Show simple item record

dc.contributor.authorBasile, G
dc.contributor.authorKulkarni, RN
dc.contributor.authorMorgan, NG
dc.date.accessioned2020-01-09T11:01:58Z
dc.date.issued2019-06-27
dc.description.abstractPurpose of Review Pancreatic β-cells play a critical role in whole-body glucose homeostasis by regulating the release of insulin in response to minute by minute alterations in metabolic demand. As such, β-cells are staunchly resilient but there are circumstances where they can become functionally compromised or physically lost due to pathophysiological changes which culminate in overt hyperglycemia and diabetes. Recent Findings In humans, β-cell mass appears to be largely defined in the postnatal period and this early replicative and generative phase is followed by a refractory state which persists throughout life. Despite this, efforts to identify physiological and pharmacological factors which might re-initiate β-cell replication (or cause the replenishment of β-cells by neogenesis or transdifferentiation) are beginning to bear fruit. Summary Controlled manipulation of β-cell mass in humans still represents a holy grail for therapeutic intervention in diabetes, but progress is being made which may lead to ultimate success.en_GB
dc.description.sponsorshipNational Institutes of Health Researchen_GB
dc.description.sponsorshipDiabetes UKen_GB
dc.description.sponsorshipJDRFen_GB
dc.identifier.citationVol. 19: 48en_GB
dc.identifier.doi10.1007/s11892-019-1176-8
dc.identifier.grantnumberDK067536en_GB
dc.identifier.grantnumberUC4 DK116278en_GB
dc.identifier.grantnumberUC4 DK116255en_GB
dc.identifier.grantnumber15/0005156en_GB
dc.identifier.grantnumber16/0005480en_GB
dc.identifier.grantnumber3-SRA-2017-492-A-Nen_GB
dc.identifier.grantnumber2-SRA-2018-474-S-Ben_GB
dc.identifier.urihttp://hdl.handle.net/10871/40313
dc.language.isoenen_GB
dc.publisherSpringeren_GB
dc.rights.embargoreasonUnder embargo until 27 June 2020 in compliance with publisher policy.en_GB
dc.rights(c) Springer Science+Business Media, LLC, part of Springer Nature 2019en_GB
dc.subjectProliferationen_GB
dc.subjectDiabetesen_GB
dc.subjectTransdifferentiationen_GB
dc.subjectIslets of Langerhansen_GB
dc.subjectbeta-Cell massen_GB
dc.subjectKi67en_GB
dc.titleHow, When, and Where Do Human beta-Cells Regenerate?en_GB
dc.typeArticleen_GB
dc.date.available2020-01-09T11:01:58Z
dc.identifier.issn1534-4827
exeter.article-numberARTN 48en_GB
dc.descriptionThis is the author accepted manuscript. The final version is available from Springer via the DOI in this record.en_GB
dc.identifier.journalCurrent Diabetes Reportsen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2019-06-27
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2019-06-27
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-01-09T10:52:17Z
refterms.versionFCDAM
refterms.panelAen_GB


Files in this item

This item appears in the following Collection(s)

Show simple item record