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dc.contributor.authorConway, James
dc.contributor.authorInce, S
dc.contributor.authorBlack, Stephanie
dc.contributor.authorKramer, Edgar
dc.date.accessioned2020-10-16T12:56:36Z
dc.date.issued2020-09-01
dc.identifier.issn0302-766X
dc.identifier.issn1432-0878
dc.identifier.urihttp://hdl.handle.net/10026.1/16547
dc.description.abstract

The glial cell line-derived neurotrophic factor (GDNF) and its canonical receptor Ret can signal both in tandem and separately to exert many vital functions in the midbrain dopamine system. It is known that Ret has effects on maintenance, physiology, protection and regeneration in the midbrain dopamine system, with the physiological functions of GDNF still somewhat unclear. Notwithstanding, Ret ligands, such as GDNF, are considered as promising candidates for neuroprotection and/or regeneration in Parkinson's disease, although data from clinical trials are so far inconclusive. In this review, we discuss the current knowledge of GDNF/Ret signaling in the dopamine system in vivo as well as crosstalk with pathology-associated proteins and their signaling in mammals.

dc.format.extent135-146
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.subjectMidbrain dopamine system
dc.subjectCell survival
dc.subjectProtection
dc.subjectRegeneration
dc.subjectRet
dc.subjectGDNF
dc.titleGDNF/RET signaling in dopamine neurons in vivo
dc.typejournal-article
dc.typeJournal Article
dc.typeReview
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000565098900001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue1
plymouth.volume382
plymouth.publication-statusPublished
plymouth.journalCell and Tissue Research
dc.identifier.doi10.1007/s00441-020-03268-9
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Arts, Humanities and Business
plymouth.organisational-group/Plymouth/Faculty of Arts, Humanities and Business/School of Art, Design and Architecture
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA32 Art and Design: History, Practice and Theory
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeGermany
dcterms.dateAccepted2020-07-23
dc.rights.embargodate2021-9-1
dc.identifier.eissn1432-0878
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1007/s00441-020-03268-9
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2020-09-01
rioxxterms.typeJournal Article/Review


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