Show simple item record

Gene expression of the insulin-like growth factors and their receptors in human neuroblastoma cell lines

dc.contributor.authorMartin, Donna M.en_US
dc.contributor.authorYee, Douglasen_US
dc.contributor.authorCarlson, Robert O.en_US
dc.contributor.authorFeldman, Eva L.en_US
dc.date.accessioned2006-04-10T15:03:17Z
dc.date.available2006-04-10T15:03:17Z
dc.date.issued1992-10en_US
dc.identifier.citationMartin, D. M., Yee, D., Carlson, R. O., Feldman, E. L. (1992/10)."Gene expression of the insulin-like growth factors and their receptors in human neuroblastoma cell lines." Molecular Brain Research 15(3-4): 241-246. <http://hdl.handle.net/2027.42/29806>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T07-4859N3B-6B/2/55031b14f84bd9e2503dcab549ea5025en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29806
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1331680&dopt=citationen_US
dc.description.abstractInsulin-like growth factors (IGF) I and II are polypeptides with both growth-promoting and insulin-like metabolic effects. The developmentally specific expression of IGF I and II in the nervous system implies a role for these growth factors in neuronal growth and differentiation. In the present study, we analyzed IGF and IGF receptor mRNA transcripts from two related human neuroblastoma cell lines, SH-SY5Y and SK-N-SH. These cell lines provide a good in vitro model of neuronal development. Northern analysis of total RNA from each cell line revealed three IGF II mRNA transcripts (6.0, 4.8, and 1.8 kb), and one mRNA transcript each for the type I (11.0 kb) and type II (9.4 kb) IGF receptors. The size distribution of these multiple transcripts is similar to that found during normal human fetal development. These results establish both cell lines as good in vitro models for investigating the mechanisms which underly IGF gene expression during nervous system development.en_US
dc.format.extent639443 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleGene expression of the insulin-like growth factors and their receptors in human neuroblastoma cell linesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Neurology and the Neuroscience Program, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumThe Mental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Neurology and the Neuroscience Program, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationotherDepartment of Medicine, Division of Oncology, University of Texas Health Science Center, San Antonio, TX 78284, USAen_US
dc.identifier.pmid1331680en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29806/1/0000152.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0169-328X(92)90114-Qen_US
dc.identifier.sourceMolecular Brain Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.