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Immunohistochemical localization of adenosine deaminase in primary afferent neurons of the rat

dc.contributor.authorNagy, J. I.en_US
dc.contributor.authorBuss, M.en_US
dc.contributor.authorLaBella, L. A.en_US
dc.contributor.authorDaddona, Peter E.en_US
dc.date.accessioned2006-04-07T18:25:41Z
dc.date.available2006-04-07T18:25:41Z
dc.date.issued1984-07-27en_US
dc.identifier.citationNagy, J. I., Buss, M., LaBella, L. A., Daddona, P. E. (1984/07/27)."Immunohistochemical localization of adenosine deaminase in primary afferent neurons of the rat." Neuroscience Letters 48(2): 133-138. <http://hdl.handle.net/2027.42/24752>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T0G-485H4WS-3C/2/ec9442a8747dd1947955be7cc5d67844en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/24752
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6090996&dopt=citationen_US
dc.description.abstractAdenosine deaminase (ADA) was detected immunohistochemically in neuronal cell bodies of dorsal root ganglia (DRG) of the rat. ADA-immunoreactivity was confined exclusively to small type B ganglion neurons in cervical, thoracic and lumbar sensory ganglia; large type A neurons in sensory ganglia were devoid of immunostaining for ADA. It was consistently found that only a small proportion of type B neurons in DRG contain immunohistochemically detectable ADA. It is suggested that the expression of high ADA levels is a distinguishing feature of a subpopulation of type B DRG neurons and, further, that ADA in these neurons may reflect their utilization of purines (adenosine or adenine nucleotides) as transmitters or cotransmitters.en_US
dc.format.extent496914 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleImmunohistochemical localization of adenosine deaminase in primary afferent neurons of the raten_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.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationotherDepartment of Physiology, Faculty of Medicine, University of Manitoba, 770 Bannatyne Avenue, Winnipeg, Man. R3E 0W3, Canadaen_US
dc.contributor.affiliationotherDepartment of Physiology, Faculty of Medicine, University of Manitoba, 770 Bannatyne Avenue, Winnipeg, Man. R3E 0W3, Canadaen_US
dc.contributor.affiliationotherDepartment of Physiology, Faculty of Medicine, University of Manitoba, 770 Bannatyne Avenue, Winnipeg, Man. R3E 0W3, Canadaen_US
dc.identifier.pmid6090996en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/24752/1/0000174.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0304-3940(84)90008-9en_US
dc.identifier.sourceNeuroscience Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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