJLLpnmRhSiq55HYaAmjJV-0xVzlQ9ZaomG18PbbyWvCSYCWxPSBny9y4e9P6_7D--dK5_</recordid><startdate>20180112</startdate><enddate>20180112</enddate><creator>Alshawaf, Abdullah Jawad</creator><creator>Viventi, Serena</creator><creator>Qiu, Wanzhi</creator><creator>D’Abaco, Giovanna</creator><creator>Nayagam, Bryony</creator><creator>Erlichster, Michael</creator><creator>Chana, Gursharan</creator><creator>Everall, Ian</creator><creator>Ivanusic, Jason</creator><creator>Skafidas, Efstratios</creator><creator>Dottori, Mirella</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4263-9972</orcidid><orcidid>https://orcid.org/0000-0003-0598-4195</orcidid></search><sort><creationdate>20180112</creationdate><title>Phenotypic and Functional Characterization of Peripheral Sensory Neurons derived from Human Embryonic Stem Cells</title><author>Alshawaf, Abdullah Jawad ; Viventi, Serena ; Qiu, Wanzhi ; D’Abaco, Giovanna ; Nayagam, Bryony ; Erlichster, Michael ; Chana, Gursharan ; Everall, Ian ; Ivanusic, Jason ; Skafidas, Efstratios ; Dottori, Mirella</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c577t-a7b1d457694b402c30e23ffa0bc20df499da9093188905bab1ac14dda7090d903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>13/100</topic><topic>13/106</topic><topic>14/19</topic><topic>38</topic><topic>38/77</topic><topic>631/136/142</topic><topic>631/378/1959/2605</topic><topic>631/378/3917</topic><topic>631/532/1360</topic><topic>82/51</topic><topic>9/30</topic><topic>Biomarkers - metabolism</topic><topic>Cell culture</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Central nervous system</topic><topic>Dorsal root ganglia</topic><topic>Embryo cells</topic><topic>Gene expression</topic><topic>Human Embryonic Stem Cells - cytology</topic><topic>Human Embryonic Stem Cells - metabolism</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Microelectrodes</topic><topic>multidisciplinary</topic><topic>Neural crest</topic><topic>Pain</topic><topic>Peripheral Nervous System - cytology</topic><topic>Phenotype</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Sensory neurons</topic><topic>Sensory Receptor Cells - cytology</topic><topic>Sensory Receptor Cells - metabolism</topic><topic>Sensory stimuli</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alshawaf, Abdullah Jawad</creatorcontrib><creatorcontrib>Viventi, Serena</creatorcontrib><creatorcontrib>Qiu, Wanzhi</creatorcontrib><creatorcontrib>D’Abaco, Giovanna</creatorcontrib><creatorcontrib>Nayagam, Bryony</creatorcontrib><creatorcontrib>Erlichster, Michael</creatorcontrib><creatorcontrib>Chana, Gursharan</creatorcontrib><creatorcontrib>Everall, Ian</creatorcontrib><creatorcontrib>Ivanusic, Jason</creatorcontrib><creatorcontrib>Skafidas, Efstratios</creatorcontrib><creatorcontrib>Dottori, Mirella</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alshawaf, Abdullah Jawad</au><au>Viventi, Serena</au><au>Qiu, Wanzhi</au><au>D’Abaco, Giovanna</au><au>Nayagam, Bryony</au><au>Erlichster, Michael</au><au>Chana, Gursharan</au><au>Everall, Ian</au><au>Ivanusic, Jason</au><au>Skafidas, Efstratios</au><au>Dottori, Mirella</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenotypic and Functional Characterization of Peripheral Sensory Neurons derived from Human Embryonic Stem Cells</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-01-12</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>603</spage><epage>12</epage><pages>603-12</pages><artnum>603</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The dorsal root ganglia (DRG) consist of a multitude of sensory neuronal subtypes that function to relay sensory stimuli, including temperature, pressure, pain and position to the central nervous system. Our knowledge of DRG sensory neurons have been predominantly driven by animal studies and considerably less is known about the human DRG. Human embryonic stem cells (hESC) are valuable resource to help close this gap. Our previous studies reported an efficient system for deriving neural crest and DRG sensory neurons from hESC. Here we show that this differentiation system gives rise to heterogeneous populations of sensory neuronal subtypes as demonstrated by phenotypic and functional analyses. Furthermore, using microelectrode arrays the maturation rate of the hESC-derived sensory neuronal cultures was monitored over 8 weeks in culture, showing their spontaneous firing activities starting at about 12 days post-differentiation and reaching maximum firing at about 6 weeks. These studies are highly valuable for developing an in vitro platform to study the diversity of sensory neuronal subtypes found within the human DRG.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29330377</pmid><doi>10.1038/s41598-017-19093-0</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4263-9972</orcidid><orcidid>https://orcid.org/0000-0003-0598-4195</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2045-2322
ispartof Scientific reports, 2018-01, Vol.8 (1), p.603-12, Article 603
issn 2045-2322
2045-2322
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5766621
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature OA Free Journals; Nature Free; PubMed Central; Free Full-Text Journals in Chemistry
subjects 13/100
13/106
14/19
38
38/77
631/136/142
631/378/1959/2605
631/378/3917
631/532/1360
82/51
9/30
Biomarkers - metabolism
Cell culture
Cell Culture Techniques - methods
Cell Differentiation
Cell Line
Central nervous system
Dorsal root ganglia
Embryo cells
Gene expression
Human Embryonic Stem Cells - cytology
Human Embryonic Stem Cells - metabolism
Humanities and Social Sciences
Humans
Microelectrodes
multidisciplinary
Neural crest
Pain
Peripheral Nervous System - cytology
Phenotype
Science
Science (multidisciplinary)
Sensory neurons
Sensory Receptor Cells - cytology
Sensory Receptor Cells - metabolism
Sensory stimuli
Stem cell transplantation
Stem cells
title Phenotypic and Functional Characterization of Peripheral Sensory Neurons derived from Human Embryonic Stem Cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T05%3A15%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Phenotypic%20and%20Functional%20Characterization%20of%20Peripheral%20Sensory%20Neurons%20derived%20from%20Human%20Embryonic%20Stem%20Cells&rft.jtitle=Scientific%20reports&rft.au=Alshawaf,%20Abdullah%20Jawad&rft.date=2018-01-12&rft.volume=8&rft.issue=1&rft.spage=603&rft.epage=12&rft.pages=603-12&rft.artnum=603&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-017-19093-0&rft_dat=%3Cproquest_pubme%3E1989580854%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1986974576&rft_id=info:pmid/29330377&rfr_iscdi=true